Compile Data Set for Download or QSAR

Found 57 hits with Last Name = 'mirand' and Initial = 'c'   

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
Low molecular weight phosphotyrosine protein phosphatase (Mus musculus)	BDBM50096252 (CHEMBL3594198) Show SMILES OP(O)(=O)Cc1ccc(CCl)cc1 Show InChI InChI=1S/C36H62N4O6/c1-5-8-9-10-11-12-13-15-21-28(42)25-30-34(44)39-32(26(4)6-2)36(46)40-24-19-18-23-31(40)35(45)37-29(33(43)38-30)22-17-14-16-20-27(41)7-3/h26,29-32H,5-25H2,1-4H3,(H,37,45)(H,38,43)(H,39,44)/t26?,29-,30-,31+,32-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	4.70E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Campinas Curated by ChEMBL					Assay Description Competitive inhibition of mouse LMW-PTP expressed in Escherichia coli using pNPP substrate by Dixon plot				Bioorg Med Chem 23: 4462-71 (2015) Article DOI: 10.1016/j.bmc.2015.06.017 BindingDB Entry DOI: 10.7270/Q2R78GZ7
					More data for this Ligand-Target Pair
Low molecular weight phosphotyrosine protein phosphatase (Mus musculus)	BDBM50096253 (CHEMBL3593255) Show SMILES OP(O)(=O)Cc1ccc(cc1)[N+]([O-])=O Show InChI InChI=1S/C35H49N5O7/c1-4-22(3)31-35(47)40-18-12-11-17-29(40)34(46)36-26(15-8-6-7-13-24(41)5-2)32(44)37-27(33(45)38-31)19-23-20-39(21-30(42)43)28-16-10-9-14-25(23)28/h9-10,14,16,20,22,26-27,29,31H,4-8,11-13,15,17-19,21H2,1-3H3,(H,36,46)(H,37,44)(H,38,45)(H,42,43)/t22?,26-,27-,29+,31-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.24E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Campinas Curated by ChEMBL					Assay Description Competitive inhibition of mouse LMW-PTP expressed in Escherichia coli using pNPP substrate by Dixon plot				Bioorg Med Chem 23: 4462-71 (2015) Article DOI: 10.1016/j.bmc.2015.06.017 BindingDB Entry DOI: 10.7270/Q2R78GZ7
					More data for this Ligand-Target Pair
Alkaline phosphatase, placental type (Homo sapiens (Human))	BDBM50080274 (Benzyl-phosphonic acid | CHEMBL299737 | Phenyl-met...) Show SMILES OP(O)(=O)Cc1ccccc1 Show InChI InChI=1S/C7H9O3P/c8-11(9,10)6-7-4-2-1-3-5-7/h1-5H,6H2,(H2,8,9,10)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	5.80E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Campinas Curated by ChEMBL					Assay Description Inhibition of human placental alkaline phosphatase using p-nitrophenyl phosphate substrate				Bioorg Med Chem 23: 4462-71 (2015) Article DOI: 10.1016/j.bmc.2015.06.017 BindingDB Entry DOI: 10.7270/Q2R78GZ7
					More data for this Ligand-Target Pair
Ectonucleotide pyrophosphatase/phosphodiesterase family member 3 (Bos taurus)	BDBM50080274 (Benzyl-phosphonic acid | CHEMBL299737 | Phenyl-met...) Show SMILES OP(O)(=O)Cc1ccccc1 Show InChI InChI=1S/C7H9O3P/c8-11(9,10)6-7-4-2-1-3-5-7/h1-5H,6H2,(H2,8,9,10)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	1.40E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Campinas Curated by ChEMBL					Assay Description Inhibition of bovine intestinal 5'-nucleotide phosphodiesterase using 4-nitrophenyl phenylphosphonate substrate by spectrophotometry				Bioorg Med Chem 23: 4462-71 (2015) Article DOI: 10.1016/j.bmc.2015.06.017 BindingDB Entry DOI: 10.7270/Q2R78GZ7
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50080274 (Benzyl-phosphonic acid | CHEMBL299737 | Phenyl-met...) Show SMILES OP(O)(=O)Cc1ccccc1 Show InChI InChI=1S/C7H9O3P/c8-11(9,10)6-7-4-2-1-3-5-7/h1-5H,6H2,(H2,8,9,10)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	3.00E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Campinas Curated by ChEMBL					Assay Description Inhibition of PTP1B (unknown origin) using nPP substrate				Bioorg Med Chem 23: 4462-71 (2015) Article DOI: 10.1016/j.bmc.2015.06.017 BindingDB Entry DOI: 10.7270/Q2R78GZ7
