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Compile Data Set for Download or QSAR

Found 383 hits of Enz. Inhib. data with enzyme = 'Angiotensin II receptor' and Substrate = 'to-be-curated'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Angiotensin II receptor


(Homo sapiens (Human))
BDBM50240609
PNG
(2-Ethoxy-3-[2'-(1H-tetrazol-5-yl)-biphenyl-4-ylmet...)
Show SMILES CCOc1nc2cccc(C(O)=O)c2n1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1
Show InChI InChI=1S/C24H20N6O3/c1-2-33-24-25-20-9-5-8-19(23(31)32)21(20)30(24)14-15-10-12-16(13-11-15)17-6-3-4-7-18(17)22-26-28-29-27-22/h3-13H,2,14H2,1H3,(H,31,32)(H,26,27,28,29)
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0.170n/an/an/an/an/an/an/an/a



Shinshu University

Curated by PDSP Ki Database




Fundam Clin Pharmacol 16: 317-23 (2002)


BindingDB Entry DOI: 10.7270/Q2697259
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM50006909
PNG
(2-Butyl-5-chloro-3-[2'-(1H-tetrazol-5-yl)-biphenyl...)
Show SMILES CCCCc1nc(Cl)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1
Show InChI InChI=1S/C22H21ClN6O2/c1-2-3-8-18-24-20(23)19(22(30)31)29(18)13-14-9-11-15(12-10-14)16-6-4-5-7-17(16)21-25-27-28-26-21/h4-7,9-12H,2-3,8,13H2,1H3,(H,30,31)(H,25,26,27,28)
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0.670n/an/an/an/an/an/an/an/a



Shinshu University

Curated by PDSP Ki Database




Fundam Clin Pharmacol 16: 317-23 (2002)


BindingDB Entry DOI: 10.7270/Q2697259
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM50287290
PNG
(CHEMBL34866 | KRH-594 | Potassium; 2-[5-ethyl-3-[2...)
Show SMILES CCc1nn(Cc2ccc(cc2)-c2ccccc2-c2nnn[nH]2)c(=NC(=O)C2=C(CCC2)C([O-])=O)s1
Show InChI InChI=1S/C25H23N7O3S/c1-2-21-29-32(25(36-21)26-23(33)19-8-5-9-20(19)24(34)35)14-15-10-12-16(13-11-15)17-6-3-4-7-18(17)22-27-30-31-28-22/h3-4,6-7,10-13H,2,5,8-9,14H2,1H3,(H,34,35)(H,27,28,30,31)/p-1
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1.24n/an/an/an/an/an/an/an/a



Shinshu University

Curated by PDSP Ki Database




Fundam Clin Pharmacol 16: 317-23 (2002)


BindingDB Entry DOI: 10.7270/Q2697259
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM50171290
PNG
(5-(4-Bromo-phenyl)-1-(2,4-dichloro-phenyl)-4-ethyl...)
Show SMILES CCc1c(nn(c1-c1ccc(Br)cc1)-c1ccc(Cl)cc1Cl)C(=O)NN1CCCCC1
Show InChI InChI=1S/C23H23BrCl2N4O/c1-2-18-21(23(31)28-29-12-4-3-5-13-29)27-30(20-11-10-17(25)14-19(20)26)22(18)15-6-8-16(24)9-7-15/h6-11,14H,2-5,12-13H2,1H3,(H,28,31)
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1.00E+3n/an/an/an/an/an/an/an/a



Sanofi-Synthelabo Recherche

Curated by PDSP Ki Database




J Pharmacol Exp Ther 310: 905-14 (2004)


Article DOI: 10.1124/jpet.104.067884
BindingDB Entry DOI: 10.7270/Q2RR1WTX
More data for this
Ligand-Target Pair
Angiotensin II receptor


(HUMAN)
BDBM50035398
PNG
((S)-1-Methyl-2-(3-methyl-isoxazol-5-yl)-pyrrolidin...)
Show SMILES CN1CCC[C@H]1c1cc(C)no1
Show InChI InChI=1S/C9H14N2O/c1-7-6-9(12-10-7)8-4-3-5-11(8)2/h6,8H,3-5H2,1-2H3/t8-/m0/s1
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>1.00E+4n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by PDSP Ki Database




J Pharmacol Exp Ther 270: 310-8 (1994)


BindingDB Entry DOI: 10.7270/Q2HH6HKJ
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM21280
PNG
(5-(4-chloro-3-methylphenyl)-1-[(4-methylphenyl)met...)
Show SMILES Cc1ccc(Cn2nc(cc2-c2ccc(Cl)c(C)c2)C(=O)NC2[C@@]3(C)CCC(C3)C2(C)C)cc1
Show InChI InChI=1S/C29H34ClN3O/c1-18-6-8-20(9-7-18)17-33-25(21-10-11-23(30)19(2)14-21)15-24(32-33)26(34)31-27-28(3,4)22-12-13-29(27,5)16-22/h6-11,14-15,22,27H,12-13,16-17H2,1-5H3,(H,31,34)/t22?,27?,29-/m0/s1
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Sanofi Recherche

Curated by PDSP Ki Database




J Pharmacol Exp Ther 284: 644-50 (1998)


Article DOI: 10.1021/acschembio.5b00817
BindingDB Entry DOI: 10.7270/Q2D50KHT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(HUMAN)
BDBM263926
PNG
(US9714224, 40 | US9714224, 41)
Show SMILES COc1ccc2CN([C@@H](Cc2c1OCc1ccccc1)C(=O)NS(=O)(=O)N(C)C)C(=O)C(c1ccccc1)c1ccccc1
Show InChI InChI=1S/C34H35N3O6S/c1-36(2)44(40,41)35-33(38)29-21-28-27(19-20-30(42-3)32(28)43-23-24-13-7-4-8-14-24)22-37(29)34(39)31(25-15-9-5-10-16-25)26-17-11-6-12-18-26/h4-20,29,31H,21-23H2,1-3H3,(H,35,38)/t29-/m0/s1
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n/an/a 10.9n/an/an/an/an/an/a



NOVARTIS AG

US Patent


Assay Description
120 μL membrane (5 mg protein/well) was incubated with 15 μL of [125I]-CGP42112A and 15 μL of compound at RT for 1.5 hrs. The binding ...


US Patent US9714224 (2017)

More data for this
Ligand-Target Pair
Angiotensin II receptor


(HUMAN)
BDBM263925
PNG
(US9714224, 34)
Show SMILES OC(=O)[C@@H]1Cc2c(CN1C(=O)C(c1ccccc1)c1ccccc1)ccc(O)c2OCc1ccccc1
Show InChI InChI=1S/C31H27NO5/c33-27-17-16-24-19-32(30(34)28(22-12-6-2-7-13-22)23-14-8-3-9-15-23)26(31(35)36)18-25(24)29(27)37-20-21-10-4-1-5-11-21/h1-17,26,28,33H,18-20H2,(H,35,36)/t26-/m0/s1
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n/an/a 33.5n/an/an/an/an/an/a



NOVARTIS AG

US Patent


Assay Description
120 μL membrane (5 mg protein/well) was incubated with 15 μL of [125I]-CGP42112A and 15 μL of compound at RT for 1.5 hrs. The binding ...


US Patent US9714224 (2017)

More data for this
Ligand-Target Pair
Angiotensin II receptor


(HUMAN)
BDBM261619
PNG
((S)-4-(1-benzyl-3-methyl-1H-pyrazol-5-yl)-1-(2,2-d...)
Show SMILES Cc1cc(N2CCN([C@@H](C2)C(O)=O)C(=O)C(c2ccccc2)c2ccccc2)n(Cc2ccccc2)n1
Show InChI InChI=1S/C30H30N4O3/c1-22-19-27(34(31-22)20-23-11-5-2-6-12-23)32-17-18-33(26(21-32)30(36)37)29(35)28(24-13-7-3-8-14-24)25-15-9-4-10-16-25/h2-16,19,26,28H,17-18,20-21H2,1H3,(H,36,37)/t26-/m0/s1
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n/an/a 40.3n/an/an/an/an/an/a



NOVARTIS AG

US Patent


Assay Description
120 μL membrane (5 mg protein/well) was incubated with 15 μL of [125I]-CGP42112A and 15 μL of compound at RT for 1.5 hrs.The binding r...


US Patent US9708275 (2017)

More data for this
Ligand-Target Pair
Angiotensin II receptor


(HUMAN)
BDBM263928
PNG
(US9714224, 48)
Show SMILES COc1ccc2CN([C@@H](Cc2c1OCC#Cc1ccccc1)C(=O)NS(=O)(=O)N(C)C)C(=O)C(c1ccccc1)c1ccccc1
Show InChI InChI=1S/C36H35N3O6S/c1-38(2)46(42,43)37-35(40)31-24-30-29(21-22-32(44-3)34(30)45-23-13-16-26-14-7-4-8-15-26)25-39(31)36(41)33(27-17-9-5-10-18-27)28-19-11-6-12-20-28/h4-12,14-15,17-22,31,33H,23-25H2,1-3H3,(H,37,40)/t31-/m0/s1
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n/an/a 79.5n/an/an/an/an/an/a



NOVARTIS AG

US Patent


Assay Description
120 μL membrane (5 mg protein/well) was incubated with 15 μL of [125I]-CGP42112A and 15 μL of compound at RT for 1.5 hrs. The binding ...


US Patent US9714224 (2017)

More data for this
Ligand-Target Pair
Angiotensin II receptor


(HUMAN)
BDBM261620
PNG
((S)-4-(1-benzyl-3-(-trifluoromethyl)-1H-pyrazol-5-...)
Show SMILES OC(=O)[C@@H]1CN(CCN1C(=O)C(c1ccccc1)c1ccccc1)c1cc(nn1Cc1ccccc1)C(F)(F)F
Show InChI InChI=1S/C30H27F3N4O3/c31-30(32,33)25-18-26(37(34-25)19-21-10-4-1-5-11-21)35-16-17-36(24(20-35)29(39)40)28(38)27(22-12-6-2-7-13-22)23-14-8-3-9-15-23/h1-15,18,24,27H,16-17,19-20H2,(H,39,40)/t24-/m0/s1
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n/an/a 93.8n/an/an/an/an/an/a



NOVARTIS AG

US Patent


Assay Description
120 μL membrane (5 mg protein/well) was incubated with 15 μL of [125I]-CGP42112A and 15 μL of compound at RT for 1.5 hrs.The binding r...


US Patent US9708275 (2017)

More data for this
Ligand-Target Pair
Angiotensin II receptor


(HUMAN)
BDBM263930
PNG
(US9714224, 50)
Show SMILES COc1ccc2CN([C@@H](Cc2c1OCC#Cc1ccccc1)C(O)=O)C(=O)C(c1ccccc1)c1ccccc1
Show InChI InChI=1S/C34H29NO5/c1-39-30-20-19-27-23-35(33(36)31(25-15-7-3-8-16-25)26-17-9-4-10-18-26)29(34(37)38)22-28(27)32(30)40-21-11-14-24-12-5-2-6-13-24/h2-10,12-13,15-20,29,31H,21-23H2,1H3,(H,37,38)/t29-/m0/s1
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n/an/a 96.2n/an/an/an/an/an/a



NOVARTIS AG

US Patent


Assay Description
120 μL membrane (5 mg protein/well) was incubated with 15 μL of [125I]-CGP42112A and 15 μL of compound at RT for 1.5 hrs. The binding ...


US Patent US9714224 (2017)

More data for this
Ligand-Target Pair
Angiotensin II receptor


(HUMAN)
BDBM263931
PNG
(US9714224, 51)
Show SMILES COc1ccc2CN([C@@H](Cc2c1OCC#Cc1ccc(F)cc1)C(O)=O)C(=O)C(c1ccccc1)c1ccccc1
Show InChI InChI=1S/C34H28FNO5/c1-40-30-19-16-26-22-36(33(37)31(24-10-4-2-5-11-24)25-12-6-3-7-13-25)29(34(38)39)21-28(26)32(30)41-20-8-9-23-14-17-27(35)18-15-23/h2-7,10-19,29,31H,20-22H2,1H3,(H,38,39)/t29-/m0/s1
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n/an/a 133n/an/an/an/an/an/a



NOVARTIS AG

US Patent


Assay Description
120 μL membrane (5 mg protein/well) was incubated with 15 μL of [125I]-CGP42112A and 15 μL of compound at RT for 1.5 hrs. The binding ...


US Patent US9714224 (2017)

More data for this
Ligand-Target Pair
Angiotensin II receptor


(HUMAN)
BDBM261615
PNG
((S)-1-(2,2-diphenylacetyl)-4-(3-methyl-1-phenyl-1H...)
Show SMILES OC(=O)[C@@H]1CN(CCCc2ccccc2)CCN1C(=O)C(c1ccccc1)c1ccccc1
Show InChI InChI=1S/C28H30N2O3/c31-27(26(23-14-6-2-7-15-23)24-16-8-3-9-17-24)30-20-19-29(21-25(30)28(32)33)18-10-13-22-11-4-1-5-12-22/h1-9,11-12,14-17,25-26H,10,13,18-21H2,(H,32,33)/t25-/m0/s1
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n/an/a 155n/an/an/an/an/an/a



NOVARTIS AG

US Patent


Assay Description
120 μL membrane (5 mg protein/well) was incubated with 15 μL of [125I]-CGP42112A and 15 μL of compound at RT for 1.5 hrs.The binding r...


