Compile Data Set for Download or QSAR

Found 63 hits with Last Name = 'bopp' and Initial = 'ba'   

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
Renin (Homo sapiens (Human))	BDBM50022647 (2-Benzyl-N-[1-(1-cyclohexylmethyl-2,3-dihydroxy-5-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C35H53N5O6/c1-24(2)17-31(41)33(43)29(19-26-11-7-4-8-12-26)38-35(45)30(21-28-22-36-23-37-28)39-34(44)27(18-25-9-5-3-6-10-25)20-32(42)40-13-15-46-16-14-40/h3,5-6,9-10,22-24,26-27,29-31,33,41,43H,4,7-8,11-21H2,1-2H3,(H,36,37)(H,38,45)(H,39,44)/t27-,29+,30+,31+,33-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.290	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022646 (CHEMBL307917 | Morpholine-4-carboxylic acid {1-[1-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](CCc1ccccc1)NC(=O)N1CCOCC1 Show InChI InChI=1S/C35H54N6O6/c1-24(2)19-31(42)32(43)29(20-26-11-7-4-8-12-26)38-34(45)30(21-27-22-36-23-37-27)39-33(44)28(14-13-25-9-5-3-6-10-25)40-35(46)41-15-17-47-18-16-41/h3,5-6,9-10,22-24,26,28-32,42-43H,4,7-8,11-21H2,1-2H3,(H,36,37)(H,38,45)(H,39,44)(H,40,46)/t28-,29-,30-,31-,32+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.300	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022650 (CHEMBL75117 | Morpholine-4-carboxylic acid {1-[1-(...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)N1CCOCC1 Show InChI InChI=1S/C34H52N6O6/c1-23(2)17-30(41)31(42)27(18-24-9-5-3-6-10-24)37-33(44)29(20-26-21-35-22-36-26)38-32(43)28(19-25-11-7-4-8-12-25)39-34(45)40-13-15-46-16-14-40/h4,7-8,11-12,21-24,27-31,41-42H,3,5-6,9-10,13-20H2,1-2H3,(H,35,36)(H,37,44)(H,38,43)(H,39,45)/t27-,28-,29-,30-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.350	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022643 (4-Hydroxy-piperidine-1-carboxylic acid {1-[1-(1-cy...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)N1CCC(O)CC1 Show InChI InChI=1S/C35H54N6O6/c1-23(2)17-31(43)32(44)28(18-24-9-5-3-6-10-24)38-34(46)30(20-26-21-36-22-37-26)39-33(45)29(19-25-11-7-4-8-12-25)40-35(47)41-15-13-27(42)14-16-41/h4,7-8,11-12,21-24,27-32,42-44H,3,5-6,9-10,13-20H2,1-2H3,(H,36,37)(H,38,46)(H,39,45)(H,40,47)/t28-,29-,30-,31-,32+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.420	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022649 (CHEMBL76458 | N-[1-(1-Cyclohexylmethyl-2,3-dihydro...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)N(C)C Show InChI InChI=1S/C32H50N6O5/c1-21(2)15-28(39)29(40)25(16-22-11-7-5-8-12-22)35-31(42)27(18-24-19-33-20-34-24)36-30(41)26(37-32(43)38(3)4)17-23-13-9-6-10-14-23/h6,9-10,13-14,19-22,25-29,39-40H,5,7-8,11-12,15-18H2,1-4H3,(H,33,34)(H,35,42)(H,36,41)(H,37,43)/t25-,26-,27-,28-,29+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.5	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022645 (CHEMBL75510 | N-[1-(1-Cyclohexylmethyl-2,3-dihydro...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)N(C)CCO Show InChI InChI=1S/C33H52N6O6/c1-22(2)16-29(41)30(42)26(17-23-10-6-4-7-11-23)36-32(44)28(19-25-20-34-21-35-25)37-31(43)27(18-24-12-8-5-9-13-24)38-33(45)39(3)14-15-40/h5,8-9,12-13,20-23,26-30,40-42H,4,6-7,10-11,14-19H2,1-3H3,(H,34,35)(H,36,44)(H,37,43)(H,38,45)/t26-,27-,28-,29-,30+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.550	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022651 (CHEMBL306274 | Morpholine-4-carboxylic acid {1-[1-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)C(Cc1ccccc1)=NC(=O)N1CCOCC1 |w:37.40| Show InChI InChI=1S/C34H50N6O6/c1-23(2)17-30(41)31(42)27(18-24-9-5-3-6-10-24)37-33(44)29(20-26-21-35-22-36-26)38-32(43)28(19-25-11-7-4-8-12-25)39-34(45)40-13-15-46-16-14-40/h4,7-8,11-12,21-24,27,29-31,41-42H,3,5-6,9-10,13-20H2,1-2H3,(H,35,36)(H,37,44)(H,38,43)/t27-,29-,30-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	0.580	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022644 (CHEMBL73712 | Piperazine-1-carboxylic acid {1-[1-(...