Compile Data Set for Download or QSAR

Found 992 hits with Last Name = 'fortin' and Initial = 'm'   

Target/Host (Institution)	Ligand	Target/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	pH	Temp °C
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470233 (CHEMBL80177) Show SMILES CCCCc1nc(SC)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)Cc1ccccc1 Show InChI InChI=1S/C30H31N3O5S2/c1-3-4-14-26-31-29(39-2)28(30(35)36)33(26)20-22-15-17-23(18-16-22)24-12-8-9-13-25(24)40(37,38)32-27(34)19-21-10-6-5-7-11-21/h5-13,15-18H,3-4,14,19-20H2,1-2H3,(H,32,34)(H,35,36)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.0800	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470229 (CHEMBL76870) Show SMILES CCCCc1nc(SC)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)c1ccccc1 Show InChI InChI=1S/C29H29N3O5S2/c1-3-4-14-25-30-28(38-2)26(29(34)35)32(25)19-20-15-17-21(18-16-20)23-12-8-9-13-24(23)39(36,37)31-27(33)22-10-6-5-7-11-22/h5-13,15-18H,3-4,14,19H2,1-2H3,(H,31,33)(H,34,35)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.0900	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470236 (CHEMBL309313) Show SMILES CCCCc1nc(SC)c(C(=O)OCc2ccccc2)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C33H38N4O5S2/c1-4-6-16-29-35-31(43-3)30(32(38)42-23-25-12-8-7-9-13-25)37(29)22-24-17-19-26(20-18-24)27-14-10-11-15-28(27)44(40,41)36-33(39)34-21-5-2/h7-15,17-20H,4-6,16,21-23H2,1-3H3,(H2,34,36,39)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.100	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470239 (CHEMBL311312) Show SMILES CCCCOC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc(SC)c2C(O)=O)cc1 Show InChI InChI=1S/C27H33N3O6S2/c1-4-6-12-23-28-25(37-3)24(26(31)32)30(23)18-19-13-15-20(16-14-19)21-10-8-9-11-22(21)38(34,35)29-27(33)36-17-7-5-2/h8-11,13-16H,4-7,12,17-18H2,1-3H3,(H,29,33)(H,31,32)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.100	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50285760 (5-alpha-hydroxyacid imidazolyl biphenyl sulfonyl u...) Show SMILES CCCCc1nc(SC)c(C(O)CC(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCc1ccccc1 Show InChI InChI=1S/C32H36N4O6S2/c1-3-4-14-28-34-31(43-2)30(26(37)19-29(38)39)36(28)21-23-15-17-24(18-16-23)25-12-8-9-13-27(25)44(41,42)35-32(40)33-20-22-10-6-5-7-11-22/h5-13,15-18,26,37H,3-4,14,19-21H2,1-2H3,(H,38,39)(H2,33,35,40)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article	n/a	n/a	0.200	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro binding affinity at Angiotensin II Type 1 receptor in rat liver membrane by [125I]AII displacement.				Bioorg Med Chem Lett 5: 2611-2616 (1995) Article DOI: 10.1016/0960-894X(95)00479-D BindingDB Entry DOI: 10.7270/Q2GT5N57
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470206 (CHEMBL445365) Show SMILES CCCCc1nc(SCSC)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C27H34N4O5S3/c1-4-6-11-23-29-25(38-18-37-3)24(26(32)33)31(23)17-19-12-14-20(15-13-19)21-9-7-8-10-22(21)39(35,36)30-27(34)28-16-5-2/h7-10,12-15H,4-6,11,16-18H2,1-3H3,(H,32,33)(H2,28,30,34)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.200	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470250 (CHEMBL77308) Show SMILES CCCCc1nc(SC)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)CCC Show InChI