Compile Data Set for Download or QSAR

Found 97 hits with Last Name = 'huang' and Initial = 'xc'   

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
Neutrophil collagenase (Homo sapiens (Human))	BDBM8465 ((2R)-N-hydroxy-2-[(4-methoxybenzene)(pyridin-3-ylm...) Show SMILES COc1ccc(cc1)S(=O)(=O)N(Cc1cccnc1)[C@H](C(C)C)C(=O)NO |r| Show InChI InChI=1S/C18H23N3O5S/c1-13(2)17(18(22)20-23)21(12-14-5-4-10-19-11-14)27(24,25)16-8-6-15(26-3)7-9-16/h4-11,13,17,23H,12H2,1-3H3,(H,20,22)/t17-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP8 (Phe21 to Gly467 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM8465 ((2R)-N-hydroxy-2-[(4-methoxybenzene)(pyridin-3-ylm...) Show SMILES COc1ccc(cc1)S(=O)(=O)N(Cc1cccnc1)[C@H](C(C)C)C(=O)NO |r| Show InChI InChI=1S/C18H23N3O5S/c1-13(2)17(18(22)20-23)21(12-14-5-4-10-19-11-14)27(24,25)16-8-6-15(26-3)7-9-16/h4-11,13,17,23H,12H2,1-3H3,(H,20,22)/t17-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP9 (Ala20 to Asp707 residues) expressed in CHO cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrate preincub...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM8465 ((2R)-N-hydroxy-2-[(4-methoxybenzene)(pyridin-3-ylm...) Show SMILES COc1ccc(cc1)S(=O)(=O)N(Cc1cccnc1)[C@H](C(C)C)C(=O)NO |r| Show InChI InChI=1S/C18H23N3O5S/c1-13(2)17(18(22)20-23)21(12-14-5-4-10-19-11-14)27(24,25)16-8-6-15(26-3)7-9-16/h4-11,13,17,23H,12H2,1-3H3,(H,20,22)/t17-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	30	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456787 (CHEMBL4215396) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1cccc(C)c1)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1cccc(C)c1 |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)42-32-39-24-25-47-51(5,26-15-27-52(47,6)50(59)55-44(30-37-18-9-7-10-19-37)48(57)53-40-22-13-16-35(3)28-40)43(39)33-46(42)62(60,61)56-45(31-38-20-11-8-12-21-38)49(58)54-41-23-14-17-36(4)29-41/h7-14,16-23,28-29,32-34,44-45,47,56H,15,24-27,30-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47+,51+,52+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	400	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456778 (CHEMBL4207542) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccc(C)cc1)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccc(C)cc1 |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)42-32-39-22-27-47-51(5,28-13-29-52(47,6)50(59)55-44(30-37-14-9-7-10-15-37)48(57)53-40-23-18-35(3)19-24-40)43(39)33-46(42)62(60,61)56-45(31-38-16-11-8-12-17-38)49(58)54-41-25-20-36(4)21-26-41/h7-12,14-21,23-26,32-34,44-45,47,56H,13,22,27-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47+,51+,52+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Neutrophil collagenase (Homo sapiens (Human))	BDBM50456787 (CHEMBL4215396) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1cccc(C)c1)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1cccc(C)c1 |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)42-32-39-24-25-47-51(5,26-15-27-52(47,6)50(59)55-44(30-37-18-9-7-10-19-37)48(57)53-40-22-13-16-35(3)28-40)43(39)33-46(42)62(60,61)56-45(31-38-20-11-8-12-21-38)49(58)54-41-23-14-17-36(4)29-41/h7-14,16-23,28-29,32-34,44-45,47,56H,15,24-27,30-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47+,51+,52+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP8 (Phe21 to Gly467 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456776 (CHEMBL4216154) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1C)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1C |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)40-32-39-26-27-47-51(5,28-17-29-52(47,6)50(59)55-44(30-37-20-9-7-10-21-37)48(57)53-42-24-15-13-18-35(42)3)41(39)33-46(40)62(60,61)56-45(31-38-22-11-8-12-23-38)49(58)54-43-25-16-14-19-36(43)4/h7-16,18-25,32-34,44-45,47,56H,17,26-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47+,51+,52+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50479039 (CHEMBL454276 | Nakafuran-8) Show SMILES [H][C@@]12C[C@H](C)[C@](C)(CCc3ccoc13)C(C)=C2 |r,c:17,TLB:10:9:2.3:14.16,12:13:2.3:14.16,THB:4:3:7.8.13.9:14.16,15:14:7.8.13.9:2.3| Show InChI InChI=1S/C15H20O/c1-10-8-13-9-11(2)15(10,3)6-4-12-5-7-16-14(12)13/h5,7-8,11,13H,4,6,9H2,1-3H3/t11-,13+,15+/m0/s1	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	8.78E+3	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of human recombinant PTP1B catalytic domain				J Nat Prod 71: 1399-403 (2008) Article DOI: 10.1021/np8002035 BindingDB Entry DOI: 10.7270/Q2VT1VW1
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456775 (CHEMBL4216220) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1 |r| Show InChI InChI=1S/C50H56N4O5S/c1-34(2)40-32-37-26-27-45-49(3,28-17-29-50(45,4)48(57)53-42(30-35-18-9-5-10-19-35)46(55)51-38-22-13-7-14-23-38)41(37)33-44(40)60(58,59)54-43(31-36-20-11-6-12-21-36)47(56)52-39-24-15-8-16-25-39/h5-16,18-25,32-34,42-43,45,54H,17,26-31H2,1-4H3,(H,51,55)(H,52,56)(H,53,57)/t42-,43-,45+,49+,50+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50456787 (CHEMBL4215396) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1cccc(C)c1)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1cccc(C)c1 |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)42-32-39-24-25-47-51(5,26-15-27-52(47,6)50(59)55-44(30-37-18-9-7-10-19-37)48(57)53-40-22-13-16-35(3)28-40)43(39)33-46(42)62(60,61)56-45(31-38-20-11-8-12-21-38)49(58)54-41-23-14-17-36(4)29-41/h7-14,16-23,28-29,32-34,44-45,47,56H,15,24-27,30-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47+,51+,52+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP9 (Ala20 to Asp707 residues) expressed in CHO cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrate preincub...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456786 (CHEMBL4213804) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@H](Cc1ccccc1)C(=O)Nc1cccc(C)c1)S(=O)(=O)N[C@H](Cc1ccccc1)C(=O)Nc1cccc(C)c1 |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)42-32-39-24-25-47-51(5,26-15-27-52(47,6)50(59)55-44(30-37-18-9-7-10-19-37)48(57)53-40-22-13-16-35(3)28-40)43(39)33-46(42)62(60,61)56-45(31-38-20-11-8-12-21-38)49(58)54-41-23-14-17-36(4)29-41/h7-14,16-23,28-29,32-34,44-45,47,56H,15,24-27,30-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47-,51-,52-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.02E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456795 (CHEMBL4215930) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccc(C)cc1)S(=O)(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccc(C)cc1 |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)42-32-39-22-27-47-51(5,28-13-29-52(47,6)50(59)55-44(30-37-14-9-7-10-15-37)48(57)53-40-23-18-35(3)19-24-40)43(39)33-46(42)62(60,61)56-45(31-38-16-11-8-12-17-38)49(58)54-41-25-20-36(4)21-26-41/h7-12,14-21,23-26,32-34,44-45,47,56H,13,22,27-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47-,51-,52-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.28E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Neutrophil collagenase (Homo sapiens (Human))	BDBM50456778 (CHEMBL4207542) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccc(C)cc1)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccc(C)cc1 |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)42-32-39-22-27-47-51(5,28-13-29-52(47,6)50(59)55-44(30-37-14-9-7-10-15-37)48(57)53-40-23-18-35(3)19-24-40)43(39)33-46(42)62(60,61)56-45(31-38-16-11-8-12-17-38)49(58)54-41-25-20-36(4)21-26-41/h7-12,14-21,23-26,32-34,44-45,47,56H,13,22,27-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47+,51+,52+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.77E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP8 (Phe21 to Gly467 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456777 (CHEMBL4206886) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccccc1)S(=O)(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccccc1 |r| Show InChI InChI=1S/C50H56N4O5S/c1-34(2)40-32-37-26-27-45-49(3,28-17-29-50(45,4)48(57)53-42(30-35-18-9-5-10-19-35)46(55)51-38-22-13-7-14-23-38)41(37)33-44(40)60(58,59)54-43(31-36-20-11-6-12-21-36)47(56)52-39-24-15-8-16-25-39/h5-16,18-25,32-34,42-43,45,54H,17,26-31H2,1-4H3,(H,51,55)(H,52,56)(H,53,57)/t42-,43-,45-,49-,50-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.96E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50456778 (CHEMBL4207542) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccc(C)cc1)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccc(C)cc1 |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)42-32-39-22-27-47-51(5,28-13-29-52(47,6)50(59)55-44(30-37-14-9-7-10-15-37)48(57)53-40-23-18-35(3)19-24-40)43(39)33-46(42)62(60,61)56-45(31-38-16-11-8-12-17-38)49(58)54-41-25-20-36(4)21-26-41/h7-12,14-21,23-26,32-34,44-45,47,56H,13,22,27-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47+,51+,52+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.09E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP9 (Ala20 to Asp707 residues) expressed in CHO cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrate preincub...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456781 (CHEMBL4210975) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccc(OC)cc1)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccc(OC)cc1 |r| Show InChI InChI=1S/C52H60N4O7S/c1-34(2)42-32-37-18-27-47-51(3,28-13-29-52(47,4)50(59)55-44(30-35-14-9-7-10-15-35)48(57)53-38-19-23-40(62-5)24-20-38)43(37)33-46(42)64(60,61)56-45(31-36-16-11-8-12-17-36)49(58)54-39-21-25-41(63-6)26-22-39/h7-12,14-17,19-26,32-34,44-45,47,56H,13,18,27-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47+,51+,52+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.13E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456791 (CHEMBL4202778) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccccc1C)S(=O)(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccccc1C |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)40-32-39-26-27-47-51(5,28-17-29-52(47,6)50(59)55-44(30-37-20-9-7-10-21-37)48(57)53-42-24-15-13-18-35(42)3)41(39)33-46(40)62(60,61)56-45(31-38-22-11-8-12-23-38)49(58)54-43-25-16-14-19-36(43)4/h7-16,18-25,32-34,44-45,47,56H,17,26-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47-,51-,52-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.15E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456797 (CHEMBL4218730) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1cccc(OC)c1)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1cccc(OC)c1 |r| Show InChI InChI=1S/C52H60N4O7S/c1-34(2)42-30-37-24-25-47-51(3,26-15-27-52(47,4)50(59)55-44(28-35-16-9-7-10-17-35)48(57)53-38-20-13-22-40(31-38)62-5)43(37)33-46(42)64(60,61)56-45(29-36-18-11-8-12-19-36)49(58)54-39-21-14-23-41(32-39)63-6/h7-14,16-23,30-34,44-45,47,56H,15,24-29H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47+,51+,52+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.26E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456790 (CHEMBL4214436) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1OC)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1OC |r| Show InChI InChI=1S/C52H60N4O7S/c1-34(2)38-32-37-26-27-47-51(3,28-17-29-52(47,4)50(59)55-42(30-35-18-9-7-10-19-35)48(57)53-40-22-13-15-24-44(40)62-5)39(37)33-46(38)64(60,61)56-43(31-36-20-11-8-12-21-36)49(58)54-41-23-14-16-25-45(41)63-6/h7-16,18-25,32-34,42-43,47,56H,17,26-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t42-,43-,47+,51+,52+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.38E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Neutrophil collagenase (Homo sapiens (Human))	BDBM50456776 (CHEMBL4216154) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1C)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1C |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)40-32-39-26-27-47-51(5,28-17-29-52(47,6)50(59)55-44(30-37-20-9-7-10-21-37)48(57)53-42-24-15-13-18-35(42)3)41(39)33-46(40)62(60,61)56-45(31-38-22-11-8-12-23-38)49(58)54-43-25-16-14-19-36(43)4/h7-16,18-25,32-34,44-45,47,56H,17,26-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47+,51+,52+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.43E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP8 (Phe21 to Gly467 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50456775 (CHEMBL4216220) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1 |r| Show InChI InChI=1S/C50H56N4O5S/c1-34(2)40-32-37-26-27-45-49(3,28-17-29-50(45,4)48(57)53-42(30-35-18-9-5-10-19-35)46(55)51-38-22-13-7-14-23-38)41(37)33-44(40)60(58,59)54-43(31-36-20-11-6-12-21-36)47(56)52-39-24-15-8-16-25-39/h5-16,18-25,32-34,42-43,45,54H,17,26-31H2,1-4H3,(H,51,55)(H,52,56)(H,53,57)/t42-,43-,45+,49+,50+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.43E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP9 (Ala20 to Asp707 residues) expressed in CHO cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrate preincub...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456771 (CHEMBL4203717) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccc(OC)cc1)S(=O)(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccc(OC)cc1 |r| Show InChI InChI=1S/C52H60N4O7S/c1-34(2)42-32-37-18-27-47-51(3,28-13-29-52(47,4)50(59)55-44(30-35-14-9-7-10-15-35)48(57)53-38-19-23-40(62-5)24-20-38)43(37)33-46(42)64(60,61)56-45(31-36-16-11-8-12-17-36)49(58)54-39-21-25-41(63-6)26-22-39/h7-12,14-17,19-26,32-34,44-45,47,56H,13,18,27-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47-,51-,52-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.49E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456789 (CHEMBL4203206) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1F)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1F |r| Show InChI InChI=1S/C50H54F2N4O5S/c1-32(2)36-30-35-24-25-45-49(3,26-15-27-50(45,4)48(59)55-42(28-33-16-7-5-8-17-33)46(57)53-40-22-13-11-20-38(40)51)37(35)31-44(36)62(60,61)56-43(29-34-18-9-6-10-19-34)47(58)54-41-23-14-12-21-39(41)52/h5-14,16-23,30-32,42-43,45,56H,15,24-29H2,1-4H3,(H,53,57)(H,54,58)(H,55,59)/t42-,43-,45+,49+,50+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.55E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456784 (CHEMBL4206821) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccccc1)S(O)(=O)=O |r| Show InChI InChI=1S/C35H42N2O5S/c1-23(2)27-21-25-16-17-31-34(3,28(25)22-30(27)43(40,41)42)18-11-19-35(31,4)33(39)37-29(20-24-12-7-5-8-13-24)32(38)36-26-14-9-6-10-15-26/h5-10,12-15,21-23,29,31H,11,16-20H2,1-4H3,(H,36,38)(H,37,39)(H,40,41,42)/t29-,31-,34-,35-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.69E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50456776 (CHEMBL4216154) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1C)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1C |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)40-32-39-26-27-47-51(5,28-17-29-52(47,6)50(59)55-44(30-37-20-9-7-10-21-37)48(57)53-42-24-15-13-18-35(42)3)41(39)33-46(40)62(60,61)56-45(31-38-22-11-8-12-23-38)49(58)54-43-25-16-14-19-36(43)4/h7-16,18-25,32-34,44-45,47,56H,17,26-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47+,51+,52+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.74E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP9 (Ala20 to Asp707 residues) expressed in CHO cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrate preincub...