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Compile Data Set for Download or QSAR

Found 199 hits with Last Name = 'mendieta' and Initial = 'a'   
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
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM8611
PNG
(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)
Show SMILES N#Cc1ccc(cc1)C1CCCc2cncn12
Show InChI InChI=1S/C14H13N3/c15-8-11-4-6-12(7-5-11)14-3-1-2-13-9-16-10-17(13)14/h4-7,9-10,14H,1-3H2
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n/an/a 0.800n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 11B1, mitochondrial


(Homo sapiens (Human))
BDBM8611
PNG
(4-{5H,6H,7H,8H-imidazo[1,5-a]pyridin-5-yl}benzonit...)
Show SMILES N#Cc1ccc(cc1)C1CCCc2cncn12
Show InChI InChI=1S/C14H13N3/c15-8-11-4-6-12(7-5-11)14-3-1-2-13-9-16-10-17(13)14/h4-7,9-10,14H,1-3H2
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n/an/a 6.30n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B1 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Cytochrome P450 17A1


(Homo sapiens (Human))
BDBM50438994
PNG
(CHEMBL2420683)
Show SMILES COc1ccc2ccc(-c3cncc(O)c3)c(Cl)c2c1
Show InChI InChI=1S/C16H12ClNO2/c1-20-13-4-2-10-3-5-14(16(17)15(10)7-13)11-6-12(19)9-18-8-11/h2-9,19H,1H3
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n/an/a 11n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP17 expressed in Escherichia coli using 1,2[3H]-progesterone as substrate in presence of NADPH


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM50438994
PNG
(CHEMBL2420683)
Show SMILES COc1ccc2ccc(-c3cncc(O)c3)c(Cl)c2c1
Show InChI InChI=1S/C16H12ClNO2/c1-20-13-4-2-10-3-5-14(16(17)15(10)7-13)11-6-12(19)9-18-8-11/h2-9,19H,1H3
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n/an/a 13n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM50438995
PNG
(CHEMBL2420682)
Show SMILES COc1cncc(c1)-c1ccc2ccc(O)cc2c1Cl
Show InChI InChI=1S/C16H12ClNO2/c1-20-13-6-11(8-18-9-13)14-5-3-10-2-4-12(19)7-15(10)16(14)17/h2-9,19H,1H3
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n/an/a 15n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 17A1


(Homo sapiens (Human))
BDBM50438993
PNG
(CHEMBL2420684)
Show SMILES Oc1ccc2ccc(-c3cncc(O)c3)c(Cl)c2c1
Show InChI InChI=1S/C15H10ClNO2/c16-15-13(10-5-12(19)8-17-7-10)4-2-9-1-3-11(18)6-14(9)15/h1-8,18-19H
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n/an/a 16n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP17 expressed in Escherichia coli using 1,2[3H]-progesterone as substrate in presence of NADPH


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM50439002
PNG
(CHEMBL2420675)
Show SMILES COc1ccc2ccc(-c3cccnc3)c(F)c2c1
Show InChI InChI=1S/C16H12FNO/c1-19-13-6-4-11-5-7-14(16(17)15(11)9-13)12-3-2-8-18-10-12/h2-10H,1H3
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n/an/a 17n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM50438991
PNG
(CHEMBL2420686)
Show SMILES Oc1ccc2ccc(-c3cncnc3)c(Cl)c2c1
Show InChI InChI=1S/C14H9ClN2O/c15-14-12(10-6-16-8-17-7-10)4-2-9-1-3-11(18)5-13(9)14/h1-8,18H
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n/an/a 22n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA)


(Homo sapiens (Human))
BDBM50321276
PNG
(4,5-Dimethoxy-2-propylphenol | CHEMBL1163691)
Show SMILES CCCc1cc(OC)c(OC)cc1O
Show InChI InChI=1S/C11H16O3/c1-4-5-8-6-10(13-2)11(14-3)7-9(8)12/h6-7,12H,4-5H2,1-3H3
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n/an/a 23n/an/an/an/an/an/a



Instituto Polit£cnico Nacional (IPN)

Curated by ChEMBL


Assay Description
Inhibition of human HMG-CoA reductase after 30 mins


Bioorg Med Chem 22: 5871-82 (2014)


