Compile Data Set for Download or QSAR

Found 52 hits with Last Name = 'ferrari' and Initial = 'bp'   

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 B (RAT)	BDBM50042235 (2-butyl-3-{[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4...) Show SMILES CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1 |t:4| Show InChI InChI=1S/C25H28N6O/c1-2-3-10-22-26-25(15-6-7-16-25)24(32)31(22)17-18-11-13-19(14-12-18)20-8-4-5-9-21(20)23-27-29-30-28-23/h4-5,8-9,11-14H,2-3,6-7,10,15-17H2,1H3,(H,27,28,29,30)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.30	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50009338 ((S)-2-((S)-1-((S)-2-((S)-2-((S)-2-((S)-2-((S)-5-(d...) Show SMILES CNCC(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(O)=O |r,wU:60.63,wD:24.23,36.36,43.43,56.59,17.16,6.5,(6.84,-31.4,;5.3,-31.4,;4.53,-30.07,;2.99,-30.07,;2.22,-31.4,;2.22,-28.73,;2.99,-27.4,;4.53,-27.4,;5.3,-26.07,;4.53,-24.73,;5.3,-23.4,;6.84,-23.4,;7.61,-24.73,;7.61,-22.07,;2.22,-26.07,;2.99,-24.73,;.68,-26.07,;-.09,-24.73,;.68,-23.4,;2.22,-23.4,;-.09,-22.07,;-1.63,-24.73,;-2.4,-23.4,;-2.4,-26.07,;-3.94,-26.07,;-4.71,-24.73,;-6.25,-24.73,;-7.02,-23.4,;-8.56,-23.4,;-9.33,-24.73,;-10.87,-24.73,;-8.56,-26.07,;-7.02,-26.07,;-4.71,-27.4,;-6.25,-27.4,;-3.94,-28.73,;-4.71,-30.07,;-6.25,-30.07,;-7.02,-28.73,;-7.02,-31.4,;-3.94,-31.4,;-2.4,-31.4,;-4.71,-32.73,;-3.94,-34.07,;-4.71,-35.4,;-6.25,-35.4,;-7.15,-34.16,;-8.62,-34.63,;-8.62,-36.17,;-7.15,-36.65,;-2.4,-34.07,;-1.63,-32.73,;-1.63,-35.4,;-2.26,-36.81,;-1.12,-37.84,;.22,-37.07,;-.1,-35.56,;.93,-34.42,;.45,-32.95,;2.42,-34.82,;3.5,-33.73,;3.11,-32.24,;5,-34.13,;6.09,-33.04,;5.39,-35.61,)| Show InChI InChI=1S/C42H65N13O10/c1-22(2)33(53-35(58)28(50-32(57)20-45-6)9-7-15-47-42(43)44)38(61)51-29(17-25-11-13-27(56)14-12-25)36(59)54-34(23(3)4)39(62)52-30(18-26-19-46-21-48-26)40(63)55-16-8-10-31(55)37(60)49-24(5)41(64)65/h11-14,19,21-24,28-31,33-34,45,56H,7-10,15-18,20H2,1-6H3,(H,46,48)(H,49,60)(H,50,57)(H,51,61)(H,52,62)(H,53,58)(H,54,59)(H,64,65)(H4,43,44,47)/t24-,28-,29-,30-,31-,33-,34-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	2.40	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042251 (4'-(2-Butyl-4-oxo-1,3-diaza-spiro[4.5]dec-1-en-3-y...) Show SMILES CCCCC1=NC2(CCCCC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C26H30N2O3/c1-2-3-11-23-27-26(16-7-4-8-17-26)25(31)28(23)18-19-12-14-20(15-13-19)21-9-5-6-10-22(21)24(29)30/h5-6,9-10,12-15H,2-4,7-8,11,16-18H2,1H3,(H,29,30)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	7.20	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042266 (4'-(2-Butyl-4-oxo-1,3-diaza-spiro[4.6]undec-1-en-3...) Show SMILES CCCCC1=NC2(CCCCCC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C27H32N2O3/c1-2-3-12-24-28-27(17-8-4-5-9-18-27)26(32)29(24)19-20-13-15-21(16-14-20)22-10-6-7-11-23(22)25(30)31/h6-7,10-11,13-16H,2-5,8-9,12,17-19H2,1H3,(H,30,31)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	8.70	