Compile Data Set for Download or QSAR

Found 542 hits with Last Name = 'belvisi' and Initial = 'l'   

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 (Bos taurus)	BDBM50029903 (3-Benzyl-6-butyl-2-methyl-5-[2'-(1H-tetrazol-5-yl)...) Show SMILES CCCCc1nc(C)n(Cc2ccccc2)c(=O)c1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1 Show InChI InChI=1S/C30H30N6O/c1-3-4-14-28-27(30(37)36(21(2)31-28)20-23-10-6-5-7-11-23)19-22-15-17-24(18-16-22)25-12-8-9-13-26(25)29-32-34-35-33-29/h5-13,15-18H,3-4,14,19-20H2,1-2H3,(H,32,33,34,35)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50029911 (2-{4-Butyl-2-methyl-6-oxo-5-[2'-(1H-tetrazol-5-yl)...) Show SMILES CCCCc1nc(C)n(Cc2ccccc2C(O)=O)c(=O)c1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1 Show InChI InChI=1S/C31H30N6O3/c1-3-4-13-28-27(30(38)37(20(2)32-28)19-23-9-5-6-11-25(23)31(39)40)18-21-14-16-22(17-15-21)24-10-7-8-12-26(24)29-33-35-36-34-29/h5-12,14-17H,3-4,13,18-19H2,1-2H3,(H,39,40)(H,33,34,35,36)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50029896 (4'-(2-Butyl-6-oxo-6H-pyrimidin-1-ylmethyl)-bipheny...) Show SMILES CCCCc1nccc(=O)n1Cc1ccc(cc1)-c1ccccc1C(O)=O Show InChI InChI=1S/C22H22N2O3/c1-2-3-8-20-23-14-13-21(25)24(20)15-16-9-11-17(12-10-16)18-6-4-5-7-19(18)22(26)27/h4-7,9-14H,2-3,8,15H2,1H3,(H,26,27)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50241491 (2-{4-Butyl-2-methyl-6-oxo-5-[2'-(1H-tetrazol-5-yl)...) Show SMILES CCCCc1nc(C)n(Cc2sccc2C(=O)OC)c(=O)c1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1 Show InChI InChI=1S/C30H30N6O3S/c1-4-5-10-26-25(29(37)36(19(2)31-26)18-27-24(15-16-40-27)30(38)39-3)17-20-11-13-21(14-12-20)22-8-6-7-9-23(22)28-32-34-35-33-28/h6-9,11-16H,4-5,10,17-18H2,1-3H3,(H,32,33,34,35)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50241501 (6-Butyl-2-methyl-5-[2'-(1H-tetrazol-5-yl)-biphenyl...) Show SMILES CCCCc1nc(C)n(Cc2cccs2)c(=O)c1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1 Show InChI InChI=1S/C28H28N6OS/c1-3-4-11-26-25(28(35)34(19(2)29-26)18-22-8-7-16-36-22)17-20-12-14-21(15-13-20)23-9-5-6-10-24(23)27-30-32-33-31-27/h5-10,12-16H,3-4,11,17-18H2,1-2H3,(H,30,31,32,33)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50029892 (2-{4-Butyl-2-methyl-6-oxo-5-[2'-(1H-tetrazol-5-yl)...) Show SMILES CCCCc1nc(C)n(Cc2sccc2C(O)=O)c(=O)c1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1 Show InChI InChI=1S/C29H28N6O3S/c1-3-4-9-25-24(28(36)35(18(2)30-25)17-26-23(29(37)38)14-15-39-26)16-19-10-12-20(13-11-19)21-7-5-6-8-22(21)27-31-33-34-32-27/h5-8,10-15H,3-4,9,16-17H2,1-2H3,(H,37,38)(H,31,32,33,34)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50029901 (2-{4-Butyl-2-methyl-6-oxo-5-[2'-(1H-tetrazol-5-yl)...) Show SMILES CCCCc1nc(C)n(Cc2occc2C(=O)OC)c(=O)c1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1 Show InChI InChI=1S/C30H30N6O4/c1-4-5-10-26-25(29(37)36(19(2)31-26)18-27-24(15-16-40-27)30(38)39-3)17-20-11-13-21(14-12-20)22-8-6-7-9-23(22)28-32-34-35-33-28/h6-9,11-16H,4-5,10,17-18H2,1-3H3,(H,32,33,34,35)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50029897 (4'-[4-Butyl-1-(4-carboxy-benzyl)-6-oxo-1,6-dihydro...) Show SMILES CCCCc1ncn(Cc2ccc(cc2)C(O)=O)c(=O)c1Cc1ccc(cc1)-c1ccccc1C(O)=O Show InChI InChI=1S/C30H28N2O5/c1-2-3-8-27-26(28(33)32(19-31-27)18-21-11-15-23(16-12-21)29(34)35)17-20-9-13-22(14-10-20)24-6-4-5-7-25(24)30(36)37/h4-7,9-16,19H,2-3,8,17-18H2,1H3,(H,34,35)(H,36,37)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50029902 (6-Butyl-2-methyl-5-[2'-(1H-tetrazol-5-yl)-biphenyl...) Show SMILES CCCCc1nc(C)[nH]c(=O)c1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1 Show InChI InChI=1S/C23H24N6O/c1-3-4-9-21-20(23(30)25-15(2)24-21)14-16-10-12-17(13-11-16)18-7-5-6-8-19(18)22-26-28-29-27-22/h5-8,10-13H,3-4,9,14H2,1-2H3,(H,24,25,30)(H,26,27,28,29)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50029904 (4'-[4-Butyl-1-(2-carboxy-benzyl)-2-methyl-6-oxo-1,...) Show SMILES CCCCc1nc(C)n(Cc2ccccc2C(O)=O)c(=O)c1Cc1ccc(cc1)-c1ccccc1C(O)=O Show InChI InChI=1S/C31H30N2O5/c1-3-4-13-28-27(18-21-14-16-22(17-15-21)24-10-7-8-12-26(24)31(37)38)29(34)33(20(2)32-28)19-23-9-5-6-11-25(23)30(35)36/h5-12,14-17H,3-4,13,18-19H2,1-2H3,(H,35,36)(H,37,38)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50029894 (4'-(4-Butyl-2-methyl-6-oxo-1,6-dihydro-pyrimidin-5...) Show SMILES CCCCc1nc(C)[nH]c(=O)c1Cc1ccc(cc1)-c1ccccc1C(O)=O