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50062351 ((R)-N*4*-Hydroxy-N*1*-[(S)-2-(1H-indol-3-yl)-1-met...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(C)C)CC(=O)NO |r| Show InChI InChI=1S/C20H28N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-7,11-13,17,22,28H,8-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/t13-,17+/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	PubMed	n/a	n/a	0.104	n/a	n/a	n/a	n/a	n/a	n/a
UMR/CNRS 6013 Curated by ChEMBL					Assay Description Inhibition of human matrix metalloproteinase-2				Bioorg Med Chem Lett 13: 2843-6 (2003) BindingDB Entry DOI: 10.7270/Q2PN952R
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50062351 ((R)-N*4*-Hydroxy-N*1*-[(S)-2-(1H-indol-3-yl)-1-met...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(C)C)CC(=O)NO |r| Show InChI InChI=1S/C20H28N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-7,11-13,17,22,28H,8-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/t13-,17+/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	PubMed	n/a	n/a	0.191	n/a	n/a	n/a	n/a	n/a	n/a
UMR/CNRS 6013 Curated by ChEMBL					Assay Description Inhibition of human matrix metalloproteinase-3				Bioorg Med Chem Lett 13: 2843-6 (2003) BindingDB Entry DOI: 10.7270/Q2PN952R
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50062351 ((R)-N*4*-Hydroxy-N*1*-[(S)-2-(1H-indol-3-yl)-1-met...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(C)C)CC(=O)NO |r| Show InChI InChI=1S/C20H28N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-7,11-13,17,22,28H,8-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/t13-,17+/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	Article PubMed	n/a	n/a	0.5	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP9				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50062351 ((R)-N*4*-Hydroxy-N*1*-[(S)-2-(1H-indol-3-yl)-1-met...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(C)C)CC(=O)NO |r| Show InChI InChI=1S/C20H28N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-7,11-13,17,22,28H,8-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/t13-,17+/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	Article PubMed	n/a	n/a	1.10	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP2				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50135601 ((S,E)-N1-(3-(1H-indol-3-yl)-1-(methylamino)-1-oxop...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(\CC(=O)NO)=C\C(C)C Show InChI InChI=1S/C20H26N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-8,11-12,17,22,28H,9-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/b13-8+/t17-/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	1.30	n/a	n/a	n/a	n/a	n/a	n/a
UMR/CNRS 6013 Curated by ChEMBL					Assay Description Inhibition of human matrix metalloprotease-2				Bioorg Med Chem Lett 13: 2843-6 (2003) BindingDB Entry DOI: 10.7270/Q2PN952R
					More data for this Ligand-Target Pair
Interstitial collagenase (Homo sapiens (Human))	BDBM50062351 ((R)-N*4*-Hydroxy-N*1*-[(S)-2-(1H-indol-3-yl)-1-met...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(C)C)CC(=O)NO |r| Show InChI InChI=1S/C20H28N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-7,11-13,17,22,28H,8-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/t13-,17+/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	Article PubMed	n/a	n/a	1.5	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP1				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50062351 ((R)-N*4*-Hydroxy-N*1*-[(S)-2-(1H-indol-3-yl)-1-met...