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)N1CCNCC1 Show InChI InChI=1S/C34H53N7O5/c1-23(2)17-30(42)31(43)27(18-24-9-5-3-6-10-24)38-33(45)29(20-26-21-36-22-37-26)39-32(44)28(19-25-11-7-4-8-12-25)40-34(46)41-15-13-35-14-16-41/h4,7-8,11-12,21-24,27-31,35,42-43H,3,5-6,9-10,13-20H2,1-2H3,(H,36,37)(H,38,45)(H,39,44)(H,40,46)/t27-,28-,29-,30-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.650	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin (pH 7.4)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022643 (4-Hydroxy-piperidine-1-carboxylic acid {1-[1-(1-cy...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)N1CCC(O)CC1 Show InChI InChI=1S/C35H54N6O6/c1-23(2)17-31(43)32(44)28(18-24-9-5-3-6-10-24)38-34(46)30(20-26-21-36-22-37-26)39-33(45)29(19-25-11-7-4-8-12-25)40-35(47)41-15-13-27(42)14-16-41/h4,7-8,11-12,21-24,27-32,42-44H,3,5-6,9-10,13-20H2,1-2H3,(H,36,37)(H,38,46)(H,39,45)(H,40,47)/t28-,29-,30-,31-,32+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.680	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022653 (CHEMBL309345 | Morpholine-4-carboxylic acid [1-[1-...) Show SMILES COc1ccc(C[C@H](NC(=O)N2CCOCC2)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N[C@@H](CC2CCCCC2)[C@@H](O)[C@@H](O)CC(C)C)cc1 Show InChI InChI=1S/C35H54N6O7/c1-23(2)17-31(42)32(43)28(18-24-7-5-4-6-8-24)38-34(45)30(20-26-21-36-22-37-26)39-33(44)29(19-25-9-11-27(47-3)12-10-25)40-35(46)41-13-15-48-16-14-41/h9-12,21-24,28-32,42-43H,4-8,13-20H2,1-3H3,(H,36,37)(H,38,45)(H,39,44)(H,40,46)/t28-,29-,30-,31-,32+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.760	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022641 (2-Benzylidene-N-[1-(1-cyclohexylmethyl-2,3-dihydro...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)C(CC(=O)N1CCOCC1)=Cc1ccccc1 |w:39.42| Show InChI InChI=1S/C35H51N5O6/c1-24(2)17-31(41)33(43)29(19-26-11-7-4-8-12-26)38-35(45)30(21-28-22-36-23-37-28)39-34(44)27(18-25-9-5-3-6-10-25)20-32(42)40-13-15-46-16-14-40/h3,5-6,9-10,18,22-24,26,29-31,33,41,43H,4,7-8,11-17,19-21H2,1-2H3,(H,36,37)(H,38,45)(H,39,44)/t29-,30-,31-,33+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	0.790	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022654 (CHEMBL265485 | Morpholine-4-carboxylic acid 1-[1-(...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCOCC1 Show InChI InChI=1S/C34H51N5O7/c1-23(2)17-29(40)31(41)27(18-24-9-5-3-6-10-24)37-32(42)28(20-26-21-35-22-36-26)38-33(43)30(19-25-11-7-4-8-12-25)46-34(44)39-13-15-45-16-14-39/h4,7-8,11-12,21-24,27-31,40-41H,3,5-6,9-10,13-20H2,1-2H3,(H,35,36)(H,37,42)(H,38,43)/t27-,28-,29-,30-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.820	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin (pH 7.4)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022650 (CHEMBL75117 | Morpholine-4-carboxylic acid {1-[1-(...