Show InChI InChI=1S/C23H24N2O3/c1-3-4-9-21-20(22(26)25-15(2)24-21)14-16-10-12-17(13-11-16)18-7-5-6-8-19(18)23(27)28/h5-8,10-13H,3-4,9,14H2,1-2H3,(H,27,28)(H,24,25,26)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50029895 (2-{4-Butyl-2-methyl-6-oxo-5-[2'-(1H-tetrazol-5-yl)...) Show SMILES CCCCc1nc(C)n(Cc2occc2C(O)=O)c(=O)c1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1 Show InChI InChI=1S/C29H28N6O4/c1-3-4-9-25-24(28(36)35(18(2)30-25)17-26-23(29(37)38)14-15-39-26)16-19-10-12-20(13-11-19)21-7-5-6-8-22(21)27-31-33-34-32-27/h5-8,10-15H,3-4,9,16-17H2,1-2H3,(H,37,38)(H,31,32,33,34)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50029905 (4'-(2-Butyl-4-methyl-6-oxo-6H-pyrimidin-1-ylmethyl...) Show SMILES CCCCc1nc(C)cc(=O)n1Cc1ccc(cc1)-c1ccccc1C(O)=O Show InChI InChI=1S/C23H24N2O3/c1-3-4-9-21-24-16(2)14-22(26)25(21)15-17-10-12-18(13-11-17)19-7-5-6-8-20(19)23(27)28/h5-8,10-14H,3-4,9,15H2,1-2H3,(H,27,28)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50029899 (3-{4-Butyl-2-methyl-6-oxo-5-[2'-(1H-tetrazol-5-yl)...) Show SMILES CCCCc1nc(C)n(Cc2ccsc2C(=O)OC)c(=O)c1Cc1ccc(cc1)-c1ccccc1-c1nnn[nH]1 Show InChI InChI=1S/C30H30N6O3S/c1-4-5-10-26-25(29(37)36(19(2)31-26)18-22-15-16-40-27(22)30(38)39-3)17-20-11-13-21(14-12-20)23-8-6-7-9-24(23)28-32-34-35-33-28/h6-9,11-16H,4-5,10,17-18H2,1-3H3,(H,32,33,34,35)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50029908 (4'-(4-Butyl-6-oxo-1-thiophen-2-ylmethyl-1,6-dihydr...) Show SMILES CCCCc1ncn(Cc2cccs2)c(=O)c1Cc1ccc(cc1)-c1ccccc1C(O)=O Show InChI InChI=1S/C27H26N2O3S/c1-2-3-10-25-24(26(30)29(18-28-25)17-21-7-6-15-33-21)16-19-11-13-20(14-12-19)22-8-4-5-9-23(22)27(31)32/h4-9,11-15,18H,2-3,10,16-17H2,1H3,(H,31,32)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50029893 (2-[4-Butyl-5-(2'-carboxy-biphenyl-4-ylmethyl)-2-me...) Show SMILES CCCCc1nc(C)n(Cc2occc2C(O)=O)c(=O)c1Cc1ccc(cc1)-c1ccccc1C(O)=O Show InChI InChI=1S/C29H28N2O6/c1-3-4-9-25-24(27(32)31(18(2)30-25)17-26-23(29(35)36)14-15-37-26)16-19-10-12-20(13-11-19)21-7-5-6-8-22(21)28(33)34/h5-8,10-15H,3-4,9,16-17H2,1-2H3,(H,33,34)(H,35,36)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50029906 (2-[4-Butyl-5-(2'-carboxy-biphenyl-4-ylmethyl)-2-me...) Show SMILES CCCCc1nc(C)n(Cc2sccc2C(O)=O)c(=O)c1Cc1ccc(cc1)-c1ccccc1C(O)=O Show InChI InChI=1S/C29H28N2O5S/c1-3-4-9-25-24(27(32)31(18(2)30-25)17-26-23(29(35)36)14-15-37-26)16-19-10-12-20(13-11-19)21-7-5-6-8-22(21)28(33)34/h5-8,10-15H,3-4,9,16-17H2,1-2H3,(H,33,34)(H,35,36)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50029909 (4'-[4-Butyl-1-(2-carboxy-benzyl)-6-oxo-1,6-dihydro...) Show SMILES CCCCc1ncn(Cc2ccccc2C(O)=O)c(=O)c1Cc1ccc(cc1)-c1ccccc1C(O)=O Show InChI InChI=1S/C30H28N2O5/c1-2-3-12-27-26(28(33)32(19-31-27)18-22-8-4-5-10-24(22)29(34)35)17-20-13-15-21(16-14-20)23-9-6-7-11-25(23)30(36)37/h4-11,13-16,19H,2-3,12,17-18H2,1H3,(H,34,35)(H,36,37)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50029907 (4'-(1-Benzyl-4-butyl-6-oxo-1,6-dihydro-pyrimidin-5...) Show SMILES CCCCc1ncn(Cc2ccccc2)c(=O)c1Cc1ccc(cc1)-c1ccccc1C(O)=O Show InChI InChI=1S/C29H28N2O3/c1-2-3-13-27-26(28(32)31(20-30-27)19-22-9-5-4-6-10-22)18-21-14-16-23(17-15-21)24-11-7-8-12-25(24)29(33)34/h4-12,14-17,20H,2-3,13,18-19H2,1H3,(H,33,34)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor (Bos taurus)	BDBM50029910 (4'-(4-Butyl-6-oxo-1,6-dihydro-pyrimidin-5-ylmethyl...) Show SMILES CCCCc1nc[nH]c(=O)c1Cc1ccc(cc1)-c1ccccc1C(O)=O Show InChI InChI=1S/C22H22N2O3/c1-2-3-8-20-19(21(25)24-14-23-20)13-15-9-11-16(12-10-15)17-6-4-5-7-18(17)22(26)27/h4-7,9-12,14H,2-3,8,13H2,1H3,(H,26,27)(H,23,24,25)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	>4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Binding affinity towards Angiotensin II type 2 receptor in bovine cerebellar cortical membranes; Inactive				J Med Chem 38: 4806-20 (1996) BindingDB Entry DOI: 10.7270/Q2JQ101N
					More data for this Ligand-Target Pair
Baculoviral IAP repeat-containing protein 3 (Homo sapiens (Human))	BDBM13211 ((3S,6S,9aS)-6-[(2S)-2-aminobutanamido]-N-(diphenyl...) Show SMILES CC[C@H](N)C(=O)N[C@H]1CCC[C@H]2CC[C@H](N2C1=O)C(=O)NC(c1ccccc1)c1ccccc1 |r| Show InChI InChI=1S/C27H34N4O3/c1-2-21(28)25(32)29-22-15-9-14-20-16-17-23(31(20)27(22)34)26(33)30-24(18-10-5-3-6-11-18)19-12-7-4-8-13-19/h3-8,10-13,20-24H,2,9,14-17,28H2,1H3,(H,29,32)(H,30,33)/t20-,21-,22-,23-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	25	-43.1	460	n/a	n/a	n/a	n/a	7.5	23