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(C)C)CC(=O)NO |r| Show InChI InChI=1S/C20H28N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-7,11-13,17,22,28H,8-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/t13-,17+/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	Article PubMed	n/a	n/a	1.90	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP3				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50135602 (CHEMBL420259 | N*1*-{2-[2-(2-Dimethylamino-ethyl)-...) Show SMILES CNC(=O)C(Cc1c(CCN(C)C)[nH]c2ccccc12)NC(=O)C(\CC(=O)NO)=C\C(C)C Show InChI InChI=1S/C24H35N5O4/c1-15(2)12-16(13-22(30)28-33)23(31)27-21(24(32)25-3)14-18-17-8-6-7-9-19(17)26-20(18)10-11-29(4)5/h6-9,12,15,21,26,33H,10-11,13-14H2,1-5H3,(H,25,32)(H,27,31)(H,28,30)/b16-12+	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	5.70	n/a	n/a	n/a	n/a	n/a	n/a
UMR/CNRS 6013 Curated by ChEMBL					Assay Description Inhibition of human matrix metalloproteinase-2				Bioorg Med Chem Lett 13: 2843-6 (2003) BindingDB Entry DOI: 10.7270/Q2PN952R
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50135600 ((S)-2-((E)-2-Hydroxycarbamoylmethyl-4-methyl-pent-...) Show SMILES CCOC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(\CC(=O)NO)=C\C(C)C Show InChI InChI=1S/C21H27N3O5/c1-4-29-21(27)18(10-15-12-22-17-8-6-5-7-16(15)17)23-20(26)14(9-13(2)3)11-19(25)24-28/h5-9,12-13,18,22,28H,4,10-11H2,1-3H3,(H,23,26)(H,24,25)/b14-9+/t18-/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	6	n/a	n/a	n/a	n/a	n/a	n/a
UMR/CNRS 6013 Curated by ChEMBL					Assay Description Inhibition of human matrix metalloproteinase-2				Bioorg Med Chem Lett 13: 2843-6 (2003) BindingDB Entry DOI: 10.7270/Q2PN952R
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50135601 ((S,E)-N1-(3-(1H-indol-3-yl)-1-(methylamino)-1-oxop...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(\CC(=O)NO)=C\C(C)C Show InChI InChI=1S/C20H26N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-8,11-12,17,22,28H,9-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/b13-8+/t17-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.20	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP2				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Matrix metalloproteinase-14 (Homo sapiens (Human))	BDBM50135601 ((S,E)-N1-(3-(1H-indol-3-yl)-1-(methylamino)-1-oxop...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(\CC(=O)NO)=C\C(C)C Show InChI InChI=1S/C20H26N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-8,11-12,17,22,28H,9-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/b13-8+/t17-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP14				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Matrix metalloproteinase-14 (Homo sapiens (Human))	BDBM50062351 ((R)-N*4*-Hydroxy-N*1*-[(S)-2-(1H-indol-3-yl)-1-met...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(C)C)CC(=O)NO |r| Show InChI InChI=1S/C20H28N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-7,11-13,17,22,28H,8-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/t13-,17+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	13	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP14				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50135601 ((S,E)-N1-(3-(1H-indol-3-yl)-1-(methylamino)-1-oxop...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(\CC(=O)NO)=C\C(C)C Show InChI InChI=1S/C20H26N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-8,11-12,17,22,28H,9-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/b13-8+/t17-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP9				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Interstitial collagenase (Homo sapiens (Human))	BDBM50135601 ((S,E)-N1-(3-(1H-indol-3-yl)-1-(methylamino)-1-oxop...