Compile Data Set for Download or QSAR

Found 40 hits with Last Name = 'tambaro' and Initial = 's'   

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
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM21278 (5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl...) Show SMILES Cc1c(nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1Cl)C(=O)NN1CCCCC1 Show InChI InChI=1S/C22H21Cl3N4O/c1-14-20(22(30)27-28-11-3-2-4-12-28)26-29(19-10-9-17(24)13-18(19)25)21(14)15-5-7-16(23)8-6-15/h5-10,13H,2-4,11-12H2,1H3,(H,27,30)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem Patents Similars	Article PubMed	1.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Neuroscienze PharmaNess S.c.a r.l. Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from CB1 receptor in CD1 mouse brain membrane without cerebellum by liquid scintillation counting analysis				Eur J Med Chem 62: 256-69 (2013) Article DOI: 10.1016/j.ejmech.2012.12.056 BindingDB Entry DOI: 10.7270/Q2TQ62W2
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM50195530 (5-(4-chlorophenyl)-3-[(E)-2-cyclohexylethenyl]-1-(...) Show SMILES Cc1c(\C=C\C2CCCCC2)nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1Cl Show InChI InChI=1S/C24H23Cl3N2/c1-16-22(13-7-17-5-3-2-4-6-17)28-29(23-14-12-20(26)15-21(23)27)24(16)18-8-10-19(25)11-9-18/h7-15,17H,2-6H2,1H3/b13-7+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	11	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Neuroscienze PharmaNess S.c.a r.l. Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from CB1 receptor in CD1 mouse brain membrane without cerebellum by liquid scintillation counting analysis				Eur J Med Chem 62: 256-69 (2013) Article DOI: 10.1016/j.ejmech.2012.12.056 BindingDB Entry DOI: 10.7270/Q2TQ62W2
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM50429403 (CHEMBL2337204) Show SMILES Cc1c(nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1Cl)C(\F)=C\C1CCCCC1 Show InChI InChI=1S/C24H22Cl3FN2/c1-15-23(21(28)13-16-5-3-2-4-6-16)29-30(22-12-11-19(26)14-20(22)27)24(15)17-7-9-18(25)10-8-17/h7-14,16H,2-6H2,1H3/b21-13-	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	26	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Neuroscienze PharmaNess S.c.a r.l. Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from CB1 receptor in CD1 mouse brain membrane without cerebellum by liquid scintillation counting analysis				Eur J Med Chem 62: 256-69 (2013) Article DOI: 10.1016/j.ejmech.2012.12.056 BindingDB Entry DOI: 10.7270/Q2TQ62W2
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM50429405 (CHEMBL2337206) Show SMILES Cc1c(nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1Cl)C(=O)CC1CCCCC1 Show InChI InChI=1S/C24H23Cl3N2O/c1-15-23(22(30)13-16-5-3-2-4-6-16)28-29(21-12-11-19(26)14-20(21)27)24(15)17-7-9-18(25)10-8-17/h7-12,14,16H,2-6,13H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	46	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Neuroscienze PharmaNess S.c.a r.l. Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from CB1 receptor in CD1 mouse brain membrane without cerebellum by liquid scintillation counting analysis				Eur J Med Chem 62: 256-69 (2013) Article DOI: 10.1016/j.ejmech.2012.12.056 BindingDB Entry DOI: 10.7270/Q2TQ62W2