Universita degli Studi di Milano					Assay Description Fluorescence polarization was measured on an Ultra plate reader (Tecan) at excitation and emission wavelengths of 485 and 530 nm, respectively. The e...				Bioorg Med Chem 17: 5834-56 (2009) Article DOI: 10.1016/j.bmc.2009.07.009 BindingDB Entry DOI: 10.7270/Q28W3BNV
					More data for this Ligand-Target Pair
Baculoviral IAP repeat-containing protein 3 (Homo sapiens (Human))	BDBM13212 ((3S,6S,9aS)-N-(diphenylmethyl)-6-[(2S)-2-(methylam...) Show SMILES CC[C@H](NC)C(=O)N[C@H]1CCC[C@H]2CC[C@H](N2C1=O)C(=O)NC(c1ccccc1)c1ccccc1 |r| Show InChI InChI=1S/C28H36N4O3/c1-3-22(29-2)26(33)30-23-16-10-15-21-17-18-24(32(21)28(23)35)27(34)31-25(19-11-6-4-7-12-19)20-13-8-5-9-14-20/h4-9,11-14,21-25,29H,3,10,15-18H2,1-2H3,(H,30,33)(H,31,34)/t21-,22-,23-,24-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	61	-40.9	530	n/a	n/a	n/a	n/a	7.5	23
Universita degli Studi di Milano					Assay Description Fluorescence polarization was measured on an Ultra plate reader (Tecan) at excitation and emission wavelengths of 485 and 530 nm, respectively. The e...				Bioorg Med Chem 17: 5834-56 (2009) Article DOI: 10.1016/j.bmc.2009.07.009 BindingDB Entry DOI: 10.7270/Q28W3BNV
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/Type-1 angiotensin II receptor B/Type-2 angiotensin II receptor (RAT)	BDBM50003399 (4'-(2-Butyl-4-chloro-5-hydroxymethyl-imidazol-1-yl...) Show SMILES CCCCc1nc(Cl)c(CO)n1Cc1ccc(cc1)-c1ccccc1C(O)=O Show InChI InChI=1S/C22H23ClN2O3/c1-2-3-8-20-24-21(23)19(14-26)25(20)13-15-9-11-16(12-10-15)17-6-4-5-7-18(17)22(27)28/h4-7,9-12,26H,2-3,8,13-14H2,1H3,(H,27,28)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	350	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Tested for the binding affinity using radioligand [125I]-Sar1 Ile8-AII in the rat adrenal capsular membranes (adrenal cortex)				J Med Chem 37: 3928-38 (1994) Article DOI: 10.1021/jm00049a012 BindingDB Entry DOI: 10.7270/Q2W098NX
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/Type-1 angiotensin II receptor B/Type-2 angiotensin II receptor (RAT)	BDBM50470054 (CHEMBL129225) Show SMILES CCCCc1nc(Cl)c(CO)n1Cc1ccc(cc1)-c1cccnc1C(O)=O Show InChI InChI=1S/C21H22ClN3O3/c1-2-3-6-18-24-20(22)17(13-26)25(18)12-14-7-9-15(10-8-14)16-5-4-11-23-19(16)21(27)28/h4-5,7-11,26H,2-3,6,12-13H2,1H3,(H,27,28)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Tested for the binding affinity using radioligand [125I]-Sar1 Ile8-AII in the rat adrenal capsular membranes (adrenal cortex)				J Med Chem 37: 3928-38 (1994) Article DOI: 10.1021/jm00049a012 BindingDB Entry DOI: 10.7270/Q2W098NX
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/Type-1 angiotensin II receptor B/Type-2 angiotensin II receptor (RAT)	BDBM50470049 (CHEMBL340682) Show SMILES CCCCc1nc(Cl)c(CO)n1Cc1ccc(cc1)-c1cnccc1C(O)=O Show InChI InChI=1S/C21H22ClN3O3/c1-2-3-4-19-24-20(22)18(13-26)25(19)12-14-5-7-15(8-6-14)17-11-23-10-9-16(17)21(27)28/h5-11,26H,2-4,12-13H2,1H3,(H,27,28)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	6.70E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Tested for the binding affinity using radioligand [125I]-Sar1 Ile8-AII in the rat adrenal capsular membranes (adrenal cortex)				J Med Chem 37: 3928-38 (1994) Article DOI: 10.1021/jm00049a012 BindingDB Entry DOI: 10.7270/Q2W098NX
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/Type-1 angiotensin II receptor B/Type-2 angiotensin II receptor (RAT)	BDBM50470051 (CHEMBL339044) Show SMILES CCCCc1nc(CO)c(Cl)n1Cc1ccc(o1)-c1ccccc1C(O)=O Show InChI InChI=1S/C20H21ClN2O4/c1-2-3-8-18-22-16(12-24)19(21)23(18)11-13-9-10-17(27-13)14-6-4-5-7-15(14)20(25)26/h4-7,9-10,24H,2-3,8,11-12H2,1H3,(H,25,26)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	9.70E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Tested for the binding affinity using radioligand [125I]-Sar1 Ile8-AII in the rat adrenal capsular membranes (adrenal cortex)				J Med Chem 37: 3928-38 (1994) Article DOI: 10.1021/jm00049a012 BindingDB Entry DOI: 10.7270/Q2W098NX
