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PDB code 4DBU

Compile Data Set for Download or QSAR

Identical Ligands in BindingDB

Found 9 hits Enzyme Inhibition Constant Data   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
17-beta-Hydroxysteroid Dehydrogenase 5 (17-beta-HSD5, AKR1C3)

  (322/323 > 99%)
(Homo sapiens (human))
BDBM50337283
PNG
(3-[N-(4-trifluoromethylphenyl)amino]benzoic acid |...)
Show SMILES OC(=O)c1cccc(Nc2ccc(cc2)C(F)(F)F)c1
Show InChI InChI=1S/C14H10F3NO2/c15-14(16,17)10-4-6-11(7-5-10)18-12-3-1-2-9(8-12)13(19)20/h1-8,18H,(H,19,20)
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PubMed
n/an/a 60n/an/an/an/an/an/a



University of Pennsylvania

Curated by ChEMBL


Assay Description
Inhibition of recombinant AKR1C3 assessed as NADP+ dependent oxidation of S-tetralol by fluorescence assay


J Med Chem 55: 2311-23 (2012)

More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
17-beta-Hydroxysteroid Dehydrogenase 5 (17-beta-HSD5, AKR1C3)

  (322/323 > 99%)
(Homo sapiens (human))
BDBM50337283
PNG
(3-[N-(4-trifluoromethylphenyl)amino]benzoic acid |...)
Show SMILES OC(=O)c1cccc(Nc2ccc(cc2)C(F)(F)F)c1
Show InChI InChI=1S/C14H10F3NO2/c15-14(16,17)10-4-6-11(7-5-10)18-12-3-1-2-9(8-12)13(19)20/h1-8,18H,(H,19,20)
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n/an/a 62n/an/an/an/an/an/a



University of Pennsylvania

Curated by ChEMBL


Assay Description
Inhibition of AKR1C3 by fluorimetric method


Bioorg Med Chem Lett 21: 1464-8 (2011)

More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
17-beta-Hydroxysteroid Dehydrogenase 5 (17-beta-HSD5, AKR1C3)

  (322/323 > 99%)
(Homo sapiens (human))
BDBM50337283
PNG
(3-[N-(4-trifluoromethylphenyl)amino]benzoic acid |...)
Show SMILES OC(=O)c1cccc(Nc2ccc(cc2)C(F)(F)F)c1
Show InChI InChI=1S/C14H10F3NO2/c15-14(16,17)10-4-6-11(7-5-10)18-12-3-1-2-9(8-12)13(19)20/h1-8,18H,(H,19,20)
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US Patent
n/an/a 62n/an/an/an/an/an/a



The Trustees of the University of Pennsylvania

US Patent


Assay Description
Compounds may be evaluated as selective reversible inhibitors of AKR1C3 by screening them against homogeneous recombinant AKR1C1-AKR1C4 expressed in ...


Citation and Details
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Aldo-keto reductase family 1 member C2

  (281/323 = 87%)
(Homo sapiens (human))
BDBM50337283
PNG
(3-[N-(4-trifluoromethylphenyl)amino]benzoic acid |...)
Show SMILES OC(=O)c1cccc(Nc2ccc(cc2)C(F)(F)F)c1
Show InChI InChI=1S/C14H10F3NO2/c15-14(16,17)10-4-6-11(7-5-10)18-12-3-1-2-9(8-12)13(19)20/h1-8,18H,(H,19,20)
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US Patent
n/an/a 1.50E+4n/an/an/an/an/an/a



The Trustees of the University of Pennsylvania

US Patent


Assay Description
Compounds may be evaluated as selective reversible inhibitors of AKR1C3 by screening them against homogeneous recombinant AKR1C1-AKR1C4 expressed in ...