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM50429404 (CHEMBL2337205) Show SMILES Cc1c(nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1Cl)C(O)CC1CCCCC1 Show InChI InChI=1S/C24H25Cl3N2O/c1-15-23(22(30)13-16-5-3-2-4-6-16)28-29(21-12-11-19(26)14-20(21)27)24(15)17-7-9-18(25)10-8-17/h7-12,14,16,22,30H,2-6,13H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	175	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Neuroscienze PharmaNess S.c.a r.l. Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from CB1 receptor in CD1 mouse brain membrane without cerebellum by liquid scintillation counting analysis				Eur J Med Chem 62: 256-69 (2013) Article DOI: 10.1016/j.ejmech.2012.12.056 BindingDB Entry DOI: 10.7270/Q2TQ62W2
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM50429401 (CHEMBL2337202) Show SMILES Cc1c(nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1Cl)C(NN1CCCCC1)C(F)(F)F Show InChI InChI=1S/C23H22Cl3F3N4/c1-14-20(22(23(27,28)29)31-32-11-3-2-4-12-32)30-33(19-10-9-17(25)13-18(19)26)21(14)15-5-7-16(24)8-6-15/h5-10,13,22,31H,2-4,11-12H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	287	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Neuroscienze PharmaNess S.c.a r.l. Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from CB1 receptor in CD1 mouse brain membrane without cerebellum by liquid scintillation counting analysis				Eur J Med Chem 62: 256-69 (2013) Article DOI: 10.1016/j.ejmech.2012.12.056 BindingDB Entry DOI: 10.7270/Q2TQ62W2
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (MOUSE)	BDBM21278 (5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl...) Show SMILES Cc1c(nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1Cl)C(=O)NN1CCCCC1 Show InChI InChI=1S/C22H21Cl3N4O/c1-14-20(22(30)27-28-11-3-2-4-12-28)26-29(19-10-9-17(24)13-18(19)25)21(14)15-5-7-16(23)8-6-15/h5-10,13H,2-4,11-12H2,1H3,(H,27,30)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem Patents Similars	Article PubMed	375	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Neuroscienze PharmaNess S.c.a r.l. Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from CB2 receptor in CD1 mouse spleen membrane by liquid scintillation counting analysis				Eur J Med Chem 62: 256-69 (2013) Article DOI: 10.1016/j.ejmech.2012.12.056 BindingDB Entry DOI: 10.7270/Q2TQ62W2
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM50429402 (CHEMBL2337203) Show SMILES Cc1c(nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1Cl)C(\F)=C/C1CCCCC1 Show InChI InChI=1S/C24H22Cl3FN2/c1-15-23(21(28)13-16-5-3-2-4-6-16)29-30(22-12-11-19(26)14-20(22)27)24(15)17-7-9-18(25)10-8-17/h7-14,16H,2-6H2,1H3/b21-13+	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	412	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Neuroscienze PharmaNess S.c.a r.l. Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from CB1 receptor in CD1 mouse brain membrane without cerebellum by liquid scintillation counting analysis				Eur J Med Chem 62: 256-69 (2013) Article DOI: 10.1016/j.ejmech.2012.12.056 BindingDB Entry DOI: 10.7270/Q2TQ62W2
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (MOUSE)	BDBM50429403 (CHEMBL2337204) Show SMILES Cc1c(nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1Cl)C(\F)=C\C1CCCCC1 Show InChI InChI=1S/C24H22Cl3FN2/c1-15-23(21(28)13-16-5-3-2-4-6-16)29-30(22-12-11-19(26)14-20(22)27)24(15)17-7-9-18(25)10-8-17/h7-14,16H,2-6H2,1H3/b21-13-	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.95E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Neuroscienze PharmaNess S.c.a r.l. Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from CB2 receptor in CD1 mouse spleen membrane by liquid scintillation counting analysis				Eur J Med Chem 62: 256-69 (2013) Article DOI: 10.1016/j.ejmech.2012.12.056 BindingDB Entry DOI: 10.7270/Q2TQ62W2
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (MOUSE)	BDBM50429405 (CHEMBL2337206) Show SMILES Cc1c(nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1Cl)C(=O)CC1CCCCC1 Show InChI InChI=1S/C24H23Cl3N2O/c1-15-23(22(30)13-16-5-3-2-4-6-16)28-29(21-12-11-19(26)14-20(21)27)24(15)17-7-9-18(25)10-8-17/h7-12,14,16H,2-6,13H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.23E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Neuroscienze PharmaNess S.c.a r.l. Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from CB2 receptor in CD1 mouse spleen membrane by liquid scintillation counting analysis				Eur J Med Chem 62: 256-69 (2013) Article DOI: 10.1016/j.ejmech.2012.12.056 BindingDB Entry DOI: 10.7270/Q2TQ62W2
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (MOUSE)	BDBM50195530 (5-(4-chlorophenyl)-3-[(E)-2-cyclohexylethenyl]-1-(...) Show SMILES Cc1c(\C=C\C2CCCCC2)nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1Cl Show InChI InChI=1S/C24H23Cl3N2/c1-16-22(13-7-17-5-3-2-4-6-17)28-29(23-14-12-20(26)15-21(23)27)24(16)18-8-10-19(25)11-9-18/h7-15,17H,2-6H2,1H3/b13-7+	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Neuroscienze PharmaNess S.c.a r.l. Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from CB2 receptor in CD1 mouse spleen membrane by liquid scintillation counting analysis				Eur J Med Chem 62: 256-69 (2013) Article DOI: 10.1016/j.ejmech.2012.12.056 BindingDB Entry DOI: 10.7270/Q2TQ62W2
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (MOUSE)	BDBM50429402 (CHEMBL2337203) Show SMILES Cc1c(nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1Cl)C(\F)=C/C1CCCCC1 Show InChI InChI=1S/C24H22Cl3FN2/c1-15-23(21(28)13-16-5-3-2-4-6-16)29-30(22-12-11-19(26)14-20(22)27)24(15)17-7-9-18(25)10-8-17/h7-14,16H,2-6H2,1H3/b21-13+	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Neuroscienze PharmaNess S.c.a r.l. Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from CB2 receptor in CD1 mouse spleen membrane by liquid scintillation counting analysis				Eur J Med Chem 62: 256-69 (2013) Article DOI: 10.1016/j.ejmech.2012.12.056 BindingDB Entry DOI: 10.7270/Q2TQ62W2
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (MOUSE)	BDBM50429404 (CHEMBL2337205) Show SMILES Cc1c(nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1Cl)C(O)CC1CCCCC1 Show InChI InChI=1S/C24H25Cl3N2O/c1-15-23(22(30)13-16-5-3-2-4-6-16)28-29(21-12-11-19(26)14-20(21)27)24(15)17-7-9-18(25)10-8-17/h7-12,14,16,22,30H,2-6,13H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	4.20E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Neuroscienze PharmaNess S.c.a r.l. Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from CB2 receptor in CD1 mouse spleen membrane by liquid scintillation counting analysis				Eur J Med Chem 62: 256-69 (2013) Article DOI: 10.1016/j.ejmech.2012.12.056 BindingDB Entry DOI: 10.7270/Q2TQ62W2
