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Compile Data Set for Download or QSAR
maximum 50k data
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
(change energy unit to
kcal/mol
)
Found
197
hits in this display
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 1.5nM
Assay Description:
Antagonistic activity of the compound was evaluated against histamine H3 receptor using [3H]- N-alpha-methylhistamine as radioligand in experiment 2
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Target
Hrh3 protein
(RAT)
Gliatech
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: 1.80nM
More data for this Ligand-Target Pair
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Target
Hrh3 protein
(RAT)
Gliatech
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.99nM
More data for this Ligand-Target Pair
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Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2nM
Assay Description:
In vitro antagonistic activity against histamine H3 receptor on rat cerebral cortex
More data for this Ligand-Target Pair
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Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2nM
Assay Description:
Binding affinity against H3 receptor in rat cerebral cortex membranes was evaluated using [3H]N-methyl-histamine as radioligand
More data for this Ligand-Target Pair
Target Info
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Target
Hrh3 protein
(RAT)
Gliatech
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2nM
More data for this Ligand-Target Pair
Target Info
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Target
Histamine H3 receptor
(GUINEA PIG)
UnitÉ
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2nM
More data for this Ligand-Target Pair
Target Info
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Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.10nM
Assay Description:
Displacement of [3H]-(R)alpha-MeHA from rat brain H3 receptor
More data for this Ligand-Target Pair
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Target
Hrh3 protein
(RAT)
Gliatech
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.10nM
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 2.70nM
Assay Description:
Inhibition of rat Histamine H3 receptor using [3H]-N-alpha-methyl histamine
More data for this Ligand-Target Pair
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Target
Hrh3 protein
(RAT)
Gliatech
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 3.21nM
More data for this Ligand-Target Pair
Target Info
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Target
Hrh3 protein
(RAT)
Gliatech
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 3.63nM
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 3.63nM
Assay Description:
In vitro binding affinity was determined as displacement of [3H]N-R-methylhistamine from C6 cell membranes expressing rat histamine H3 receptor
More data for this Ligand-Target Pair
Target Info
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Article
PubMed
Copy BDB DOI
Target
Hrh3 protein
(RAT)
Gliatech
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 3.98nM
More data for this Ligand-Target Pair
Target Info
KEGG
UniProtKB/TrEMBL
GoogleScholar
Ligand Info
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CHEMBL
MMDB
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Article
PubMed
Copy BDB DOI
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 3.98nM
Assay Description:
Binding affinity to rat cortical histamine H3 receptor
More data for this Ligand-Target Pair
Target Info
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In Depth
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PubMed
Copy BDB DOI
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 3.98nM
Assay Description:
In vitro antagonistic activity tested against Histamine H3 receptor on synaptosomes from rat cerebral cortex
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
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GoogleScholar
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CHEMBL
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In Depth
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Article
PubMed
Copy BDB DOI
Target
Histamine H3 receptor
(GUINEA PIG)
UnitÉ
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 3.98nM
Assay Description:
Antagonistic activity for Histamine H3 receptor on electrically evoked guinea-pig ileum contraction
More data for this Ligand-Target Pair
Target Info
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MMDB
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Copy BDB DOI
Target
Hrh3 protein
(RAT)
Gliatech
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 3.98nM
More data for this Ligand-Target Pair
Target Info
KEGG
UniProtKB/TrEMBL
GoogleScholar
Ligand Info
Purchase
CHEMBL
MMDB
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PC sid
PDB
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In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Hrh3 protein
(RAT)
Gliatech
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4nM
More data for this Ligand-Target Pair
Target Info
KEGG
UniProtKB/TrEMBL
GoogleScholar
Ligand Info
Purchase
CHEMBL
MMDB
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PC sid
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In Depth
Details
PubMed
Copy BDB DOI
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4nM
Assay Description:
In vitro antagonistic activity against histamine H3-receptor in an assay with K+-evoked depolarisation-induced release of [3H]histamine of synaptosom...