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)N1CCOCC1 Show InChI InChI=1S/C34H52N6O6/c1-23(2)17-30(41)31(42)27(18-24-9-5-3-6-10-24)37-33(44)29(20-26-21-35-22-36-26)38-32(43)28(19-25-11-7-4-8-12-25)39-34(45)40-13-15-46-16-14-40/h4,7-8,11-12,21-24,27-31,41-42H,3,5-6,9-10,13-20H2,1-2H3,(H,35,36)(H,37,44)(H,38,43)(H,39,45)/t27-,28-,29-,30-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.890	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin (pH 7.4)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022642 (CHEMBL74765 | Morpholine-4-carboxylic acid (1-{[1-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)N(C)C(=O)[C@H](Cc1ccccc1)NC(=O)N1CCOCC1 Show InChI InChI=1S/C35H54N6O6/c1-24(2)18-31(42)32(43)28(19-25-10-6-4-7-11-25)38-33(44)30(21-27-22-36-23-37-27)40(3)34(45)29(20-26-12-8-5-9-13-26)39-35(46)41-14-16-47-17-15-41/h5,8-9,12-13,22-25,28-32,42-43H,4,6-7,10-11,14-21H2,1-3H3,(H,36,37)(H,38,44)(H,39,46)/t28-,29-,30-,31-,32+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.940	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin (pH 7.4)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022645 (CHEMBL75510 | N-[1-(1-Cyclohexylmethyl-2,3-dihydro...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)N(C)CCO Show InChI InChI=1S/C33H52N6O6/c1-22(2)16-29(41)30(42)26(17-23-10-6-4-7-11-23)36-32(44)28(19-25-20-34-21-35-25)37-31(43)27(18-24-12-8-5-9-13-24)38-33(45)39(3)14-15-40/h5,8-9,12-13,20-23,26-30,40-42H,4,6-7,10-11,14-19H2,1-3H3,(H,34,35)(H,36,44)(H,37,43)(H,38,45)/t26-,27-,28-,29-,30+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.980	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin (pH 7.4)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022647 (2-Benzyl-N-[1-(1-cyclohexylmethyl-2,3-dihydroxy-5-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](CC(=O)N1CCOCC1)Cc1ccccc1 Show InChI InChI=1S/C35H53N5O6/c1-24(2)17-31(41)33(43)29(19-26-11-7-4-8-12-26)38-35(45)30(21-28-22-36-23-37-28)39-34(44)27(18-25-9-5-3-6-10-25)20-32(42)40-13-15-46-16-14-40/h3,5-6,9-10,22-24,26-27,29-31,33,41,43H,4,7-8,11-21H2,1-2H3,(H,36,37)(H,38,45)(H,39,44)/t27-,29+,30+,31+,33-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.30	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022646 (CHEMBL307917 | Morpholine-4-carboxylic acid {1-[1-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](CCc1ccccc1)NC(=O)N1CCOCC1 Show InChI InChI=1S/C35H54N6O6/c1-24(2)19-31(42)32(43)29(20-26-11-7-4-8-12-26)38-34(45)30(21-27-22-36-23-37-27)39-33(44)28(14-13-25-9-5-3-6-10-25)40-35(46)41-15-17-47-18-16-41/h3,5-6,9-10,22-24,26,28-32,42-43H,4,7-8,11-21H2,1-2H3,(H,36,37)(H,38,45)(H,39,44)(H,40,46)/t28-,29-,30-,31-,32+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin (pH 7.4)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022353 (CHEMBL3142231 | {1-[1-[1-Cyclohexylmethyl-2-hydrox...) Show SMILES CC(C)S(=O)(=O)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C Show InChI InChI=1S/C33H51N5O7S/c1-22(2)46(43,44)20-29(39)26(16-23-12-8-6-9-13-23)36-31(41)28(18-25-19-34-21-35-25)37-30(40)27(17-24-14-10-7-11-15-24)38-32(42)45-33(3,4)5/h7,10-11,14-15,19,21-23,26-29,39H,6,8-9,12-13,16-18,20H2,1-5H3,(H,34,35)(H,36,41)(H,37,40)(H,38,42)/t26-,27?,28?,29-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022641 (2-Benzylidene-N-[1-(1-cyclohexylmethyl-2,3-dihydro...