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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
7
hits in this display
Target
Amine oxidase [flavin-containing] A
(Homo sapiens (Human))
Fudan University
Curated by
ChEMBL
Ligand
BDBM50524013
((-)-(R)-MELLEIN | (R)-Mellein)
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Affinity Data
IC50: 6.20E+3nM
Assay Description:
Inhibition of human recombinant MAOA using kynuramine as substrate incubated for 10 mins by UPLC-ESI-MS/MS analysis
More data for this Ligand-Target Pair
Target Info
PDB
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UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
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Article
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Target
Amine oxidase [flavin-containing] A
(Homo sapiens (Human))
Fudan University
Curated by
ChEMBL
Ligand
BDBM50524012
(CHEMBL4438912)
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Copy InChI
Affinity Data
IC50: 7.50E+3nM
Assay Description:
Inhibition of human recombinant MAOA using kynuramine as substrate incubated for 10 mins by UPLC-ESI-MS/MS analysis
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
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PC cid
PC sid
In Depth
Details
Article
PubMed
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Target
Amine oxidase [flavin-containing] B
(Homo sapiens (Human))
Fudan University
Curated by
ChEMBL
Ligand
BDBM50524012
(CHEMBL4438912)
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Affinity Data
IC50: 2.40E+4nM
Assay Description:
Inhibition of human recombinant MAOB using kynuramine as substrate incubated for 10 mins by UPLC-ESI-MS/MS analysis
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
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PC cid
PC sid
In Depth
Details
Article
PubMed
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Target
Amine oxidase [flavin-containing] B
(Homo sapiens (Human))
Fudan University
Curated by
ChEMBL
Ligand
BDBM50524013
((-)-(R)-MELLEIN | (R)-Mellein)
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Copy InChI
Affinity Data
IC50: 5.00E+4nM
Assay Description:
Inhibition of human recombinant MAOB using kynuramine as substrate incubated for 10 mins by UPLC-ESI-MS/MS analysis
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
Purchase
PC cid
PC sid
In Depth
Details
Article
PubMed
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Target
DNA polymerase lambda
(Homo sapiens (Human))
Science University Of Tokyo
Curated by
ChEMBL
Ligand
BDBM50208249
(3-methyl-8-hydroxy-3,4-dihydroisocoumarin | CHEMBL...)
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Affinity Data
IC50: 3.16E+5nM
Assay Description:
Inhibition of human DNA polymerase lambda
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
Ligand Info
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ChEBI
CHEMBL
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In Depth
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Article
PubMed
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Target
DNA polymerase delta catalytic subunit
(Homo sapiens (Human))
Science University Of Tokyo
Curated by
ChEMBL
Ligand
BDBM50208249
(3-methyl-8-hydroxy-3,4-dihydroisocoumarin | CHEMBL...)
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Affinity Data
IC50: >1.00E+6nM
Assay Description:
Inhibition of human DNA polymerase delta
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
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ChEBI
CHEMBL
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PC sid
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In Depth
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Article
PubMed
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Target
DNA polymerase beta
(Rattus norvegicus)
Science University Of Tokyo
Curated by
ChEMBL
Ligand
BDBM50208249
(3-methyl-8-hydroxy-3,4-dihydroisocoumarin | CHEMBL...)
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Affinity Data
IC50: >1.00E+6nM
Assay Description:
Inhibition of rat DNA polymerase beta
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
Ligand Info
Purchase
ChEBI
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI