Compile Data Set for Download or QSAR

Found 521 hits with Last Name = 'beckett' and Initial = 'p'   

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
Acidic mammalian chitinase (Mus musculus)	BDBM50243745 (CHEMBL4076989) Show SMILES CC(C)CN(CCc1ccc(Cl)cc1)C1CCN(CC1)c1nc(N)n[nH]1 Show InChI InChI=1S/C19H29ClN6/c1-14(2)13-26(10-7-15-3-5-16(20)6-4-15)17-8-11-25(12-9-17)19-22-18(21)23-24-19/h3-6,14,17H,7-13H2,1-2H3,(H3,21,22,23,24)	PDB KEGG 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
OncoArendi Therapeutics SA Curated by ChEMBL					Assay Description Inhibition of mouse recombinant full length C-terminal His-tagged acidic mammalian chitinase expressed in CHO-K1 cells using 4-methylumbelliferyl-bet...				J Med Chem 61: 695-710 (2018) Article DOI: 10.1021/acs.jmedchem.7b01051 BindingDB Entry DOI: 10.7270/Q2J105J5
					More data for this Ligand-Target Pair
Acidic mammalian chitinase (Homo sapiens (Human))	BDBM50243745 (CHEMBL4076989) Show SMILES CC(C)CN(CCc1ccc(Cl)cc1)C1CCN(CC1)c1nc(N)n[nH]1 Show InChI InChI=1S/C19H29ClN6/c1-14(2)13-26(10-7-15-3-5-16(20)6-4-15)17-8-11-25(12-9-17)19-22-18(21)23-24-19/h3-6,14,17H,7-13H2,1-2H3,(H3,21,22,23,24)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	14	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
OncoArendi Therapeutics SA Curated by ChEMBL					Assay Description Inhibition of human recombinant full length C-terminal His-tagged acidic mammalian chitinase expressed in CHO-K1 cells using 4-methylumbelliferyl-bet...				J Med Chem 61: 695-710 (2018) Article DOI: 10.1021/acs.jmedchem.7b01051 BindingDB Entry DOI: 10.7270/Q2J105J5
					More data for this Ligand-Target Pair
Peptide deformylase, mitochondrial (Homo sapiens (Human))	BDBM50121445 ((S)-2-Mercaptomethyl-hexanoic acid [(S)-5-amino-1-...) Show SMILES CCCC[C@H](CS)C(=O)N[C@@H](CCCCN)C(=O)Nc1ccc(cc1)[N+]([O-])=O Show InChI InChI=1S/C19H30N4O4S/c1-2-3-6-14(13-28)18(24)22-17(7-4-5-12-20)19(25)21-15-8-10-16(11-9-15)23(26)27/h8-11,14,17,28H,2-7,12-13,20H2,1H3,(H,21,25)(H,22,24)/t14-,17+/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	19	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Compound was evaluated for inhibition of peptide deformylase, PDF.Fe of Escherichia coli				Bioorg Med Chem Lett 12: 3595-9 (2002) BindingDB Entry DOI: 10.7270/Q2FJ2G4H
					More data for this Ligand-Target Pair
Chitotriosidase-1 (Homo sapiens (Human))	BDBM50243745 (CHEMBL4076989) Show SMILES CC(C)CN(CCc1ccc(Cl)cc1)C1CCN(CC1)c1nc(N)n[nH]1 Show InChI InChI=1S/C19H29ClN6/c1-14(2)13-26(10-7-15-3-5-16(20)6-4-15)17-8-11-25(12-9-17)19-22-18(21)23-24-19/h3-6,14,17H,7-13H2,1-2H3,(H3,21,22,23,24)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	312	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
OncoArendi Therapeutics SA Curated by ChEMBL					Assay Description Inhibition of human recombinant full length C-terminal His-tagged chitotriosidase expressed in CHO-K1 cells using 4-methylumbelliferyl-beta-D-N,N',N\...				J Med Chem 61: 695-710 (2018) Article DOI: 10.1021/acs.jmedchem.7b01051 BindingDB Entry DOI: 10.7270/Q2J105J5
					More data for this Ligand-Target Pair
Peptide deformylase, mitochondrial (Homo sapiens (Human))	BDBM50121442 (5-Guanidino-2-(2-mercaptomethyl-hexanoylamino)-pen...) Show SMILES CCCCC(CS)C(=O)NC(CCCNC(N)=N)C(=O)OC Show InChI InChI=1S/C14H28N4O3S/c1-3-4-6-10(9-22)12(19)18-11(13(20)21-2)7-5-8-17-14(15)16/h10-11,22H,3-9H2,1-2H3,(H,18,19)(H4,15,16,17)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	2.50E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Compound was evaluated for inhibition of peptide deformylase, PDF.Ni of Escherichia coli				Bioorg Med Chem Lett 12: 3595-9 (2002) BindingDB Entry DOI: 10.7270/Q2FJ2G4H