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
GoogleScholar
Ligand Info
Purchase
CHEMBL
MMDB
PC cid
PC sid
PDB
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In Depth
Details
Article
Copy BDB DOI
Target
Hrh3 protein
(RAT)
Gliatech
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4nM
More data for this Ligand-Target Pair
Target Info
KEGG
UniProtKB/TrEMBL
GoogleScholar
Ligand Info
Purchase
CHEMBL
MMDB
PC cid
PC sid
PDB
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In Depth
Details
PubMed
Copy BDB DOI
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4nM
Assay Description:
Effect on histamine H3 receptors in vitro, on synaptosomes of rat cerebral cortex for the release of [3H]histamine
More data for this Ligand-Target Pair
Target Info
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PubMed
Copy BDB DOI
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4nM
Assay Description:
In vitro binding affinity against rat histamine H3 receptor
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4nM
Assay Description:
In vitro inhibitory activity against against histamine H3 receptor using [3H]-Histamine as radioligand from rat cerebral cortex synaptosomes
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4nM
Assay Description:
In vitro inhibitory activity against Histamine H3 receptor for K+ evoked depolarization-induced release of [3H]-histamine from synaptosomes of rat ce...
More data for this Ligand-Target Pair
Target Info
PDB
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KEGG
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In Depth
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Copy BDB DOI
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4nM
Assay Description:
Histamine H3 receptor antagonist activity in an assay with K+ evoked depolarization-induced release of [3H]-histamine from rat synaptosomes.
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4nM
Assay Description:
Effect at histamine H3 receptors (in vitro) on synaptosomes of rat cerebral cortex assayed by functional H3-receptor assay.
More data for this Ligand-Target Pair
Target Info
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KEGG
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CHEMBL
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Copy BDB DOI
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4nM
Assay Description:
In vitro antagonistic activity of the compound against Histamine H3 receptor on Synaptosomes of rat cerebral cortex.
More data for this Ligand-Target Pair
Target Info
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KEGG
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CHEMBL
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Copy BDB DOI
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4nM
Assay Description:
Rat Histamine H3 receptor antagonism determined by [K+] - evoked depolarization-induced release of [3H]-histamine from rat cerebral cortex synaptosom...
More data for this Ligand-Target Pair
Target Info
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PubMed
Copy BDB DOI
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4nM
Assay Description:
In vitro antagonist potency at Histamine H3 receptor measured as K+-evoked [3H]-histamine release from synaptosomes of rat cerebral cortex.
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4nM
Assay Description:
In vitro Histamine H3 receptor antagonist activity in an assay with K+-evoked depolarization-induced release of [3H]-histamine from synaptosomes of r...
More data for this Ligand-Target Pair
Target Info
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KEGG
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Copy BDB DOI
Target
Hrh3 protein
(RAT)
Gliatech
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4.20nM
More data for this Ligand-Target Pair
Target Info
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Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4.30nM
Assay Description:
Histamine H3 receptor affinity of compound was determined in rat cortical membranes using the H3 selective agonist ligand, [3H]N-alpha-methylhistamin...
More data for this Ligand-Target Pair
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Copy BDB DOI
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4.30nM
Assay Description:
Antagonistic activity of the compound was evaluated against histamine H3 receptor using [3H]- N-alpha-methylhistamine as radioligand in experiment 1
More data for this Ligand-Target Pair
Target Info
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Copy BDB DOI
Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4.30nM
Assay Description:
In vitro antagonism of the histamine H3-receptor in the rat cerebral cortex.
More data for this Ligand-Target Pair
Target Info
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CHEMBL
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PubMed
Copy BDB DOI
Target
Hrh3 protein
(RAT)
Gliatech
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 4.30nM
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Target
Histamine H3 receptor
(GUINEA PIG)
UnitÉ
Curated by
PDSP K
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Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 4.57nM
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Target
Histamine H3 receptor
(Mus musculus)
Tsukuba Research Institute
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 4.80nM
Assay Description:
Displacement of 3-([1,1,1-3H]methyl)-2-(4-{[3-(1-pyrrolidinyl)propyl]oxy}phenyl)-4(3H)-quinazolinone from mouse histamine H3 receptor expressed in HE...