US Patent US9708275 (2017)

More data for this
Ligand-Target Pair
Angiotensin II receptor


(HUMAN)
BDBM263929
PNG
(US9714224, 49)
Show SMILES COc1ccc2CN([C@@H](Cc2c1OCC#Cc1ccc(F)cc1)C(=O)NS(=O)(=O)N(C)C)C(=O)C(c1ccccc1)c1ccccc1
Show InChI InChI=1S/C36H34FN3O6S/c1-39(2)47(43,44)38-35(41)31-23-30-28(18-21-32(45-3)34(30)46-22-10-11-25-16-19-29(37)20-17-25)24-40(31)36(42)33(26-12-6-4-7-13-26)27-14-8-5-9-15-27/h4-9,12-21,31,33H,22-24H2,1-3H3,(H,38,41)/t31-/m0/s1
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n/an/a 206n/an/an/an/an/an/a



NOVARTIS AG

US Patent


Assay Description
120 μL membrane (5 mg protein/well) was incubated with 15 μL of [125I]-CGP42112A and 15 μL of compound at RT for 1.5 hrs. The binding ...


US Patent US9714224 (2017)

More data for this
Ligand-Target Pair
Angiotensin II receptor


(HUMAN)
BDBM261613
PNG
((S)-4-benzyl-1-(2,2-diphenylacetyl)piperazine-2-ca...)
Show SMILES OC(=O)[C@@H]1CN(Cc2ccccc2)CCN1C(=O)C(c1ccccc1)c1ccccc1
Show InChI InChI=1S/C26H26N2O3/c29-25(24(21-12-6-2-7-13-21)22-14-8-3-9-15-22)28-17-16-27(19-23(28)26(30)31)18-20-10-4-1-5-11-20/h1-15,23-24H,16-19H2,(H,30,31)/t23-/m0/s1
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n/an/a 383n/an/an/an/an/an/a



NOVARTIS AG

US Patent


Assay Description
120 μL membrane (5 mg protein/well) was incubated with 15 μL of [125I]-CGP42112A and 15 μL of compound at RT for 1.5 hrs.The binding r...


US Patent US9708275 (2017)

More data for this
Ligand-Target Pair
Angiotensin II receptor


(HUMAN)
BDBM261612
PNG
((S)-1-(2,2-diphenylacetyl)-4-phenylpiperazine-2-ca...)
Show SMILES OC(=O)[C@@H]1CN(CCN1C(=O)C(c1ccccc1)c1ccccc1)c1ccccc1
Show InChI InChI=1S/C25H24N2O3/c28-24(23(19-10-4-1-5-11-19)20-12-6-2-7-13-20)27-17-16-26(18-22(27)25(29)30)21-14-8-3-9-15-21/h1-15,22-23H,16-18H2,(H,29,30)/t22-/m0/s1
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n/an/a 408n/an/an/an/an/an/a



NOVARTIS AG

US Patent


Assay Description
120 μL membrane (5 mg protein/well) was incubated with 15 μL of [125I]-CGP42112A and 15 μL of compound at RT for 1.5 hrs.The binding r...


US Patent US9708275 (2017)

More data for this
Ligand-Target Pair
Angiotensin II receptor


(HUMAN)
BDBM263923
PNG
(US9714221, Example 219N/A*: Not available. Prodrug...)
Show SMILES CC(F)(F)c1ccc(cc1)C1=C(c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c2ccc(cc2CCC1)C(O)=O
Show InChI InChI=1S/C33H34F3NO3/c1-33(35,36)26-11-6-22(7-12-26)29-5-2-4-24-20-25(32(38)39)10-15-30(24)31(29)23-8-13-27(14-9-23)40-28-16-19-37(21-28)18-3-17-34/h6-15,20,28H,2-5,16-19,21H2,1H3,(H,38,39)/t28-/m0/s1
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n/an/a 431n/an/an/an/an/an/a



NOVARTIS AG

US Patent


Assay Description
120 μL membrane (5 mg protein/well) was incubated with 15 μL of [125I]-CGP42112A and 15 μL of compound at RT for 1.5 hrs. The binding ...