Article DOI: 10.1016/j.bmc.2014.09.022
BindingDB Entry DOI: 10.7270/Q2833TM8
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM50438996
PNG
(CHEMBL2420681)
Show SMILES COc1ccc2ccc(-c3cncc(OC)c3)c(Cl)c2c1
Show InChI InChI=1S/C17H14ClNO2/c1-20-13-5-3-11-4-6-15(17(18)16(11)8-13)12-7-14(21-2)10-19-9-12/h3-10H,1-2H3
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n/an/a 24n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM50438999
PNG
(CHEMBL2420678)
Show SMILES Oc1ccc2ccc(-c3cccnc3)c(Cl)c2c1F
Show InChI InChI=1S/C15H9ClFNO/c16-14-11(10-2-1-7-18-8-10)5-3-9-4-6-12(19)15(17)13(9)14/h1-8,19H
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n/an/a 25n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA)


(Homo sapiens (Human))
BDBM50030652
PNG
(CHEMBL3344536)
Show SMILES CCC(=O)c1cc(OC)c(OC)cc1O
Show InChI InChI=1S/C11H14O4/c1-4-8(12)7-5-10(14-2)11(15-3)6-9(7)13/h5-6,13H,4H2,1-3H3
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n/an/a 25n/an/an/an/an/an/a



Instituto Polit£cnico Nacional (IPN)

Curated by ChEMBL


Assay Description
Inhibition of human HMG-CoA reductase after 30 mins


Bioorg Med Chem 22: 5871-82 (2014)


Article DOI: 10.1016/j.bmc.2014.09.022
BindingDB Entry DOI: 10.7270/Q2833TM8
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM50439003
PNG
(CHEMBL2420674)
Show SMILES Oc1ccc2ccc(-c3cccnc3)c(Cl)c2c1
Show InChI InChI=1S/C15H10ClNO/c16-15-13(11-2-1-7-17-9-11)6-4-10-3-5-12(18)8-14(10)15/h1-9,18H
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n/an/a 26n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM50438993
PNG
(CHEMBL2420684)
Show SMILES Oc1ccc2ccc(-c3cncc(O)c3)c(Cl)c2c1
Show InChI InChI=1S/C15H10ClNO2/c16-15-13(10-5-12(19)8-17-7-10)4-2-9-1-3-11(18)6-14(9)15/h1-8,18-19H
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n/an/a 27n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 17A1


(Homo sapiens (Human))
BDBM8913
PNG
(3-(1-Chloro-7-methoxy-2-naphthyl)pyridine | 3-(1-c...)
Show SMILES COc1ccc2ccc(-c3cccnc3)c(Cl)c2c1
Show InChI InChI=1S/C16H12ClNO/c1-19-13-6-4-11-5-7-14(16(17)15(11)9-13)12-3-2-8-18-10-12/h2-10H,1H3
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n/an/a 27n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP17


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM8904
PNG
(3-(2-Naphthyl)pyridine | 3-(naphthalen-2-yl)pyridi...)
Show SMILES c1ccc2cc(ccc2c1)-c1cccnc1
Show InChI InChI=1S/C15H11N/c1-2-5-13-10-14(8-7-12(13)4-1)15-6-3-9-16-11-15/h1-11H
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n/an/a 28n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM50439000
PNG
(CHEMBL2420677)
Show SMILES COc1ccc2ccc(-c3cccnc3)c(Cl)c2c1F
Show InChI InChI=1S/C16H11ClFNO/c1-20-13-7-5-10-4-6-12(11-3-2-8-19-9-11)15(17)14(10)16(13)18/h2-9H,1H3
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n/an/a 28n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM8913
PNG
(3-(1-Chloro-7-methoxy-2-naphthyl)pyridine | 3-(1-c...)
Show SMILES COc1ccc2ccc(-c3cccnc3)c(Cl)c2c1
Show InChI InChI=1S/C16H12ClNO/c1-19-13-6-4-11-5-7-14(16(17)15(11)9-13)12-3-2-8-18-10-12/h2-10H,1H3
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n/an/a 29n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM50439001
PNG
(CHEMBL2420676)
Show SMILES Oc1ccc2ccc(-c3cccnc3)c(F)c2c1
Show InChI InChI=1S/C15H10FNO/c16-15-13(11-2-1-7-17-9-11)6-4-10-3-5-12(18)8-14(10)15/h1-9,18H
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n/an/a 30n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM50438997
PNG
(CHEMBL2420680)
Show SMILES Oc1ccc2ccc(-c3cncc(F)c3)c(Cl)c2c1
Show InChI InChI=1S/C15H9ClFNO/c16-15-13(10-5-11(17)8-18-7-10)4-2-9-1-3-12(19)6-14(9)15/h1-8,19H
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n/an/a 33n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA)


(Homo sapiens (Human))
BDBM50240783
PNG
(1,2,4-Trimethoxy-5-propenyl-benzene | 17-(1,5-Dime...)
Show SMILES COc1cc(OC)c(\C=C\C)cc1OC
Show InChI InChI=1S/C12H16O3/c1-5-6-9-7-11(14-3)12(15-4)8-10(9)13-2/h5-8H,1-4H3/b6-5+
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n/an/a 36n/an/an/an/an/an/a



Instituto Polit£cnico Nacional (IPN)

Curated by ChEMBL


Assay Description
Inhibition of human HMG-CoA reductase after 30 mins


Bioorg Med Chem 22: 5871-82 (2014)


Article DOI: 10.1016/j.bmc.2014.09.022
BindingDB Entry DOI: 10.7270/Q2833TM8
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM50438998
PNG
(CHEMBL2420679)
Show SMILES COc1ccc2ccc(-c3cncc(F)c3)c(Cl)c2c1
Show InChI InChI=1S/C16H11ClFNO/c1-20-13-4-2-10-3-5-14(16(17)15(10)7-13)11-6-12(18)9-19-8-11/h2-9H,1H3
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n/an/a 38n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA)


(Homo sapiens (Human))
BDBM50139181
PNG
((1S,3R,7S,8S,8aR)-8-{2-[(2R,4R)-4-hydroxy-6-oxotet...)
Show SMILES CCC(C)(C)C(=O)O[C@H]1C[C@@H](C)C=C2C=C[C@H](C)[C@H](CC[C@@H]3C[C@@H](O)CC(=O)O3)[C@@H]12 |r,c:14,t:12|
Show InChI InChI=1S/C25H38O5/c1-6-25(4,5)24(28)30-21-12-15(2)11-17-8-7-16(3)20(23(17)21)10-9-19-13-18(26)14-22(27)29-19/h7-8,11,15-16,18-21,23,26H,6,9-10,12-14H2,1-5H3/t15-,16-,18+,19+,20-,21-,23-/m0/s1
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n/an/a 40n/an/an/an/an/an/a



Instituto Polit£cnico Nacional (IPN)

Curated by ChEMBL


Assay Description
Inhibition of human HMG-CoA reductase after 30 mins


Bioorg Med Chem 22: 5871-82 (2014)


Article DOI: 10.1016/j.bmc.2014.09.022
BindingDB Entry DOI: 10.7270/Q2833TM8
More data for this
Ligand-Target Pair
3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA)


(Homo sapiens (Human))
BDBM50321274
PNG
(CHEMBL1163189 | Methyl 2-(5-hydroxy-2-methoxy-4-pr...)
Show SMILES CCCc1cc(OC)c(OCC(=O)OC)cc1O
Show InChI InChI=1S/C13H18O5/c1-4-5-9-6-11(16-2)12(7-10(9)14)18-8-13(15)17-3/h6-7,14H,4-5,8H2,1-3H3
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n/an/a 40n/an/an/an/an/an/a



Instituto Polit£cnico Nacional (IPN)

Curated by ChEMBL


Assay Description
Inhibition of human HMG-CoA reductase after 30 mins


Bioorg Med Chem 22: 5871-82 (2014)


Article DOI: 10.1016/j.bmc.2014.09.022
BindingDB Entry DOI: 10.7270/Q2833TM8
More data for this
Ligand-Target Pair
3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA)