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/Type-1 angiotensin II receptor B/Type-2 angiotensin II receptor (RAT)	BDBM50470050 (CHEMBL129170) Show SMILES CCCCc1nc(Cl)c(CO)n1Cc1ccc(cc1)-c1ncccc1C(O)=O Show InChI InChI=1S/C21H22ClN3O3/c1-2-3-6-18-24-20(22)17(13-26)25(18)12-14-7-9-15(10-8-14)19-16(21(27)28)5-4-11-23-19/h4-5,7-11,26H,2-3,6,12-13H2,1H3,(H,27,28)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	9.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Tested for the binding affinity using radioligand [125I]-Sar1 Ile8-AII in the rat adrenal capsular membranes (adrenal cortex)				J Med Chem 37: 3928-38 (1994) Article DOI: 10.1021/jm00049a012 BindingDB Entry DOI: 10.7270/Q2W098NX
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/Type-1 angiotensin II receptor B/Type-2 angiotensin II receptor (RAT)	BDBM50470052 (CHEMBL127108) Show SMILES CCCCc1nc(Cl)c(CO)n1Cc1ccc(cc1)-c1ccoc1C(O)=O Show InChI InChI=1S/C20H21ClN2O4/c1-2-3-4-17-22-19(21)16(12-24)23(17)11-13-5-7-14(8-6-13)15-9-10-27-18(15)20(25)26/h5-10,24H,2-4,11-12H2,1H3,(H,25,26)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Tested for the binding affinity using radioligand [125I]-Sar1 Ile8-AII in the rat adrenal capsular membranes (adrenal cortex)				J Med Chem 37: 3928-38 (1994) Article DOI: 10.1021/jm00049a012 BindingDB Entry DOI: 10.7270/Q2W098NX
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/Type-1 angiotensin II receptor B/Type-2 angiotensin II receptor (RAT)	BDBM50470055 (CHEMBL125790) Show SMILES CCCCc1nc(CO)c(Cl)n1Cc1ccc(cc1)-c1ncccc1C(O)=O Show InChI InChI=1S/C21H22ClN3O3/c1-2-3-6-18-24-17(13-26)20(22)25(18)12-14-7-9-15(10-8-14)19-16(21(27)28)5-4-11-23-19/h4-5,7-11,26H,2-3,6,12-13H2,1H3,(H,27,28)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Tested for the binding affinity using radioligand [125I]-Sar1 Ile8-AII in the rat adrenal capsular membranes (adrenal cortex)				J Med Chem 37: 3928-38 (1994) Article DOI: 10.1021/jm00049a012 BindingDB Entry DOI: 10.7270/Q2W098NX
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/Type-1 angiotensin II receptor B/Type-2 angiotensin II receptor (RAT)	BDBM50470047 (CHEMBL50135) Show SMILES CCCCc1nc(Cl)c(CO)n1Cc1ccc(s1)-c1ccccc1C(O)=O Show InChI InChI=1S/C20H21ClN2O3S/c1-2-3-8-18-22-19(21)16(12-24)23(18)11-13-9-10-17(27-13)14-6-4-5-7-15(14)20(25)26/h4-7,9-10,24H,2-3,8,11-12H2,1H3,(H,25,26)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Tested for the binding affinity using radioligand [125I]-Sar1 Ile8-AII in the rat adrenal capsular membranes (adrenal cortex)				J Med Chem 37: 3928-38 (1994) Article DOI: 10.1021/jm00049a012 BindingDB Entry DOI: 10.7270/Q2W098NX
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/Type-1 angiotensin II receptor B/Type-2 angiotensin II receptor (RAT)	BDBM50470058 (CHEMBL129005) Show SMILES CCCCc1nc(Cl)c(CO)n1Cc1ccc(o1)-c1ccccc1C(O)=O Show InChI InChI=1S/C20H21ClN2O4/c1-2-3-8-18-22-19(21)16(12-24)23(18)11-13-9-10-17(27-13)14-6-4-5-7-15(14)20(25)26/h4-7,9-10,24H,2-3,8,11-12H2,1H3,(H,25,26)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Tested for the binding affinity using radioligand [125I]-Sar1 Ile8-AII in the rat adrenal capsular membranes (adrenal cortex)				J Med Chem 37: 3928-38 (1994) Article DOI: 10.1021/jm00049a012 BindingDB Entry DOI: 10.7270/Q2W098NX
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/Type-1 angiotensin II receptor B/Type-2 angiotensin II receptor (RAT)	BDBM50470048 (CHEMBL128291) Show SMILES CCCCc1nc(CO)c(Cl)n1Cc1ccc(cc1)-c1ccoc1C(O)=O Show InChI InChI=1S/C20H21ClN2O4/c1-2-3-4-17-22-16(12-24)19(21)23(17)11-13-5-7-14(8-6-13)15-9-10-27-18(15)20(25)26/h5-10,24H,2-4,11-12H2,1H3,(H,25,26)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Tested for the binding affinity using radioligand [125I]-Sar1 Ile8-AII in the rat adrenal capsular membranes (adrenal cortex)				J Med Chem 37: 3928-38 (1994) Article DOI: 10.1021/jm00049a012 BindingDB Entry DOI: 10.7270/Q2W098NX
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/Type-1 angiotensin II receptor B/Type-2 angiotensin II receptor (RAT)	BDBM50470057 (CHEMBL129336) Show SMILES CCCCc1nc(CO)c(Cl)n1Cc1ccc(cc1)-c1nc(C)sc1C(O)=O Show InChI InChI=1S/C20H22ClN3O3S/c1-3-4-5-16-23-15(11-25)19(21)24(16)10-13-6-8-14(9-7-13)17-18(20(26)27)28-12(2)22-17/h6-9,25H,3-5,10-11H2,1-2H3,(H,26,27)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Tested for the binding affinity using radioligand [125I]-Sar1 Ile8-AII in the rat adrenal capsular membranes (adrenal cortex)				J Med Chem 37: 3928-38 (1994) Article DOI: 10.1021/jm00049a012 BindingDB Entry DOI: 10.7270/Q2W098NX