					More data for this Ligand-Target Pair
Chitotriosidase-1 (Mus musculus)	BDBM50243745 (CHEMBL4076989) Show SMILES CC(C)CN(CCc1ccc(Cl)cc1)C1CCN(CC1)c1nc(N)n[nH]1 Show InChI InChI=1S/C19H29ClN6/c1-14(2)13-26(10-7-15-3-5-16(20)6-4-15)17-8-11-25(12-9-17)19-22-18(21)23-24-19/h3-6,14,17H,7-13H2,1-2H3,(H3,21,22,23,24)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.40E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
OncoArendi Therapeutics SA Curated by ChEMBL					Assay Description Inhibition of mouse recombinant full length C-terminal His-tagged chitotriosidase expressed in CHO-K1 cells using 4-methylumbelliferyl-beta-D-N,N',N\...				J Med Chem 61: 695-710 (2018) Article DOI: 10.1021/acs.jmedchem.7b01051 BindingDB Entry DOI: 10.7270/Q2J105J5
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50290436 ((R)-N*1*-((S)-2,2-Dimethyl-1-methylcarbamoyl-propy...) Show SMILES CCCCCCCCC[C@H](CC(=O)NO)C(=O)N[C@H](C(=O)NC)C(C)(C)C Show InChI InChI=1S/C20H39N3O4/c1-6-7-8-9-10-11-12-13-15(14-16(24)23-27)18(25)22-17(19(26)21-5)20(2,3)4/h15,17,27H,6-14H2,1-5H3,(H,21,26)(H,22,25)(H,23,24)/t15-,17-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	<0.150	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound concentration for 50% inhibition of human recombinant gelatinase A (MMP-2).				Bioorg Med Chem Lett 7: 193-198 (1997) Article DOI: 10.1016/S0960-894X(96)00602-6 BindingDB Entry DOI: 10.7270/Q2057FXG
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50031790 ((R)-N*4*-Hydroxy-N*1*-((S)-1-methylcarbamoyl-2-phe...) Show SMILES CNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CCCCCOc1ccccc1)CC(=O)NO Show InChI InChI=1S/C25H33N3O5/c1-26-25(31)22(17-19-11-5-2-6-12-19)27-24(30)20(18-23(29)28-32)13-7-4-10-16-33-21-14-8-3-9-15-21/h2-3,5-6,8-9,11-12,14-15,20,22,32H,4,7,10,13,16-18H2,1H3,(H,26,31)(H,27,30)(H,28,29)/t20-,22+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	0.310	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound concentration for 50% inhibition of human recombinant gelatinase A (MMP-2).				Bioorg Med Chem Lett 7: 193-198 (1997) Article DOI: 10.1016/S0960-894X(96)00602-6 BindingDB Entry DOI: 10.7270/Q2057FXG
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137332 ((R)-2-Cyclopentylmethyl-N-[(S)-1-(4,5-difluoro-2-m...) Show SMILES CC(C)(C)[C@H](NC(=O)[C@H](CC1CCCC1)CN(O)C=O)C(=O)c1cc(F)c(F)cc1N1CCOCC1 Show InChI InChI=1S/C26H37F2N3O5/c1-26(2,3)24(29-25(34)18(15-31(35)16-32)12-17-6-4-5-7-17)23(33)19-13-20(27)21(28)14-22(19)30-8-10-36-11-9-30/h13-14,16-18,24,35H,4-12,15H2,1-3H3,(H,29,34)/t18-,24-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.5	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50290448 ((R)-N*1*-((S)-2,2-Dimethyl-1-methylcarbamoyl-propy...) Show SMILES CNC(=O)[C@@H](NC(=O)[C@H](CCCCCCCCCCCCCCO)CC(=O)NO)C(C)(C)C Show InChI InChI=1S/C25H49N3O5/c1-25(2,3)22(24(32)26-4)27-23(31)20(19-21(30)28-33)17-15-13-11-9-7-5-6-8-10-12-14-16-18-29/h20,22,29,33H,5-19H2,1-4H3,(H,26,32)(H,27,31)(H,28,30)/t20-,22-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound concentration for 50% inhibition of human recombinant gelatinase A (MMP-2).				Bioorg Med Chem Lett 7: 193-198 (1997) Article DOI: 10.1016/S0960-894X(96)00602-6 BindingDB Entry DOI: 10.7270/Q2057FXG
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50290441 ((R)-N*1*-((S)-2,2-Dimethyl-1-methylcarbamoyl-propy...) Show SMILES CCCCCCCCCCCCCCCC[C@H](CC(=O)NO)C(=O)N[C@H](C(=O)NC)C(C)(C)C Show InChI InChI=1S/C27H53N3O4/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-22(21-23(31)30-34)25(32)29-24(26(33)28-5)27(2,3)4/h22,24,34H,6-21H2,1-5H3,(H,28,33)(H,29,32)(H,30,31)/t22-,24-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.600	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound concentration for 50% inhibition of human recombinant gelatinase A (MMP-2).				Bioorg Med Chem Lett 7: 193-198 (1997) Article DOI: 10.1016/S0960-894X(96)00602-6 BindingDB Entry DOI: 10.7270/Q2057FXG
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50290442 ((R)-N*4*-Hydroxy-N*1*-((S)-1-methylcarbamoyl-2-phe...) Show SMILES CCCCCCCC[C@H](CC(=O)NO)C(=O)N[C@@H](Cc1ccccc1)C(=O)NC Show InChI InChI=1S/C22H35N3O4/c1-3-4-5-6-7-11-14-18(16-20(26)25-29)21(27)24-19(22(28)23-2)15-17-12-9-8-10-13-17/h8-10,12-13,18-19,29H,3-7,11,14-16H2,1-2H3,(H,23,28)(H,24,27)(H,25,26)/t18-,19+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.600	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound concentration for 50% inhibition of human recombinant gelatinase A (MMP-2).				Bioorg Med Chem Lett 7: 193-198 (1997) Article DOI: 10.1016/S0960-894X(96)00602-6 BindingDB Entry DOI: 10.7270/Q2057FXG
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137327 ((R)-2-Cyclopentylmethyl-N-[(S)-1-(3-fluoro-4-morph...) Show SMILES CC(C)(C)[C@H](NC(=O)[C@H](CC1CCCC1)CN(O)C=O)C(=O)c1ccc(N2CCOCC2)c(F)c1 Show InChI InChI=1S/C26H38FN3O5/c1-26(2,3)24(28-25(33)20(16-30(34)17-31)14-18-6-4-5-7-18)23(32)19-8-9-22(21(27)15-19)29-10-12-35-13-11-29/h8-9,15,17-18,20,24,34H,4-7,10-14,16H2,1-3H3,(H,28,33)/t20-,24-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	0.600	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50290439 ((R)-N*1*-((S)-2,2-Dimethyl-1-methylcarbamoyl-propy...) Show SMILES CCCCCCCC[C@H](CC(=O)NO)C(=O)N[C@H](C(=O)NC)C(C)(C)C Show InChI InChI=1S/C19H37N3O4/c1-6-7-8-9-10-11-12-14(13-15(23)22-26)17(24)21-16(18(25)20-5)19(2,3)4/h14,16,26H,6-13H2,1-5H3,(H,20,25)(H,21,24)(H,22,23)/t14-,16-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.700	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound concentration for 50% inhibition of human recombinant gelatinase A (MMP-2).				Bioorg Med Chem Lett 7: 193-198 (1997) Article DOI: 10.1016/S0960-894X(96)00602-6 BindingDB Entry DOI: 10.7270/Q2057FXG
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50290449 ((R)-N*1*-((S)-2,2-Dimethyl-1-methylcarbamoyl-propy...) Show SMILES CCCCCCCCCCCCCC[C@H](CC(=O)NO)C(=O)N[C@H](C(=O)NC)C(C)(C)C Show InChI InChI=1S/C25H49N3O4/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-20(19-21(29)28-32)23(30)27-22(24(31)26-5)25(2,3)4/h20,22,32H,6-19H2,1-5H3,(H,26,31)(H,27,30)(H,28,29)/t20-,22-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	0.800	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound concentration for 50% inhibition of human recombinant gelatinase A (MMP-2).				Bioorg Med Chem Lett 7: 193-198 (1997) Article DOI: 10.1016/S0960-894X(96)00602-6 BindingDB Entry DOI: 10.7270/Q2057FXG
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50290450 ((R)-2-Dodecyl-N*4*-hydroxy-N*1*-((S)-1-methylcarba...) Show SMILES CCCCCCCCCCCC[C@H](CC(=O)NO)C(=O)N[C@@H](Cc1ccccc1)C(=O)NC Show InChI InChI=1S/C26H43N3O4/c1-3-4-5-6-7-8-9-10-11-15-18-22(20-24(30)29-33)25(31)28-23(26(32)27-2)19-21-16-13-12-14-17-21/h12-14,16-17,22-23,33H,3-11,15,18-20H2,1-2H3,(H,27,32)(H,28,31)(H,29,30)/t22-,23+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound concentration for 50% inhibition of human recombinant gelatinase A (MMP-2).				Bioorg Med Chem Lett 7: 193-198 (1997) Article DOI: 10.1016/S0960-894X(96)00602-6 BindingDB Entry DOI: 10.7270/Q2057FXG