(Homo sapiens (Human))
BDBM50030656
PNG
(CHEMBL3344540)
Show SMILES CCCC(=O)c1cc(OC)c(OCC(=O)OC)cc1O
Show InChI InChI=1S/C14H18O6/c1-4-5-10(15)9-6-12(18-2)13(7-11(9)16)20-8-14(17)19-3/h6-7,16H,4-5,8H2,1-3H3
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n/an/a 45n/an/an/an/an/an/a



Instituto Polit£cnico Nacional (IPN)

Curated by ChEMBL


Assay Description
Inhibition of human HMG-CoA reductase after 30 mins


Bioorg Med Chem 22: 5871-82 (2014)


Article DOI: 10.1016/j.bmc.2014.09.022
BindingDB Entry DOI: 10.7270/Q2833TM8
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM50438990
PNG
(CHEMBL2420687)
Show SMILES COc1ccc2ccc(c(Cl)c2c1)-c1cncc2ccccc12
Show InChI InChI=1S/C20H14ClNO/c1-23-15-8-6-13-7-9-17(20(21)18(13)10-15)19-12-22-11-14-4-2-3-5-16(14)19/h2-12H,1H3
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n/an/a 54n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 17A1


(Homo sapiens (Human))
BDBM25457
PNG
(2-fluoro-4-[5-(pyridin-4-yl)-5,6,7,8-tetrahydronap...)
Show SMILES Oc1ccc(cc1F)-c1ccc2C(CCCc2c1)c1ccncc1
Show InChI InChI=1S/C21H18FNO/c22-20-13-16(5-7-21(20)24)15-4-6-19-17(12-15)2-1-3-18(19)14-8-10-23-11-9-14/h4-13,18,24H,1-3H2
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n/an/a 64n/an/an/an/a7.437



Saarland University



Assay Description
The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...


J Med Chem 51: 5009-18 (2008)


Article DOI: 10.1021/jm800355c
BindingDB Entry DOI: 10.7270/Q2TB156N
More data for this
Ligand-Target Pair
Cytochrome P450 17A1


(Homo sapiens (Human))
BDBM50439003
PNG
(CHEMBL2420674)
Show SMILES Oc1ccc2ccc(-c3cccnc3)c(Cl)c2c1
Show InChI InChI=1S/C15H10ClNO/c16-15-13(11-2-1-7-17-9-11)6-4-10-3-5-12(18)8-14(10)15/h1-9,18H
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n/an/a 64n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP17 expressed in Escherichia coli using 1,2[3H]-progesterone as substrate in presence of NADPH


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM50438989
PNG
(CHEMBL2420688)
Show SMILES Oc1ccc2ccc(c(Cl)c2c1)-c1cncc2ccccc12
Show InChI InChI=1S/C19H12ClNO/c20-19-16(8-6-12-5-7-14(22)9-17(12)19)18-11-21-10-13-3-1-2-4-15(13)18/h1-11,22H
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n/an/a 66n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM8610
PNG
(1-[4-(4-{[(2R,4S)-2-(2,4-dichlorophenyl)-2-(1H-imi...)
Show SMILES [H][C@]1(COc2ccc(cc2)N2CCN(CC2)C(C)=O)CO[C@@](Cn2ccnc2)(O1)c1ccc(Cl)cc1Cl |r|
Show InChI InChI=1S/C26H28Cl2N4O4/c1-19(33)31-10-12-32(13-11-31)21-3-5-22(6-4-21)34-15-23-16-35-26(36-23,17-30-9-8-29-18-30)24-7-2-20(27)14-25(24)28/h2-9,14,18,23H,10-13,15-17H2,1H3/t23-,26-/m0/s1
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n/an/a 67n/an/an/an/an/an/a



Saarland University



Assay Description
The enzyme activity was assayed by monitoring the conversion of deoxycorticosterone to corticosterone in the presence of inhibitor compounds. The pro...


J Med Chem 51: 5009-18 (2008)


Article DOI: 10.1021/jm800355c
BindingDB Entry DOI: 10.7270/Q2TB156N
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM50439004
PNG
(CHEMBL193863)
Show SMILES COc1ccc2ccc(cc2c1)-c1cccnc1
Show InChI InChI=1S/C16H13NO/c1-18-16-7-6-12-4-5-13(9-15(12)10-16)14-3-2-8-17-11-14/h2-11H,1H3
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n/an/a 68n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 3A


(Homo sapiens (Human))
BDBM8610
PNG
(1-[4-(4-{[(2R,4S)-2-(2,4-dichlorophenyl)-2-(1H-imi...)
Show SMILES [H][C@]1(COc2ccc(cc2)N2CCN(CC2)C(C)=O)CO[C@@](Cn2ccnc2)(O1)c1ccc(Cl)cc1Cl |r|
Show InChI InChI=1S/C26H28Cl2N4O4/c1-19(33)31-10-12-32(13-11-31)21-3-5-22(6-4-21)34-15-23-16-35-26(36-23,17-30-9-8-29-18-30)24-7-2-20(27)14-25(24)28/h2-9,14,18,23H,10-13,15-17H2,1H3/t23-,26-/m0/s1
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n/an/a 72n/an/an/an/an/an/a



Saarland University



Assay Description
To measure CYP3A4 activity, the product of testosterone 6-hydroxylation, 6beta-hydroxytestosterone was determined. After incubation, the reaction was...


J Med Chem 51: 5009-18 (2008)


Article DOI: 10.1021/jm800355c
BindingDB Entry DOI: 10.7270/Q2TB156N
More data for this
Ligand-Target Pair
Cytochrome P450 17A1


(Homo sapiens (Human))
BDBM25458
PNG
((1S,2R,5S,10R,11S,15S)-2,15-dimethyl-14-(pyridin-3...)
Show SMILES [H][C@@]12CC=C(c3cccnc3)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2C[C@@H](O)CC[C@]12C |t:3,23|
Show InChI InChI=1S/C24H31NO/c1-23-11-9-18(26)14-17(23)5-6-19-21-8-7-20(16-4-3-13-25-15-16)24(21,2)12-10-22(19)23/h3-5,7,13,15,18-19,21-22,26H,6,8-12,14H2,1-2H3/t18-,19-,21-,22-,23-,24+/m0/s1
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n/an/a 72n/an/an/an/an/an/a



Saarland University

Curated by ChEMBL


Assay Description
Inhibition of human CYP17 expressed in Escherichia coli co-expressed with NADPH-P450 reductase


Bioorg Med Chem 16: 1992-2010 (2008)


Article DOI: 10.1016/j.bmc.2007.10.094
BindingDB Entry DOI: 10.7270/Q29W0GBN
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Cytochrome P450 17A1


(Homo sapiens (Human))
BDBM25458
PNG
((1S,2R,5S,10R,11S,15S)-2,15-dimethyl-14-(pyridin-3...)
Show SMILES [H][C@@]12CC=C(c3cccnc3)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2C[C@@H](O)CC[C@]12C |t:3,23|
Show InChI InChI=1S/C24H31NO/c1-23-11-9-18(26)14-17(23)5-6-19-21-8-7-20(16-4-3-13-25-15-16)24(21,2)12-10-22(19)23/h3-5,7,13,15,18-19,21-22,26H,6,8-12,14H2,1-2H3/t18-,19-,21-,22-,23-,24+/m0/s1
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n/an/a 72n/an/an/an/a7.437



Saarland University



Assay Description
The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...


J Med Chem 51: 5009-18 (2008)


Article DOI: 10.1021/jm800355c
BindingDB Entry DOI: 10.7270/Q2TB156N
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Cytochrome P450 17A1


(Homo sapiens (Human))
BDBM25458
PNG
((1S,2R,5S,10R,11S,15S)-2,15-dimethyl-14-(pyridin-3...)
Show SMILES [H][C@@]12CC=C(c3cccnc3)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2C[C@@H](O)CC[C@]12C |t:3,23|
Show InChI InChI=1S/C24H31NO/c1-23-11-9-18(26)14-17(23)5-6-19-21-8-7-20(16-4-3-13-25-15-16)24(21,2)12-10-22(19)23/h3-5,7,13,15,18-19,21-22,26H,6,8-12,14H2,1-2H3/t18-,19-,21-,22-,23-,24+/m0/s1
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n/an/a 72n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP17 expressed in Escherichia coli using 1,2[3H]-progesterone as substrate in presence of NADPH