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/Type-1 angiotensin II receptor B/Type-2 angiotensin II receptor (RAT)	BDBM50470059 (CHEMBL338840) Show SMILES CCCCc1nc(Cl)c(CO)n1Cc1ccc(cc1)-c1nc(C)sc1C(O)=O Show InChI InChI=1S/C20H22ClN3O3S/c1-3-4-5-16-23-19(21)15(11-25)24(16)10-13-6-8-14(9-7-13)17-18(20(26)27)28-12(2)22-17/h6-9,25H,3-5,10-11H2,1-2H3,(H,26,27)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Tested for the binding affinity using radioligand [125I]-Sar1 Ile8-AII in the rat adrenal capsular membranes (adrenal cortex)				J Med Chem 37: 3928-38 (1994) Article DOI: 10.1021/jm00049a012 BindingDB Entry DOI: 10.7270/Q2W098NX
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/Type-1 angiotensin II receptor B/Type-2 angiotensin II receptor (RAT)	BDBM50470060 (CHEMBL125789) Show SMILES CCCCc1nc(CO)c(Cl)n1Cc1ccc(cc1)-c1cccnc1C(O)=O Show InChI InChI=1S/C21H22ClN3O3/c1-2-3-6-18-24-17(13-26)20(22)25(18)12-14-7-9-15(10-8-14)16-5-4-11-23-19(16)21(27)28/h4-5,7-11,26H,2-3,6,12-13H2,1H3,(H,27,28)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Tested for the binding affinity using radioligand [125I]-Sar1 Ile8-AII in the rat adrenal capsular membranes (adrenal cortex)				J Med Chem 37: 3928-38 (1994) Article DOI: 10.1021/jm00049a012 BindingDB Entry DOI: 10.7270/Q2W098NX
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/Type-1 angiotensin II receptor B/Type-2 angiotensin II receptor (RAT)	BDBM50470053 (CHEMBL125621) Show SMILES CCCCc1nc(CO)c(Cl)n1Cc1ccc(s1)-c1ccccc1C(O)=O Show InChI InChI=1S/C20H21ClN2O3S/c1-2-3-8-18-22-16(12-24)19(21)23(18)11-13-9-10-17(27-13)14-6-4-5-7-15(14)20(25)26/h4-7,9-10,24H,2-3,8,11-12H2,1H3,(H,25,26)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.16E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Tested for the binding affinity using radioligand [125I]-Sar1 Ile8-AII in the rat adrenal capsular membranes (adrenal cortex)				J Med Chem 37: 3928-38 (1994) Article DOI: 10.1021/jm00049a012 BindingDB Entry DOI: 10.7270/Q2W098NX
					More data for this Ligand-Target Pair
Type-1 angiotensin II receptor A/Type-1 angiotensin II receptor B/Type-2 angiotensin II receptor (RAT)	BDBM50470056 (CHEMBL129006) Show SMILES CCCCc1nc(Cl)c(CO)n1Cc1ccc(cc1)-c1ccsc1C(O)=O Show InChI InChI=1S/C20H21ClN2O3S/c1-2-3-4-17-22-19(21)16(12-24)23(17)11-13-5-7-14(8-6-13)15-9-10-27-18(15)20(25)26/h5-10,24H,2-4,11-12H2,1H3,(H,25,26)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.45E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Istituto Lusofarmaco Curated by ChEMBL					Assay Description Tested for the binding affinity using radioligand [125I]-Sar1 Ile8-AII in the rat adrenal capsular membranes (adrenal cortex)				J Med Chem 37: 3928-38 (1994) Article DOI: 10.1021/jm00049a012 BindingDB Entry DOI: 10.7270/Q2W098NX
					More data for this Ligand-Target Pair
Integrin alpha-V/beta-5 (Homo sapiens (Human))	BDBM50237601 (CHEMBL411941 | CycloRGDfV | [(2S,5R,8S,11S)-5-Benz...) Show SMILES [#6]-[#6](-[#6])-[#6@@H]-1-[#7]-[#6](=O)-[#6@@H](-[#6]-c2ccccc2)-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#8])=O)-[#7]-[#6](=O)-[#6]-[#7]-[#6](=O)-[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](/[#7])-[#7])-[#7]-[#6]-1=O |r| Show InChI InChI=1S/C26H38N8O7/c1-14(2)21-25(41)32-16(9-6-10-29-26(27)28)22(38)30-13-19(35)31-18(12-20(36)37)23(39)33-17(24(40)34-21)11-15-7-4-3-5-8-15/h3-5,7-8,14,16-18,21H,6,9-13H2,1-2H3,(H,30,38)(H,31,35)(H,32,41)(H,33,39)(H,34,40)(H,36,37)(H4,27,28,29)/t16-,17+,18-,21-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.110	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ di Parma Curated by ChEMBL					Assay Description Displacement of [125I]-echistatin from alpha-v-beta-5 integrin receptor				J Med Chem 48: 7675-87 (2005) Article DOI: 10.1021/jm050698x BindingDB Entry DOI: 10.7270/Q2GX4CBT
					More data for this Ligand-Target Pair