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (MOUSE)	BDBM50429401 (CHEMBL2337202) Show SMILES Cc1c(nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1Cl)C(NN1CCCCC1)C(F)(F)F Show InChI InChI=1S/C23H22Cl3F3N4/c1-14-20(22(23(27,28)29)31-32-11-3-2-4-12-32)30-33(19-10-9-17(25)13-18(19)26)21(14)15-5-7-16(24)8-6-15/h5-10,13,22,31H,2-4,11-12H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	>5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Neuroscienze PharmaNess S.c.a r.l. Curated by ChEMBL					Assay Description Displacement of [3H]CP55940 from CB2 receptor in CD1 mouse spleen membrane by liquid scintillation counting analysis				Eur J Med Chem 62: 256-69 (2013) Article DOI: 10.1016/j.ejmech.2012.12.056 BindingDB Entry DOI: 10.7270/Q2TQ62W2
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Homo sapiens (Human))	BDBM21642 ((2S)-1-[(2S)-2-methyl-3-sulfanylpropanoyl]pyrrolid...) Show SMILES C[C@H](CS)C(=O)N1CCC[C@H]1C(O)=O Show InChI InChI=1S/C9H15NO3S/c1-6(5-14)8(11)10-4-2-3-7(10)9(12)13/h6-7,14H,2-5H2,1H3,(H,12,13)/t6-,7+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	DrugBank PDB Article PubMed	n/a	n/a	0.120	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of human recombinant ACE by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair				3D Structure (crystal)
Neprilysin [1-24] (Sus scrofa)	BDBM21641 (2-(2-benzyl-3-sulfanylpropanamido)acetic acid | CH...) Show SMILES OC(=O)CNC(=O)C(CS)Cc1ccccc1 Show InChI InChI=1S/C12H15NO3S/c14-11(15)7-13-12(16)10(8-17)6-9-4-2-1-3-5-9/h1-5,10,17H,6-8H2,(H,13,16)(H,14,15)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	6.20	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of pig kidney NEP by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Endothelin-converting enzyme 1 (Homo sapiens (Human))	BDBM50251742 ((3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydro...) Show SMILES CC(C)C[C@H](NP(O)(=O)O[C@@H]1O[C@@H](C)[C@H](O)[C@@H](O)[C@H]1O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(O)=O |r| Show InChI InChI=1S/C23H34N3O10P/c1-11(2)8-16(26-37(33,34)36-23-20(29)19(28)18(27)12(3)35-23)21(30)25-17(22(31)32)9-13-10-24-15-7-5-4-6-14(13)15/h4-7,10-12,16-20,23-24,27-29H,8-9H2,1-3H3,(H,25,30)(H,31,32)(H2,26,33,34)/t12-,16-,17-,18-,19+,20+,23-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of human recombinant ECE1 by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair				3D Structure (crystal)
Neprilysin [1-24] (Sus scrofa)	BDBM50046261 (2-(3-Mercapto-5-methyl-hexanoylamino)-3-phenyl-pro...) Show SMILES CC(C)CC(S)CC(=O)NC(Cc1ccccc1)C(O)=O Show InChI InChI=1S/C16H23NO3S/c1-11(2)8-13(21)10-15(18)17-14(16(19)20)9-12-6-4-3-5-7-12/h3-7,11,13-14,21H,8-10H2,1-2H3,(H,17,18)(H,19,20)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	41	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of pig kidney NEP by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Neprilysin [1-24] (Sus scrofa)	BDBM50046258 (3-(4-Hydroxy-phenyl)-2-[2-(3-mercapto-5-methyl-hex...) Show SMILES CC(C)CC(S)CC(=O)NC(Cc1ccccc1)C(=O)NC(Cc1ccc(O)cc1)C(O)=O Show InChI InChI=1S/C25H32N2O5S/c1-16(2)12-20(33)15-23(29)26-21(13-17-6-4-3-5-7-17)24(30)27-22(25(31)32)14-18-8-10-19(28)11-9-18/h3-11,16,20-22,28,33H,12-15H2,1-2H3,(H,26,29)(H,27,30)(H,31,32)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	50	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of pig kidney NEP by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Neprilysin [1-24] (Sus scrofa)	BDBM50298107 (3-(4-Hydroxy-phenyl)-2-(4,4,4-trifluoro-3-mercapto...) Show