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456796 (CHEMBL4210262) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccc(OC)cc1)S(O)(=O)=O |r| Show InChI InChI=1S/C36H44N2O6S/c1-23(2)28-21-25-12-17-32-35(3,29(25)22-31(28)45(41,42)43)18-9-19-36(32,4)34(40)38-30(20-24-10-7-6-8-11-24)33(39)37-26-13-15-27(44-5)16-14-26/h6-8,10-11,13-16,21-23,30,32H,9,12,17-20H2,1-5H3,(H,37,39)(H,38,40)(H,41,42,43)/t30-,32+,35+,36+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Neutrophil collagenase (Homo sapiens (Human))	BDBM50456775 (CHEMBL4216220) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1 |r| Show InChI InChI=1S/C50H56N4O5S/c1-34(2)40-32-37-26-27-45-49(3,28-17-29-50(45,4)48(57)53-42(30-35-18-9-5-10-19-35)46(55)51-38-22-13-7-14-23-38)41(37)33-44(40)60(58,59)54-43(31-36-20-11-6-12-21-36)47(56)52-39-24-15-8-16-25-39/h5-16,18-25,32-34,42-43,45,54H,17,26-31H2,1-4H3,(H,51,55)(H,52,56)(H,53,57)/t42-,43-,45+,49+,50+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.82E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP8 (Phe21 to Gly467 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456798 (CHEMBL4211708) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccccc1OC)S(=O)(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccccc1OC |r| Show InChI InChI=1S/C52H60N4O7S/c1-34(2)38-32-37-26-27-47-51(3,28-17-29-52(47,4)50(59)55-42(30-35-18-9-7-10-19-35)48(57)53-40-22-13-15-24-44(40)62-5)39(37)33-46(38)64(60,61)56-43(31-36-20-11-8-12-21-36)49(58)54-41-23-14-16-25-45(41)63-6/h7-16,18-25,32-34,42-43,47,56H,17,26-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t42-,43-,47-,51-,52-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.02E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50479041 (CHEMBL469255 | Microcionin-4) Show SMILES C[C@@H]1CCCC(=C)[C@]1(C)CCc1ccoc1 |r| Show InChI InChI=1S/C15H22O/c1-12-5-4-6-13(2)15(12,3)9-7-14-8-10-16-11-14/h8,10-11,13H,1,4-7,9H2,2-3H3/t13-,15+/m1/s1	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	3.11E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of human recombinant PTP1B catalytic domain				J Nat Prod 71: 1399-403 (2008) Article DOI: 10.1021/np8002035 BindingDB Entry DOI: 10.7270/Q2VT1VW1
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50479038 (Lingshuiperoxide) Show SMILES [H][C@]12OO[C@](C)(C=C1)[C@@](C)(CCC1=CC(O)OC1=O)[C@@H]2C |r,c:6,t:13| Show InChI InChI=1S/C15H20O5/c1-9-11-5-7-15(3,20-19-11)14(9,2)6-4-10-8-12(16)18-13(10)17/h5,7-9,11-12,16H,4,6H2,1-3H3/t9-,11+,12?,14+,15-/m1/s1	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	3.13E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of human recombinant PTP1B catalytic domain				J Nat Prod 71: 1399-403 (2008) Article DOI: 10.1021/np8002035 BindingDB Entry DOI: 10.7270/Q2VT1VW1
					More data for this Ligand-Target Pair
Neutrophil collagenase (Homo sapiens (Human))	BDBM50456791 (CHEMBL4202778) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccccc1C)S(=O)(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccccc1C |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)40-32-39-26-27-47-51(5,28-17-29-52(47,6)50(59)55-44(30-37-20-9-7-10-21-37)48(57)53-42-24-15-13-18-35(42)3)41(39)33-46(40)62(60,61)56-45(31-38-22-11-8-12-23-38)49(58)54-43-25-16-14-19-36(43)4/h7-16,18-25,32-34,44-45,47,56H,17,26-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47-,51-,52-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.34E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP8 (Phe21 to Gly467 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50456791 (CHEMBL4202778) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccccc1C)S(=O)(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccccc1C |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)40-32-39-26-27-47-51(5,28-17-29-52(47,6)50(59)55-44(30-37-20-9-7-10-21-37)48(57)53-42-24-15-13-18-35(42)3)41(39)33-46(40)62(60,61)56-45(31-38-22-11-8-12-23-38)49(58)54-43-25-16-14-19-36(43)4/h7-16,18-25,32-34,44-45,47,56H,17,26-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47-,51-,52-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.36E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP9 (Ala20 to Asp707 residues) expressed in CHO cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrate preincub...