Integrin alpha-V/beta-5 (Homo sapiens (Human))	BDBM50235980 (2-((2S,5R,8S,11S)-5-benzyl-11-(3-guanidinopropyl)-...) Show SMILES [#6]-[#6](-[#6])-[#6@@H]-1-[#7](-[#6])-[#6](=O)-[#6@@H](-[#6]-c2ccccc2)-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#8])=O)-[#7]-[#6](=O)-[#6]-[#7]-[#6](=O)-[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#7]-[#6]-1=O |r| Show InChI InChI=1S/C27H40N8O7/c1-15(2)22-25(41)33-17(10-7-11-30-27(28)29)23(39)31-14-20(36)32-18(13-21(37)38)24(40)34-19(26(42)35(22)3)12-16-8-5-4-6-9-16/h4-6,8-9,15,17-19,22H,7,10-14H2,1-3H3,(H,31,39)(H,32,36)(H,33,41)(H,34,40)(H,37,38)(H4,28,29,30)/t17-,18-,19+,22-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MMDB PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.130	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ di Parma Curated by ChEMBL					Assay Description Displacement of [125I]-echistatin from alpha-v-beta-5 integrin receptor				J Med Chem 48: 7675-87 (2005) Article DOI: 10.1021/jm050698x BindingDB Entry DOI: 10.7270/Q2GX4CBT
					More data for this Ligand-Target Pair
Integrin alpha-V/beta-3 (Homo sapiens (Human))	BDBM50399923 (CHEMBL2180979) Show SMILES [#7]\[#6](-[#7])=[#7]\[#6]-[#6]-[#6]-[#6@@H]-1-[#7]-[#6](=O)-[#6]-[#6@@H]-2-[#7](-[#6]-c3ccccc3)-[#6](=O)-[#6@@H](-[#6]-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#8])=O)-[#7]-[#6](=O)-[#6]-[#7]-[#6]-1=O)-[#7](-[#6]-c1ccccc1)-[#6]-2=O |r| Show InChI InChI=1S/C33H41N9O8/c34-33(35)36-13-7-12-22-29(47)38-17-27(44)40-23(14-28(45)46)30(48)37-16-25-32(50)41(18-20-8-3-1-4-9-20)24(15-26(43)39-22)31(49)42(25)19-21-10-5-2-6-11-21/h1-6,8-11,22-25H,7,12-19H2,(H,37,48)(H,38,47)(H,39,43)(H,40,44)(H,45,46)(H4,34,35,36)/t22-,23-,24-,25+/m0/s1	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.200	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Milano Curated by ChEMBL					Assay Description Competitive inhibition of biotinylated vitronectin to integrin alphaVbeta3 receptor after 3 hrs by microplate reader analysis				J Med Chem 55: 10460-74 (2012) Article DOI: 10.1021/jm301058f BindingDB Entry DOI: 10.7270/Q2WD41Q5
					More data for this Ligand-Target Pair
Integrin alpha-V/beta-3 (Homo sapiens (Human))	BDBM50399922 (CHEMBL2180974) Show SMILES [#7]\[#6](-[#7])=[#7]\[#6]-[#6]-[#6]-[#6@@H]-1-[#7]-[#6](=O)-[#6]-[#6@H]-2-[#7](-[#6]-c3ccccc3)-[#6](=O)-[#6@H](-[#6]-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#8])=O)-[#7]-[#6](=O)-[#6]-[#7]-[#6]-1=O)-[#7](-[#6]-c1ccccc1)-[#6]-2=O |r| Show InChI InChI=1S/C33H41N9O8/c34-33(35)36-13-7-12-22-29(47)38-17-27(44)40-23(14-28(45)46)30(48)37-16-25-32(50)41(18-20-8-3-1-4-9-20)24(15-26(43)39-22)31(49)42(25)19-21-10-5-2-6-11-21/h1-6,8-11,22-25H,7,12-19H2,(H,37,48)(H,38,47)(H,39,43)(H,40,44)(H,45,46)(H4,34,35,36)/t22-,23-,24+,25-/m0/s1	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.200	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Milano Curated by ChEMBL					Assay Description Competitive inhibition of biotinylated vitronectin to integrin alphaVbeta3 receptor after 3 hrs by microplate reader analysis				J Med Chem 55: 10460-74 (2012) Article DOI: 10.1021/jm301058f BindingDB Entry DOI: 10.7270/Q2WD41Q5
					More data for this Ligand-Target Pair
Integrin alpha-V/beta-3 (Homo sapiens (Human))	BDBM50399922 (CHEMBL2180974) Show SMILES [#7]\[#6](-[#7])=[#7]\[#6]-[#6]-[#6]-[#6@@H]-1-[#7]-[#6](=O)-[#6]-[#6@H]-2-[#7](-[#6]-c3ccccc3)-[#6](=O)-[#6@H](-[#6]-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#8])=O)-[#7]-[#6](=O)-[#6]-[#7]-[#6]-1=O)-[#7](-[#6]-c1ccccc1)-[#6]-2=O |r| Show InChI InChI=1S/C33H41N9O8/c34-33(35)36-13-7-12-22-29(47)38-17-27(44)40-23(14-28(45)46)30(48)37-16-25-32(50)41(18-20-8-3-1-4-9-20)24(15-26(43)39-22)31(49)42(25)19-21-10-5-2-6-11-21/h1-6,8-11,22-25H,7,12-19H2,(H,37,48)(H,38,47)(H,39,43)(H,40,44)(H,45,46)(H4,34,35,36)/t22-,23-,24+,25-/m0/s1	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.200	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Milano Curated by ChEMBL					Assay Description Competitive inhibition of biotinylated vitronectin to integrin alphaVbeta3 receptor after 3 hrs by microplate reader analysis				J Med Chem 55: 10460-74 (2012) Article DOI: 10.1021/jm301058f BindingDB Entry DOI: 10.7270/Q2WD41Q5
					More data for this Ligand-Target Pair
Integrin alpha-L/beta-2 (Homo sapiens (Human))	BDBM50550223 (CHEMBL4794300) Show SMILES OC(=O)C(F)(F)F.Nc1ccc(CNC(=O)N2C(CC(O)=O)CC2=O)cc1 Show InChI	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	PubMed	n/a	n/a	0.390	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Antagonist activity at alphaLbeta2 in human Jurkat E6.1 cells assessed as reduction in cell adhesion to ICAM1 pre-incubated for 30 mins before ICAM1 ...				Citation and Details BindingDB Entry DOI: 10.7270/Q2154MPK