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Target
Hrh3 protein
(RAT)
Gliatech
Curated by
PDSP K
i
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Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 6.46nM
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 6.5nM
Assay Description:
Displacement of [125I]-iodoproxyfan from human striatal full length H3 receptor expressed in CHOK1 cells after 60 mins
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Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 6.5nM
Assay Description:
Binding affinity of the compound to rat Histamine H3 receptor in CHO-K1 cells using [125I]-iodoproxyfan as radioligand
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Target
Histamine receptor H3
(Dog)
Abbott Laboratories
Curated by
PDSP K
i
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Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 6.76nM
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Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 7nM
Assay Description:
Competition radioligand binding assays were performed with increasing concentrations of test compound in the presence of [3H]ligand. All binding reac...
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Target
Hrh3 protein
(RAT)
Gliatech
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 7.08nM
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Target
Histamine H3 receptor
(GUINEA PIG)
UnitÉ
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 7.30nM
Assay Description:
Binding affinity against H3 receptor in guinea pig brain using [3H]-N-alpha-methyl histamine as radioligand
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Target
Histamine H3 receptor
(GUINEA PIG)
UnitÉ
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 7.30nM
Assay Description:
Inhibition of N-alpha-methylhistamine binding to histamine H3 receptor of guinea pig brain membranes
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Target
Hrh3 protein
(RAT)
Gliatech
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 7.5nM
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Target
Hrh3 protein
(RAT)
Gliatech
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 10.2nM
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 14nM
Assay Description:
Antagonist potency against human histamine H3 receptor expressed in CHO cells was determined by GTPgamma-S-assay
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 14nM
Assay Description:
Antagonist potency against human H3 receptor in GTPgamma[S]-Assay
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Target
Hrh3 protein
(RAT)
Gliatech
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 16nM
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Target
Histamine H3 receptor
(Rattus norvegicus (rat))
Gliatech
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 23nM
Assay Description:
Displacement of N-alpha-[methyl-3H]-methylhistamine dihydrochloride from Sprague-Dawley rat brain membrane histamine H3 receptor assessed as inhibiti...
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 25nM
Assay Description:
Binding affinity to the human histamine H3 receptor
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 25nM
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
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Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 27nM
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 27nM
Assay Description:
Displacement of [3H]histamine human recombinant histamine H4 receptor
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 27nM
Assay Description:
Binding affinity to the human histamine H4 receptor
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 28.8nM
Assay Description:
Mean binding affinity for human H3 receptor
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 29.5nM
Assay Description:
Displacement of [3H]N-alpha-methylhistamine from human histamine H3 receptor expressed in HEK293 cells after 60 mins by liquid scintillation counting
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 31.6nM
Assay Description:
Displacement of [3H]N-alpha-methylhistamine from human histamine H3 receptor expressed in SK-N-MC cells
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 39.8nM
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 40nM
Assay Description:
Displacement of [3H]-UR-PI294 from Galphai2/Gbeta1gamma2-coupled human recombinant H3R expressed in baculovirus infected Sf9 insect cell membranes co...
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
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Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 43nM
Assay Description:
Displacement of [3H]histamine from human full-length histamine H4 receptor expressed in HEK293 cells after 60 mins
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 43nM
Assay Description:
Displacement of [3H]histamine from human histamine H4 receptor expressed in HEK293 cells
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 44nM
Assay Description:
Inhibition of UR-DEBa242 binding to human recombinant NLuc/GPCR-fused H3R expressed in HEK293T cells measured after 30 mins by furimazine substrate b...
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 47.8nM
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 47.9nM
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 48nM
Assay Description:
Competition radioligand binding assays were performed with increasing concentrations of test compound in the presence of [3H]ligand. All binding reac...