Citation and Details
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Aldo-keto reductase family 1 member C2

  (281/323 = 87%)
(Homo sapiens (human))
BDBM50337283
PNG
(3-[N-(4-trifluoromethylphenyl)amino]benzoic acid |...)
Show SMILES OC(=O)c1cccc(Nc2ccc(cc2)C(F)(F)F)c1
Show InChI InChI=1S/C14H10F3NO2/c15-14(16,17)10-4-6-11(7-5-10)18-12-3-1-2-9(8-12)13(19)20/h1-8,18H,(H,19,20)
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PubMed
n/an/a 1.50E+4n/an/an/an/an/an/a



University of Pennsylvania

Curated by ChEMBL


Assay Description
Inhibition of AKR1C2 by fluorimetric method


Bioorg Med Chem Lett 21: 1464-8 (2011)

More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Aldo-keto reductase family 1 member C2

  (281/323 = 87%)
(Homo sapiens (human))
BDBM50337283
PNG
(3-[N-(4-trifluoromethylphenyl)amino]benzoic acid |...)
Show SMILES OC(=O)c1cccc(Nc2ccc(cc2)C(F)(F)F)c1
Show InChI InChI=1S/C14H10F3NO2/c15-14(16,17)10-4-6-11(7-5-10)18-12-3-1-2-9(8-12)13(19)20/h1-8,18H,(H,19,20)
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Article
PubMed
n/an/a 1.54E+4n/an/an/an/an/an/a



University of Pennsylvania

Curated by ChEMBL


Assay Description
Inhibition of recombinant AKR1C2 assessed as NADP+ dependent oxidation of S-tetralol by fluorescence assay


J Med Chem 55: 2311-23 (2012)

More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Aldo-keto reductase family 1 member C1

  (284/323 = 88%)
(Homo sapiens (human))
BDBM50337283
PNG
(3-[N-(4-trifluoromethylphenyl)amino]benzoic acid |...)
Show SMILES OC(=O)c1cccc(Nc2ccc(cc2)C(F)(F)F)c1
Show InChI InChI=1S/C14H10F3NO2/c15-14(16,17)10-4-6-11(7-5-10)18-12-3-1-2-9(8-12)13(19)20/h1-8,18H,(H,19,20)
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Article
PubMed
n/an/a 2.27E+4n/an/an/an/an/an/a



Perelman School of Medicine University of Pennsylvania

Curated by ChEMBL


Assay Description
Inhibition of recombinant AKR1C1 assessed as enzyme catalyzed oxidation of S-tetralol by fluorimetric assay


Bioorg Med Chem Lett 22: 3492-7 (2012)

More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Aldo-keto reductase family 1 member C1

  (284/323 = 88%)
(Homo sapiens (human))
BDBM50337283
PNG
(3-[N-(4-trifluoromethylphenyl)amino]benzoic acid |...)
Show SMILES OC(=O)c1cccc(Nc2ccc(cc2)C(F)(F)F)c1
Show InChI InChI=1S/C14H10F3NO2/c15-14(16,17)10-4-6-11(7-5-10)18-12-3-1-2-9(8-12)13(19)20/h1-8,18H,(H,19,20)
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Article
PubMed
n/an/a 2.27E+4n/an/an/an/an/an/a



University of Pennsylvania

Curated by ChEMBL


Assay Description
Inhibition of recombinant AKR1C1 assessed as NADP+ dependent oxidation of S-tetralol by fluorescence assay


J Med Chem 55: 2311-23 (2012)

More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Aldo-keto reductase family 1 member C1

  (284/323 = 88%)
(Homo sapiens (human))
BDBM50337283
PNG
(3-[N-(4-trifluoromethylphenyl)amino]benzoic acid |...)
Show SMILES OC(=O)c1cccc(Nc2ccc(cc2)C(F)(F)F)c1
Show InChI InChI=1S/C14H10F3NO2/c15-14(16,17)10-4-6-11(7-5-10)18-12-3-1-2-9(8-12)13(19)20/h1-8,18H,(H,19,20)
PDB
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US Patent
n/an/a 2.27E+4n/an/an/an/an/an/a



The Trustees of the University of Pennsylvania

US Patent


Assay Description
Compounds may be evaluated as selective reversible inhibitors of AKR1C3 by screening them against homogeneous recombinant AKR1C1-AKR1C4 expressed in ...


Citation and Details
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)

Search BindingMOAD for More Affinity Data:

* indicates data uncertainty>20%
* 0.9 Tanimoto similarity
Identities from BLAST output