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042234 (4'-(2-Butyl-4-oxo-1,3-diaza-spiro[4.4]non-1-en-3-y...) Show SMILES CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C25H28N2O3/c1-2-3-10-22-26-25(15-6-7-16-25)24(30)27(22)17-18-11-13-19(14-12-18)20-8-4-5-9-21(20)23(28)29/h4-5,8-9,11-14H,2-3,6-7,10,15-17H2,1H3,(H,28,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50009714 (CHEMBL191 | {2-Butyl-5-chloro-3-[2'-(2H-tetrazol-5...) Show SMILES CCCCC1=NC(Cl)C(CO)N1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1 |t:4| Show InChI InChI=1S/C22H25ClN6O/c1-2-3-8-20-24-21(23)19(14-30)29(20)13-15-9-11-16(12-10-15)17-6-4-5-7-18(17)22-25-27-28-26-22/h4-7,9-12,19,21,30H,2-3,8,13-14H2,1H3,(H,25,26,27,28)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042243 (4'-(8-Acetyl-2-butyl-4-oxo-1,3,8-triaza-spiro[4.5]...) Show SMILES CCCCC1=NC2(CCN(CC2)C(C)=O)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C27H31N3O4/c1-3-4-9-24-28-27(14-16-29(17-15-27)19(2)31)26(34)30(24)18-20-10-12-21(13-11-20)22-7-5-6-8-23(22)25(32)33/h5-8,10-13H,3-4,9,14-18H2,1-2H3,(H,32,33)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	18	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042261 (4'-(2-Butyl-4,4-diisopropyl-5-oxo-4,5-dihydro-imid...) Show SMILES CCCCC1=NC(C(C)C)(C(C)C)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C27H34N2O3/c1-6-7-12-24-28-27(18(2)3,19(4)5)26(32)29(24)17-20-13-15-21(16-14-20)22-10-8-9-11-23(22)25(30)31/h8-11,13-16,18-19H,6-7,12,17H2,1-5H3,(H,30,31)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042225 (4'-(4-Oxo-2-pentyl-1,3-diaza-spiro[4.4]non-1-en-3-...) Show SMILES CCCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:5| Show InChI InChI=1S/C26H30N2O3/c1-2-3-4-11-23-27-26(16-7-8-17-26)25(31)28(23)18-19-12-14-20(15-13-19)21-9-5-6-10-22(21)24(29)30/h5-6,9-10,12-15H,2-4,7-8,11,16-18H2,1H3,(H,29,30)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	24	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042249 (4'-(4-Oxo-2-propyl-1,3-diaza-spiro[4.4]non-1-en-3-...) Show SMILES CCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:3| Show InChI InChI=1S/C24H26N2O3/c1-2-7-21-25-24(14-5-6-15-24)23(29)26(21)16-17-10-12-18(13-11-17)19-8-3-4-9-20(19)22(27)28/h3-4,8-13H,2,5-7,14-16H2,1H3,(H,27,28)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	27	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042244 (4'-(2-Butyl-4,4-dimethyl-5-oxo-4,5-dihydro-imidazo...) Show SMILES CCCCC1=NC(C)(C)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C23H26N2O3/c1-4-5-10-20-24-23(2,3)22(28)25(20)15-16-11-13-17(14-12-16)18-8-6-7-9-19(18)21(26)27/h6-9,11-14H,4-5,10,15H2,1-3H3,(H,26,27)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	35	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042238 (4'-(6-Butyl-8-oxo-5,7-diaza-spiro[3.4]oct-5-en-7-y...) Show SMILES