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)C(CC(=O)N1CCOCC1)=Cc1ccccc1 |w:39.42| Show InChI InChI=1S/C35H51N5O6/c1-24(2)17-31(41)33(43)29(19-26-11-7-4-8-12-26)38-35(45)30(21-28-22-36-23-37-28)39-34(44)27(18-25-9-5-3-6-10-25)20-32(42)40-13-15-46-16-14-40/h3,5-6,9-10,18,22-24,26,29-31,33,41,43H,4,7-8,11-17,19-21H2,1-2H3,(H,36,37)(H,38,45)(H,39,44)/t29-,30-,31-,33+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	2.10	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022653 (CHEMBL309345 | Morpholine-4-carboxylic acid [1-[1-...) Show SMILES COc1ccc(C[C@H](NC(=O)N2CCOCC2)C(=O)N[C@@H](Cc2cnc[nH]2)C(=O)N[C@@H](CC2CCCCC2)[C@@H](O)[C@@H](O)CC(C)C)cc1 Show InChI InChI=1S/C35H54N6O7/c1-23(2)17-31(42)32(43)28(18-24-7-5-4-6-8-24)38-34(45)30(20-26-21-36-22-37-26)39-33(44)29(19-25-9-11-27(47-3)12-10-25)40-35(46)41-13-15-48-16-14-41/h9-12,21-24,28-32,42-43H,4-8,13-20H2,1-3H3,(H,36,37)(H,38,45)(H,39,44)(H,40,46)/t28-,29-,30-,31-,32+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.40	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin (pH 7.4)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022642 (CHEMBL74765 | Morpholine-4-carboxylic acid (1-{[1-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)N(C)C(=O)[C@H](Cc1ccccc1)NC(=O)N1CCOCC1 Show InChI InChI=1S/C35H54N6O6/c1-24(2)18-31(42)32(43)28(19-25-10-6-4-7-11-25)38-33(44)30(21-27-22-36-23-37-27)40(3)34(45)29(20-26-12-8-5-9-13-26)39-35(46)41-14-16-47-17-15-41/h5,8-9,12-13,22-25,28-32,42-43H,4,6-7,10-11,14-21H2,1-3H3,(H,36,37)(H,38,44)(H,39,46)/t28-,29-,30-,31-,32+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.5	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin (pH 7.4)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022370 (CHEMBL3142232 | {1-[1-(3-Cyclohexanesulfonyl-1-cyc...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CS(=O)(=O)C1CCCCC1 Show InChI InChI=1S/C36H55N5O7S/c1-36(2,3)48-35(45)41-30(20-26-15-9-5-10-16-26)33(43)40-31(21-27-22-37-24-38-27)34(44)39-29(19-25-13-7-4-8-14-25)32(42)23-49(46,47)28-17-11-6-12-18-28/h5,9-10,15-16,22,24-25,28-32,42H,4,6-8,11-14,17-21,23H2,1-3H3,(H,37,38)(H,39,44)(H,40,43)(H,41,45)/t29-,30?,31?,32-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.5	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022652 (CHEMBL305865 | Morpholine-4-carboxylic acid {1-[1-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)N1CCOCC1)C(C)(C)c1ccccc1 Show InChI InChI=1S/C36H56N6O6/c1-24(2)19-30(43)31(44)28(20-25-11-7-5-8-12-25)39-33(45)29(21-27-22-37-23-38-27)40-34(46)32(36(3,4)26-13-9-6-10-14-26)41-35(47)42-15-17-48-18-16-42/h6,9-10,13-14,22-25,28-32,43-44H,5,7-8,11-12,15-21H2,1-4H3,(H,37,38)(H,39,45)(H,40,46)(H,41,47)/t28-,29-,30-,31+,32+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.60	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin (pH 7.4)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50226408 (CHEMBL3142220) Show SMILES CC(C)S(=O)(=O)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)CC(C)(C)C |r| Show InChI InChI=1S/C34H53N5O6S/c1-23(2)46(44,45)21-30(40)27(16-24-12-8-6-9-13-24)38-33(43)29(18-26-20-35-22-36-26)39-32(42)28(17-25-14-10-7-11-15-25)37-31(41)19-34(3,4)5/h7,10-11,14-15,20,22-24,27-30,40H,6,8-9,12-13,16-19,21H2,1-5H3,(H,35,36)(H,37,41)(H,38,43)(H,39,42)/t27-,28-,29-,30-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022379 (CHEMBL3142221 | [1-[1-[1-Cyclohexylmethyl-2-hydrox...) Show SMILES COc1ccc(C[C@H](NC(=O)OC(C)(C)C)C(=O)N[C@@H](Cc2c[nH]cn2)C(=O)N[C@@H](CC2CCCCC2)[C@@H](O)CS(=O)(=O)C(C)C)cc1 Show InChI InChI=1S/C34H53N5O8S/c1-22(2)48(44,45)20-30(40)27(16-23-10-8-7-9-11-23)37-32(42)29(18-25-19-35-21-36-25)38-31(41)28(39-33(43)47-34(3,4)5)17-24-12-14-26(46-6)15-13-24/h12-15,19,21-23,27-30,40H,7-11,16-18,20H2,1-6H3,(H,35,36)(H,37,42)(H,38,41)(H,39,43)/t27-,28?,29?,30-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022654 (CHEMBL265485 | Morpholine-4-carboxylic acid 1-[1-(...