SMILES OC(=O)C(Cc1ccc(O)cc1)NC(=O)CC(S)C(F)(F)F Show InChI InChI=1S/C13H14F3NO4S/c14-13(15,16)10(22)6-11(19)17-9(12(20)21)5-7-1-3-8(18)4-2-7/h1-4,9-10,18,22H,5-6H2,(H,17,19)(H,20,21)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	80	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of pig kidney NEP by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Homo sapiens (Human))	BDBM50298107 (3-(4-Hydroxy-phenyl)-2-(4,4,4-trifluoro-3-mercapto...) Show SMILES OC(=O)C(Cc1ccc(O)cc1)NC(=O)CC(S)C(F)(F)F Show InChI InChI=1S/C13H14F3NO4S/c14-13(15,16)10(22)6-11(19)17-9(12(20)21)5-7-1-3-8(18)4-2-7/h1-4,9-10,18,22H,5-6H2,(H,17,19)(H,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	160	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of human recombinant ACE by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Neprilysin [1-24] (Sus scrofa)	BDBM50298108 (3-(4-Fluoro-phenyl)-2-(4,4,4-trifluoro-3-mercapto-...) Show SMILES OC(=O)C(Cc1ccc(F)cc1)NC(=O)CC(S)C(F)(F)F Show InChI InChI=1S/C13H13F4NO3S/c14-8-3-1-7(2-4-8)5-9(12(20)21)18-11(19)6-10(22)13(15,16)17/h1-4,9-10,22H,5-6H2,(H,18,19)(H,20,21)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	230	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of pig kidney NEP by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Homo sapiens (Human))	BDBM50298111 (3-(4-Hydroxy-phenyl)-2-[3-phenyl-2-(4,4,4-trifluor...) Show SMILES OC(=O)C(Cc1ccc(O)cc1)NC(=O)C(Cc1ccccc1)NC(=O)CC(S)C(F)(F)F Show InChI InChI=1S/C22H23F3N2O5S/c23-22(24,25)18(33)12-19(29)26-16(10-13-4-2-1-3-5-13)20(30)27-17(21(31)32)11-14-6-8-15(28)9-7-14/h1-9,16-18,28,33H,10-12H2,(H,26,29)(H,27,30)(H,31,32)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	280	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of human recombinant ACE by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Neprilysin [1-24] (Sus scrofa)	BDBM50298106 (3-phenyl-2-(4,4,4-trifluoro-3-mercaptobutanamido)p...) Show SMILES OC(=O)C(Cc1ccccc1)NC(=O)CC(S)C(F)(F)F Show InChI InChI=1S/C13H14F3NO3S/c14-13(15,16)10(21)7-11(18)17-9(12(19)20)6-8-4-2-1-3-5-8/h1-5,9-10,21H,6-7H2,(H,17,18)(H,19,20)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	300	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of pig kidney NEP by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Homo sapiens (Human))	BDBM50298108 (3-(4-Fluoro-phenyl)-2-(4,4,4-trifluoro-3-mercapto-...) Show SMILES OC(=O)C(Cc1ccc(F)cc1)NC(=O)CC(S)C(F)(F)F Show InChI InChI=1S/C13H13F4NO3S/c14-8-3-1-7(2-4-8)5-9(12(20)21)18-11(19)6-10(22)13(15,16)17/h1-4,9-10,22H,5-6H2,(H,18,19)(H,20,21)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	300	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of human recombinant ACE by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Homo sapiens (Human))	BDBM50298109 (3-(1H-Indol-3-yl)-2-(4,4,4-trifluoro-3-mercapto-bu...) Show SMILES OC(=O)C(Cc1c[nH]c2ccccc12)NC(=O)CC(S)C(F)(F)F Show InChI InChI=1S/C15H15F3N2O3S/c16-15(17,18)12(24)6-13(21)20-11(14(22)23)5-8-7-19-10-4-2-1-3-9(8)10/h1-4,7,11-12,19,24H,5-6H2,(H,20,21)(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	400	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of human recombinant ACE by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Neprilysin [1-24] (Sus scrofa)	BDBM50298111 (3-(4-Hydroxy-phenyl)-2-[3-phenyl-2-(4,4,4-trifluor...) Show