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(\CC(=O)NO)=C\C(C)C Show InChI InChI=1S/C20H26N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-8,11-12,17,22,28H,9-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/b13-8+/t17-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	18	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP1				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50451552 (CHEMBL2111573) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(CC(=O)NO)=CC(C)C Show InChI InChI=1S/C20H26N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-8,11-12,17,22,28H,9-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/t17-/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
UMR/CNRS 6013 Curated by ChEMBL					Assay Description Inhibition of human matrix metalloproteinase-2				Bioorg Med Chem Lett 13: 2843-6 (2003) BindingDB Entry DOI: 10.7270/Q2PN952R
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50213416 ((2E)-3-(N-hydroxycarbamoyl)-2-[(2E)-3-phenylprop-2...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(CC(=O)NO)=CC=Cc1ccccc1 |w:24.26,26.28| Show InChI InChI=1S/C25H26N4O4/c1-26-25(32)22(14-19-16-27-21-13-6-5-12-20(19)21)28-24(31)18(15-23(30)29-33)11-7-10-17-8-3-2-4-9-17/h2-13,16,22,27,33H,14-15H2,1H3,(H,26,32)(H,28,31)(H,29,30)/t22-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	38	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP9				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Histone deacetylase 6 (Homo sapiens (Human))	BDBM19149 (CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...) Show SMILES ONC(=O)CCCCCCC(=O)Nc1ccccc1 Show InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18)	PDB MMDB NCI pathway 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 Article PubMed	n/a	n/a	42	n/a	n/a	n/a	n/a	n/a	n/a
University of Bras£lia Curated by ChEMBL					Assay Description Inhibition of human recombinant HDAC6 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence method				ACS Med Chem Lett 10: 671-676 (2019) Article DOI: 10.1021/acsmedchemlett.9b00071 BindingDB Entry DOI: 10.7270/Q2BP068P
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50213419 ((2E)-3-(N-hydroxycarbamoyl)-2-(3-phenylpropylidene...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(CC(=O)NO)=CCCc1ccccc1 |w:24.26| Show InChI InChI=1S/C25H28N4O4/c1-26-25(32)22(14-19-16-27-21-13-6-5-12-20(19)21)28-24(31)18(15-23(30)29-33)11-7-10-17-8-3-2-4-9-17/h2-6,8-9,11-13,16,22,27,33H,7,10,14-15H2,1H3,(H,26,32)(H,28,31)(H,29,30)/t22-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	45	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP9				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Neutrophil collagenase (Homo sapiens (Human))	BDBM50213418 ((2E)-3-(N-hydroxycarbamoyl)-2-heptylidenepropionyl...) Show SMILES CCCCCC\C=C(/CC(=O)NO)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)NC Show InChI InChI=1S/C23H32N4O4/c1-3-4-5-6-7-10-16(14-21(28)27-31)22(29)26-20(23(30)24-2)13-17-15-25-19-12-9-8-11-18(17)19/h8-12,15,20,25,31H,3-7,13-14H2,1-2H3,(H,24,30)(H,26,29)(H,27,28)/b16-10+/t20-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	101	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP8				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50213416 ((2E)-3-(N-hydroxycarbamoyl)-2-[(2E)-3-phenylprop-2...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(CC(=O)NO)=CC=Cc1ccccc1 |w:24.26,26.28| Show InChI InChI=1S/C25H26N4O4/c1-26-25(32)22(14-19-16-27-21-13-6-5-12-20(19)21)28-24(31)18(15-23(30)29-33)11-7-10-17-8-3-2-4-9-17/h2-13,16,22,27,33H,14-15H2,1H3,(H,26,32)(H,28,31)(H,29,30)/t22-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	120	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP2				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Histone deacetylase 1 (Homo sapiens (Human))	BDBM19149 (CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...) Show SMILES ONC(=O)CCCCCCC(=O)Nc1ccccc1 Show InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18)	PDB MMDB NCI pathway 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	120	n/a	n/a	n/a	n/a	n/a	n/a