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50290456 ((R)-2-Heptyl-N*4*-hydroxy-N*1*-((S)-1-methylcarbam...) Show SMILES CCCCCCC[C@H](CC(=O)NO)C(=O)N[C@@H](Cc1ccccc1)C(=O)NC Show InChI InChI=1S/C21H33N3O4/c1-3-4-5-6-10-13-17(15-19(25)24-28)20(26)23-18(21(27)22-2)14-16-11-8-7-9-12-16/h7-9,11-12,17-18,28H,3-6,10,13-15H2,1-2H3,(H,22,27)(H,23,26)(H,24,25)/t17-,18+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound concentration for 50% inhibition of human recombinant gelatinase A (MMP-2).				Bioorg Med Chem Lett 7: 193-198 (1997) Article DOI: 10.1016/S0960-894X(96)00602-6 BindingDB Entry DOI: 10.7270/Q2057FXG
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50290433 ((R)-N*4*-Hydroxy-N*1*-((S)-1-methylcarbamoyl-2-phe...) Show SMILES CCCCCCCCC[C@H](CC(=O)NO)C(=O)N[C@@H](Cc1ccccc1)C(=O)NC Show InChI InChI=1S/C23H37N3O4/c1-3-4-5-6-7-8-12-15-19(17-21(27)26-30)22(28)25-20(23(29)24-2)16-18-13-10-9-11-14-18/h9-11,13-14,19-20,30H,3-8,12,15-17H2,1-2H3,(H,24,29)(H,25,28)(H,26,27)/t19-,20+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound concentration for 50% inhibition of human recombinant gelatinase A (MMP-2).				Bioorg Med Chem Lett 7: 193-198 (1997) Article DOI: 10.1016/S0960-894X(96)00602-6 BindingDB Entry DOI: 10.7270/Q2057FXG
					More data for this Ligand-Target Pair
Peptide deformylase, mitochondrial (Homo sapiens (Human))	BDBM50121444 ((R)-2-Butyl-N*1*-((S)-1-dimethylcarbamoyl-2,2-dime...) Show SMILES CCCC[C@H](CC(=O)NO)C(=O)N[C@H](C(=O)N(C)C)C(C)(C)C Show InChI InChI=1S/C16H31N3O4/c1-7-8-9-11(10-12(20)18-23)14(21)17-13(16(2,3)4)15(22)19(5)6/h11,13,23H,7-10H2,1-6H3,(H,17,21)(H,18,20)/t11-,13-/m1/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Compound was evaluated for inhibition of peptide deformylase, PDF.Ni of Escherichia coli				Bioorg Med Chem Lett 12: 3595-9 (2002) BindingDB Entry DOI: 10.7270/Q2FJ2G4H
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137345 ((R)-2-[(Formyl-hydroxy-amino)-methyl]-hexanoic aci...) Show SMILES CCCC[C@H](CN(O)C=O)C(=O)N[C@H](C(=O)c1ccc(OC)cc1)C(C)(C)C Show InChI InChI=1S/C21H32N2O5/c1-6-7-8-16(13-23(27)14-24)20(26)22-19(21(2,3)4)18(25)15-9-11-17(28-5)12-10-15/h9-12,14,16,19,27H,6-8,13H2,1-5H3,(H,22,26)/t16-,19-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137341 ((R)-2-Cyclopentylmethyl-N-((S)-1-{3-fluoro-4-[4-(2...) Show SMILES CC(C)(C)[C@H](NC(=O)[C@H](CC1CCCC1)CN(O)C=O)C(=O)c1ccc(N2CCN(CCO)CC2)c(F)c1 Show InChI InChI=1S/C28H43FN4O5/c1-28(2,3)26(30-27(37)22(18-33(38)19-35)16-20-6-4-5-7-20)25(36)21-8-9-24(23(29)17-21)32-12-10-31(11-13-32)14-15-34/h8-9,17,19-20,22,26,34,38H,4-7,10-16,18H2,1-3H3,(H,30,37)/t22-,26-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137324 ((R)-2-Cyclopentylmethyl-N-{(S)-1-[4,5-difluoro-2-(...) Show SMILES CC(C)(C)[C@H](NC(=O)[C@H](CC1CCCC1)CN(O)C=O)C(=O)c1cc(F)c(F)cc1N1CCC(O)CC1 Show InChI InChI=1S/C27H39F2N3O5/c1-27(2,3)25(30-26(36)18(15-32(37)16-33)12-17-6-4-5-7-17)24(35)20-13-21(28)22(29)14-23(20)31-10-8-19(34)9-11-31/h13-14,16-19,25,34,37H,4-12,15H2,1-3H3,(H,30,36)/t18-,25-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50290436 ((R)-N*1*-((S)-2,2-Dimethyl-1-methylcarbamoyl-propy...) Show SMILES CCCCCCCCC[C@H](CC(=O)NO)C(=O)N[C@H](C(=O)NC)C(C)(C)C Show InChI InChI=1S/C20H39N3O4/c1-6-7-8-9-10-11-12-13-15(14-16(24)23-27)18(25)22-17(19(26)21-5)20(2,3)4/h15,17,27H,6-14H2,1-5H3,(H,21,26)(H,22,25)(H,23,24)/t15-,17-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	1.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of human recombinant Gelatinase B (MMP-9)				Bioorg Med Chem Lett 7: 193-198 (1997) Article DOI: 10.1016/S0960-894X(96)00602-6 BindingDB Entry DOI: 10.7270/Q2057FXG