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)OC(=O)N1CCOCC1 Show InChI InChI=1S/C34H51N5O7/c1-23(2)17-29(40)31(41)27(18-24-9-5-3-6-10-24)37-32(42)28(20-26-21-35-22-36-26)38-33(43)30(19-25-11-7-4-8-12-25)46-34(44)39-13-15-45-16-14-39/h4,7-8,11-12,21-24,27-31,40-41H,3,5-6,9-10,13-20H2,1-2H3,(H,35,36)(H,37,42)(H,38,43)/t27-,28-,29-,30-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin (pH 7.4)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022649 (CHEMBL76458 | N-[1-(1-Cyclohexylmethyl-2,3-dihydro...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)N(C)C Show InChI InChI=1S/C32H50N6O5/c1-21(2)15-28(39)29(40)25(16-22-11-7-5-8-12-22)35-31(42)27(18-24-19-33-20-34-24)36-30(41)26(37-32(43)38(3)4)17-23-13-9-6-10-14-23/h6,9-10,13-14,19-22,25-29,39-40H,5,7-8,11-12,15-18H2,1-4H3,(H,33,34)(H,35,42)(H,36,41)(H,37,43)/t25-,26-,27-,28-,29+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.30	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin (pH 7.4)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022350 (CHEMBL3143950 | N-{1-[1-[1-Cyclohexylmethyl-2-hydr...) Show SMILES Cl.CC(C)S(=O)(=O)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)CC(C)(C)C |r| Show InChI InChI=1S/C34H53N5O6S/c1-23(2)46(44,45)21-30(40)27(16-24-12-8-6-9-13-24)38-33(43)29(18-26-20-35-22-36-26)39-32(42)28(17-25-14-10-7-11-15-25)37-31(41)19-34(3,4)5/h7,10-11,14-15,20,22-24,27-30,40H,6,8-9,12-13,16-19,21H2,1-5H3,(H,35,36)(H,37,41)(H,38,43)(H,39,42)/t27-,28?,29?,30-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.5	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair				3D Structure (docked)
Renin (Homo sapiens (Human))	BDBM50022356 (CHEMBL309127 | {1-[1-(1-Cyclohexylmethyl-3-cyclohe...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CSC1CCCCC1 Show InChI InChI=1S/C36H55N5O5S/c1-36(2,3)46-35(45)41-30(20-26-15-9-5-10-16-26)33(43)40-31(21-27-22-37-24-38-27)34(44)39-29(19-25-13-7-4-8-14-25)32(42)23-47-28-17-11-6-12-18-28/h5,9-10,15-16,22,24-25,28-32,42H,4,6-8,11-14,17-21,23H2,1-3H3,(H,37,38)(H,39,44)(H,40,43)(H,41,45)/t29-,30?,31?,32-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022372 (CHEMBL357302 | {1-[1-(1-Cyclohexylmethyl-2-hydroxy...) Show SMILES CC(C)SC[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C Show InChI InChI=1S/C33H51N5O5S/c1-22(2)44-20-29(39)26(16-23-12-8-6-9-13-23)36-31(41)28(18-25-19-34-21-35-25)37-30(40)27(17-24-14-10-7-11-15-24)38-32(42)43-33(3,4)5/h7,10-11,14-15,19,21-23,26-29,39H,6,8-9,12-13,16-18,20H2,1-5H3,(H,34,35)(H,36,41)(H,37,40)(H,38,42)/t26-,27?,28?,29-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022376 ((1-{1-[1-Cyclohexylmethyl-2-hydroxy-3-(propane-2-s...) Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CS(=O)(=O)C(C)C Show InChI InChI=1S/C33H55N3O7S/c1-22(2)18-27(35-31(39)28(20-25-16-12-9-13-17-25)36-32(40)43-33(5,6)7)30(38)34-26(19-24-14-10-8-11-15-24)29(37)21-44(41,42)23(3)4/h9,12-13,16-17,22-24,26-29,37H,8,10-11,14-15,18-21H2,1-7H3,(H,34,38)(H,35,39)(H,36,40)/t26-,27?,28?,29-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022644 (CHEMBL73712 | Piperazine-1-carboxylic acid {1-[1-(...