University of Bras£lia Curated by ChEMBL					Assay Description Inhibition of human recombinant HDAC1 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence method				ACS Med Chem Lett 10: 671-676 (2019) Article DOI: 10.1021/acsmedchemlett.9b00071 BindingDB Entry DOI: 10.7270/Q2BP068P
					More data for this Ligand-Target Pair				3D Structure (crystal)
Collagenase 3 (Homo sapiens (Human))	BDBM50213418 ((2E)-3-(N-hydroxycarbamoyl)-2-heptylidenepropionyl...) Show SMILES CCCCCC\C=C(/CC(=O)NO)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)NC Show InChI InChI=1S/C23H32N4O4/c1-3-4-5-6-7-10-16(14-21(28)27-31)22(29)26-20(23(30)24-2)13-17-15-25-19-12-9-8-11-18(17)19/h8-12,15,20,25,31H,3-7,13-14H2,1-2H3,(H,24,30)(H,26,29)(H,27,28)/b16-10+/t20-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	122	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP13				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50213418 ((2E)-3-(N-hydroxycarbamoyl)-2-heptylidenepropionyl...) Show SMILES CCCCCC\C=C(/CC(=O)NO)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)NC Show InChI InChI=1S/C23H32N4O4/c1-3-4-5-6-7-10-16(14-21(28)27-31)22(29)26-20(23(30)24-2)13-17-15-25-19-12-9-8-11-18(17)19/h8-12,15,20,25,31H,3-7,13-14H2,1-2H3,(H,24,30)(H,26,29)(H,27,28)/b16-10+/t20-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	123	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP2				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50135601 ((S,E)-N1-(3-(1H-indol-3-yl)-1-(methylamino)-1-oxop...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(\CC(=O)NO)=C\C(C)C Show InChI InChI=1S/C20H26N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-8,11-12,17,22,28H,9-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/b13-8+/t17-/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	179	n/a	n/a	n/a	n/a	n/a	n/a
UMR/CNRS 6013 Curated by ChEMBL					Assay Description Inhibition of PKD2 ( assessed as residual activity at 1 uM ) by TR-FRET assay				Bioorg Med Chem Lett 13: 2843-6 (2003) BindingDB Entry DOI: 10.7270/Q2PN952R
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50135601 ((S,E)-N1-(3-(1H-indol-3-yl)-1-(methylamino)-1-oxop...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(\CC(=O)NO)=C\C(C)C Show InChI InChI=1S/C20H26N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-8,11-12,17,22,28H,9-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/b13-8+/t17-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	179	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP3				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Histone deacetylase 6 (Homo sapiens (Human))	BDBM50535444 (CHEMBL4463058) Show SMILES COc1cccc(CCCCCCCC(=O)NO)c1 Show InChI InChI=1S/C15H23NO3/c1-19-14-10-7-9-13(12-14)8-5-3-2-4-6-11-15(17)16-18/h7,9-10,12,18H,2-6,8,11H2,1H3,(H,16,17)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	190	n/a	n/a	n/a	n/a	n/a	n/a
University of Bras£lia Curated by ChEMBL					Assay Description Inhibition of human recombinant HDAC6 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence method				ACS Med Chem Lett 10: 671-676 (2019) Article DOI: 10.1021/acsmedchemlett.9b00071 BindingDB Entry DOI: 10.7270/Q2BP068P
					More data for this Ligand-Target Pair
Histone deacetylase 6 (Homo sapiens (Human))	BDBM50535445 (CHEMBL4455730) Show SMILES COC(=O)c1c(CCCCCCCC(=O)NO)cccc1OC Show InChI InChI=1S/C17H25NO5/c1-22-14-11-8-10-13(16(14)17(20)23-2)9-6-4-3-5-7-12-15(19)18-21/h8,10-11,21H,3-7,9,12H2,1-2H3,(H,18,19)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	215	n/a	n/a	n/a	n/a	n/a	n/a