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 50nM
Assay Description:
Displacement of [3H]-N-alpha-methylhistamine from human recombinant H3R expressed in human SK-N-MC cell membranes
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 50nM
Assay Description:
Displacement of clobenpropit-BODIPY-630/650 from recombinant human NLuc-fused H3R expressed in HEK293T cells by Nano-BRET assay
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 50nM
Assay Description:
Ligand displacement assays were performed on The SK-N-MC/hH3R cell homogenates. Retained radioactivity was determined by liquid scintillation countin...
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 50nM
Assay Description:
Binding affinity in Nluc-hH3R assessed in HEK293T cells by NanoBRET binding assay
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Target
Histamine H4 receptor
(Rattus norvegicus (rat))
TBA
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 50.1nM
Assay Description:
Binding affinity to rat histamine H4 receptor
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 50.1nM
Assay Description:
Displacement of [3H]N-alpha-methylhistamine from human histamine H3 receptor expressed in human SK-N-MC cells by liquid scintillation counting
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 50.1nM
Assay Description:
Binding affinity to human histamine H3 receptor
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 51.1nM
Assay Description:
Displacement of [3H]N-alpha-methyl-histamine from human histamine H3 receptor expressed in human HEK293-EBNA cells
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 51.1nM
Assay Description:
Displacement of [3H]Nalpha-methylhistamine form human H3 receptor
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 52nM
Assay Description:
Binding affinity in Nluc-hH3R assessed in HEK293 cells by NanoBRET binding assay
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 58nM
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 60nM
Assay Description:
Binding affinity of the compound to human Histamine H3 receptor in CHO-K1 cells using [125I]-iodoproxyfan as radioligand
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 60nM
Assay Description:
Displacement of [125I]iodoproxyfan from human histamine H3 receptor expressing CHO cells
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 60nM
Assay Description:
Displacement of [125I]iodoproxyfan from human full-length histamine H3 receptor expressed in HEK293 cells after 60 mins
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 60nM
Assay Description:
Displacement of [3H]iodoproxyfan from human histamine H3 receptor expressed in CHO-K1 cells
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 61.3nM
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 63nM
Assay Description:
Displacement of [3H]histamine from human H4 receptor expressed in Sf9 cell membrane co-transfected with Galphai2 and Gbeta1gamma2 after 60 mins by li...
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 63nM
Assay Description:
Displacement of [3H]N-alpha-methylhistamine from human histamine H3 receptor expressed in SK-N-MC cells
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Copy InChI
Affinity Data
Ki: 63nM
Assay Description:
Displacement of clobenpropit-BODIPY-630/650 from recombinant human NLuc-fused H4R expressed in HEK293T cells by Nano-BRET assay
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 63nM
Assay Description:
Displacement of [3H]histamine from human histamine H4 receptor expressed in HEK293T cells
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 63nM
Assay Description:
Antagonist activity at human H4 receptor expressed in HEK293T cells assessed as inhibition of histamine-induced [35S]GTPgammaS binding
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 63.1nM
Assay Description:
Displacement of [3H]histamine from human histamine H4 receptor expressed in HEK293 cells after 60 mins by liquid scintillation counting
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 63.1nM
Assay Description:
Displacement of [3H]histamine from human histamine H4 receptor expressed in HEK293T cells
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Target
Histamine H4 receptor
(Mus musculus (mouse))
University Of Regensburg
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 66nM
Assay Description:
Inhibition of UR-DEBa242 binding to mouse recombinant NLuc/GPCR-fused H4R expressed in HEK293T cells measured after 30 mins by furimazine substrate b...
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Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 66.1nM
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 66.1nM
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 71nM
Assay Description:
Displacement of [3H]N-alpha-methylhistamine from human H3 receptor expressed in HEK-293 cell membrane after 90 mins by liquid scintillation counting ...
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 72nM ΔG°: -40.8kJ/mole
pH: 7.4 T: 2°C
Assay Description:
Competition radioligand binding assays were performed with increasing concentrations of test compound in the presence of [3H]ligand. All binding reac...