					More data for this Ligand-Target Pair
Collagenase 3 (Homo sapiens (Human))	BDBM50063917 ((2S,3R)-N(4)-[(2S)-3,3-dimethyl-1-(methylamino)-1-...) Show SMILES CNC(=O)[C@@H](NC(=O)[C@H](CC(C)C)[C@H](O)C(=O)NO)C(C)(C)C |r| Show InChI InChI=1S/C15H29N3O5/c1-8(2)7-9(10(19)13(21)18-23)12(20)17-11(14(22)16-6)15(3,4)5/h8-11,19,23H,7H2,1-6H3,(H,16,22)(H,17,20)(H,18,21)/t9-,10+,11-/m1/s1	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 PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibition of Coll-3 MMP-13				Bioorg Med Chem Lett 9: 2887-92 (1999) BindingDB Entry DOI: 10.7270/Q25H7FGN
					More data for this Ligand-Target Pair
Interstitial collagenase (Homo sapiens (Human))	BDBM50081851 ((2R,3R)-3-(cyclopentylmethyl)-2-((1-(dimethylamino...) Show SMILES CN(C)c1cccc2c(cccc12)S(=O)(=O)N(C)C[C@@H]([C@@H](CC1CCCC1)C(=O)N1CCCCC1)C(=O)NO Show InChI InChI=1S/C29H42N4O5S/c1-31(2)26-15-9-14-23-22(26)13-10-16-27(23)39(37,38)32(3)20-25(28(34)30-36)24(19-21-11-5-6-12-21)29(35)33-17-7-4-8-18-33/h9-10,13-16,21,24-25,36H,4-8,11-12,17-20H2,1-3H3,(H,30,34)/t24-,25+/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	2	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibition of HFC MMP-1				Bioorg Med Chem Lett 9: 2887-92 (1999) BindingDB Entry DOI: 10.7270/Q25H7FGN
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137334 ((R)-2-Cyclopentylmethyl-N-((S)-2,2-dimethyl-1-{4-[...) Show SMILES CC(C)(C)[C@H](NC(=O)[C@H](CC1CCCC1)CN(O)C=O)C(=O)c1ccc(cc1)N1CCN(CCN2CCOCC2)CC1 Show InChI InChI=1S/C32H51N5O5/c1-32(2,3)30(33-31(40)27(23-37(41)24-38)22-25-6-4-5-7-25)29(39)26-8-10-28(11-9-26)36-16-14-34(15-17-36)12-13-35-18-20-42-21-19-35/h8-11,24-25,27,30,41H,4-7,12-23H2,1-3H3,(H,33,40)/t27-,30-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137328 ((R)-2-Cyclopentylmethyl-3-(formyl-hydroxy-amino)-N...) Show SMILES CC(C)(C)[C@H](NC(=O)[C@H](CC1CCCC1)CN(O)C=O)C(=O)c1ccc(O)cc1 Show InChI InChI=1S/C22H32N2O5/c1-22(2,3)20(19(27)16-8-10-18(26)11-9-16)23-21(28)17(13-24(29)14-25)12-15-6-4-5-7-15/h8-11,14-15,17,20,26,29H,4-7,12-13H2,1-3H3,(H,23,28)/t17-,20-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137320 ((R)-2-Cyclopentylmethyl-N-{(S)-1-[4,5-difluoro-2-(...) Show SMILES CC(C)(C)[C@H](NC(=O)[C@H](CC1CCCC1)CN(O)C=O)C(=O)c1cc(F)c(F)cc1N1CCC[C@H]1CO Show InChI InChI=1S/C27H39F2N3O5/c1-27(2,3)25(30-26(36)18(14-31(37)16-34)11-17-7-4-5-8-17)24(35)20-12-21(28)22(29)13-23(20)32-10-6-9-19(32)15-33/h12-13,16-19,25,33,37H,4-11,14-15H2,1-3H3,(H,30,36)/t18-,19+,25-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
Neutrophil collagenase (Homo sapiens (Human))	BDBM50063917 ((2S,3R)-N(4)-[(2S)-3,3-dimethyl-1-(methylamino)-1-...) Show SMILES CNC(=O)[C@@H](NC(=O)[C@H](CC(C)C)[C@H](O)C(=O)NO)C(C)(C)C |r| Show InChI InChI=1S/C15H29N3O5/c1-8(2)7-9(10(19)13(21)18-23)12(20)17-11(14(22)16-6)15(3,4)5/h8-11,19,23H,7H2,1-6H3,(H,16,22)(H,17,20)(H,18,21)/t9-,10+,11-/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 PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibition of HNC MMP-8				Bioorg Med Chem Lett 9: 2887-92 (1999) BindingDB Entry DOI: 10.7270/Q25H7FGN
					More data for this Ligand-Target Pair