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](Cc1ccccc1)NC(=O)N1CCNCC1 Show InChI InChI=1S/C34H53N7O5/c1-23(2)17-30(42)31(43)27(18-24-9-5-3-6-10-24)38-33(45)29(20-26-21-36-22-37-26)39-32(44)28(19-25-11-7-4-8-12-25)40-34(46)41-15-13-35-14-16-41/h4,7-8,11-12,21-24,27-31,35,42-43H,3,5-6,9-10,13-20H2,1-2H3,(H,36,37)(H,38,45)(H,39,44)(H,40,46)/t27-,28-,29-,30-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	4.5	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of human plasma renin (pH 7.4)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022381 (CHEMBL3142207 | {1-[1-[1-Cyclohexylmethyl-2-hydrox...) Show SMILES CCOC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CS(=O)(=O)C(C)C Show InChI InChI=1S/C31H47N5O7S/c1-4-43-31(40)36-26(16-23-13-9-6-10-14-23)29(38)35-27(17-24-18-32-20-33-24)30(39)34-25(15-22-11-7-5-8-12-22)28(37)19-44(41,42)21(2)3/h6,9-10,13-14,18,20-22,25-28,37H,4-5,7-8,11-12,15-17,19H2,1-3H3,(H,32,33)(H,34,39)(H,35,38)(H,36,40)/t25-,26?,27?,28-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022651 (CHEMBL306274 | Morpholine-4-carboxylic acid {1-[1-...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)C(Cc1ccccc1)=NC(=O)N1CCOCC1 |w:37.40| Show InChI InChI=1S/C34H50N6O6/c1-23(2)17-30(41)31(42)27(18-24-9-5-3-6-10-24)37-33(44)29(20-26-21-35-22-36-26)38-32(43)28(19-25-11-7-4-8-12-25)39-34(45)40-13-15-46-16-14-40/h4,7-8,11-12,21-24,27,29-31,41-42H,3,5-6,9-10,13-20H2,1-2H3,(H,35,36)(H,37,44)(H,38,43)/t27-,29-,30-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	5.30	n/a	n/a	n/a	n/a	7.4	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022364 (CHEMBL3142204 | {2-Benzyloxy-1-[1-[1-cyclohexylmet...) Show SMILES CC(C)S(=O)(=O)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@@H](NC(=O)OC(C)(C)C)[C@@H](C)OCc1ccccc1 Show InChI InChI=1S/C35H55N5O8S/c1-23(2)49(45,46)21-30(41)28(17-25-13-9-7-10-14-25)38-32(42)29(18-27-19-36-22-37-27)39-33(43)31(40-34(44)48-35(4,5)6)24(3)47-20-26-15-11-8-12-16-26/h8,11-12,15-16,19,22-25,28-31,41H,7,9-10,13-14,17-18,20-21H2,1-6H3,(H,36,37)(H,38,42)(H,39,43)(H,40,44)/t24?,28-,29?,30-,31?/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022373 ((1-{2-Benzyloxy-1-[1-cyclohexylmethyl-2-hydroxy-3-...) Show SMILES CC(C)S(=O)(=O)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)[C@@H](C)OCc1ccccc1 Show InChI InChI=1S/C38H57N3O8S/c1-26(2)50(46,47)25-33(42)31(22-28-16-10-7-11-17-28)39-36(44)34(27(3)48-24-30-20-14-9-15-21-30)41-35(43)32(23-29-18-12-8-13-19-29)40-37(45)49-38(4,5)6/h8-9,12-15,18-21,26-28,31-34,42H,7,10-11,16-17,22-25H2,1-6H3,(H,39,44)(H,40,45)(H,41,43)/t27?,31-,32?,33-,34?/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	6	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022382 (CHEMBL3142219 | {1-[1-(1-Cyclohexylmethyl-2-hydrox...) Show SMILES CC(C)CSC[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C Show InChI InChI=1S/C34H53N5O5S/c1-23(2)20-45-21-30(40)27(16-24-12-8-6-9-13-24)37-32(42)29(18-26-19-35-22-36-26)38-31(41)28(17-25-14-10-7-11-15-25)39-33(43)44-34(3,4)5/h7,10-11,14-15,19,22-24,27-30,40H,6,8-9,12-13,16-18,20-21H2,1-5H3,(H,35,36)(H,37,42)(H,38,41)(H,39,43)/t27-,28?,29?,30-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	6.5	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022368 ((1-{1-[1-Cyclohexylmethyl-2-hydroxy-3-(propane-2-s...) Show SMILES C[C@@H](O)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CS(=O)(=O)C(C)C Show InChI InChI=1S/C31H51N3O8S/c1-20(2)43(40,41)19-26(36)24(17-22-13-9-7-10-14-22)32-29(38)27(21(3)35)34-28(37)25(18-23-15-11-8-12-16-23)33-30(39)42-31(4,5)6/h8,11-12,15-16,20-22,24-27,35-36H,7,9-10,13-14,17-19H2,1-6H3,(H,32,38)(H,33,39)(H,34,37)/t21?,24-,25?,26-,27?