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Cytochrome P450 17A1


(Homo sapiens (Human))
BDBM25458
PNG
((1S,2R,5S,10R,11S,15S)-2,15-dimethyl-14-(pyridin-3...)
Show SMILES [H][C@@]12CC=C(c3cccnc3)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2C[C@@H](O)CC[C@]12C |t:3,23|
Show InChI InChI=1S/C24H31NO/c1-23-11-9-18(26)14-17(23)5-6-19-21-8-7-20(16-4-3-13-25-15-16)24(21,2)12-10-22(19)23/h3-5,7,13,15,18-19,21-22,26H,6,8-12,14H2,1-2H3/t18-,19-,21-,22-,23-,24+/m0/s1
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n/an/a 72n/an/an/an/an/an/a



Saarland University

Curated by ChEMBL


Assay Description
Inhibition of human CYP17 expressed in Escherichia coli


Bioorg Med Chem Lett 18: 267-73 (2008)


Article DOI: 10.1016/j.bmcl.2007.10.079
BindingDB Entry DOI: 10.7270/Q2833RSP
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM50438992
PNG
(CHEMBL2420685)
Show SMILES COc1ccc2ccc(-c3cncnc3)c(Cl)c2c1
Show InChI InChI=1S/C15H11ClN2O/c1-19-12-4-2-10-3-5-13(15(16)14(10)6-12)11-7-17-9-18-8-11/h2-9H,1H3
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n/an/a 72n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B2 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 17A1


(Homo sapiens (Human))
BDBM50438996
PNG
(CHEMBL2420681)
Show SMILES COc1ccc2ccc(-c3cncc(OC)c3)c(Cl)c2c1
Show InChI InChI=1S/C17H14ClNO2/c1-20-13-5-3-11-4-6-15(17(18)16(11)8-13)12-7-14(21-2)10-19-9-12/h3-10H,1-2H3
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n/an/a 94n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP17 expressed in Escherichia coli using 1,2[3H]-progesterone as substrate in presence of NADPH


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 17A1


(Homo sapiens (Human))
BDBM50439002
PNG
(CHEMBL2420675)
Show SMILES COc1ccc2ccc(-c3cccnc3)c(F)c2c1
Show InChI InChI=1S/C16H12FNO/c1-19-13-6-4-11-5-7-14(16(17)15(11)9-13)12-3-2-8-18-10-12/h2-10H,1H3
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n/an/a 106n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP17 expressed in Escherichia coli using 1,2[3H]-progesterone as substrate in presence of NADPH


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 11B2 (CYP11B2)


(Homo sapiens (Human))
BDBM25448
PNG
(4-[6-(4-fluorophenyl)-3,4-dihydronaphthalen-1-yl]p...)
Show SMILES Fc1ccc(cc1)-c1ccc2C(=CCCc2c1)c1ccncc1 |c:12|
Show InChI InChI=1S/C21H16FN/c22-19-7-4-15(5-8-19)17-6-9-21-18(14-17)2-1-3-20(21)16-10-12-23-13-11-16/h3-14H,1-2H2
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n/an/a 121n/an/an/an/an/an/a



Saarland University



Assay Description
The enzyme activity was assayed by monitoring the conversion of deoxycorticosterone to corticosterone in the presence of inhibitor compounds. The pro...


J Med Chem 51: 5009-18 (2008)


Article DOI: 10.1021/jm800355c
BindingDB Entry DOI: 10.7270/Q2TB156N
More data for this
Ligand-Target Pair
Cytochrome P450 11B1, mitochondrial


(Homo sapiens (Human))
BDBM8610
PNG
(1-[4-(4-{[(2R,4S)-2-(2,4-dichlorophenyl)-2-(1H-imi...)
Show SMILES [H][C@]1(COc2ccc(cc2)N2CCN(CC2)C(C)=O)CO[C@@](Cn2ccnc2)(O1)c1ccc(Cl)cc1Cl |r|
Show InChI InChI=1S/C26H28Cl2N4O4/c1-19(33)31-10-12-32(13-11-31)21-3-5-22(6-4-21)34-15-23-16-35-26(36-23,17-30-9-8-29-18-30)24-7-2-20(27)14-25(24)28/h2-9,14,18,23H,10-13,15-17H2,1H3/t23-,26-/m0/s1
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n/an/a 127n/an/an/an/an/an/a



Saarland University



Assay Description
The enzyme activity was assayed by monitoring the conversion of deoxycorticosterone to corticosterone in the presence of inhibitor compounds. The pro...