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 72nM
Assay Description:
In vitro binding affinity was determined as displacement of [3H]N-R-methylhistamine from C6 cell membranes expressing human histamine H3 receptor
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 72.4nM
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 72.6nM
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Target
Histamine H4 receptor
(Mus musculus (mouse))
University Of Regensburg
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 79nM
Assay Description:
Displacement of UR-DEBa176 from mouse recombinant H4R expressed in HEK293T-SF-His6-CRE-Luc cells
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 79nM
Assay Description:
Displacement of [3H]histamine from human H4 receptor expressed in HEK cell membranes
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: 79.4nM
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5-hydroxytryptamine receptor 3A
(GUINEA PIG)
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Ki: 120nM
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Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
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Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 124nM
Assay Description:
Displacement of [3H]histamine form human H4 receptor
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Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 125nM
Assay Description:
Displacement of [3H]histamine from human histamine H4 receptor expressed in human SK-N-MC cell membrane incubated for 60 mins
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Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 126nM
Assay Description:
Binding affinity to human histamine H4 receptor
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Alpha-2A adrenergic receptor
(Homo sapiens (Human))
Abbott Laboratories
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Ki: 126nM
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 126nM
Assay Description:
Displacement of [3H]histamine from human histamine H4 receptor expressed in human SK-N-MC cells by liquid scintillation counting
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Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 126nM
Assay Description:
Ligand displacement assays were performed on The SK-N-MC/hH4R cell homogenates. Retained radioactivity was determined by liquid scintillation countin...
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Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 155nM
Assay Description:
Inhibition of UR-DEBa242 binding to human recombinant NLuc/GPCR-fused H4R expressed in HEK293T cells measured after 30 mins by furimazine substrate b...
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Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 178nM
Assay Description:
Displacement of [3H]histamine from human histamine H4 receptor expressed in sf9 cells co-expressing mammalian Galphai2 and Gbeta1gamma2
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Target
Sigma non-opioid intracellular receptor 1
(RAT)
Vrije Universiteit
Curated by
PDSP K
i
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Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Ki: 180nM
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Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 191nM
Assay Description:
Displacement of N-alpha-[methyl-3H]-methylhistamine dihydrochloride from recombinant human histamine H3 receptor expressed in CHO-K1 cells assessed a...
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Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 328nM
Assay Description:
Displacement of [3H]histamine from human histamine H4 receptor expressed in SK-NM-C cells
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Alpha-2C adrenergic receptor
(Homo sapiens (Human))
Abbott Laboratories
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Ki: 347nM
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Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 427nM
Assay Description:
Displacement of [3H]histamine from human histamine H4 receptor expressed in Sf9 cells co-expressing Gai2 and Gb1c2 subunit
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 501nM
Assay Description:
Displacement of [3H]-histamine from human recombinant H4R expressed in HEK293T cell homogenates
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 501nM
Assay Description:
Displacement of UR-DEBa176 from human recombinant H4R expressed in HEK293T-SF-His6-CRE-Luc cells
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 501nM
Assay Description:
Displacement of [3H]-histamine from Galphai2/Gbeta1gamma2-coupled human recombinant H4R expressed in baculovirus infected Sf9 insect cell membranes c...
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 501nM
Assay Description:
Displacement of [3H]-histamine from human recombinant H4R stably expressed in human SK-N-MC cell homogenates
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 501nM
Assay Description:
Displacement of [3H]-UR-PI294 from Galphai2/Gbeta1gamma2-coupled human recombinant H4R expressed in baculovirus infected Sf9 insect cell membranes co...