CCCCC1=NC2(CCC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C24H26N2O3/c1-2-3-9-21-25-24(14-6-15-24)23(29)26(21)16-17-10-12-18(13-11-17)19-7-4-5-8-20(19)22(27)28/h4-5,7-8,10-13H,2-3,6,9,14-16H2,1H3,(H,27,28)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	38	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042248 (4'-(2-Butyl-4-oxo-8-oxa-1,3-diaza-spiro[4.5]dec-1-...) Show SMILES CCCCC1=NC2(CCOCC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C25H28N2O4/c1-2-3-8-22-26-25(13-15-31-16-14-25)24(30)27(22)17-18-9-11-19(12-10-18)20-6-4-5-7-21(20)23(28)29/h4-7,9-12H,2-3,8,13-17H2,1H3,(H,28,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	47	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042264 (4'-(8-Benzoyl-2-butyl-4-oxo-1,3,8-triaza-spiro[4.5...) Show SMILES CCCCC1=NC2(CCN(CC2)C(=O)c2ccccc2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C32H33N3O4/c1-2-3-13-28-33-32(18-20-34(21-19-32)29(36)25-9-5-4-6-10-25)31(39)35(28)22-23-14-16-24(17-15-23)26-11-7-8-12-27(26)30(37)38/h4-12,14-17H,2-3,13,18-22H2,1H3,(H,37,38)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	49	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042240 (4'-(2-Butyl-4,4-diethyl-5-oxo-4,5-dihydro-imidazol...) Show SMILES CCCCC1=NC(CC)(CC)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C25H30N2O3/c1-4-7-12-22-26-25(5-2,6-3)24(30)27(22)17-18-13-15-19(16-14-18)20-10-8-9-11-21(20)23(28)29/h8-11,13-16H,4-7,12,17H2,1-3H3,(H,28,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	56	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042237 (4'-[2-Butyl-8-(2-carboxy-acetyl)-4-oxo-1,3,8-triaz...) Show SMILES CCCCC1=NC2(CCN(CC2)C(=O)CC(O)=O)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C28H31N3O6/c1-2-3-8-23-29-28(13-15-30(16-14-28)24(32)17-25(33)34)27(37)31(23)18-19-9-11-20(12-10-19)21-6-4-5-7-22(21)26(35)36/h4-7,9-12H,2-3,8,13-18H2,1H3,(H,33,34)(H,35,36)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	59	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042232 (2-{4-[2-butyl-5-oxospiro[4,5-dihydro-1H-imidazole-...) Show SMILES CCCCC1=NC2(Cc3ccccc3C2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C29H28N2O3/c1-2-3-12-26-30-29(17-22-8-4-5-9-23(22)18-29)28(34)31(26)19-20-13-15-21(16-14-20)24-10-6-7-11-25(24)27(32)33/h4-11,13-16H,2-3,12,17-19H2,1H3,(H,32,33)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042259 (2-[4-(2-butyl-5-oxospiro[4,5-dihydro-1H-imidazole-...) Show SMILES CCCCC1=NC2(C3CC4CC(C3)CC2C4)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4,TLB:15:14:12:9.8.10,5:6:9.8.15:11.12.13,THB:15:9:12:6.14.13,16:6:9.8.15:11.12.13,5:6:12:9.8.10,10:9:6:11.12.13,10:11:6:9.8.15,(3.07,-11.48,;4.4,-10.72,;4.4,-9.18,;5.71,-8.41,;5.73,-6.86,;4.47,-5.97,;4.95,-4.5,;3.57,-3.93,;3.55,-2.36,;4.59,-1.15,;3.25,-1.6,;3.26,-3.09,;2.08,-4.36,;4.57,-3.58,;5.97,-3.23,;5.97,-1.72,;6.5,-4.49,;7.4,-3.25,;6.98,-5.97,;8.06,-7.04,;9.6,-7.04,;10.35,-5.7,;11.88,-5.7,;12.66,-7.04,;11.89,-8.38,;10.35,-8.38,;14.21,-7.04,;14.95,-5.7,;16.5,-5.68,;17.28,-7.02,;16.51,-8.36,;14.97,-8.36,;14.21,-9.72,;12.66,-9.72,;14.97,-11.03,)| Show