J Med Chem 51: 5009-18 (2008)


Article DOI: 10.1021/jm800355c
BindingDB Entry DOI: 10.7270/Q2TB156N
More data for this
Ligand-Target Pair
Cytochrome P450 17A1


(Homo sapiens (Human))
BDBM25456
PNG
(4-[5-(pyridin-4-yl)-5,6,7,8-tetrahydronaphthalen-2...)
Show SMILES Oc1ccc(cc1O)-c1ccc2C(CCCc2c1)c1ccncc1
Show InChI InChI=1S/C21H19NO2/c23-20-7-5-16(13-21(20)24)15-4-6-19-17(12-15)2-1-3-18(19)14-8-10-22-11-9-14/h4-13,18,23-24H,1-3H2
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n/an/a 144n/an/an/an/a7.437



Saarland University



Assay Description
The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...


J Med Chem 51: 5009-18 (2008)


Article DOI: 10.1021/jm800355c
BindingDB Entry DOI: 10.7270/Q2TB156N
More data for this
Ligand-Target Pair
Cytochrome P450 17A1


(Homo sapiens (Human))
BDBM50439000
PNG
(CHEMBL2420677)
Show SMILES COc1ccc2ccc(-c3cccnc3)c(Cl)c2c1F
Show InChI InChI=1S/C16H11ClFNO/c1-20-13-7-5-10-4-6-12(11-3-2-8-19-9-11)15(17)14(10)16(13)18/h2-9H,1H3
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n/an/a 147n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP17 expressed in Escherichia coli using 1,2[3H]-progesterone as substrate in presence of NADPH


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 3A


(Homo sapiens (Human))
BDBM25446
PNG
(4-[6-(4-fluorophenyl)-1H-inden-3-yl]pyridine | Abi...)
Show SMILES Fc1ccc(cc1)-c1ccc2C(=CCc2c1)c1ccncc1 |c:12|
Show InChI InChI=1S/C20H14FN/c21-18-5-1-14(2-6-18)16-3-7-20-17(13-16)4-8-19(20)15-9-11-22-12-10-15/h1-3,5-13H,4H2
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MMDB

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n/an/a 159n/an/an/an/an/an/a



Saarland University



Assay Description
To measure CYP3A4 activity, the product of testosterone 6-hydroxylation, 6beta-hydroxytestosterone was determined. After incubation, the reaction was...


J Med Chem 51: 5009-18 (2008)


Article DOI: 10.1021/jm800355c
BindingDB Entry DOI: 10.7270/Q2TB156N
More data for this
Ligand-Target Pair
Cytochrome P450 17A1


(Homo sapiens (Human))
BDBM25454
PNG
(4-[6-(4-fluorophenyl)-1,2,3,4-tetrahydronaphthalen...)
Show SMILES Fc1ccc(cc1)-c1ccc2C(CCCc2c1)c1ccncc1
Show InChI InChI=1S/C21H18FN/c22-19-7-4-15(5-8-19)17-6-9-21-18(14-17)2-1-3-20(21)16-10-12-23-13-11-16/h4-14,20H,1-3H2
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n/an/a 163n/an/an/an/a7.437



Saarland University



Assay Description
The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...