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 501nM
Assay Description:
Displacement of [3H]-histamine from Galphai2/Gbeta1gamma2-coupled human recombinant H4R expressed in baculovirus infected Sf9 insect cell membranes
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 501nM
Assay Description:
Displacement of [3H]-histamine from human recombinant H4R stably expressed in human SK-N-MC cell membranes
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 603nM
Assay Description:
Displacement of [125I]iodoproxyfan from human histamine H3 receptor expressed in CHO-K1 cells
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Target
5-hydroxytryptamine receptor 3A
(RAT)
Abbott Laboratories
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 2.29E+3nM
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Target
5-hydroxytryptamine receptor 4
(GUINEA PIG)
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Ki: 2.80E+3nM
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Target
Alpha-2C adrenergic receptor
(RAT)
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 4.00E+3nM
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Target
Muscarinic acetylcholine receptor M1
(RAT)
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 4.60E+3nM
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5-hydroxytryptamine receptor 1A
(Rattus norvegicus (rat))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: 6.40E+3nM
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Target
Alpha-1A adrenergic receptor
(Rattus norvegicus (Rat))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: >1.00E+4nM
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Target
Beta-2 adrenergic receptor
(Rattus norvegicus)
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: >1.00E+4nM
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Target
Voltage-dependent L-type calcium channel subunit alpha-1C
(RAT)
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Ki: >1.00E+4nM
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Target
Calcium release-activated calcium channel protein 1
(Homo sapiens (Human))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Ki: >1.00E+4nM
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Target
Calcium release-activated calcium channel protein 1
(Homo sapiens (Human))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Ki: >1.00E+4nM
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Target
Cholecystokinin receptor type A
(RAT)
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: >1.00E+4nM
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Target
Cholecystokinin receptor type A
(RAT)
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: >1.00E+4nM
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Target
Muscarinic acetylcholine receptor M2
(RAT)
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: >1.00E+4nM
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Target
Muscarinic acetylcholine receptor M3
(Homo sapiens (Human))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: >1.00E+4nM
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Target
D(1A) dopamine receptor
(RAT)
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: >1.00E+4nM
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Target
D(3) dopamine receptor
(Rattus norvegicus (Rat))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM
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Target
Gamma-aminobutyric acid receptor subunit alpha-1
(Rattus norvegicus (Rat))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM
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Target
Gamma-aminobutyric acid receptor subunit alpha-1
(Rattus norvegicus (Rat))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM
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Target
Glutamate receptor ionotropic, NMDA 1
(RAT)
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: >1.00E+4nM
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Target
Glycine amidinotransferase, mitochondrial
(RAT)
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM
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Target
Glycine receptor subunit alpha-1
(RAT)
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM
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Target
Histamine H1 receptor
(Cavia porcellus (domestic guinea pig))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM
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Target
Histamine H2 receptor
(Cavia porcellus (domestic guinea pig))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM
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Target
Nischarin
(RAT)
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM
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Target
Melatonin receptor type 1B
(Chick)
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM
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Target
Delta-type opioid receptor
(Rattus norvegicus (rat))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM
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Target
Kappa-type opioid receptor
(Rattus norvegicus (rat))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM
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Target
Mu-type opioid receptor
(Rattus norvegicus (rat))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM
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Target
Histamine H1 receptor
(Homo sapiens (Human))
UniversitÉ
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM
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Target
Sodium channel protein type 10 subunit alpha
(Rattus norvegicus (Rat))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM
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Target
Protachykinin-1
(Homo sapiens (Human))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: >1.00E+4nM
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Target
Histamine H1 receptor
(Homo sapiens (Human))
UniversitÉ
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM
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Target
Histamine H2 receptor
(Homo sapiens (Human))
Abbott Laboratories
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Ki: >1.00E+4nM
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Target
Histamine H2 receptor
(Homo sapiens (Human))
Abbott Laboratories
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM ΔG°: >-28.5kJ/mole
pH: 7.4 T: 2°C
Assay Description:
Competition radioligand binding assays were performed with increasing concentrations of test compound in the presence of [3H]ligand. All binding reac...