InChI=1S/C26H31N3O5S2/c1-4-6-12-22-27-25(35-3)24(26(31)32)29(22)17-18-13-15-19(16-14-18)20-10-7-8-11-21(20)36(33,34)28-23(30)9-5-2/h7-8,10-11,13-16H,4-6,9,12,17H2,1-3H3,(H,28,30)(H,31,32)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.200	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50213557 (CHEMBL309602) Show SMILES CCCCc1nc(SC)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCC Show InChI InChI=1S/C25H30N4O5S2/c1-4-6-11-21-27-23(35-3)22(24(30)31)29(21)16-17-12-14-18(15-13-17)19-9-7-8-10-20(19)36(33,34)28-25(32)26-5-2/h7-10,12-15H,4-6,11,16H2,1-3H3,(H,30,31)(H2,26,28,32)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.200	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50031491 (2-propyl-4-(methythio)-1-[[[2'-[(propylamino)carbo...) Show SMILES CCCNC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCC)nc(SC)c2C(O)=O)cc1 Show InChI InChI=1S/C25H30N4O5S2/c1-4-8-21-27-23(35-3)22(24(30)31)29(21)16-17-11-13-18(14-12-17)19-9-6-7-10-20(19)36(33,34)28-25(32)26-15-5-2/h6-7,9-14H,4-5,8,15-16H2,1-3H3,(H,30,31)(H2,26,28,32)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	0.200	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50213569 (CHEMBL78866) Show SMILES CCCCNC(=O)NS(=O)(=O)c1ccccc1-c1ccc(Cn2c(CCCC)nc(SC)c2C(O)=O)cc1 Show InChI InChI=1S/C27H34N4O5S2/c1-4-6-12-23-29-25(37-3)24(26(32)33)31(23)18-19-13-15-20(16-14-19)21-10-8-9-11-22(21)38(35,36)30-27(34)28-17-7-5-2/h8-11,13-16H,4-7,12,17-18H2,1-3H3,(H,32,33)(H2,28,30,34)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.200	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50285761 (5-alpha-hydroxyacid imidazolyl biphenyl sulfonyl u...) Show SMILES CCCCc1nc(SC)c(C(=O)C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCc1ccccc1 Show InChI InChI=1S/C31H32N4O6S2/c1-3-4-14-26-33-29(42-2)27(28(36)30(37)38)35(26)20-22-15-17-23(18-16-22)24-12-8-9-13-25(24)43(40,41)34-31(39)32-19-21-10-6-5-7-11-21/h5-13,15-18H,3-4,14,19-20H2,1-2H3,(H,37,38)(H2,32,34,39)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.200	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro binding affinity at Angiotensin II Type 1 receptor in rat liver membrane by [125I]AII displacement.				Bioorg Med Chem Lett 5: 2611-2616 (1995) Article DOI: 10.1016/0960-894X(95)00479-D BindingDB Entry DOI: 10.7270/Q2GT5N57
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470225 (CHEMBL80700) Show SMILES CCCCc1nc(SCCCO)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C28H36N4O6S2/c1-3-5-11-24-30-26(39-18-8-17-33)25(27(34)35)32(24)19-20-12-14-21(15-13-20)22-9-6-7-10-23(22)40(37,38)31-28(36)29-16-4-2/h6-7,9-10,12-15,33H,3-5,8,11,16-19H2,1-2H3,(H,34,35)(H2,29,31,36)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.200	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470226 (CHEMBL311827) Show SMILES CCCCc1nc(Sc2cccs2)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C29H32N4O5S3/c1-3-5-11-24-31-27(40-25-12-8-18-39-25)26(28(34)35)33(24)19-20-13-15-21(16-14-20)22-9-6-7-10-23(22)41(37,38)32-29(36)30-17-4-2/h6-10,12-16,18H,3-5,11,17,19H2,1-2H3,(H,34,35)(H2,30,32,36)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.200	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470235 (CHEMBL308135) Show SMILES CCCCc1nc(SC)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)OCC(C)C Show InChI InChI=1S/C27H33N3O6S2/c1-5-6-11-23-28-25(37-4)24(26(31)32)30(23)16-19-12-14-20(15-13-19)21-9-7-8-10-22(21)38(34,35)29-27(33)36-17-18(2)3/h7-10,12-15,18H,5-6,11,16-17H2,1-4H3,(H,29,33)(H,31,32)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.200	