J Med Chem 51: 5009-18 (2008)


Article DOI: 10.1021/jm800355c
BindingDB Entry DOI: 10.7270/Q2TB156N
More data for this
Ligand-Target Pair
Cytochrome P450 17A1


(Homo sapiens (Human))
BDBM50438995
PNG
(CHEMBL2420682)
Show SMILES COc1cncc(c1)-c1ccc2ccc(O)cc2c1Cl
Show InChI InChI=1S/C16H12ClNO2/c1-20-13-6-11(8-18-9-13)14-5-3-10-2-4-12(19)7-15(10)16(14)17/h2-9,19H,1H3
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n/an/a 185n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP17 expressed in Escherichia coli using 1,2[3H]-progesterone as substrate in presence of NADPH


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 17A1


(Homo sapiens (Human))
BDBM25451
PNG
(2-fluoro-4-[5-(pyridin-4-yl)-7,8-dihydronaphthalen...)
Show SMILES Oc1ccc(cc1F)-c1ccc2C(=CCCc2c1)c1ccncc1 |c:13|
Show InChI InChI=1S/C21H16FNO/c22-20-13-16(5-7-21(20)24)15-4-6-19-17(12-15)2-1-3-18(19)14-8-10-23-11-9-14/h3-13,24H,1-2H2
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n/an/a 188n/an/an/an/a7.437



Saarland University



Assay Description
The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...


J Med Chem 51: 5009-18 (2008)


Article DOI: 10.1021/jm800355c
BindingDB Entry DOI: 10.7270/Q2TB156N
More data for this
Ligand-Target Pair
Cytochrome P450 17A1


(Rattus norvegicus (Rat))
BDBM25458
PNG
((1S,2R,5S,10R,11S,15S)-2,15-dimethyl-14-(pyridin-3...)
Show SMILES [H][C@@]12CC=C(c3cccnc3)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2C[C@@H](O)CC[C@]12C |t:3,23|
Show InChI InChI=1S/C24H31NO/c1-23-11-9-18(26)14-17(23)5-6-19-21-8-7-20(16-4-3-13-25-15-16)24(21,2)12-10-22(19)23/h3-5,7,13,15,18-19,21-22,26H,6,8-12,14H2,1-2H3/t18-,19-,21-,22-,23-,24+/m0/s1
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n/an/a 220n/an/an/an/an/an/a



Saarland University

Curated by ChEMBL


Assay Description
Inhibition of Sprague-Dawley rat testicular CYP17


Bioorg Med Chem 16: 1992-2010 (2008)


Article DOI: 10.1016/j.bmc.2007.10.094
BindingDB Entry DOI: 10.7270/Q29W0GBN
More data for this
Ligand-Target Pair
Cytochrome P450 11B1, mitochondrial


(Homo sapiens (Human))
BDBM50438999
PNG
(CHEMBL2420678)
Show SMILES Oc1ccc2ccc(-c3cccnc3)c(Cl)c2c1F
Show InChI InChI=1S/C15H9ClFNO/c16-14-11(10-2-1-7-18-8-10)5-3-9-4-6-12(19)15(17)13(9)14/h1-8,19H
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n/an/a 224n/an/an/an/an/an/a



Saarland University& Helmholtz Institute for Pharmaceutical Research Saarland (HIPS)

Curated by ChEMBL


Assay Description
Inhibition of human CYP11B1 expressed in hamster V79MZh cells using [1,2-3H]-11-deoxycorticosterone as substrate


J Med Chem 56: 6101-7 (2013)


Article DOI: 10.1021/jm400484p
BindingDB Entry DOI: 10.7270/Q2CJ8FX2
More data for this
Ligand-Target Pair
Cytochrome P450 17A1


(Homo sapiens (Human))
BDBM25453
PNG
(4-[5-(4-fluorophenyl)-2,3-dihydro-1H-inden-1-yl]py...)
Show SMILES Fc1ccc(cc1)-c1ccc2C(CCc2c1)c1ccncc1
Show InChI InChI=1S/C20H16FN/c21-18-5-1-14(2-6-18)16-3-7-20-17(13-16)4-8-19(20)15-9-11-22-12-10-15/h1-3,5-7,9-13,19H,4,8H2
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n/an/a 233n/an/an/an/a7.437



Saarland University



Assay Description
The 17 alpha-hydroxylase activity of CYP 17 was determined by measuring the conversion of progesterone into 17 alpha-hydroxyprogesterone and the bypr...


J Med Chem 51: 5009-18 (2008)


Article DOI: 10.1021/jm800355c
BindingDB Entry DOI: 10.7270/Q2TB156N
More data for this
Ligand-Target Pair
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