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Target
Histamine H1 receptor
(Homo sapiens (Human))
UniversitÉ
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM
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Target
Histamine H2 receptor
(Homo sapiens (Human))
Abbott Laboratories
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM
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Target
Histamine H1 receptor
(Homo sapiens (Human))
UniversitÉ
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: <1.00E+4nM
Assay Description:
Displacement of [3H]pyrilamine from human H1 receptor expressed in CHO cell membrane after 120 mins by liquid scintillation counting analysis
More data for this Ligand-Target Pair
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Target
Histamine H1 receptor
(Homo sapiens (Human))
UniversitÉ
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM ΔG°: >-28.5kJ/mole
pH: 7.4 T: 2°C
Assay Description:
Competition radioligand binding assays were performed with increasing concentrations of test compound in the presence of [3H]ligand. All binding reac...
More data for this Ligand-Target Pair
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Target
5-hydroxytryptamine receptor 2C
(Rattus norvegicus (Rat))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
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Affinity Data
Ki: >1.00E+4nM
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Target
5-hydroxytryptamine receptor 2A
(Rattus norvegicus (rat))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM
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Target
5-hydroxytryptamine receptor 1D
(RAT)
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM
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Target
5-hydroxytryptamine receptor 1B
(Rattus norvegicus (Rat))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM
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Target
Sodium-dependent serotonin transporter
(GUINEA PIG)
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM
More data for this Ligand-Target Pair
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Target
5-hydroxytryptamine receptor 1A
(Rattus norvegicus (rat))
Vrije Universiteit
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 16nM
Assay Description:
Antagonist activity at human H3 receptor expressed in 293-EBNA cells assessed as inhibition of histamine agonist activity by luciferase reporter gene...
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Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
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Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
IC50: 19nM
Assay Description:
Antagonist activity at human H4 receptor expressed in CHO-K1 cells co-expressing G protein alpha16 assessed as inhibition of histamine-induced calciu...
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Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
IC50: 20nM
Assay Description:
Inverse agonist activity at human H3R expressed in HEK293T-SP-FLAG-hH3R-CRE-CBR cells assessed as reduction in histamine-induced inhibition of forsko...
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Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
IC50: 120nM
Assay Description:
Antagonist activity at human histamine H3 receptor expressed in HEK293 cells assessed by forskolin induced cAMP response element activation after 5 h...
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Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
IC50: 140nM
Assay Description:
Histamine-3 membranes were prepared from recombinant CHO-k1 cells expressing human histamine-3 receptor or rat histamine-3 receptor. Radioligand (RS)...
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
IC50: 140nM
Assay Description:
Inverse agonist activity at recombinant human Histamine 3 receptor expressed in CHO-K1 cells assessed as inhibition of RAMH-induced agonist activity ...
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
IC50: 296nM
Assay Description:
Antagonist activity at human histamine H3 receptor expressed in CHO-K1 cells assessed as inhibition of imetit-stimulation ERK1/2 phosphorylation by E...
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Target
Cholesterol 24-hydroxylase
(Homo sapiens (Human))
Takeda Pharmaceutical
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
IC50: 430nM
Assay Description:
Inhibition of CH24H expressing human 293-F cells for 15 minutes using [14C] cholesterol as substrate and measured after 5 hrs by trypan blue staining...
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Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
IC50: 490nM
Assay Description:
Inverse agonist activity at human H4R expressed in HEK293 cells co-expressing ELucC/ELucN-beta-arrestin2 assessed as inhibition of histamine-induced ...
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Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
IC50: 518nM
Assay Description:
Antagonist activity at histamine H3 receptor expressed in HEK293 cells co-transfected with pCRE-Luc gene assessed as inhibition of forskolin/histamin...
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Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
IC50: 667nM
Assay Description:
Antagonist activity at histamine H4 receptor expressed in HEK293 cells co-transfected with pCRE-Luc gene assessed as inhibition of forskolin/histamin...
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Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
IC50: 680nM
Assay Description:
Antagonist activity at human H4 receptor expressed in 293-EBNA cells assessed as inhibition of histamine agonist activity by luciferase reporter gene...