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50285769 (5-alpha-hydroxyacid imidazolyl biphenyl sulfonyl u...) Show SMILES CCCCc1nc(SC)c(C(=O)n2cnnn2)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCc1ccccc1 Show InChI InChI=1S/C31H32N8O4S2/c1-3-4-14-27-34-29(44-2)28(30(40)39-21-33-36-37-39)38(27)20-23-15-17-24(18-16-23)25-12-8-9-13-26(25)45(42,43)35-31(41)32-19-22-10-6-5-7-11-22/h5-13,15-18,21H,3-4,14,19-20H2,1-2H3,(H2,32,35,41)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.200	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro binding affinity at Angiotensin II Type 1 receptor in rat liver membrane by [125I]AII displacement.				Bioorg Med Chem Lett 5: 2611-2616 (1995) Article DOI: 10.1016/0960-894X(95)00479-D BindingDB Entry DOI: 10.7270/Q2GT5N57
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50031537 (2-Butyl-3-(N'-propylureidylsulfonyl-biphenyl-4-ylm...) Show SMILES CCCCc1nc(SC)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C26H32N4O5S2/c1-4-6-11-22-28-24(36-3)23(25(31)32)30(22)17-18-12-14-19(15-13-18)20-9-7-8-10-21(20)37(34,35)29-26(33)27-16-5-2/h7-10,12-15H,4-6,11,16-17H2,1-3H3,(H,31,32)(H2,27,29,33)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	0.300	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470249 (CHEMBL309845) Show SMILES CCCCc1nc(SCC(F)(F)C(F)(F)CO)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C29H34F4N4O6S2/c1-3-5-10-23-35-25(44-18-29(32,33)28(30,31)17-38)24(26(39)40)37(23)16-19-11-13-20(14-12-19)21-8-6-7-9-22(21)45(42,43)36-27(41)34-15-4-2/h6-9,11-14,38H,3-5,10,15-18H2,1-2H3,(H,39,40)(H2,34,36,41)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.300	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470223 (CHEMBL312386) Show SMILES CCCCc1nc(Sc2ccccc2)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C31H34N4O5S2/c1-3-5-15-27-33-29(41-24-11-7-6-8-12-24)28(30(36)37)35(27)21-22-16-18-23(19-17-22)25-13-9-10-14-26(25)42(39,40)34-31(38)32-20-4-2/h6-14,16-19H,3-5,15,20-21H2,1-2H3,(H,36,37)(H2,32,34,38)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.300	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470227 (CHEMBL76538) Show SMILES CCCCc1nc(SC)c(C(=O)NC(C(C)CC)C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C32H43N5O6S2/c1-6-9-14-26-34-30(44-5)28(29(38)35-27(31(39)40)21(4)8-3)37(26)20-22-15-17-23(18-16-22)24-12-10-11-13-25(24)45(42,43)36-32(41)33-19-7-2/h10-13,15-18,21,27H,6-9,14,19-20H2,1-5H3,(H,35,38)(H,39,40)(H2,33,36,41)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.300	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470241 (CHEMBL305638) Show SMILES CCCCc1nc(SCCCCOC(C)=O)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C31H40N4O7S2/c1-4-6-13-27-33-29(43-20-10-9-19-42-22(3)36)28(30(37)38)35(27)21-23-14-16-24(17-15-23)25-11-7-8-12-26(25)44(40,41)34-31(39)32-18-5-2/h7-8,11-12,14-17H,4-6,9-10,13,18-21H2,1-3H3,(H,37,38)(H2,32,34,39)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.300	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50285767 (5-alpha-hydroxyacid imidazolyl biphenyl sulfonyl u...) Show SMILES CCCCc1nc(SC)c(n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCc1ccccc1)C(O)(C(O)=O)C(F)(F)F Show InChI InChI=1S/C32H33F3N4O6S2/c1-3-4-14-26-37-28(46-2)27(31(43,29(40)41)32(33,34)35)39(26)20-22-15-17-23(18-16-22)24-12-8-9-13-25(24)47(44,45)38-30(42)36-19-21-10-6-5-7-11-21/h5-13,15-18,43H,3-4,14,19-20H2,1-2H3,(H,40,41)(H2,36,38,42)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.300	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro binding affinity at Angiotensin II Type 1 receptor in rat liver membrane by [125I]AII displacement.				Bioorg Med Chem Lett 5: 2611-2616 (1995) Article DOI: 10.1016/0960-894X(95)00479-D BindingDB Entry DOI: 10.7270/Q2GT5N57
