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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
4
hits in this display
Target
5-hydroxytryptamine receptor 1A
(Rattus norvegicus (rat))
TBA
Curated by
ChEMBL
Ligand
BDBM50285312
(3-(4-{4-[4-(5-carbamoyl-1H-3-indolyl)-3-cyclohexen...)
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Affinity Data
IC50: 14.5nM
Assay Description:
Inhibitory activity against 5-hydroxytryptamine 1A receptor receptor subtype
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
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Target
5-hydroxytryptamine receptor 1D
(Homo sapiens (Human))
TBA
Curated by
ChEMBL
Ligand
BDBM50285312
(3-(4-{4-[4-(5-carbamoyl-1H-3-indolyl)-3-cyclohexen...)
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Affinity Data
IC50: 20.3nM
Assay Description:
Inhibitory activity against 5-hydroxytryptamine 1D receptor subtype
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
Copy BDB DOI
Target
Sodium-dependent serotonin transporter
(Rattus norvegicus (rat))
TBA
Curated by
ChEMBL
Ligand
BDBM50285312
(3-(4-{4-[4-(5-carbamoyl-1H-3-indolyl)-3-cyclohexen...)
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Affinity Data
IC50: 47.8nM
Assay Description:
Ability to inhibit Serotonin transporter
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
Copy BDB DOI
Target
5-hydroxytryptamine receptor 1E
(Homo sapiens (Human))
TBA
Curated by
ChEMBL
Ligand
BDBM50285312
(3-(4-{4-[4-(5-carbamoyl-1H-3-indolyl)-3-cyclohexen...)
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Copy InChI
Affinity Data
IC50: >1.00E+3nM
Assay Description:
Inhibitory activity against 5-hydroxytryptamine 1E receptor subtype
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
Copy BDB DOI