SMILES OC(=O)C(Cc1ccc(O)cc1)NC(=O)C(Cc1ccccc1)NC(=O)CC(S)C(F)(F)F Show InChI InChI=1S/C22H23F3N2O5S/c23-22(24,25)18(33)12-19(29)26-16(10-13-4-2-1-3-5-13)20(30)27-17(21(31)32)11-14-6-8-15(28)9-7-14/h1-9,16-18,28,33H,10-12H2,(H,26,29)(H,27,30)(H,31,32)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	430	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of pig kidney NEP by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Neprilysin [1-24] (Sus scrofa)	BDBM50298109 (3-(1H-Indol-3-yl)-2-(4,4,4-trifluoro-3-mercapto-bu...) Show SMILES OC(=O)C(Cc1c[nH]c2ccccc12)NC(=O)CC(S)C(F)(F)F Show InChI InChI=1S/C15H15F3N2O3S/c16-15(17,18)12(24)6-13(21)20-11(14(22)23)5-8-7-19-10-4-2-1-3-9(8)10/h1-4,7,11-12,19,24H,5-6H2,(H,20,21)(H,22,23)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	580	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of pig kidney NEP by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Homo sapiens (Human))	BDBM50298106 (3-phenyl-2-(4,4,4-trifluoro-3-mercaptobutanamido)p...) Show SMILES OC(=O)C(Cc1ccccc1)NC(=O)CC(S)C(F)(F)F Show InChI InChI=1S/C13H14F3NO3S/c14-13(15,16)10(21)7-11(18)17-9(12(19)20)6-8-4-2-1-3-5-8/h1-5,9-10,21H,6-7H2,(H,17,18)(H,19,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	830	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of human recombinant ACE by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Homo sapiens (Human))	BDBM50298110 (2-(4,4,5,5,5-Pentafluoro-3-mercapto-pentanoylamino...) Show SMILES OC(=O)C(Cc1ccccc1)NC(=O)CC(S)C(F)(F)C(F)(F)F Show InChI InChI=1S/C14H14F5NO3S/c15-13(16,14(17,18)19)10(24)7-11(21)20-9(12(22)23)6-8-4-2-1-3-5-8/h1-5,9-10,24H,6-7H2,(H,20,21)(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.01E+3	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of human recombinant ACE by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Neprilysin [1-24] (Sus scrofa)	BDBM50298110 (2-(4,4,5,5,5-Pentafluoro-3-mercapto-pentanoylamino...) Show SMILES OC(=O)C(Cc1ccccc1)NC(=O)CC(S)C(F)(F)C(F)(F)F Show InChI InChI=1S/C14H14F5NO3S/c15-13(16,14(17,18)19)10(24)7-11(21)20-9(12(22)23)6-8-4-2-1-3-5-8/h1-5,9-10,24H,6-7H2,(H,20,21)(H,22,23)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.15E+3	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of pig kidney NEP by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Endothelin-converting enzyme 1 (Homo sapiens (Human))	BDBM50298110 (2-(4,4,5,5,5-Pentafluoro-3-mercapto-pentanoylamino...) Show SMILES OC(=O)C(Cc1ccccc1)NC(=O)CC(S)C(F)(F)C(F)(F)F Show InChI InChI=1S/C14H14F5NO3S/c15-13(16,14(17,18)19)10(24)7-11(21)20-9(12(22)23)6-8-4-2-1-3-5-8/h1-5,9-10,24H,6-7H2,(H,20,21)(H,22,23)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.42E+3	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of human recombinant ECE1 by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Homo sapiens (Human))	BDBM50046258 (3-(4-Hydroxy-phenyl)-2-[2-(3-mercapto-5-methyl-hex...) Show SMILES CC(C)CC(S)CC(=O)NC(Cc1ccccc1)C(=O)NC(Cc1ccc(O)cc1)C(O)=O Show InChI InChI=1S/C25H32N2O5S/c1-16(2)12-20(33)15-23(29)26-21(13-17-6-4-3-5-7-17)24(30)27-22(25(31)32)14-18-8-10-19(28)11-9-18/h3-11,16,20-22,28,33H,12-15H2,1-2H3,(H,26,29)(H,27,30)(H,31,32)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of human recombinant ACE by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Endothelin-converting