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
IC50: 977nM
Assay Description:
Antagonist activity at human H4 receptor expressed in HEK293T cells assessed as inhibition of histamine-induced [35S]GTPgammaS binding
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Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
IC50: 1.03E+3nM
Assay Description:
Inhibition of human H3R expressed in methylhistamine-induced human H3-bla U2OS cells incubated for 30 mins by beta-lactamase complementation technolo...
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Cytochrome P450 3A4
(Homo sapiens (Human))
Jadavpur University
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
IC50: 6.10E+3nM
Assay Description:
Inhibition of CYP3A4
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Histamine H4 receptor
(Mus musculus (mouse))
University Of Regensburg
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
EC50: 28nM
Assay Description:
Antagonist activity at mouse H4R expressed in HEK293 cells co-expressing ELucC/ELucN-beta-arrestin2 assessed as inhibition of histamine-induced beta-...
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Histamine H4 receptor
(Mus musculus (mouse))
University Of Regensburg
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
EC50: 302nM
Assay Description:
Agonist activity at mouse H4R expressed in HEK293-SF-mH4R-His6-CRE-Luc cells incubated for 5 hrs by luciferase reporter gene assay
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Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
EC50: 120nM
Assay Description:
Agonist activity at human H4R expressed in HEK293-SF-hH4R-His6-CRE-Luc cells incubated for 5 hrs by luciferase reporter gene assay
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
EC50: 110nM
Assay Description:
Agonist activity at human histamine H4 receptor expressed in Sf9 cells coexpressing RGS19 protein by steady-state GTPase assay
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
EC50: 97.7nM
Assay Description:
Agonist activity at human histamine H3 receptor expressed in Sf9 cells coexpressing Gialpha-2-Gbeta-1-gamma-2 and RGS4 proteins protein by steady-sta...
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Target
Histamine H3 receptor
(GUINEA PIG)
UnitÉ
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
Kd: 1.26nM
Assay Description:
Displacement of [3H]Nalpha-methylhistamine from histamine H3 receptors in homogenates of rat cerebral cortex
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Histamine H3 receptor
(Mus musculus)
Tsukuba Research Institute
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
EC50: 11nM
Assay Description:
Inverse agonist activity at mouse histamine H3 receptor overexpressed in HEK293 cells by [35S]GTPgammaS binding assay
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Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
EC50: 417nM
Assay Description:
Antagonist activity at human histamine 4 receptor expressed in Sf9 cell membranes co-expressing Galphai2 and Gbeta1gamma2 assessed as [35S]GTPgammaS ...
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
EC50: 110nM
Assay Description:
Agonist activity at human H4 receptor expressed in insect Sf9 cells co-expressing RGS19 fusion protein and Gialpha2, Gbeta1gamma2 assessed as gamma[3...
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
EC50: 98nM
Assay Description:
Agonist activity at human H3 receptor expressed in insect Sf9 cells co-expressing Gialpha2, Gbeta1gamma2 and RGS4 assessed as gamma[32P]GTP binding b...
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
EC50: 34nM
Assay Description:
Inverse agonist activity at recombinant human histamine H3 receptor expressed in CHO-K1 cells preincubated for 10 mins followed by [35S]GTPgammaS add...
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Target
Histamine H4 receptor
(Homo sapiens (Human))
The R. W. Johnson Pharmaceutical Research Institute
Curated by
PDSP K
i
Database
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
EC50: 79.4nM
Assay Description:
Inverse agonist activity at human histamine H4 receptor expressed in HEK293 cells assessed by forskolin induced cAMP response element activation by l...
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Target
Histamine H3 receptor
(Homo sapiens (Human))
Jagiellonian University Medical College
Curated by
ChEMBL
Ligand
BDBM22914
(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
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Affinity Data
EC50: 39.8nM
Assay Description:
Inverse agonist activity at human histamine H3 receptor expressed in HEK293 cells assessed by forskolin induced cAMP response element activation by l...
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