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50285752 (5-alpha-hydroxyacid imidazolyl biphenyl sulfonyl u...) Show SMILES CCCCCCC(O)(C(O)=O)c1c(SC)nc(CCC)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCc1ccccc1 Show InChI InChI=1S/C36H44N4O6S2/c1-4-6-7-13-23-36(44,34(41)42)32-33(47-3)38-31(14-5-2)40(32)25-27-19-21-28(22-20-27)29-17-11-12-18-30(29)48(45,46)39-35(43)37-24-26-15-9-8-10-16-26/h8-12,15-22,44H,4-7,13-14,23-25H2,1-3H3,(H,41,42)(H2,37,39,43)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro binding affinity at Angiotensin II Type 1 receptor in rat liver membrane by [125I]AII displacement.				Bioorg Med Chem Lett 5: 2611-2616 (1995) Article DOI: 10.1016/0960-894X(95)00479-D BindingDB Entry DOI: 10.7270/Q2GT5N57
					More data for this Ligand-Target Pair
Polymerase basic protein 2 (Influenza A virus (strain A/WS/1933 H1N1))	BDBM552303 (US11312727, Compound 123A) Show SMILES Oc1c2C(=O)N3CN([C@H](c4ccccc4C4CC4)c4cccc(Cl)c4OC\C=C\C3)n2ccc1=O |r,t:30| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description EN PA FRET inhibition assay was performed using a 19 nucleotide synthetic oligoribonucleotide substrate: 5′-FAM-AUUUUGUUUUUAAUAUUUC-BHQ-3′...				Citation and Details BindingDB Entry DOI: 10.7270/Q2P272BG
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470228 (CHEMBL80971) Show SMILES CCCCc1nc(SC)c(C(=O)OCC)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C28H36N4O5S2/c1-5-8-13-24-30-26(38-4)25(27(33)37-7-3)32(24)19-20-14-16-21(17-15-20)22-11-9-10-12-23(22)39(35,36)31-28(34)29-18-6-2/h9-12,14-17H,5-8,13,18-19H2,1-4H3,(H2,29,31,34)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470234 (CHEMBL76948) Show SMILES CCCCc1nc(SCCCCO)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C29H38N4O6S2/c1-3-5-12-25-31-27(40-19-9-8-18-34)26(28(35)36)33(25)20-21-13-15-22(16-14-21)23-10-6-7-11-24(23)41(38,39)32-29(37)30-17-4-2/h6-7,10-11,13-16,34H,3-5,8-9,12,17-20H2,1-2H3,(H,35,36)(H2,30,32,37)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50031530 (2-Butyl-4-(methylthio)-1-[[2'-[[[(propylamino)carb...) Show SMILES CCCCc1nc(SC)c(C([O-])=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C26H32N4O5S2/c1-4-6-11-22-28-24(36-3)23(25(31)32)30(22)17-18-12-14-19(15-13-18)20-9-7-8-10-21(20)37(34,35)29-26(33)27-16-5-2/h7-10,12-15H,4-6,11,16-17H2,1-3H3,(H,31,32)(H2,27,29,33)/p-1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.480	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50031530 (2-Butyl-4-(methylthio)-1-[[2'-[[[(propylamino)carb...) Show SMILES CCCCc1nc(SC)c(C([O-])=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C26H32N4O5S2/c1-4-6-11-22-28-24(36-3)23(25(31)32)30(22)17-18-12-14-19(15-13-18)20-9-7-8-10-21(20)37(34,35)29-26(33)27-16-5-2/h7-10,12-15H,4-6,11,16-17H2,1-3H3,(H,31,32)(H2,27,29,33)/p-1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro binding affinity at Angiotensin II Type 1 receptor in rat liver membrane by [125I]AII displacement.				Bioorg Med Chem Lett 5: 2611-2616 (1995) Article DOI: 10.1016/0960-894X(95)00479-D BindingDB Entry DOI: 10.7270/Q2GT5N57