enzyme 1 (Homo sapiens (Human))	BDBM50298108 (3-(4-Fluoro-phenyl)-2-(4,4,4-trifluoro-3-mercapto-...) Show SMILES OC(=O)C(Cc1ccc(F)cc1)NC(=O)CC(S)C(F)(F)F Show InChI InChI=1S/C13H13F4NO3S/c14-8-3-1-7(2-4-8)5-9(12(20)21)18-11(19)6-10(22)13(15,16)17/h1-4,9-10,22H,5-6H2,(H,18,19)(H,20,21)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of human recombinant ECE1 by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Endothelin-converting enzyme 1 (Homo sapiens (Human))	BDBM50298109 (3-(1H-Indol-3-yl)-2-(4,4,4-trifluoro-3-mercapto-bu...) Show SMILES OC(=O)C(Cc1c[nH]c2ccccc12)NC(=O)CC(S)C(F)(F)F Show InChI InChI=1S/C15H15F3N2O3S/c16-15(17,18)12(24)6-13(21)20-11(14(22)23)5-8-7-19-10-4-2-1-3-9(8)10/h1-4,7,11-12,19,24H,5-6H2,(H,20,21)(H,22,23)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of human recombinant ECE1 by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Endothelin-converting enzyme 1 (Homo sapiens (Human))	BDBM50298106 (3-phenyl-2-(4,4,4-trifluoro-3-mercaptobutanamido)p...) Show SMILES OC(=O)C(Cc1ccccc1)NC(=O)CC(S)C(F)(F)F Show InChI InChI=1S/C13H14F3NO3S/c14-13(15,16)10(21)7-11(18)17-9(12(19)20)6-8-4-2-1-3-5-8/h1-5,9-10,21H,6-7H2,(H,17,18)(H,19,20)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of human recombinant ECE1 by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Endothelin-converting enzyme 1 (Homo sapiens (Human))	BDBM50046261 (2-(3-Mercapto-5-methyl-hexanoylamino)-3-phenyl-pro...) Show SMILES CC(C)CC(S)CC(=O)NC(Cc1ccccc1)C(O)=O Show InChI InChI=1S/C16H23NO3S/c1-11(2)8-13(21)10-15(18)17-14(16(19)20)9-12-6-4-3-5-7-12/h3-7,11,13-14,21H,8-10H2,1-2H3,(H,17,18)(H,19,20)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of human recombinant ECE1 by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Angiotensin-converting enzyme (Homo sapiens (Human))	BDBM50046261 (2-(3-Mercapto-5-methyl-hexanoylamino)-3-phenyl-pro...) Show SMILES CC(C)CC(S)CC(=O)NC(Cc1ccccc1)C(O)=O Show InChI InChI=1S/C16H23NO3S/c1-11(2)8-13(21)10-15(18)17-14(16(19)20)9-12-6-4-3-5-7-12/h3-7,11,13-14,21H,8-10H2,1-2H3,(H,17,18)(H,19,20)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of human recombinant ACE by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Endothelin-converting enzyme 1 (Homo sapiens (Human))	BDBM50298111 (3-(4-Hydroxy-phenyl)-2-[3-phenyl-2-(4,4,4-trifluor...) Show SMILES OC(=O)C(Cc1ccc(O)cc1)NC(=O)C(Cc1ccccc1)NC(=O)CC(S)C(F)(F)F Show InChI InChI=1S/C22H23F3N2O5S/c23-22(24,25)18(33)12-19(29)26-16(10-13-4-2-1-3-5-13)20(30)27-17(21(31)32)11-14-6-8-15(28)9-7-14/h1-9,16-18,28,33H,10-12H2,(H,26,29)(H,27,30)(H,31,32)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of human recombinant ECE1 by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair
Endothelin-converting enzyme 1 (Homo sapiens (Human))	BDBM50298107 (3-(4-Hydroxy-phenyl)-2-(4,4,4-trifluoro-3-mercapto...) Show SMILES OC(=O)C(Cc1ccc(O)cc1)NC(=O)CC(S)C(F)(F)F Show InChI InChI=1S/C13H14F3NO4S/c14-13(15,16)10(22)6-11(19)17-9(12(20)21)5-7-1-3-8(18)4-2-7/h1-4,9-10,18,22H,5-6H2,(H,17,19)(H,20,21)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Dipartimento di Chimica Curated by ChEMBL					Assay Description Inhibition of human recombinant ECE1 by fluorimetry				Bioorg Med Chem Lett 19: 4715-9 (2009) Article DOI: 10.1016/j.bmcl.2009.06.064 BindingDB Entry DOI: 10.7270/Q2GH9JWT
					More data for this Ligand-Target Pair