/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	8	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022375 (BDBM50022873 | CHEMBL348469 | {1-[1-(1-Cyclohexylm...) Show SMILES CC(C)SC[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](C)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C Show InChI InChI=1S/C30H49N3O5S/c1-20(2)39-19-26(34)24(17-22-13-9-7-10-14-22)32-27(35)21(3)31-28(36)25(18-23-15-11-8-12-16-23)33-29(37)38-30(4,5)6/h8,11-12,15-16,20-22,24-26,34H,7,9-10,13-14,17-19H2,1-6H3,(H,31,36)(H,32,35)(H,33,37)/t21?,24-,25?,26-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	9.90	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022358 (CHEMBL3142234 | {1-[1-(1-Cyclohexylmethyl-2-hydrox...) Show SMILES CSC[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C Show InChI InChI=1S/C31H47N5O5S/c1-31(2,3)41-30(40)36-25(16-22-13-9-6-10-14-22)28(38)35-26(17-23-18-32-20-33-23)29(39)34-24(27(37)19-42-4)15-21-11-7-5-8-12-21/h6,9-10,13-14,18,20-21,24-27,37H,5,7-8,11-12,15-17,19H2,1-4H3,(H,32,33)(H,34,39)(H,35,38)(H,36,40)/t24-,25?,26?,27-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022359 (3-Benzyloxy-N-[1-[1-cyclohexylmethyl-2-hydroxy-3-(...) Show SMILES CC(C)C(=O)N[C@@H]([C@@H](C)OCc1ccccc1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CS(=O)(=O)C(C)C Show InChI InChI=1S/C34H53N5O7S/c1-22(2)32(41)39-31(24(5)46-19-26-14-10-7-11-15-26)34(43)38-29(17-27-18-35-21-36-27)33(42)37-28(16-25-12-8-6-9-13-25)30(40)20-47(44,45)23(3)4/h7,10-11,14-15,18,21-25,28-31,40H,6,8-9,12-13,16-17,19-20H2,1-5H3,(H,35,36)(H,37,42)(H,38,43)(H,39,41)/t24?,28-,29?,30-,31?/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022648 (CHEMBL74875 | Morpholine-4-carboxylic acid {1-[1-(...) Show SMILES CC(C)C[C@H](O)[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)N1CCOCC1 Show InChI InChI=1S/C34H52N6O6/c1-23(2)17-30(41)31(42)27(18-24-9-5-3-6-10-24)37-33(44)29(20-26-21-35-22-36-26)38-32(43)28(19-25-11-7-4-8-12-25)39-34(45)40-13-15-46-16-14-40/h4,7-8,11-12,21-24,27-31,41-42H,3,5-6,9-10,13-20H2,1-2H3,(H,35,36)(H,37,44)(H,38,43)(H,39,45)/t27-,28+,29-,30-,31+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	6.0	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Inhibition of purified human renin (pH 6.0)				J Med Chem 31: 2277-88 (1989) BindingDB Entry DOI: 10.7270/Q2PG1QQ4
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022383 (CHEMBL3142208 | {1-[1-(1-Benzyl-3-cyclohexylsulfan...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)CSC1CCCCC1 Show InChI InChI=1S/C36H49N5O5S/c1-36(2,3)46-35(45)41-30(20-26-15-9-5-10-16-26)33(43)40-31(21-27-22-37-24-38-27)34(44)39-29(19-25-13-7-4-8-14-25)32(42)23-47-28-17-11-6-12-18-28/h4-5,7-10,13-16,22,24,28-32,42H,6,11-12,17-21,23H2,1-3H3,(H,37,38)(H,39,44)(H,40,43)(H,41,45)/t29-,30?,31?,32-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	15	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022354 (2-Benzyl-N-[1-(1-cyclohexylmethyl-3-cyclohexylsulf...) Show SMILES O[C@@H](CSC1CCCCC1)[C@H](CC1CCCCC1)NC(=O)C(Cc1cnc[nH]1)NC(=O)C(Cc1ccccc1)Cc1ccccc1 Show InChI InChI=1S/C38H52N4O3S/c43-36(26-46-33-19-11-4-12-20-33)34(23-30-17-9-3-10-18-30)41-38(45)35(24-32-25-39-27-40-32)42-37(44)31(21-28-13-5-1-6-14-28)22-29-15-7-2-8-16-29/h1-2,5-8,13-16,25,27,30-31,33-36,43H,3-4,9-12,17-24,26H2,(H,39,40)(H,41,45)(H,42,44)/t34-,35?,36-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia 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