Neutrophil collagenase (Homo sapiens (Human))	BDBM50081851 ((2R,3R)-3-(cyclopentylmethyl)-2-((1-(dimethylamino...) Show SMILES CN(C)c1cccc2c(cccc12)S(=O)(=O)N(C)C[C@@H]([C@@H](CC1CCCC1)C(=O)N1CCCCC1)C(=O)NO Show InChI InChI=1S/C29H42N4O5S/c1-31(2)26-15-9-14-23-22(26)13-10-16-27(23)39(37,38)32(3)20-25(28(34)30-36)24(19-21-11-5-6-12-21)29(35)33-17-7-4-8-18-33/h9-10,13-16,21,24-25,36H,4-8,11-12,17-20H2,1-3H3,(H,30,34)/t24-,25+/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	2	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibition of HNC MMP-8				Bioorg Med Chem Lett 9: 2887-92 (1999) BindingDB Entry DOI: 10.7270/Q25H7FGN
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137326 ((R)-2-Cyclopentylmethyl-3-(formyl-hydroxy-amino)-N...) Show SMILES CC(C)(C)[C@H](NC(=O)[C@H](CC1CCCC1)CN(O)C=O)C(=O)c1ccc(cc1)N1CCN(CCO)CC1 Show InChI InChI=1S/C28H44N4O5/c1-28(2,3)26(29-27(36)23(19-32(37)20-34)18-21-6-4-5-7-21)25(35)22-8-10-24(11-9-22)31-14-12-30(13-15-31)16-17-33/h8-11,20-21,23,26,33,37H,4-7,12-19H2,1-3H3,(H,29,36)/t23-,26-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137342 ((R)-2-Cyclopentylmethyl-N-((S)-1-{4,5-difluoro-2-[...) Show SMILES CC(C)(C)[C@H](NC(=O)[C@H](CC1CCCC1)CN(O)C=O)C(=O)c1cc(F)c(F)cc1N1CCN(CCO)CC1 Show InChI InChI=1S/C28H42F2N4O5/c1-28(2,3)26(31-27(38)20(17-34(39)18-36)14-19-6-4-5-7-19)25(37)21-15-22(29)23(30)16-24(21)33-10-8-32(9-11-33)12-13-35/h15-16,18-20,26,35,39H,4-14,17H2,1-3H3,(H,31,38)/t20-,26-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137339 ((R)-2-Cyclopentylmethyl-3-(formyl-hydroxy-amino)-N...) Show SMILES CC(C)(C)[C@H](NC(=O)[C@H](CC1CCCC1)CN(O)C=O)C(=O)c1ccc(cc1)N1CCC(O)CC1 Show InChI InChI=1S/C27H41N3O5/c1-27(2,3)25(28-26(34)21(17-30(35)18-31)16-19-6-4-5-7-19)24(33)20-8-10-22(11-9-20)29-14-12-23(32)13-15-29/h8-11,18-19,21,23,25,32,35H,4-7,12-17H2,1-3H3,(H,28,34)/t21-,25-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137329 ((R)-2-Cyclopentylmethyl-N-((S)-1-{4,5-difluoro-2-[...) Show SMILES CC(C)(C)[C@H](NC(=O)[C@H](CC1CCCC1)CN(O)C=O)C(=O)c1cc(F)c(F)cc1N1CCN(CCN2CCOCC2)CC1 Show InChI InChI=1S/C32H49F2N5O5/c1-32(2,3)30(35-31(42)24(21-39(43)22-40)18-23-6-4-5-7-23)29(41)25-19-26(33)27(34)20-28(25)38-12-10-36(11-13-38)8-9-37-14-16-44-17-15-37/h19-20,22-24,30,43H,4-18,21H2,1-3H3,(H,35,42)/t24-,30-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137316 ((R)-2-Cyclopentylmethyl-N-((S)-1-{4,5-difluoro-2-[...) Show SMILES CC(C)(C)[C@H](NC(=O)[C@H](CC1CCCC1)CN(O)C=O)C(=O)c1cc(F)c(F)cc1N1CCN(CCN2CCCC2)CC1 Show InChI InChI=1S/C32H49F2N5O4/c1-32(2,3)30(35-31(42)24(21-39(43)22-40)18-23-8-4-5-9-23)29(41)25-19-26(33)27(34)20-28(25)38-16-14-37(15-17-38)13-12-36-10-6-7-11-36/h19-20,22-24,30,43H,4-18,21H2,1-3H3,(H,35,42)/t24-,30-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137333 ((R)-2-Cyclopentylmethyl-N-{(S)-1-[3-fluoro-4-((S)-...) Show SMILES CC(C)(C)[C@H](NC(=O)[C@H](CC1CCCC1)CN(O)C=O)C(=O)c1ccc(N2CCC[C@H]2CO)c(F)c1 Show InChI InChI=1S/C27H40FN3O5/c1-27(2,3)25(29-26(35)20(15-30(36)17-33)13-18-7-4-5-8-18)24(34)19-10-11-23(22(28)14-19)31-12-6-9-21(31)16-32/h10-11,14,17-18,20-21,25,32,36H,4-9,12-13,15-16H2,1-3H3,(H,29,35)/t20-,21+,25-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137314 ((R)-2-Cyclopentylmethyl-N-{(S)-1-[3-fluoro-4-(4-hy...) Show SMILES CC(C)(C)[C@H](NC(=O)[C@H](CC1CCCC1)CN(O)C=O)C(=O)c1ccc(N2CCC(O)CC2)c(F)c1 Show InChI InChI=1S/C27H40FN3O5/c1-27(2,3)25(29-26(35)20(16-31(36)17-32)14-18-6-4-5-7-18)24(34)19-8-9-23(22(28)15-19)30-12-10-21(33)11-13-30/h8-9,15,17-18,20-21,25,33,36H,4-7,10-14,16H2,1-3H3,(H,29,35)/t20-,25-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50290453 ((R)-2-Decyl-N*4*-hydroxy-N*1*-((S)-1-methylcarbamo...) Show SMILES CCCCCCCCCC[C@H](CC(=O)NO)C(=O)N[C@@H](Cc1ccccc1)C(=O)NC Show InChI InChI=1S/C24H39N3O4/c1-3-4-5-6-7-8-9-13-16-20(18-22(28)27-31)23(29)26-21(24(30)25-2)17-19-14-11-10-12-15-19/h10-12,14-15,20-21,31H,3-9,13,16-18H2,1-2H3,(H,25,30)(H,26,29)(H,27,28)/t20-,21+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound concentration for 50% inhibition of human recombinant gelatinase A (MMP-2).				Bioorg Med Chem Lett 7: 193-198 (1997) Article DOI: 10.1016/S0960-894X(96)00602-6 BindingDB Entry DOI: 10.7270/Q2057FXG