US Patent US9714224 (2017)

More data for this
Ligand-Target Pair
Angiotensin II receptor


(HUMAN)
BDBM261615
PNG
((S)-1-(2,2-diphenylacetyl)-4-(3-methyl-1-phenyl-1H...)
Show SMILES OC(=O)[C@@H]1CN(CCCc2ccccc2)CCN1C(=O)C(c1ccccc1)c1ccccc1
Show InChI InChI=1S/C28H30N2O3/c31-27(26(23-14-6-2-7-15-23)24-16-8-3-9-17-24)30-20-19-29(21-25(30)28(32)33)18-10-13-22-11-4-1-5-12-22/h1-9,11-12,14-17,25-26H,10,13,18-21H2,(H,32,33)/t25-/m0/s1
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n/an/a 517n/an/an/an/an/an/a



NOVARTIS AG

US Patent


Assay Description
120 μL membrane (5 mg protein/well) was incubated with 15 μL of [125I]-CGP42112A and 15 μL of compound at RT for 1.5 hrs.The binding r...


US Patent US9708275 (2017)

More data for this
Ligand-Target Pair
Angiotensin II receptor


(HUMAN)
BDBM261616
PNG
((S)-1-(2,2-diphenylacetyl)-4-phenethylpiperazine-2...)
Show SMILES OC(=O)[C@@H]1CN(CCc2ccccc2)CCN1C(=O)C(c1ccccc1)c1ccccc1
Show InChI InChI=1S/C27H28N2O3/c30-26(25(22-12-6-2-7-13-22)23-14-8-3-9-15-23)29-19-18-28(20-24(29)27(31)32)17-16-21-10-4-1-5-11-21/h1-15,24-25H,16-20H2,(H,31,32)/t24-/m0/s1
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n/an/a 1.27E+3n/an/an/an/an/an/a



NOVARTIS AG

US Patent


Assay Description
120 μL membrane (5 mg protein/well) was incubated with 15 μL of [125I]-CGP42112A and 15 μL of compound at RT for 1.5 hrs.The binding r...


US Patent US9708275 (2017)

More data for this
Ligand-Target Pair
Angiotensin II receptor


(HUMAN)
BDBM261623
PNG
((S)-1-(2,2-diphenylacetyl)-4-(4-phenylbut-3-yn-1-y...)
Show SMILES OC(=O)[C@@H]1CN(CCC#Cc2ccccc2)CCN1C(=O)C(c1ccccc1)c1ccccc1
Show InChI InChI=1S/C29H28N2O3/c32-28(27(24-15-6-2-7-16-24)25-17-8-3-9-18-25)31-21-20-30(22-26(31)29(33)34)19-11-10-14-23-12-4-1-5-13-23/h1-9,12-13,15-18,26-27H,11,19-22H2,(H,33,34)/t26-/m0/s1
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n/an/a 1.32E+3n/an/an/an/an/an/a



NOVARTIS AG

US Patent


Assay Description
120 μL membrane (5 mg protein/well) was incubated with 15 μL of [125I]-CGP42112A and 15 μL of compound at RT for 1.5 hrs.The binding r...


US Patent US9708275 (2017)

More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM54371
PNG
(2-Hydroxy-benzoic acid [1-quinolin-8-yl-meth-(E)-y...)
Show SMILES Oc1ccccc1C(=O)NN=Cc1cccc2cccnc12
Show InChI InChI=1S/C17H13N3O2/c21-15-9-2-1-8-14(15)17(22)20-19-11-13-6-3-5-12-7-4-10-18-16(12)13/h1-11,21H,(H,20,22)
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n/an/a 1.56E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM63210
PNG
(3-({7-[(4-methylphenyl)thio]-4-nitro-2,1,3-benzoxa...)
Show SMILES CC(=O)OCCCNc1cc(Sc2ccc(C)cc2)c2nonc2c1[N+]([O-])=O
Show InChI InChI=1S/C18H18N4O5S/c1-11-4-6-13(7-5-11)28-15-10-14(19-8-3-9-26-12(2)23)18(22(24)25)17-16(15)20-27-21-17/h4-7,10,19H,3,8-9H2,1-2H3
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n/an/a 1.56E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM38931
PNG
(6-methyl-2-[3-methyl-5-(4-methylanilino)-1-pyrazol...)
Show SMILES Cc1cc(Nc2ccc(C)cc2)n(n1)-c1nc(C)cc(=O)[nH]1
Show InChI InChI=1S/C16H17N5O/c1-10-4-6-13(7-5-10)18-14-8-12(3)20-21(14)16-17-11(2)9-15(22)19-16/h4-9,18H,1-3H3,(H,17,19,22)
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n/an/a 1.77E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(HUMAN)
BDBM263926
PNG
(US9714224, 40 | US9714224, 41)
Show SMILES COc1ccc2CN([C@@H](Cc2c1OCc1ccccc1)C(=O)NS(=O)(=O)N(C)C)C(=O)C(c1ccccc1)c1ccccc1
Show InChI InChI=1S/C34H35N3O6S/c1-36(2)44(40,41)35-33(38)29-21-28-27(19-20-30(42-3)32(28)43-23-24-13-7-4-8-14-24)22-37(29)34(39)31(25-15-9-5-10-16-25)26-17-11-6-12-18-26/h4-20,29,31H,21-23H2,1-3H3,(H,35,38)/t29-/m0/s1
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n/an/a 1.79E+3n/an/an/an/an/an/a