InChI InChI=1S/C30H34N2O3/c1-2-3-8-27-31-30(23-14-20-13-21(16-23)17-24(30)15-20)29(35)32(27)18-19-9-11-22(12-10-19)25-6-4-5-7-26(25)28(33)34/h4-7,9-12,20-21,23-24H,2-3,8,13-18H2,1H3,(H,33,34)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	62	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042228 (4'-(2-Butyl-8-methyl-4-oxo-1,3-diaza-spiro[4.5]dec...) Show SMILES CCCCC1=NC2(CCC(C)CC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4,(3.07,-11.48,;4.4,-10.72,;4.4,-9.18,;5.71,-8.41,;5.74,-6.86,;4.47,-5.97,;4.95,-4.5,;3.44,-4.66,;2.55,-3.42,;3.17,-2.02,;2.27,-.78,;4.69,-1.86,;5.59,-3.1,;6.5,-4.49,;7.4,-3.25,;6.98,-5.97,;8.06,-7.04,;9.6,-7.04,;10.36,-5.7,;11.88,-5.7,;12.66,-7.04,;11.9,-8.38,;10.36,-8.38,;14.21,-7.04,;14.95,-5.7,;16.5,-5.68,;17.28,-7.02,;16.52,-8.36,;14.98,-8.36,;14.21,-9.72,;12.66,-9.72,;14.98,-11.04,)| Show InChI InChI=1S/C27H32N2O3/c1-3-4-9-24-28-27(16-14-19(2)15-17-27)26(32)29(24)18-20-10-12-21(13-11-20)22-7-5-6-8-23(22)25(30)31/h5-8,10-13,19H,3-4,9,14-18H2,1-2H3,(H,30,31)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	66	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042258 (4'-(2-Butyl-4-thioxo-1,3-diaza-spiro[4.4]non-1-en-...) Show SMILES CCCCC1=NC2(CCCC2)C(=S)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C25H28N2O2S/c1-2-3-10-22-26-25(15-6-7-16-25)24(30)27(22)17-18-11-13-19(14-12-18)20-8-4-5-9-21(20)23(28)29/h4-5,8-9,11-14H,2-3,6-7,10,15-17H2,1H3,(H,28,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	80	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042239 (4'-(2-Butyl-4,4-dicyclopropyl-5-oxo-4,5-dihydro-im...) Show SMILES CCCCC1=NC(C2CC2)(C2CC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C27H30N2O3/c1-2-3-8-24-28-27(20-13-14-20,21-15-16-21)26(32)29(24)17-18-9-11-19(12-10-18)22-6-4-5-7-23(22)25(30)31/h4-7,9-12,20-21H,2-3,8,13-17H2,1H3,(H,30,31)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	80	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042229 (4'-(8-Benzyl-2-butyl-4-oxo-1,3,8-triaza-spiro[4.5]...) Show SMILES CCCCC1=NC2(CCN(Cc3ccccc3)CC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C32H35N3O3/c1-2-3-13-29-33-32(18-20-34(21-19-32)22-24-9-5-4-6-10-24)31(38)35(29)23-25-14-16-26(17-15-25)27-11-7-8-12-28(27)30(36)37/h4-12,14-17H,2-3,13,18-23H2,1H3,(H,36,37)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	110	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042231 (4'-[2-Butyl-4-oxo-8-(2,2,2-trifluoro-acetyl)-1,3,8...) Show SMILES CCCCC1=NC2(CCN(CC2)C(=O)C(F)(F)F)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C27H28F3N3O4/c1-2-3-8-22-31-26(13-15-32(16-14-26)25(37)27(28,29)30)24(36)33(22)17-18-9-11-19(12-10-18)20-6-4-5-7-21(20)23(34)35/h4-7,9-12H,2-3,8,13-17H2,1H3,(H,34,35)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	140	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042267 (4'-(2-Butyl-5-oxo-4,4-dipropyl-4,5-dihydro-imidazo...) Show SMILES