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137323 ((R)-2-Cyclopentylmethyl-N-((S)-2,2-dimethyl-1-{4-[...) Show SMILES CC(C)(C)[C@H](NC(=O)[C@H](CC1CCCC1)CN(O)C=O)C(=O)c1ccc(cc1)N1CCN(CCN2CCCC2)CC1 Show InChI InChI=1S/C32H51N5O4/c1-32(2,3)30(33-31(40)27(23-37(41)24-38)22-25-8-4-5-9-25)29(39)26-10-12-28(13-11-26)36-20-18-35(19-21-36)17-16-34-14-6-7-15-34/h10-13,24-25,27,30,41H,4-9,14-23H2,1-3H3,(H,33,40)/t27-,30-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137318 ((R)-2-Cyclopentylmethyl-3-(formyl-hydroxy-amino)-N...) Show SMILES COc1ccc(cc1)C(=O)[C@@H](NC(=O)[C@H](CC1CCCC1)CN(O)C=O)C(C)(C)C Show InChI InChI=1S/C23H34N2O5/c1-23(2,3)21(20(27)17-9-11-19(30-4)12-10-17)24-22(28)18(14-25(29)15-26)13-16-7-5-6-8-16/h9-12,15-16,18,21,29H,5-8,13-14H2,1-4H3,(H,24,28)/t18-,21-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137346 ((R)-2-Cyclopentylmethyl-N-[(S)-1-(4-fluoro-benzoyl...) Show SMILES CC(C)(C)[C@H](NC(=O)[C@H](CC1CCCC1)CN(O)C=O)C(=O)c1ccc(F)cc1 Show InChI InChI=1S/C22H31FN2O4/c1-22(2,3)20(19(27)16-8-10-18(23)11-9-16)24-21(28)17(13-25(29)14-26)12-15-6-4-5-7-15/h8-11,14-15,17,20,29H,4-7,12-13H2,1-3H3,(H,24,28)/t17-,20-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137330 ((R)-2-[(Formyl-hydroxy-amino)-methyl]-hexanoic aci...) Show SMILES CCCC[C@H](CN(O)C=O)C(=O)N[C@H](C(=O)c1ccccc1)C(C)(C)C Show InChI InChI=1S/C20H30N2O4/c1-5-6-10-16(13-22(26)14-23)19(25)21-18(20(2,3)4)17(24)15-11-8-7-9-12-15/h7-9,11-12,14,16,18,26H,5-6,10,13H2,1-4H3,(H,21,25)/t16-,18-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50290440 ((R)-N*1*-((S)-2,2-Dimethyl-1-methylcarbamoyl-propy...) Show SMILES CCCCCCCCCCCCC[C@H](CC(=O)NO)C(=O)N[C@H](C(=O)NC)C(C)(C)C Show InChI InChI=1S/C24H47N3O4/c1-6-7-8-9-10-11-12-13-14-15-16-17-19(18-20(28)27-31)22(29)26-21(23(30)25-5)24(2,3)4/h19,21,31H,6-18H2,1-5H3,(H,25,30)(H,26,29)(H,27,28)/t19-,21-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound concentration for 50% inhibition of human recombinant gelatinase A (MMP-2).				Bioorg Med Chem Lett 7: 193-198 (1997) Article DOI: 10.1016/S0960-894X(96)00602-6 BindingDB Entry DOI: 10.7270/Q2057FXG
					More data for this Ligand-Target Pair
Neutrophil collagenase (Homo sapiens (Human))	BDBM50081869 ((2R,3R)-3-(cyclopentylmethyl)-N-hydroxy-2-((4-meth...) Show SMILES COc1ccc(cc1)S(=O)(=O)N(C)C[C@@H]([C@@H](CC1CCCC1)C(=O)N1CCCCC1)C(=O)NO Show InChI InChI=1S/C24H37N3O6S/c1-26(34(31,32)20-12-10-19(33-2)11-13-20)17-22(23(28)25-30)21(16-18-8-4-5-9-18)24(29)27-14-6-3-7-15-27/h10-13,18,21-22,30H,3-9,14-17H2,1-2H3,(H,25,28)/t21-,22+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibition of HNC MMP-8				Bioorg Med Chem Lett 9: 2887-92 (1999) BindingDB Entry DOI: 10.7270/Q25H7FGN
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137348 ((R)-2-[(Formyl-hydroxy-amino)-methyl]-hexanoic aci...) Show SMILES CCCC[C@H](CN(O)C=O)C(=O)N[C@H](C(=O)c1ccc(F)cc1)C(C)(C)C Show InChI InChI=1S/C20H29FN2O4/c1-5-6-7-15(12-23(27)13-24)19(26)22-18(20(2,3)4)17(25)14-8-10-16(21)11-9-14/h8-11,13,15,18,27H,5-7,12H2,1-4H3,(H,22,26)/t15-,18-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