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022362 ((1-{1-[1-Cyclohexylmethyl-2-hydroxy-3-(propane-2-s...) Show SMILES CC(C)S(=O)(=O)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](CCO)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C Show InChI InChI=1S/C31H51N3O8S/c1-21(2)43(40,41)20-27(36)25(18-22-12-8-6-9-13-22)33-28(37)24(16-17-35)32-29(38)26(19-23-14-10-7-11-15-23)34-30(39)42-31(3,4)5/h7,10-11,14-15,21-22,24-27,35-36H,6,8-9,12-13,16-20H2,1-5H3,(H,32,38)(H,33,37)(H,34,39)/t24?,25-,26?,27-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia 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
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022371 (CHEMBL3142206 | {2-Benzyloxy-1-[1-[1-cyclohexylmet...) Show SMILES CCOC(=O)N[C@@H]([C@@H](C)OCc1ccccc1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CS(=O)(=O)C(C)C Show InChI InChI=1S/C33H51N5O8S/c1-5-45-33(42)38-30(23(4)46-19-25-14-10-7-11-15-25)32(41)37-28(17-26-18-34-21-35-26)31(40)36-27(16-24-12-8-6-9-13-24)29(39)20-47(43,44)22(2)3/h7,10-11,14-15,18,21-24,27-30,39H,5-6,8-9,12-13,16-17,19-20H2,1-4H3,(H,34,35)(H,36,40)(H,37,41)(H,38,42)/t23?,27-,28?,29-,30?/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022369 (2-(2-Benzyl-3-phenyl-propionylamino)-4-methyl-pent...) Show SMILES CC(C)CC(NC(=O)C(Cc1ccccc1)Cc1ccccc1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CS(=O)(=O)C(C)C Show InChI InChI=1S/C35H52N2O5S/c1-25(2)20-32(37-34(39)30(21-27-14-8-5-9-15-27)22-28-16-10-6-11-17-28)35(40)36-31(23-29-18-12-7-13-19-29)33(38)24-43(41,42)26(3)4/h5-6,8-11,14-17,25-26,29-33,38H,7,12-13,18-24H2,1-4H3,(H,36,40)(H,37,39)/t31-,32?,33-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	25	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022378 ((1-{1-[1-Cyclohexylmethyl-2-hydroxy-3-(propane-2-s...) Show SMILES CC(C)S(=O)(=O)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OC(C)(C)C Show InChI InChI=1S/C36H53N3O7S/c1-25(2)47(44,45)24-32(40)29(21-26-15-9-6-10-16-26)37-33(41)30(22-27-17-11-7-12-18-27)38-34(42)31(23-28-19-13-8-14-20-28)39-35(43)46-36(3,4)5/h7-8,11-14,17-20,25-26,29-32,40H,6,9-10,15-16,21-24H2,1-5H3,(H,37,41)(H,38,42)(H,39,43)/t29-,30?,31?,32-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	30	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair
Renin (Homo sapiens (Human))	BDBM50022363 (2-Benzyl-N-[1-(3-cyclohexanesulfonyl-1-cyclohexylm...) Show SMILES O[C@@H](CS(=O)(=O)C1CCCCC1)[C@H](CC1CCCCC1)NC(=O)C(Cc1cnc[nH]1)NC(=O)C(Cc1ccccc1)Cc1ccccc1 Show InChI InChI=1S/C38H52N4O5S/c43-36(26-48(46,47)33-19-11-4-12-20-33)34(23-30-17-9-3-10-18-30)41-38(45)35(24-32-25-39-27-40-32)42-37(44)31(21-28-13-5-1-6-14-28)22-29-15-7-2-8-16-29/h1-2,5-8,13-16,25,27,30-31,33-36,43H,3-4,9-12,17-24,26H2,(H,39,40)(H,41,45)(H,42,44)/t34-,35?,36-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	40	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair				3D Structure (docked)
Renin (Homo sapiens (Human))	BDBM50022377 (CHEMBL3142224 | {1-[1-(1-Cyclohexylmethyl-2-hydrox...) Show SMILES CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CC1CCCCC1)[C@@H](O)CS(C)(=O)=O Show InChI InChI=1S/C31H47N5O7S/c1-31(2,3)43-30(40)36-25(16-22-13-9-6-10-14-22)28(38)35-26(17-23-18-32-20-33-23)29(39)34-24(27(37)19-44(4,41)42)15-21-11-7-5-8-12-21/h6,9-10,13-14,18,20-21,24-27,37H,5,7-8,11-12,15-17,19H2,1-4H3,(H,32,33)(H,34,39)(H,35,38)(H,36,40)/t24-,25?,26?,27-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	n/a	n/a	40	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Evaluated in vitro for inhibitory potency against renin.				J Med Chem 30: 2137-44 (1987) BindingDB Entry DOI: 10.7270/Q2RJ4K2D
					More data for this Ligand-Target Pair

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