CCCCC1=NC(CCC)(CCC)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C27H34N2O3/c1-4-7-12-24-28-27(17-5-2,18-6-3)26(32)29(24)19-20-13-15-21(16-14-20)22-10-8-9-11-23(22)25(30)31/h8-11,13-16H,4-7,12,17-19H2,1-3H3,(H,30,31)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	150	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042230 (2-Butyl-3-[2'-(1-methyl-1H-tetrazol-5-yl)-biphenyl...) Show SMILES CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1-c1nnnn1C |t:4| Show InChI InChI=1S/C26H30N6O/c1-3-4-11-23-27-26(16-7-8-17-26)25(33)32(23)18-19-12-14-20(15-13-19)21-9-5-6-10-22(21)24-28-29-30-31(24)2/h5-6,9-10,12-15H,3-4,7-8,11,16-18H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	150	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042255 (4'-(2-Butyl-4-oxo-1,3-diaza-spiro[4.4]non-3-ylmeth...) Show SMILES CCCCC1NC2(CCCC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O Show InChI InChI=1S/C25H30N2O3/c1-2-3-10-22-26-25(15-6-7-16-25)24(30)27(22)17-18-11-13-19(14-12-18)20-8-4-5-9-21(20)23(28)29/h4-5,8-9,11-14,22,26H,2-3,6-7,10,15-17H2,1H3,(H,28,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	190	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042224 (4'-[8-(2-Amino-5-guanidino-pentanoyl)-2-butyl-4-ox...) Show SMILES CCCCC1=NC2(CCN(CC2)C(=O)C(N)CCCNC(N)=N)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C31H41N7O4/c1-2-3-10-26-36-31(15-18-37(19-16-31)27(39)25(32)9-6-17-35-30(33)34)29(42)38(26)20-21-11-13-22(14-12-21)23-7-4-5-8-24(23)28(40)41/h4-5,7-8,11-14,25H,2-3,6,9-10,15-20,32H2,1H3,(H,40,41)(H4,33,34,35)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	220	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042270 (4'-[8-(2-Amino-3-mercapto-propionyl)-2-butyl-4-oxo...) Show SMILES CCCCC1=NC2(CCN(CC2)C(=O)C(N)CS)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C28H34N4O4S/c1-2-3-8-24-30-28(13-15-31(16-14-28)25(33)23(29)18-37)27(36)32(24)17-19-9-11-20(12-10-19)21-6-4-5-7-22(21)26(34)35/h4-7,9-12,23,37H,2-3,8,13-18,29H2,1H3,(H,34,35)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	250	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042245 (4'-(2-Butyl-4-oxo-8-phenyl-1,3-diaza-spiro[4.5]dec...) Show SMILES CCCCC1=NC2(CCC(CC2)c2ccccc2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4,(3.08,-11.51,;4.41,-10.74,;4.41,-9.2,;5.73,-8.43,;5.75,-6.88,;4.48,-5.98,;4.96,-4.51,;5.6,-3.11,;4.71,-1.86,;3.17,-2.02,;2.56,-3.43,;3.45,-4.67,;2.28,-.78,;.78,-.94,;-.12,.31,;.51,1.71,;2.02,1.85,;2.92,.61,;6.52,-4.5,;7.42,-3.26,;7,-5.98,;8.08,-7.06,;9.63,-7.06,;10.38,-8.4,;11.93,-8.4,;12.69,-7.06,;11.92,-5.72,;10.38,-5.72,;14.25,-7.06,;14.99,-5.72,;16.55,-5.7,;17.32,-7.04,;16.56,-8.38,;15.01,-8.38,;14.25,-9.74,;12.69,-9.74,;15.01,-11.06,)| Show InChI InChI=1S/C32H34N2O3/c1-2-3-13-29-33-32(20-18-25(19-21-32)24-9-5-4-6-10-24)31(37)34(29)22-23-14-16-26(17-15-23)27-11-7-8-12-28(27)30(35)36/h4-12,14-17,25H,2-3,13,18-22H2,1H3,(H,35,36)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	260	