Peptide deformylase (Escherichia coli)	BDBM50137319 ((R)-2-[(Formyl-hydroxy-amino)-methyl]-hexanoic aci...) Show SMILES CCCC[C@H](CN(O)C=O)C(=O)N[C@H](C(=O)c1ccccn1)C(C)(C)C Show InChI InChI=1S/C19H29N3O4/c1-5-6-9-14(12-22(26)13-23)18(25)21-17(19(2,3)4)16(24)15-10-7-8-11-20-15/h7-8,10-11,13-14,17,26H,5-6,9,12H2,1-4H3,(H,21,25)/t14-,17-/m1/s1	PDB MMDB KEGG UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibitory activity against Escherichia coli peptide deformylase (PDF) Nickel containing enzyme				Bioorg Med Chem Lett 14: 59-62 (2003) BindingDB Entry DOI: 10.7270/Q2T43SHT
					More data for this Ligand-Target Pair
Neutrophil collagenase (Homo sapiens (Human))	BDBM50081866 ((2R,3R)-3-(cyclopentylmethyl)-N-hydroxy-2-((4-meth...) Show SMILES COc1ccc(cc1)S(=O)(=O)N(C)C[C@@H]([C@@H](CC1CCCC1)C(=O)N1CCOCC1)C(=O)NO Show InChI InChI=1S/C23H35N3O7S/c1-25(34(30,31)19-9-7-18(32-2)8-10-19)16-21(22(27)24-29)20(15-17-5-3-4-6-17)23(28)26-11-13-33-14-12-26/h7-10,17,20-21,29H,3-6,11-16H2,1-2H3,(H,24,27)/t20-,21+/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	3	n/a	n/a	n/a	n/a	n/a	n/a
British Biotech Pharmaceuticals Limited Curated by ChEMBL					Assay Description Inhibition of HNC MMP-8				Bioorg Med Chem Lett 9: 2887-92 (1999) BindingDB Entry DOI: 10.7270/Q25H7FGN
					More data for this Ligand-Target Pair
Acidic mammalian chitinase (Homo sapiens (Human))	BDBM50243685 (CHEMBL4084573) Show SMILES Nc1n[nH]c(n1)N1CCC(CC1)N(CCc1ccc(Cl)cc1)Cc1cccc2ccccc12 Show InChI InChI=1S/C26H29ClN6/c27-22-10-8-19(9-11-22)12-15-33(18-21-6-3-5-20-4-1-2-7-24(20)21)23-13-16-32(17-14-23)26-29-25(28)30-31-26/h1-11,23H,12-18H2,(H3,28,29,30,31)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.40	n/a	n/a	n/a	n/a	n/a	n/a
OncoArendi Therapeutics SA Curated by ChEMBL					Assay Description Inhibition of human recombinant full length C-terminal His-tagged acidic mammalian chitinase expressed in CHO-K1 cells using 4-methylumbelliferyl-bet...				J Med Chem 61: 695-710 (2018) Article DOI: 10.1021/acs.jmedchem.7b01051 BindingDB Entry DOI: 10.7270/Q2J105J5
					More data for this Ligand-Target Pair
Acidic mammalian chitinase (Homo sapiens (Human))	BDBM50243795 (CHEMBL4077644) Show SMILES Nc1n[nH]c(n1)N1CCC(CC1)N(CCc1ccc(Cl)cc1)Cc1ccccc1Cl Show InChI InChI=1S/C22H26Cl2N6/c23-18-7-5-16(6-8-18)9-12-30(15-17-3-1-2-4-20(17)24)19-10-13-29(14-11-19)22-26-21(25)27-28-22/h1-8,19H,9-15H2,(H3,25,26,27,28)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.5	n/a	n/a	n/a	n/a	n/a	n/a
OncoArendi Therapeutics SA Curated by ChEMBL					Assay Description Inhibition of human recombinant full length C-terminal His-tagged acidic mammalian chitinase expressed in CHO-K1 cells using 4-methylumbelliferyl-bet...				J Med Chem 61: 695-710 (2018) Article DOI: 10.1021/acs.jmedchem.7b01051 BindingDB Entry DOI: 10.7270/Q2J105J5
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50063918 ((2R,3S)-N*4*-Hydroxy-2-isobutyl-N*1*-((S)-1-methyl...) Show SMILES CNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(C)C)[C@H](CSc1cccs1)C(=O)NO Show InChI InChI=1S/C23H31N3O4S2/c1-15(2)12-17(18(22(28)26-30)14-32-20-10-7-11-31-20)21(27)25-19(23(29)24-3)13-16-8-5-4-6-9-16/h4-11,15,17-19,30H,12-14H2,1-3H3,(H,24,29)(H,25,27)(H,26,28)/t17-,18+,19+/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	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound concentration for 50% inhibition of human recombinant gelatinase A (MMP-2).				Bioorg Med Chem Lett 7: 193-198 (1997) Article DOI: 10.1016/S0960-894X(96)00602-6 BindingDB Entry DOI: 10.7270/Q2057FXG
					More data for this Ligand-Target Pair

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