University of Bras£lia Curated by ChEMBL					Assay Description Inhibition of human recombinant HDAC6 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence method				ACS Med Chem Lett 10: 671-676 (2019) Article DOI: 10.1021/acsmedchemlett.9b00071 BindingDB Entry DOI: 10.7270/Q2BP068P
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50213419 ((2E)-3-(N-hydroxycarbamoyl)-2-(3-phenylpropylidene...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(CC(=O)NO)=CCCc1ccccc1 |w:24.26| Show InChI InChI=1S/C25H28N4O4/c1-26-25(32)22(14-19-16-27-21-13-6-5-12-20(19)21)28-24(31)18(15-23(30)29-33)11-7-10-17-8-3-2-4-9-17/h2-6,8-9,11-13,16,22,27,33H,7,10,14-15H2,1H3,(H,26,32)(H,28,31)(H,29,30)/t22-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL 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
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP2				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Histone deacetylase 1 (Homo sapiens (Human))	BDBM50535444 (CHEMBL4463058) Show SMILES COc1cccc(CCCCCCCC(=O)NO)c1 Show InChI InChI=1S/C15H23NO3/c1-19-14-10-7-9-13(12-14)8-5-3-2-4-6-11-15(17)16-18/h7,9-10,12,18H,2-6,8,11H2,1H3,(H,16,17)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	316	n/a	n/a	n/a	n/a	n/a	n/a
University of Bras£lia Curated by ChEMBL					Assay Description Inhibition of human recombinant HDAC1 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence method				ACS Med Chem Lett 10: 671-676 (2019) Article DOI: 10.1021/acsmedchemlett.9b00071 BindingDB Entry DOI: 10.7270/Q2BP068P
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50135602 (CHEMBL420259 | N*1*-{2-[2-(2-Dimethylamino-ethyl)-...) Show SMILES CNC(=O)C(Cc1c(CCN(C)C)[nH]c2ccccc12)NC(=O)C(\CC(=O)NO)=C\C(C)C Show InChI InChI=1S/C24H35N5O4/c1-15(2)12-16(13-22(30)28-33)23(31)27-21(24(32)25-3)14-18-17-8-6-7-9-19(17)26-20(18)10-11-29(4)5/h6-9,12,15,21,26,33H,10-11,13-14H2,1-5H3,(H,25,32)(H,27,31)(H,28,30)/b16-12+	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	665	n/a	n/a	n/a	n/a	n/a	n/a
UMR/CNRS 6013 Curated by ChEMBL					Assay Description Inhibition of human matrix metalloproteinase-3				Bioorg Med Chem Lett 13: 2843-6 (2003) BindingDB Entry DOI: 10.7270/Q2PN952R
					More data for this Ligand-Target Pair
Histone deacetylase 1 (Homo sapiens (Human))	BDBM50535445 (CHEMBL4455730) Show SMILES COC(=O)c1c(CCCCCCCC(=O)NO)cccc1OC Show InChI InChI=1S/C17H25NO5/c1-22-14-11-8-10-13(16(14)17(20)23-2)9-6-4-3-5-7-12-15(19)18-21/h8,10-11,21H,3-7,9,12H2,1-2H3,(H,18,19)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	775	n/a	n/a	n/a	n/a	n/a	n/a
University of Bras£lia Curated by ChEMBL					Assay Description Inhibition of human recombinant HDAC1 using ZMAL (Z-(Ac)Lys-AMC fluorogenic substrate incubated for 90 mins by fluorescence method				ACS Med Chem Lett 10: 671-676 (2019) Article DOI: 10.1021/acsmedchemlett.9b00071 BindingDB Entry DOI: 10.7270/Q2BP068P
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50451552 (CHEMBL2111573) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(CC(=O)NO)=CC(C)C Show InChI InChI=1S/C20H26N4O4/c1-12(2)8-13(10-18(25)24-28)19(26)23-17(20(27)21-3)9-14-11-22-16-7-5-4-6-15(14)16/h4-8,11-12,17,22,28H,9-10H2,1-3H3,(H,21,27)(H,23,26)(H,24,25)/t17-/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	910	n/a	n/a	n/a	n/a	n/a	n/a
UMR/CNRS 6013 Curated by ChEMBL					Assay Description Inhibition of human matrix metalloproteinase-3				Bioorg Med Chem Lett 13: 2843-6 (2003) BindingDB Entry DOI: 10.7270/Q2PN952R
					More data for this Ligand-Target Pair