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042265 (4'-(5-Butyl-7-oxo-4,6-diaza-spiro[2.4]hept-4-en-6-...) Show SMILES CCCCC1=NC2(CC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C23H24N2O3/c1-2-3-8-20-24-23(13-14-23)22(28)25(20)15-16-9-11-17(12-10-16)18-6-4-5-7-19(18)21(26)27/h4-7,9-12H,2-3,8,13-15H2,1H3,(H,26,27)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	260	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042221 (4'-(2-Butyl-4-oxo-1,3-diaza-spiro[4.10]pentadec-1-...) Show SMILES CCCCC1=NC2(CCCCCCCCCC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C31H40N2O3/c1-2-3-16-28-32-31(21-12-8-6-4-5-7-9-13-22-31)30(36)33(28)23-24-17-19-25(20-18-24)26-14-10-11-15-27(26)29(34)35/h10-11,14-15,17-20H,2-9,12-13,16,21-23H2,1H3,(H,34,35)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	350	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042246 (4'-(2-Cyclopentyl-4-oxo-1,3-diaza-spiro[4.4]non-1-...) Show SMILES OC(=O)c1ccccc1-c1ccc(CN2C(=NC3(CCCC3)C2=O)C2CCCC2)cc1 |c:16| Show InChI InChI=1S/C26H28N2O3/c29-24(30)22-10-4-3-9-21(22)19-13-11-18(12-14-19)17-28-23(20-7-1-2-8-20)27-26(25(28)31)15-5-6-16-26/h3-4,9-14,20H,1-2,5-8,15-17H2,(H,29,30)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	410	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042242 (4'-(2-Butyl-4-oxo-1,3-diaza-spiro[4.4]non-1-en-3-y...) Show SMILES CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C#N |t:4| Show InChI InChI=1S/C25H27N3O/c1-2-3-10-23-27-25(15-6-7-16-25)24(29)28(23)18-19-11-13-20(14-12-19)22-9-5-4-8-21(22)17-26/h4-5,8-9,11-14H,2-3,6-7,10,15-16,18H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	440	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042262 (4'-[2-Butyl-8-(2-carboxy-benzoyl)-4-oxo-1,3,8-tria...) Show SMILES CCCCC1=NC2(CCN(CC2)C(=O)c2ccccc2C(O)=O)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C33H33N3O6/c1-2-3-12-28-34-33(17-19-35(20-18-33)29(37)25-9-5-7-11-27(25)31(40)41)32(42)36(28)21-22-13-15-23(16-14-22)24-8-4-6-10-26(24)30(38)39/h4-11,13-16H,2-3,12,17-21H2,1H3,(H,38,39)(H,40,41)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	480	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042223 (2-Butyl-3-[2'-(2-methyl-2H-tetrazol-5-yl)-biphenyl...) Show SMILES CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1-c1nnn(C)n1 |t:4| Show InChI InChI=1S/C26H30N6O/c1-3-4-11-23-27-26(16-7-8-17-26)25(33)32(23)18-19-12-14-20(15-13-19)21-9-5-6-10-22(21)24-28-30-31(2)29-24/h5-6,9-10,12-15H,3-4,7-8,11,16-18H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	660	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042254 (4'-[8-(2-Amino-3-methyl-pentanoyl)-2-butyl-4-oxo-1...) Show SMILES CCCCC1=NC2(CCN(CC2)C(=O)C(N)C(C)CC)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C31H40N4O4/c1-4-6-11-26-33-31(16-18-34(19-17-31)28(36)27(32)21(3)5-2)30(39)35(26)20-22-12-14-23(15-13-22)24-9-7-8-10-25(24)29(37)38/h7-10,12-15,21,27H,4-6,11,16-20,32H2,1-3H3,(H,37,38)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	