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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
11
hits in this display
Target
Aldo-keto reductase family 1 member C3
(Homo sapiens (Human))
University Of Pennsylvania
Curated by
ChEMBL
Ligand
BDBM50337284
(3-[N-(4-chlorophenyl)amino]benzoic acid | CHEMBL16...)
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Affinity Data
IC50: 130nM
Assay Description:
Inhibition of AKR1C3 by fluorimetric method
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Aldo-keto reductase family 1 member C3
(Homo sapiens (Human))
University Of Pennsylvania
Curated by
ChEMBL
Ligand
BDBM50337284
(3-[N-(4-chlorophenyl)amino]benzoic acid | CHEMBL16...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 130nM
Assay Description:
Compounds may be evaluated as selective reversible inhibitors of AKR1C3 by screening them against homogeneous recombinant AKR1C1-AKR1C4 expressed in ...
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
US Patent
Copy BDB DOI
Target
Aldo-keto reductase family 1 member C3
(Homo sapiens (Human))
University Of Pennsylvania
Curated by
ChEMBL
Ligand
BDBM50337284
(3-[N-(4-chlorophenyl)amino]benzoic acid | CHEMBL16...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 140nM
Assay Description:
Inhibition of recombinant AKR1C3 assessed as NADP+ dependent oxidation of S-tetralol by fluorescence assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Aldo-keto reductase family 1 member C2
(Homo sapiens (Human))
University Of Pennsylvania
US Patent
Ligand
BDBM50337284
(3-[N-(4-chlorophenyl)amino]benzoic acid | CHEMBL16...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 1.90E+4nM
Assay Description:
Compounds may be evaluated as selective reversible inhibitors of AKR1C3 by screening them against homogeneous recombinant AKR1C1-AKR1C4 expressed in ...
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
US Patent
Copy BDB DOI
Target
Aldo-keto reductase family 1 member C2
(Homo sapiens (Human))
University Of Pennsylvania
US Patent
Ligand
BDBM50337284
(3-[N-(4-chlorophenyl)amino]benzoic acid | CHEMBL16...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 1.90E+4nM
Assay Description:
Inhibition of AKR1C2 by fluorimetric method
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Aldo-keto reductase family 1 member C2
(Homo sapiens (Human))
University Of Pennsylvania
US Patent
Ligand
BDBM50337284
(3-[N-(4-chlorophenyl)amino]benzoic acid | CHEMBL16...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 1.91E+4nM
Assay Description:
Inhibition of recombinant AKR1C2 assessed as NADP+ dependent oxidation of S-tetralol by fluorescence assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Aldo-keto reductase family 1 member C1
(Homo sapiens (Human))
University Of Pennsylvania
Curated by
ChEMBL
Ligand
BDBM50337284
(3-[N-(4-chlorophenyl)amino]benzoic acid | CHEMBL16...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 3.02E+4nM
Assay Description:
Inhibition of recombinant AKR1C1 assessed as NADP+ dependent oxidation of S-tetralol by fluorescence assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Aldo-keto reductase family 1 member C1
(Homo sapiens (Human))
University Of Pennsylvania
Curated by
ChEMBL
Ligand
BDBM50337284
(3-[N-(4-chlorophenyl)amino]benzoic acid | CHEMBL16...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 3.02E+4nM
Assay Description:
Compounds may be evaluated as selective reversible inhibitors of AKR1C3 by screening them against homogeneous recombinant AKR1C1-AKR1C4 expressed in ...
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
US Patent
Copy BDB DOI
Target
Aldo-keto reductase family 1 member C4
(Homo sapiens (Human))
University Of Pennsylvania
US Patent
Ligand
BDBM50337284
(3-[N-(4-chlorophenyl)amino]benzoic acid | CHEMBL16...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 4.87E+4nM
Assay Description:
Compounds may be evaluated as selective reversible inhibitors of AKR1C3 by screening them against homogeneous recombinant AKR1C1-AKR1C4 expressed in ...
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
US Patent
Copy BDB DOI
Target
Aldo-keto reductase family 1 member C4
(Homo sapiens (Human))
University Of Pennsylvania
US Patent
Ligand
BDBM50337284
(3-[N-(4-chlorophenyl)amino]benzoic acid | CHEMBL16...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 4.87E+4nM
Assay Description:
Inhibition of recombinant AKR1C4 assessed as NADP+ dependent oxidation of S-tetralol by fluorescence assay
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Prostaglandin G/H synthase 1
(Homo sapiens (Human))
University Of Pennsylvania
US Patent
Ligand
BDBM50337284
(3-[N-(4-chlorophenyl)amino]benzoic acid | CHEMBL16...)
Copy SMILES
Copy InChI
Affinity Data
IC50: >1.00E+5nM
Assay Description:
Compounds may be evaluated as selective reversible inhibitors of AKR1C3 by screening them against homogeneous recombinant AKR1C1-AKR1C4 expressed in ...
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Similars
In Depth
Details
US Patent
Copy BDB DOI