NOVARTIS AG

US Patent


Assay Description
120 μL membrane (5 mg protein/well) was incubated with 15 μL of [125I]-CGP42112A and 15 μL of compound at RT for 1.5 hrs. The binding ...


US Patent US9714224 (2017)

More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM33098
PNG
(2-[[7-(1,3-benzothiazol-2-ylsulfanyl)-4-nitro-2,1,...)
Show SMILES OCCNc1cc(Sc2nc3ccccc3s2)c2nonc2c1[N+]([O-])=O
Show InChI InChI=1S/C15H11N5O4S2/c21-6-5-16-9-7-11(12-13(19-24-18-12)14(9)20(22)23)26-15-17-8-3-1-2-4-10(8)25-15/h1-4,7,16,21H,5-6H2
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n/an/a 1.90E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM67337
PNG
(4-fluoranyl-N-(1-pyridin-2-ylethylideneamino)benza...)
Show SMILES CC(=NNC(=O)c1ccc(F)cc1)c1ccccn1
Show InChI InChI=1S/C14H12FN3O/c1-10(13-4-2-3-9-16-13)17-18-14(19)11-5-7-12(15)8-6-11/h2-9H,1H3,(H,18,19)
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n/an/a 1.96E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM33096
PNG
(3-[[7-(1,3-benzothiazol-2-ylsulfanyl)-4-nitro-2,1,...)
Show SMILES OCCCNc1cc(Sc2nc3ccccc3s2)c2nonc2c1[N+]([O-])=O
Show InChI InChI=1S/C16H13N5O4S2/c22-7-3-6-17-10-8-12(13-14(20-25-19-13)15(10)21(23)24)27-16-18-9-4-1-2-5-11(9)26-16/h1-2,4-5,8,17,22H,3,6-7H2
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n/an/a 2.05E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM33097
PNG
(3-[[7-(1,3-benzothiazol-2-ylsulfanyl)-4-nitro-2,1,...)
Show SMILES CC(=O)OCCCNc1cc(Sc2nc3ccccc3s2)c2nonc2c1[N+]([O-])=O
Show InChI InChI=1S/C18H15N5O5S2/c1-10(24)27-8-4-7-19-12-9-14(15-16(22-28-21-15)17(12)23(25)26)30-18-20-11-5-2-3-6-13(11)29-18/h2-3,5-6,9,19H,4,7-8H2,1H3
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n/an/a 2.06E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM33081
PNG
(2-[[7-(1,3-benzothiazol-2-ylsulfanyl)-4-nitro-2,1,...)
Show SMILES CN(CCO)c1cc(Sc2nc3ccccc3s2)c2nonc2c1[N+]([O-])=O
Show InChI InChI=1S/C16H13N5O4S2/c1-20(6-7-22)10-8-12(13-14(19-25-18-13)15(10)21(23)24)27-16-17-9-4-2-3-5-11(9)26-16/h2-5,8,22H,6-7H2,1H3
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n/an/a 2.08E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM67315
PNG
(4-(4-bromophenyl)-2-hydrazino-6-phenylpyrimidine |...)
Show SMILES NNc1nc(cc(n1)-c1ccc(Br)cc1)-c1ccccc1
Show InChI InChI=1S/C16H13BrN4/c17-13-8-6-12(7-9-13)15-10-14(19-16(20-15)21-18)11-4-2-1-3-5-11/h1-10H,18H2,(H,19,20,21)
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n/an/a 2.09E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM59072
PNG
(5-chloranyl-2-ethylsulfonyl-N-[4-(3-methylpiperidi...)
Show SMILES CCS(=O)(=O)c1ncc(Cl)c(n1)C(=O)Nc1ccc(cc1)S(=O)(=O)N1CCCC(C)C1
Show InChI InChI=1S/C19H23ClN4O5S2/c1-3-30(26,27)19-21-11-16(20)17(23-19)18(25)22-14-6-8-15(9-7-14)31(28,29)24-10-4-5-13(2)12-24/h6-9,11,13H,3-5,10,12H2,1-2H3,(H,22,25)
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n/an/a 2.18E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM67266
PNG
(4-chloranyl-1-ethyl-3-nitro-quinolin-2-one | 4-chl...)
Show SMILES CCn1c2ccccc2c(Cl)c([N+]([O-])=O)c1=O
Show InChI InChI=1S/C11H9ClN2O3/c1-2-13-8-6-4-3-5-7(8)9(12)10(11(13)15)14(16)17/h3-6H,2H2,1H3