730	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042253 (4'-[8-(2-Amino-3-carboxy-propionyl)-2-butyl-4-oxo-...) Show SMILES CCCCC1=NC2(CCN(CC2)C(=O)C(N)CC(O)=O)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C29H34N4O6/c1-2-3-8-24-31-29(13-15-32(16-14-29)26(36)23(30)17-25(34)35)28(39)33(24)18-19-9-11-20(12-10-19)21-6-4-5-7-22(21)27(37)38/h4-7,9-12,23H,2-3,8,13-18,30H2,1H3,(H,34,35)(H,37,38)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	800	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042257 (4'-(2-Butyl-4-oxo-1,3,8-triaza-spiro[4.5]dec-1-en-...) Show SMILES CCCCC1=NC2(CCNCC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C25H29N3O3/c1-2-3-8-22-27-25(13-15-26-16-14-25)24(31)28(22)17-18-9-11-19(12-10-18)20-6-4-5-7-21(20)23(29)30/h4-7,9-12,26H,2-3,8,13-17H2,1H3,(H,29,30)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	890	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042269 (4'-(2-Butyl-8-carboxymethyl-4-oxo-1,3,8-triaza-spi...) Show SMILES CCCCC1=NC2(CCN(CC(O)=O)CC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C27H31N3O5/c1-2-3-8-23-28-27(13-15-29(16-14-27)18-24(31)32)26(35)30(23)17-19-9-11-20(12-10-19)21-6-4-5-7-22(21)25(33)34/h4-7,9-12H,2-3,8,13-18H2,1H3,(H,31,32)(H,33,34)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	950	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042222 (4'-(2,4,4-Tributyl-5-oxo-4,5-dihydro-imidazol-1-yl...) Show SMILES CCCCC1=NC(CCCC)(CCCC)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C29H38N2O3/c1-4-7-14-26-30-29(19-8-5-2,20-9-6-3)28(34)31(26)21-22-15-17-23(18-16-22)24-12-10-11-13-25(24)27(32)33/h10-13,15-18H,4-9,14,19-21H2,1-3H3,(H,32,33)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042227 (4'-(2-Butyl-4-oxo-1,3-diaza-spiro[4.4]non-2-en-1-y...) Show SMILES CCCCC1=NC(=O)C2(CCCC2)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C25H28N2O3/c1-2-3-10-22-26-24(30)25(15-6-7-16-25)27(22)17-18-11-13-19(14-12-18)20-8-4-5-9-21(20)23(28)29/h4-5,8-9,11-14H,2-3,6-7,10,15-17H2,1H3,(H,28,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042247 (4'-(2-Butyl-4-oxo-1,3-diaza-spiro[4.4]non-1-en-3-y...) Show SMILES CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(=O)OC |t:4| Show InChI InChI=1S/C26H30N2O3/c1-3-4-11-23-27-26(16-7-8-17-26)25(30)28(23)18-19-12-14-20(15-13-19)21-9-5-6-10-22(21)24(29)31-2/h5-6,9-10,12-15H,3-4,7-8,11,16-18H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042241 (4'-(2-Butyl-4,4-diisobutyl-5-oxo-4,5-dihydro-imida...) Show SMILES CCCCC1=NC(CC(C)C)(CC(C)C)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:4| Show InChI InChI=1S/C29H38N2O3/c1-6-7-12-26-30-29(17-20(2)3,18-21(4)5)28(34)31(26)19-22-13-15-23(16-14-22)24-10-8-9-11-25(24)27(32)33/h8-11,13-16,20-21H,6-7,12,17-19H2,1-5H3,(H,32,33)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042236 (4'-(2-Benzyl-4-oxo-1,3-diaza-spiro[4.4]non-1-en-3-...) Show SMILES