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50285762 (5-alpha-hydroxyacid imidazolyl biphenyl sulfonyl u...) Show SMILES CCCCC(O)(C(O)=O)c1c(SC)nc(CCC)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCc1ccccc1 Show InChI InChI=1S/C34H40N4O6S2/c1-4-6-21-34(42,32(39)40)30-31(45-3)36-29(12-5-2)38(30)23-25-17-19-26(20-18-25)27-15-10-11-16-28(27)46(43,44)37-33(41)35-22-24-13-8-7-9-14-24/h7-11,13-20,42H,4-6,12,21-23H2,1-3H3,(H,39,40)(H2,35,37,41)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro binding affinity at Angiotensin II Type 1 receptor in rat liver membrane by [125I]AII displacement.				Bioorg Med Chem Lett 5: 2611-2616 (1995) Article DOI: 10.1016/0960-894X(95)00479-D BindingDB Entry DOI: 10.7270/Q2GT5N57
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50285770 (5-alpha-hydroxyacid imidazolyl biphenyl sulfonyl u...) Show SMILES CCCCc1nc(SC)c(n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCc1ccccc1)C(C)(O)C(O)=O Show InChI InChI=1S/C32H36N4O6S2/c1-4-5-15-27-34-29(43-3)28(32(2,40)30(37)38)36(27)21-23-16-18-24(19-17-23)25-13-9-10-14-26(25)44(41,42)35-31(39)33-20-22-11-7-6-8-12-22/h6-14,16-19,40H,4-5,15,20-21H2,1-3H3,(H,37,38)(H2,33,35,39)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro binding affinity at Angiotensin II Type 1 receptor in rat liver membrane by [125I]AII displacement.				Bioorg Med Chem Lett 5: 2611-2616 (1995) Article DOI: 10.1016/0960-894X(95)00479-D BindingDB Entry DOI: 10.7270/Q2GT5N57
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50285768 (5-alpha-hydroxyacid imidazolyl biphenyl sulfonyl u...) Show SMILES CCCCc1nc(SC)c(C(O)n2cnnn2)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCc1ccccc1 Show InChI InChI=1S/C31H34N8O4S2/c1-3-4-14-27-34-29(44-2)28(30(40)39-21-33-36-37-39)38(27)20-23-15-17-24(18-16-23)25-12-8-9-13-26(25)45(42,43)35-31(41)32-19-22-10-6-5-7-11-22/h5-13,15-18,21,30,40H,3-4,14,19-20H2,1-2H3,(H2,32,35,41)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro binding affinity at Angiotensin II Type 1 receptor in rat liver membrane by [125I]AII displacement.				Bioorg Med Chem Lett 5: 2611-2616 (1995) Article DOI: 10.1016/0960-894X(95)00479-D BindingDB Entry DOI: 10.7270/Q2GT5N57
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470243 (CHEMBL306157) Show SMILES CCCCc1nc(SC(F)F)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C26H30F2N4O5S2/c1-3-5-10-21-30-23(38-25(27)28)22(24(33)34)32(21)16-17-11-13-18(14-12-17)19-8-6-7-9-20(19)39(36,37)31-26(35)29-15-4-2/h6-9,11-14,25H,3-5,10,15-16H2,1-2H3,(H,33,34)(H2,29,31,35)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.5	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470212 (CHEMBL80622) Show SMILES CCCCc1nc(SC)c(C(=O)OC(C)(C)C)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C30H40N4O5S2/c1-7-9-14-25-32-27(40-6)26(28(35)39-30(3,4)5)34(25)20-21-15-17-22(18-16-21)23-12-10-11-13-24(23)41(37,38)33-29(36)31-19-8-2/h10-13,15-18H,7-9,14,19-20H2,1-6H3,(H2,31,33,36)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.600	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470219 (CHEMBL305604) Show SMILES