Matrix metalloproteinase-14 (Homo sapiens (Human))	BDBM50213417 ((2E)-3-(N-hydroxycarbamoyl)-2-[(2E)-but-2-en-1-yli...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(CC=CC)=CC(=O)NO |w:23.25,21.23| Show InChI InChI=1S/C20H24N4O4/c1-3-4-7-13(11-18(25)24-28)19(26)23-17(20(27)21-2)10-14-12-22-16-9-6-5-8-15(14)16/h3-6,8-9,11-12,17,22,28H,7,10H2,1-2H3,(H,21,27)(H,23,26)(H,24,25)/t17-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	913	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP14				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50213417 ((2E)-3-(N-hydroxycarbamoyl)-2-[(2E)-but-2-en-1-yli...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(CC=CC)=CC(=O)NO |w:23.25,21.23| Show InChI InChI=1S/C20H24N4O4/c1-3-4-7-13(11-18(25)24-28)19(26)23-17(20(27)21-2)10-14-12-22-16-9-6-5-8-15(14)16/h3-6,8-9,11-12,17,22,28H,7,10H2,1-2H3,(H,21,27)(H,23,26)(H,24,25)/t17-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	974	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP9				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Interstitial collagenase (Homo sapiens (Human))	BDBM50213417 ((2E)-3-(N-hydroxycarbamoyl)-2-[(2E)-but-2-en-1-yli...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(CC=CC)=CC(=O)NO |w:23.25,21.23| Show InChI InChI=1S/C20H24N4O4/c1-3-4-7-13(11-18(25)24-28)19(26)23-17(20(27)21-2)10-14-12-22-16-9-6-5-8-15(14)16/h3-6,8-9,11-12,17,22,28H,7,10H2,1-2H3,(H,21,27)(H,23,26)(H,24,25)/t17-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	984	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP1				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Interstitial collagenase (Homo sapiens (Human))	BDBM50213416 ((2E)-3-(N-hydroxycarbamoyl)-2-[(2E)-3-phenylprop-2...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(CC(=O)NO)=CC=Cc1ccccc1 |w:24.26,26.28| Show InChI InChI=1S/C25H26N4O4/c1-26-25(32)22(14-19-16-27-21-13-6-5-12-20(19)21)28-24(31)18(15-23(30)29-33)11-7-10-17-8-3-2-4-9-17/h2-13,16,22,27,33H,14-15H2,1H3,(H,26,32)(H,28,31)(H,29,30)/t22-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.24E+3	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP1				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50213419 ((2E)-3-(N-hydroxycarbamoyl)-2-(3-phenylpropylidene...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(CC(=O)NO)=CCCc1ccccc1 |w:24.26| Show InChI InChI=1S/C25H28N4O4/c1-26-25(32)22(14-19-16-27-21-13-6-5-12-20(19)21)28-24(31)18(15-23(30)29-33)11-7-10-17-8-3-2-4-9-17/h2-6,8-9,11-13,16,22,27,33H,7,10,14-15H2,1H3,(H,26,32)(H,28,31)(H,29,30)/t22-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.92E+3	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP3				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50135600 ((S)-2-((E)-2-Hydroxycarbamoylmethyl-4-methyl-pent-...) Show SMILES CCOC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(\CC(=O)NO)=C\C(C)C Show InChI InChI=1S/C21H27N3O5/c1-4-29-21(27)18(10-15-12-22-17-8-6-5-7-16(15)17)23-20(26)14(9-13(2)3)11-19(25)24-28/h5-9,12-13,18,22,28H,4,10-11H2,1-3H3,(H,23,26)(H,24,25)/b14-9+/t18-/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	2.34E+3	n/a	n/a	n/a	n/a	n/a	n/a
UMR/CNRS 6013 Curated by ChEMBL					Assay Description Inhibition of human matrix metalloproteinase-3				Bioorg Med Chem Lett 13: 2843-6 (2003) BindingDB Entry DOI: 10.7270/Q2PN952R
					More data for this Ligand-Target Pair