					More data for this Ligand-Target Pair
Integrin alpha-V/beta-5 (Homo sapiens (Human))	BDBM50177887 (CHEMBL269913 | CHEMBL556402 | c-[-Arg-Gly-Asp-Acpc...) Show SMILES [#7]\[#6](-[#7])=[#7]\[#6]-[#6]-[#6]-[#6@@H]-1-[#7]-[#6](=O)-[#6@@H]-2-[#6]-[#6]-[#6@H](-[#6]-2)-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#8])=O)-[#7]-[#6](=O)-[#6]-[#7]-[#6]-1=O Show InChI InChI=1S/C18H29N7O6/c19-18(20)21-5-1-2-11-16(30)22-8-13(26)24-12(7-14(27)28)17(31)23-10-4-3-9(6-10)15(29)25-11/h9-12H,1-8H2,(H,22,30)(H,23,31)(H,24,26)(H,25,29)(H,27,28)(H4,19,20,21)/t9-,10-,11+,12+/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.590	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ di Parma Curated by ChEMBL					Assay Description Displacement of [125I]-echistatin from alpha-v-beta-5 integrin receptor				J Med Chem 48: 7675-87 (2005) Article DOI: 10.1021/jm050698x BindingDB Entry DOI: 10.7270/Q2GX4CBT
					More data for this Ligand-Target Pair
Integrin alpha-V/beta-3 (Homo sapiens (Human))	BDBM50439683 (CHEMBL2418221) Show SMILES [#6]-[#6@@H](-[#8])-[#6@H](-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#8])=O)-[#7]-[#6](=O)-[#6]-[#7]-[#6](=O)-[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#7]-[#6](=O)-[#6]-[#7])-[#6](=O)-[#7]-1-[#6]-[#6]-[#6]-[#6@H]-1-[#6](-[#8])=O |r| Show InChI InChI=1S/C23H39N9O10/c1-11(33)18(21(40)32-7-3-5-14(32)22(41)42)31-20(39)13(8-17(36)37)30-16(35)10-28-19(38)12(29-15(34)9-24)4-2-6-27-23(25)26/h11-14,18,33H,2-10,24H2,1H3,(H,28,38)(H,29,34)(H,30,35)(H,31,39)(H,36,37)(H,41,42)(H4,25,26,27)/t11-,12+,13+,14+,18+/m1/s1	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.620	n/a	n/a	n/a	n/a	n/a	n/a
University of Bologna Curated by ChEMBL					Assay Description Inhibition of alphaVbeta3 integrin-mediated human SK-MEL-24 cell adhesion to fibronectin incubated for 30 mins before plating measured after 1 hr				Eur J Med Chem 66: 258-68 (2013) Article DOI: 10.1016/j.ejmech.2013.05.050 BindingDB Entry DOI: 10.7270/Q21Z45VC
					More data for this Ligand-Target Pair
Integrin alpha-5/beta-1 (Homo sapiens (Human))	BDBM50439683 (CHEMBL2418221) Show SMILES [#6]-[#6@@H](-[#8])-[#6@H](-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#8])=O)-[#7]-[#6](=O)-[#6]-[#7]-[#6](=O)-[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#7]-[#6](=O)-[#6]-[#7])-[#6](=O)-[#7]-1-[#6]-[#6]-[#6]-[#6@H]-1-[#6](-[#8])=O |r| Show InChI InChI=1S/C23H39N9O10/c1-11(33)18(21(40)32-7-3-5-14(32)22(41)42)31-20(39)13(8-17(36)37)30-16(35)10-28-19(38)12(29-15(34)9-24)4-2-6-27-23(25)26/h11-14,18,33H,2-10,24H2,1H3,(H,28,38)(H,29,34)(H,30,35)(H,31,39)(H,36,37)(H,41,42)(H4,25,26,27)/t11-,12+,13+,14+,18+/m1/s1	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.670	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Antagonist activity at alpha5beta1 in human K562 cells assessed as reduction in cell adhesion to fibronectin pre-incubated for 30 mins before fibrone...				Citation and Details BindingDB Entry DOI: 10.7270/Q2154MPK
					More data for this Ligand-Target Pair
Integrin alpha-L/beta-2 (Homo sapiens (Human))	BDBM50074661 ((S)-1-{(S)-2-[(S)-3-Carboxy-2-((S)-4-methyl-2-{2-[...) Show SMILES CC(C)C[C@H](NC(=O)Cc1ccc(NC(=O)Nc2ccccc2C)cc1)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@H]1C(O)=O Show InChI InChI=1S/C36H48N6O9/c1-20(2)17-26(38-29(43)18-23-12-14-24(15-13-23)37-36(51)40-25-10-7-6-9-22(25)5)32(46)39-27(19-30(44)45)33(47)41-31(21(3)4)34(48)42-16-8-11-28(42)35(49)50/h6-7,9-10,12-15,20-21,26-28,31H,8,11,16-19H2,1-5H3,(H,38,43)(H,39,46)(H,41,47)(H,44,45)(H,49,50)(H2,37,40,51)/t26-,27-,28-,31-/m0/s1	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.840	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Antagonist activity at alphaLbeta2 in human Jurkat E6.1 cells assessed as reduction in cell adhesion to ICAM1 pre-incubated for 30 mins before ICAM1 ...				Citation and Details BindingDB Entry DOI: 10.7270/Q2154MPK
					More data for this Ligand-Target Pair