CCCCc1nc(SCC(F)(F)F)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C27H31F3N4O5S2/c1-3-5-10-22-32-24(40-17-27(28,29)30)23(25(35)36)34(22)16-18-11-13-19(14-12-18)20-8-6-7-9-21(20)41(38,39)33-26(37)31-15-4-2/h6-9,11-14H,3-5,10,15-17H2,1-2H3,(H,35,36)(H2,31,33,37)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.600	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50285763 (5-alpha-hydroxyacid imidazolyl biphenyl sulfonyl u...) Show SMILES CCCc1nc(SC)c(n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCc1ccccc1)C(O)(Cc1ccccc1)C(O)=O Show InChI InChI=1S/C37H38N4O6S2/c1-3-12-32-39-34(48-2)33(37(45,35(42)43)23-26-13-6-4-7-14-26)41(32)25-28-19-21-29(22-20-28)30-17-10-11-18-31(30)49(46,47)40-36(44)38-24-27-15-8-5-9-16-27/h4-11,13-22,45H,3,12,23-25H2,1-2H3,(H,42,43)(H2,38,40,44)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.600	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro binding affinity at Angiotensin II Type 1 receptor in rat liver membrane by [125I]AII displacement.				Bioorg Med Chem Lett 5: 2611-2616 (1995) Article DOI: 10.1016/0960-894X(95)00479-D BindingDB Entry DOI: 10.7270/Q2GT5N57
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50285754 (5-alpha-hydroxyacid imidazolyl biphenyl sulfonyl u...) Show SMILES CCCc1nc(SC)c(n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCc1ccccc1)C(O)(C(O)=O)c1ccccc1 Show InChI InChI=1S/C36H36N4O6S2/c1-3-12-31-38-33(47-2)32(36(44,34(41)42)28-15-8-5-9-16-28)40(31)24-26-19-21-27(22-20-26)29-17-10-11-18-30(29)48(45,46)39-35(43)37-23-25-13-6-4-7-14-25/h4-11,13-22,44H,3,12,23-24H2,1-2H3,(H,41,42)(H2,37,39,43)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.700	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro binding affinity at Angiotensin II Type 1 receptor in rat liver membrane by [125I]AII displacement.				Bioorg Med Chem Lett 5: 2611-2616 (1995) Article DOI: 10.1016/0960-894X(95)00479-D BindingDB Entry DOI: 10.7270/Q2GT5N57
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470214 (CHEMBL77360) Show SMILES CCCCc1nc(SC)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NS(=O)(=O)C(F)(F)F Show InChI InChI=1S/C23H24F3N3O6S3/c1-3-4-9-19-27-21(36-2)20(22(30)31)29(19)14-15-10-12-16(13-11-15)17-7-5-6-8-18(17)37(32,33)28-38(34,35)23(24,25)26/h5-8,10-13,28H,3-4,9,14H2,1-2H3,(H,30,31)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.800	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470217 (CHEMBL77138) Show SMILES CCCCc1nc(SC(F)(F)F)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C26H29F3N4O5S2/c1-3-5-10-21-31-23(39-26(27,28)29)22(24(34)35)33(21)16-17-11-13-18(14-12-17)19-8-6-7-9-20(19)40(37,38)32-25(36)30-15-4-2/h6-9,11-14H,3-5,10,15-16H2,1-2H3,(H,34,35)(H2,30,32,36)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.800	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470240 (CHEMBL432158) Show SMILES CCCCc1nc(SC)c(C(=O)NS(=O)(=O)c2ccccc2)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C32H37N5O6S3/c1-4-6-16-28-34-31(44-3)29(30(38)35-45(40,41)25-12-8-7-9-13-25)37(28)22-23-17-19-24(20-18-23)26-14-10-11-15-27(26)46(42,43)36-32(39)33-21-5-2/h7-15,17-20H,4-6,16,21-22H2,1-3H3,(H,35,38)(H2,33,36,39)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.800	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470230 (CHEMBL76799) Show SMILES CCCCc1nc(SC)c(C(=O)NCC(=O)OC)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C29H37N5O6S2/c1-5-7-12-24-32-28(41-4)26(27(36)31-18-25(35)40-3)34(24)19-20-13-15-21(16-14-20)22-10-8-9-11-23(22)42(38,39)33-29(37)30-17-6-2/h8-11,13-16H,5-7,12,17-19H2,1-4H3,(H,31,36)(H2,30,33,37)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.800	