OC(=O)c1ccccc1-c1ccc(CN2C(Cc3ccccc3)=NC3(CCCC3)C2=O)cc1 |c:24| Show InChI InChI=1S/C28H26N2O3/c31-26(32)24-11-5-4-10-23(24)22-14-12-21(13-15-22)19-30-25(18-20-8-2-1-3-9-20)29-28(27(30)33)16-6-7-17-28/h1-5,8-15H,6-7,16-19H2,(H,31,32)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042256 (4'-(2-Butyl-5-oxo-4,4-diphenyl-4,5-dihydro-imidazo...) Show SMILES CCCCC1=NC(C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O)(c1ccccc1)c1ccccc1 |t:4| Show InChI InChI=1S/C33H30N2O3/c1-2-3-18-30-34-33(26-12-6-4-7-13-26,27-14-8-5-9-15-27)32(38)35(30)23-24-19-21-25(22-20-24)28-16-10-11-17-29(28)31(36)37/h4-17,19-22H,2-3,18,23H2,1H3,(H,36,37)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042226 (4'-(2-Butyl-4-oxo-1,3-diaza-spiro[4.4]non-1-en-3-y...) Show SMILES CCCCC1=NC2(CCCC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(=O)OC(C)(C)C |t:4| Show InChI InChI=1S/C29H36N2O3/c1-5-6-13-25-30-29(18-9-10-19-29)27(33)31(25)20-21-14-16-22(17-15-21)23-11-7-8-12-24(23)26(32)34-28(2,3)4/h7-8,11-12,14-17H,5-6,9-10,13,18-20H2,1-4H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042250 (4'-(2-Butyl-4-oxo-1,3-diaza-spiro[4.4]non-1-ylmeth...) Show SMILES CCCCC1NC(=O)C2(CCCC2)N1Cc1ccc(cc1)-c1ccccc1C(O)=O Show InChI InChI=1S/C25H30N2O3/c1-2-3-10-22-26-24(30)25(15-6-7-16-25)27(22)17-18-11-13-19(14-12-18)20-8-4-5-9-21(20)23(28)29/h4-5,8-9,11-14,22H,2-3,6-7,10,15-17H2,1H3,(H,26,30)(H,28,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042263 (4'-(4-Oxo-2-phenyl-1,3-diaza-spiro[4.4]non-1-en-3-...) Show SMILES OC(=O)c1ccccc1-c1ccc(CN2C(=O)C3(CCCC3)N=C2c2ccccc2)cc1 |c:24| Show InChI InChI=1S/C27H24N2O3/c30-25(31)23-11-5-4-10-22(23)20-14-12-19(13-15-20)18-29-24(21-8-2-1-3-9-21)28-27(26(29)32)16-6-7-17-27/h1-5,8-15H,6-7,16-18H2,(H,30,31)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042233 (4'-(2-Methyl-4-oxo-1,3-diaza-spiro[4.4]non-1-en-3-...) Show SMILES CC1=NC2(CCCC2)C(=O)N1Cc1ccc(cc1)-c1ccccc1C(O)=O |t:1| Show InChI InChI=1S/C22H22N2O3/c1-15-23-22(12-4-5-13-22)21(27)24(15)14-16-8-10-17(11-9-16)18-6-2-3-7-19(18)20(25)26/h2-3,6-11H,4-5,12-14H2,1H3,(H,25,26)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	7.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor B (RAT)	BDBM50042252 (4'-(2-Heptafluoropropyl-4-oxo-1,3-diaza-spiro[4.4]...) Show SMILES OC(=O)c1ccccc1-c1ccc(CN2C(=O)C3(CCCC3)N=C2C(F)(F)C(F)(F)C(F)(F)F)cc1 |c:24| Show InChI InChI=1S/C24H19F7N2O3/c25-22(26,23(27,28)24(29,30)31)19-32-21(11-3-4-12-21)20(36)33(19)13-14-7-9-15(10-8-14)16-5-1-2-6-17(16)18(34)35/h1-2,5-10H,3-4,11-13H2,(H,34,35)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Sanofi Recherche Curated by ChEMBL					Assay Description Binding affinity for Angiotensin II receptor, type 1 measured by ability to displace [125I]- A II from its specific binding site in rat liver membran...				J Med Chem 36: 3371-80 (1993) BindingDB Entry DOI: 10.7270/Q22Z14M0
					More data for this Ligand-Target Pair

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