Matrix metalloproteinase-14 (Homo sapiens (Human))	BDBM50213416 ((2E)-3-(N-hydroxycarbamoyl)-2-[(2E)-3-phenylprop-2...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(CC(=O)NO)=CC=Cc1ccccc1 |w:24.26,26.28| Show InChI InChI=1S/C25H26N4O4/c1-26-25(32)22(14-19-16-27-21-13-6-5-12-20(19)21)28-24(31)18(15-23(30)29-33)11-7-10-17-8-3-2-4-9-17/h2-13,16,22,27,33H,14-15H2,1H3,(H,26,32)(H,28,31)(H,29,30)/t22-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.49E+3	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP14				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Matrix metalloproteinase-14 (Homo sapiens (Human))	BDBM50213418 ((2E)-3-(N-hydroxycarbamoyl)-2-heptylidenepropionyl...) Show SMILES CCCCCC\C=C(/CC(=O)NO)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)NC Show InChI InChI=1S/C23H32N4O4/c1-3-4-5-6-7-10-16(14-21(28)27-31)22(29)26-20(23(30)24-2)13-17-15-25-19-12-9-8-11-18(17)19/h8-12,15,20,25,31H,3-7,13-14H2,1-2H3,(H,24,30)(H,26,29)(H,27,28)/b16-10+/t20-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.66E+3	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP14				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50213417 ((2E)-3-(N-hydroxycarbamoyl)-2-[(2E)-but-2-en-1-yli...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(CC=CC)=CC(=O)NO |w:23.25,21.23| Show InChI InChI=1S/C20H24N4O4/c1-3-4-7-13(11-18(25)24-28)19(26)23-17(20(27)21-2)10-14-12-22-16-9-6-5-8-15(14)16/h3-6,8-9,11-12,17,22,28H,7,10H2,1-2H3,(H,21,27)(H,23,26)(H,24,25)/t17-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.61E+3	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP3				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Interstitial collagenase (Homo sapiens (Human))	BDBM50213419 ((2E)-3-(N-hydroxycarbamoyl)-2-(3-phenylpropylidene...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(CC(=O)NO)=CCCc1ccccc1 |w:24.26| Show InChI InChI=1S/C25H28N4O4/c1-26-25(32)22(14-19-16-27-21-13-6-5-12-20(19)21)28-24(31)18(15-23(30)29-33)11-7-10-17-8-3-2-4-9-17/h2-6,8-9,11-13,16,22,27,33H,7,10,14-15H2,1H3,(H,26,32)(H,28,31)(H,29,30)/t22-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.13E+3	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP1				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50213416 ((2E)-3-(N-hydroxycarbamoyl)-2-[(2E)-3-phenylprop-2...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(CC(=O)NO)=CC=Cc1ccccc1 |w:24.26,26.28| Show InChI InChI=1S/C25H26N4O4/c1-26-25(32)22(14-19-16-27-21-13-6-5-12-20(19)21)28-24(31)18(15-23(30)29-33)11-7-10-17-8-3-2-4-9-17/h2-13,16,22,27,33H,14-15H2,1H3,(H,26,32)(H,28,31)(H,29,30)/t22-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP3				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Interstitial collagenase (Homo sapiens (Human))	BDBM50213418 ((2E)-3-(N-hydroxycarbamoyl)-2-heptylidenepropionyl...) Show SMILES CCCCCC\C=C(/CC(=O)NO)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)NC Show InChI InChI=1S/C23H32N4O4/c1-3-4-5-6-7-10-16(14-21(28)27-31)22(29)26-20(23(30)24-2)13-17-15-25-19-12-9-8-11-18(17)19/h8-12,15,20,25,31H,3-7,13-14H2,1-2H3,(H,24,30)(H,26,29)(H,27,28)/b16-10+/t20-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP1				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair
Matrix metalloproteinase-14 (Homo sapiens (Human))	BDBM50213419 ((2E)-3-(N-hydroxycarbamoyl)-2-(3-phenylpropylidene...) Show SMILES CNC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)C(CC(=O)NO)=CCCc1ccccc1 |w:24.26| Show InChI InChI=1S/C25H28N4O4/c1-26-25(32)22(14-19-16-27-21-13-6-5-12-20(19)21)28-24(31)18(15-23(30)29-33)11-7-10-17-8-3-2-4-9-17/h2-6,8-9,11-13,16,22,27,33H,7,10,14-15H2,1H3,(H,26,32)(H,28,31)(H,29,30)/t22-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.31E+4	n/a	n/a	n/a	n/a	n/a	n/a
Université de Reims-Champagne-Ardenne Curated by ChEMBL					Assay Description Inhibition of MMP14				Bioorg Med Chem 15: 4753-66 (2007) Article DOI: 10.1016/j.bmc.2007.05.001 BindingDB Entry DOI: 10.7270/Q2Q23ZXN
					More data for this Ligand-Target Pair

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