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Endothelin-1 receptor (RAT)	BDBM50093978 (2-(4-Carboxy-cyclohexylmethyl)-4-(6-chloro-benzo[1...) Show SMILES OC(=O)C1CCC(Cn2nc(c(Cc3cc4OCOc4cc3Cl)c2C(O)=O)-c2cccs2)CC1 |(3.14,-11.22,;4.56,-11.81,;4.77,-13.34,;5.78,-10.87,;7.2,-11.46,;8.43,-10.52,;8.23,-8.98,;9.53,-8.16,;9.46,-6.62,;8.16,-5.78,;8.57,-4.28,;10.12,-4.21,;10.96,-2.92,;12.48,-2.92,;13.25,-4.24,;14.81,-4.24,;15.84,-5.36,;17.23,-4.73,;17.06,-3.21,;15.56,-2.9,;14.77,-1.57,;13.25,-1.59,;12.46,-.26,;10.66,-5.65,;12.15,-6.06,;12.55,-7.55,;13.25,-4.98,;7.67,-3.04,;8.15,-1.57,;6.9,-.65,;5.66,-1.57,;6.13,-3.04,;6.81,-8.41,;5.58,-9.35,)| Show InChI InChI=1S/C24H23ClN2O6S/c25-17-10-19-18(32-12-33-19)9-15(17)8-16-21(20-2-1-7-34-20)26-27(22(16)24(30)31)11-13-3-5-14(6-4-13)23(28)29/h1-2,7,9-10,13-14H,3-6,8,11-12H2,(H,28,29)(H,30,31)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.810	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Marion Roussel Curated by ChEMBL					Assay Description In vitro binding affinity to endothelin A receptor in rat heart ventricles				Bioorg Med Chem Lett 10: 2575-8 (2001) BindingDB Entry DOI: 10.7270/Q22R3QW9
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470248 (CHEMBL311847) Show SMILES CCCCc1nc(SC)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCc1cccnc1 Show InChI InChI=1S/C29H31N5O5S2/c1-3-4-11-25-32-27(40-2)26(28(35)36)34(25)19-20-12-14-22(15-13-20)23-9-5-6-10-24(23)41(38,39)33-29(37)31-18-21-8-7-16-30-17-21/h5-10,12-17H,3-4,11,18-19H2,1-2H3,(H,35,36)(H2,31,33,37)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.900	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470224 (CHEMBL311189) Show SMILES CCCCc1nc(SC)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)OC Show InChI InChI=1S/C24H27N3O6S2/c1-4-5-10-20-25-22(34-3)21(23(28)29)27(20)15-16-11-13-17(14-12-16)18-8-6-7-9-19(18)35(31,32)26-24(30)33-2/h6-9,11-14H,4-5,10,15H2,1-3H3,(H,26,30)(H,28,29)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.900	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470208 (CHEMBL80900) Show SMILES CCCCc1nc(SC)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)OCC Show InChI InChI=1S/C25H29N3O6S2/c1-4-6-11-21-26-23(35-3)22(24(29)30)28(21)16-17-12-14-18(15-13-17)19-9-7-8-10-20(19)36(32,33)27-25(31)34-5-2/h7-10,12-15H,4-6,11,16H2,1-3H3,(H,27,31)(H,29,30)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.900	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-2 angiotensin II receptor (Homo sapiens (Human))	BDBM50285762 (5-alpha-hydroxyacid imidazolyl biphenyl sulfonyl u...) Show SMILES CCCCC(O)(C(O)=O)c1c(SC)nc(CCC)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCc1ccccc1 Show InChI InChI=1S/C34H40N4O6S2/c1-4-6-21-34(42,32(39)40)30-31(45-3)36-29(12-5-2)38(30)23-25-17-19-26(20-18-25)27-15-10-11-16-28(27)46(43,44)37-33(41)35-22-24-13-8-7-9-14-24/h7-11,13-20,42H,4-6,12,21-23H2,1-3H3,(H,39,40)(H2,35,37,41)	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.900	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro binding affinity at Angiotensin II Type 2 receptor in rabbit uterus membrane by [125I]-AII displacement.				Bioorg Med Chem Lett 5: 2611-2616 (1995) Article DOI: 10.1016/0960-894X(95)00479-D BindingDB Entry DOI: 10.7270/Q2GT5N57