Integrin alpha-V/beta-3 (Homo sapiens (Human))	BDBM50399919 (CHEMBL2180983) Show SMILES CC(=O)O[C@@H]1C2=C(C)[C@H](C[C@@](O)([C@@H](OC(=O)c3ccccc3)[C@@H]3[C@@]4(CO[C@@H]4C[C@H](O)[C@@]3(C)C1=O)OC(C)=O)C2(C)C)OC(=O)[C@H](OC(=O)CCC(=O)NCc1ccc(CN2[C@H]3CC(=O)N[C@@H](CCCN=C(N)N)C(=O)NCC(=O)N[C@@H](CC(O)=O)C(=O)NC[C@@H](NC3=O)C2=O)cc1)[C@@H](NC(=O)c1ccccc1)c1ccccc1 |r,wU:65.70,80.85,22.23,26.26,4.3,10.10,30.33,28.30,60.64,wD:97.105,12.12,8.45,23.37,44.49,89.94,c:5,(3.53,-26.48,;3.49,-24.94,;2.14,-24.21,;4.81,-24.14,;6.16,-24.86,;6.22,-27.9,;6.24,-29.43,;4.92,-30.22,;7.59,-30.2,;8.91,-29.4,;8.88,-27.87,;10.23,-28.61,;10.21,-27.08,;11.56,-27.82,;11.57,-29.38,;10.26,-30.14,;12.91,-30.11,;14.22,-29.31,;15.57,-30.05,;15.6,-31.61,;14.28,-32.4,;12.94,-31.65,;10.17,-25.54,;11.49,-24.75,;13.04,-24.72,;13.01,-23.19,;11.46,-23.19,;10.11,-22.45,;8.78,-23.26,;8.73,-21.72,;8.82,-24.8,;9.24,-26.26,;7.47,-24.06,;7.43,-22.52,;11.9,-26.23,;13.25,-26.97,;14.58,-26.18,;13.27,-28.52,;7.54,-27.11,;6.72,-25.81,;8.29,-25.76,;7.6,-31.72,;6.28,-32.51,;4.95,-31.76,;6.3,-34.04,;7.64,-34.8,;8.97,-34.03,;8.96,-32.49,;10.31,-34.79,;11.64,-34.01,;12.98,-34.77,;12.99,-36.31,;14.31,-33.99,;15.65,-34.75,;16.97,-33.97,;18.31,-34.74,;19.64,-33.97,;19.63,-32.42,;20.96,-31.64,;22.3,-32.4,;23.61,-31.62,;23.6,-30.08,;24.92,-29.29,;24.9,-27.75,;26.27,-30.04,;27.59,-29.25,;27.57,-27.71,;26.22,-26.96,;26.2,-25.42,;24.86,-24.67,;24.83,-23.13,;23.49,-22.38,;26.15,-22.34,;28.94,-30,;30.26,-29.21,;28.96,-31.54,;30.3,-32.29,;30.33,-33.83,;31.67,-34.58,;29,-34.62,;29.03,-36.16,;30.37,-36.91,;30.4,-38.45,;29.07,-39.24,;31.74,-39.2,;27.71,-36.95,;27.73,-38.49,;25.04,-36.99,;23.64,-36.24,;23.63,-34.7,;24.96,-33.93,;24.95,-32.39,;26.29,-31.61,;22.3,-33.94,;20.97,-34.72,;18.28,-31.66,;16.96,-32.44,;4.97,-34.83,;3.63,-34.09,;2.32,-34.86,;2.34,-36.42,;.98,-34.13,;.96,-32.57,;-.39,-31.83,;-1.7,-32.63,;-1.69,-34.16,;-.35,-34.92,;5,-36.36,;6.35,-37.1,;6.37,-38.66,;5.04,-39.45,;3.7,-38.69,;3.68,-37.16,)| Show InChI InChI=1S/C78H91N11O24/c1-40-52(34-78(107)66(112-72(105)47-21-14-9-15-22-47)64-76(6,53(92)33-54-77(64,39-108-54)113-42(3)91)65(99)62(109-41(2)90)60(40)75(78,4)5)110-73(106)63(61(45-17-10-7-11-18-45)88-67(100)46-19-12-8-13-20-46)111-59(98)29-28-55(93)82-35-43-24-26-44(27-25-43)38-89-51-32-56(94)85-48(23-16-30-81-74(79)80)68(101)84-37-57(95)86-49(31-58(96)97)69(102)83-36-50(71(89)104)87-70(51)103/h7-15,17-22,24-27,48-54,61-64,66,92,107H,16,23,28-39H2,1-6H3,(H,82,93)(H,83,102)(H,84,101)(H,85,94)(H,86,95)(H,87,103)(H,88,100)(H,96,97)(H4,79,80,81)/t48-,49-,50+,51-,52-,53-,54+,61-,62+,63+,64-,66-,76+,77-,78+/m0/s1	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	0.900	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Milano Curated by ChEMBL					Assay Description Competitive inhibition of biotinylated vitronectin to integrin alphaVbeta3 receptor after 3 hrs by microplate reader analysis				J Med Chem 55: 10460-74 (2012) Article DOI: 10.1021/jm301058f BindingDB Entry DOI: 10.7270/Q2WD41Q5
					More data for this Ligand-Target Pair
Integrin alpha-V/beta-3 (Homo sapiens (Human))	BDBM50177879 (CHEMBL200182 | ST-1646) Show SMILES [#7]\[#6](-[#7])=[#7]\[#6]-[#6]-[#6]-[#6@@H]-1-[#7]-[#6](=O)-[#6@@H]-2-[#6]-[#6]-[#6@H]-3-[#6]-[#6]-[#6]-[#6@@H](-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#8])=O)-[#7]-[#6](=O)-[#6]-[#7]-[#6]-1=O)-[#6](=O)-[#7]-2-3 Show InChI InChI=1S/C22H34N8O7/c23-22(24)25-8-2-5-12-18(34)26-10-16(31)27-14(9-17(32)33)19(35)29-13-4-1-3-11-6-7-15(20(36)28-12)30(11)21(13)37/h11-15H,1-10H2,(H,26,34)(H,27,31)(H,28,36)(H,29,35)(H,32,33)(H4,23,24,25)/t11-,12+,13-,14+,15+/m1/s1	PDB UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Milano Curated by ChEMBL					Assay Description Competitive inhibition of biotinylated vitronectin to integrin alphaVbeta3 receptor after 3 hrs by microplate reader analysis				J Med Chem 55: 10460-74 (2012) Article DOI: 10.1021/jm301058f BindingDB Entry DOI: 10.7270/Q2WD41Q5
					More data for this Ligand-Target Pair
Integrin alpha-4/beta-1 (Homo sapiens (Human))	BDBM50505781 (CHEMBL4461668) Show SMILES Cc1ccccc1NC(=O)N1[C@@H](CC1=O)C(O)=O |r| Show InChI InChI=1S/C12H12N2O4/c1-7-4-2-3-5-8(7)13-12(18)14-9(11(16)17)6-10(14)15/h2-5,9H,6H2,1H3,(H,13,18)(H,16,17)/t9-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	PubMed	n/a	n/a	1.10	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of fibronectin binding to alpha4bbeta1 isolated from human Jurkat E6.1 cells incubated for 1 hr by scintillation-proximity assay based com...				Citation and Details BindingDB Entry DOI: 10.7270/Q2154MPK
					More data for this Ligand-Target Pair

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