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n/an/a 2.22E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM49381
PNG
((3-Methyl-pyridin-2-yl)-(4-pyridin-2-yl-thiazol-2-...)
Show SMILES Cc1cccnc1Nc1nc(cs1)-c1ccccn1
Show InChI InChI=1S/C14H12N4S/c1-10-5-4-8-16-13(10)18-14-17-12(9-19-14)11-6-2-3-7-15-11/h2-9H,1H3,(H,16,17,18)
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n/an/a 2.24E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM54825
PNG
(MLS000776291 | N-(4-chloranyl-3-ethyl-5-methanoyl-...)
Show SMILES CCn1c(Cl)c(C=O)sc1=NS(=O)(=O)c1ccccc1
Show InChI InChI=1S/C12H11ClN2O3S2/c1-2-15-11(13)10(8-16)19-12(15)14-20(17,18)9-6-4-3-5-7-9/h3-8H,2H2,1H3
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n/an/a 2.24E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM41591
PNG
((Z)-2,3-bis(chloranyl)-N-(6-methoxypyridin-3-yl)-3...)
Show SMILES COc1ccc(NC(=O)C(Cl)=C(Cl)S(=O)Cc2ccc(C)cc2)cn1
Show InChI InChI=1S/C17H16Cl2N2O3S/c1-11-3-5-12(6-4-11)10-25(23)16(19)15(18)17(22)21-13-7-8-14(24-2)20-9-13/h3-9H,10H2,1-2H3,(H,21,22)
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n/an/a 2.26E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM60275
PNG
(4-Chloro-benzoic acid (1-pyridin-2-yl-ethylidene)-...)
Show SMILES CC(=NNC(=O)c1ccc(Cl)cc1)c1ccccn1
Show InChI InChI=1S/C14H12ClN3O/c1-10(13-4-2-3-9-16-13)17-18-14(19)11-5-7-12(15)8-6-11/h2-9H,1H3,(H,18,19)
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n/an/a 2.26E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM54814
PNG
(4-[(7-chloranyl-4-nitro-2,1,3-benzoxadiazol-5-yl)a...)
Show SMILES Cc1c(Nc2cc(Cl)c3nonc3c2[N+]([O-])=O)c(=O)n(-c2ccccc2)n1C
Show InChI InChI=1S/C17H13ClN6O4/c1-9-13(17(25)23(22(9)2)10-6-4-3-5-7-10)19-12-8-11(18)14-15(21-28-20-14)16(12)24(26)27/h3-8,19H,1-2H3
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n/an/a 2.33E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM58565
PNG
(MLS001125540 | N-(2-methyl-8-quinolinyl)benzenesul...)
Show SMILES Cc1ccc2cccc(NS(=O)(=O)c3ccccc3)c2n1
Show InChI InChI=1S/C16H14N2O2S/c1-12-10-11-13-6-5-9-15(16(13)17-12)18-21(19,20)14-7-3-2-4-8-14/h2-11,18H,1H3
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n/an/a 2.35E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM43465
PNG
((Z)-2,3-bis(chloranyl)-3-[(4-chlorophenyl)methylsu...)
Show SMILES COc1ccc(NC(=O)C(Cl)=C(Cl)S(=O)Cc2ccc(Cl)cc2)cn1
Show InChI InChI=1S/C16H13Cl3N2O3S/c1-24-13-7-6-12(8-20-13)21-16(22)14(18)15(19)25(23)9-10-2-4-11(17)5-3-10/h2-8H,9H2,1H3,(H,21,22)
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n/an/a 2.35E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM67310
PNG
(3,5-bis(chloranyl)-N'-[4-(1,2,3-thiadiazol-4-yl)ph...)
Show SMILES Clc1cc(Cl)cc(c1)C(=O)NNc1ccc(cc1)-c1csnn1
Show InChI InChI=1S/C15H10Cl2N4OS/c16-11-5-10(6-12(17)7-11)15(22)20-18-13-3-1-9(2-4-13)14-8-23-21-19-14/h1-8,18H,(H,20,22)
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n/an/a 2.43E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM67302
PNG
(MLS000830852 | N'-(3-chloro-4-methylphenyl)-4-...)
Show SMILES CCc1ccc(cc1)C(=O)NNc1ccc(C)c(Cl)c1
Show InChI InChI=1S/C16H17ClN2O/c1-3-12-5-7-13(8-6-12)16(20)19-18-14-9-4-11(2)15(17)10-14/h4-10,18H,3H2,1-2H3,(H,19,20)