					More data for this Ligand-Target Pair
Polymerase basic protein 2 (Influenza A virus (strain A/WS/1933 H1N1))	BDBM552356 ((17a*R,*E)-24,25-difluoro-12-hydroxy-2,6,9,17a-tet...) Show SMILES Oc1c2C(=O)N3CN([C@@H]4c5ccccc5SCc5c(F)c(F)cc(OC\C=C/C3)c45)n2ccc1=O |r,c:27| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description EN PA FRET inhibition assay was performed using a 19 nucleotide synthetic oligoribonucleotide substrate: 5′-FAM-AUUUUGUUUUUAAUAUUUC-BHQ-3′...				Citation and Details BindingDB Entry DOI: 10.7270/Q2P272BG
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470231 (CHEMBL76613) Show SMILES CCCCc1nc(Cl)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C25H29ClN4O5S/c1-3-5-10-21-28-23(26)22(24(31)32)30(21)16-17-11-13-18(14-12-17)19-8-6-7-9-20(19)36(34,35)29-25(33)27-15-4-2/h6-9,11-14H,3-5,10,15-16H2,1-2H3,(H,31,32)(H2,27,29,33)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470237 (CHEMBL306778) Show SMILES CCCCc1nc(SC)c(C(O)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(C)=O Show InChI InChI=1S/C24H27N3O5S2/c1-4-5-10-21-25-23(33-3)22(24(29)30)27(21)15-17-11-13-18(14-12-17)19-8-6-7-9-20(19)34(31,32)26-16(2)28/h6-9,11-14H,4-5,10,15H2,1-3H3,(H,26,28)(H,29,30)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Polymerase basic protein 2 (Influenza A virus (strain A/WS/1933 H1N1))	BDBM552337 (US11312727, Compound 136A) Show SMILES Oc1c2C(=O)N3CN([C@H](c4ccccc4C4CC4)c4ccc(F)c(F)c4OC\C=C/C3)n2ccc1=O |r,c:31| Show InChI	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description EN PA FRET inhibition assay was performed using a 19 nucleotide synthetic oligoribonucleotide substrate: 5′-FAM-AUUUUGUUUUUAAUAUUUC-BHQ-3′...				Citation and Details BindingDB Entry DOI: 10.7270/Q2P272BG
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50470246 (CHEMBL306085) Show SMILES CCCCc1nc(SC)c(C(N)=O)n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCCC Show InChI InChI=1S/C26H33N5O4S2/c1-4-6-11-22-29-25(36-3)23(24(27)32)31(22)17-18-12-14-19(15-13-18)20-9-7-8-10-21(20)37(34,35)30-26(33)28-16-5-2/h7-10,12-15H,4-6,11,16-17H2,1-3H3,(H2,27,32)(H2,28,30,33)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst Roussel PGU Cardiovascular Agents Curated by ChEMBL					Assay Description Specific binding inhibition of [125I]AII to Angiotensin II receptor, type 1 in rat liver membrane				J Med Chem 38: 2357-77 (1995) Article DOI: 10.1021/jm00013a013 BindingDB Entry DOI: 10.7270/Q2KK9FH8
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/B (RAT)	BDBM50285764 (5-alpha-hydroxyacid imidazolyl biphenyl sulfonyl u...) Show SMILES CCCCc1nc(SC)c(n1Cc1ccc(cc1)-c1ccccc1S(=O)(=O)NC(=O)NCC1CCCCC1)C(O)(C(O)=O)C(F)(F)F Show InChI InChI=1S/C32H39F3N4O6S2/c1-3-4-14-26-37-28(46-2)27(31(43,29(40)41)32(33,34)35)39(26)20-22-15-17-23(18-16-22)24-12-8-9-13-25(24)47(44,45)38-30(42)36-19-21-10-6-5-7-11-21/h8-9,12-13,15-18,21,43H,3-7,10-11,14,19-20H2,1-2H3,(H,40,41)(H2,36,38,42)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description In vitro binding affinity at Angiotensin II Type 1 receptor in rat liver membrane by [125I]AII displacement.				Bioorg Med Chem Lett 5: 2611-2616 (1995) Article DOI: 10.1016/0960-894X(95)00479-D BindingDB Entry DOI: 10.7270/Q2GT5N57
					More data for this Ligand-Target Pair

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