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n/an/a 2.55E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM67300
PNG
(MLS000860444 | N'-[4-(tert-butyl)phenyl]-4-met...)
Show SMILES Cc1nnsc1C(=O)NNc1ccc(cc1)C(C)(C)C
Show InChI InChI=1S/C14H18N4OS/c1-9-12(20-18-15-9)13(19)17-16-11-7-5-10(6-8-11)14(2,3)4/h5-8,16H,1-4H3,(H,17,19)
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n/an/a 2.56E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM60264
PNG
(2-(4-Bromo-phenyl)-quinoline-4-carboxylic acid [1-...)
Show SMILES Brc1ccc(cc1)-c1cc(C(=O)NN=Cc2ccccn2)c2ccccc2n1
Show InChI InChI=1S/C22H15BrN4O/c23-16-10-8-15(9-11-16)21-13-19(18-6-1-2-7-20(18)26-21)22(28)27-25-14-17-5-3-4-12-24-17/h1-14H,(H,27,28)
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n/an/a 2.58E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM67191
PNG
(2-chloranyl-N'-(6-chloranylpyridin-2-yl)ethanehydr...)
Show SMILES ClCC(=O)NNc1cccc(Cl)n1
Show InChI InChI=1S/C7H7Cl2N3O/c8-4-7(13)12-11-6-3-1-2-5(9)10-6/h1-3H,4H2,(H,10,11)(H,12,13)
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n/an/a 2.72E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM50227494
PNG
(CHEMBL257286 | N-(quinolin-8-yl)benzenesulfonamide...)
Show SMILES O=S(=O)(Nc1cccc2cccnc12)c1ccccc1
Show InChI InChI=1S/C15H12N2O2S/c18-20(19,13-8-2-1-3-9-13)17-14-10-4-6-12-7-5-11-16-15(12)14/h1-11,17H
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n/an/a 2.75E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM40197
PNG
((2Z)-2-[(8-quinolinylamino)methylidene]-1-benzothi...)
Show SMILES Oc1c(C=Nc2cccc3cccnc23)sc2ccccc12
Show InChI InChI=1S/C18H12N2OS/c21-18-13-7-1-2-9-15(13)22-16(18)11-20-14-8-3-5-12-6-4-10-19-17(12)14/h1-11,21H
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n/an/a 2.78E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM21629
PNG
(3-(4-methylphenyl)-5H-indeno[1,2-c]pyridazin-5-one...)
Show SMILES Cc1ccc(cc1)-c1cc2C(=O)c3ccccc3-c2nn1
Show InChI InChI=1S/C18H12N2O/c1-11-6-8-12(9-7-11)16-10-15-17(20-19-16)13-4-2-3-5-14(13)18(15)21/h2-10H,1H3
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n/an/a 2.89E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM67244
PNG
(6-ethyl-2-(2-pyridinyl)-3H-thieno[2,3-d]pyrimidin-...)
Show SMILES CCc1cc2c(nc([nH]c2=O)-c2ccccn2)s1
Show InChI InChI=1S/C13H11N3OS/c1-2-8-7-9-12(17)15-11(16-13(9)18-8)10-5-3-4-6-14-10/h3-7H,2H2,1H3,(H,15,16,17)
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n/an/a 2.91E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
Angiotensin II receptor


(Homo sapiens (Human))
BDBM43463
PNG
((Z)-2,3-bis(chloranyl)-3-[(4-methoxyphenyl)methyls...)
Show SMILES COc1ccc(CS(=O)C(Cl)=C(Cl)C(=O)Nc2ccc(OC)nc2)cc1
Show InChI InChI=1S/C17H16Cl2N2O4S/c1-24-13-6-3-11(4-7-13)10-26(23)16(19)15(18)17(22)21-12-5-8-14(25-2)20-9-12/h3-9H,10H2,1-2H3,(H,21,22)
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n/an/a 2.92E+3n/an/an/an/an/an/a



Burnham Center for Chemical Genomics

Curated by PubChem BioAssay


Assay Description
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute(SBMRI, San Diego, C...


PubChem Bioassay (2010)


BindingDB Entry DOI: 10.7270/Q2CJ8BXT
More data for this
Ligand-Target Pair
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