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50456786 (CHEMBL4213804) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@H](Cc1ccccc1)C(=O)Nc1cccc(C)c1)S(=O)(=O)N[C@H](Cc1ccccc1)C(=O)Nc1cccc(C)c1 |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)42-32-39-24-25-47-51(5,26-15-27-52(47,6)50(59)55-44(30-37-18-9-7-10-19-37)48(57)53-40-22-13-16-35(3)28-40)43(39)33-46(42)62(60,61)56-45(31-38-20-11-8-12-21-38)49(58)54-41-23-14-17-36(4)29-41/h7-14,16-23,28-29,32-34,44-45,47,56H,15,24-27,30-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47-,51-,52-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.48E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP9 (Ala20 to Asp707 residues) expressed in CHO cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrate preincub...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456788 (CHEMBL4212449) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccccc1F)S(=O)(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccccc1F |r| Show InChI InChI=1S/C50H54F2N4O5S/c1-32(2)36-30-35-24-25-45-49(3,26-15-27-50(45,4)48(59)55-42(28-33-16-7-5-8-17-33)46(57)53-40-22-13-11-20-38(40)51)37(35)31-44(36)62(60,61)56-43(29-34-18-9-6-10-19-34)47(58)54-41-23-14-12-21-39(41)52/h5-14,16-23,30-32,42-43,45,56H,15,24-29H2,1-4H3,(H,53,57)(H,54,58)(H,55,59)/t42-,43-,45-,49-,50-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.53E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50456796 (CHEMBL4210262) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccc(OC)cc1)S(O)(=O)=O |r| Show InChI InChI=1S/C36H44N2O6S/c1-23(2)28-21-25-12-17-32-35(3,29(25)22-31(28)45(41,42)43)18-9-19-36(32,4)34(40)38-30(20-24-10-7-6-8-11-24)33(39)37-26-13-15-27(44-5)16-14-26/h6-8,10-11,13-16,21-23,30,32H,9,12,17-20H2,1-5H3,(H,37,39)(H,38,40)(H,41,42,43)/t30-,32+,35+,36+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.63E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP9 (Ala20 to Asp707 residues) expressed in CHO cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrate preincub...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Neutrophil collagenase (Homo sapiens (Human))	BDBM50456796 (CHEMBL4210262) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccc(OC)cc1)S(O)(=O)=O |r| Show InChI InChI=1S/C36H44N2O6S/c1-23(2)28-21-25-12-17-32-35(3,29(25)22-31(28)45(41,42)43)18-9-19-36(32,4)34(40)38-30(20-24-10-7-6-8-11-24)33(39)37-26-13-15-27(44-5)16-14-26/h6-8,10-11,13-16,21-23,30,32H,9,12,17-20H2,1-5H3,(H,37,39)(H,38,40)(H,41,42,43)/t30-,32+,35+,36+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.94E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP8 (Phe21 to Gly467 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456785 (CHEMBL4211771) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1cccc(Br)c1)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1cccc(Br)c1 |r| Show InChI InChI=1S/C50H54Br2N4O5S/c1-32(2)40-28-35-22-23-45-49(3,24-13-25-50(45,4)48(59)55-42(26-33-14-7-5-8-15-33)46(57)53-38-20-11-18-36(51)29-38)41(35)31-44(40)62(60,61)56-43(27-34-16-9-6-10-17-34)47(58)54-39-21-12-19-37(52)30-39/h5-12,14-21,28-32,42-43,45,56H,13,22-27H2,1-4H3,(H,53,57)(H,54,58)(H,55,59)/t42-,43-,45+,49+,50+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.97E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Neutrophil collagenase (Homo sapiens (Human))	BDBM50456786 (CHEMBL4213804) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@H](Cc1ccccc1)C(=O)Nc1cccc(C)c1)S(=O)(=O)N[C@H](Cc1ccccc1)C(=O)Nc1cccc(C)c1 |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)42-32-39-24-25-47-51(5,26-15-27-52(47,6)50(59)55-44(30-37-18-9-7-10-19-37)48(57)53-40-22-13-16-35(3)28-40)43(39)33-46(42)62(60,61)56-45(31-38-20-11-8-12-21-38)49(58)54-41-23-14-17-36(4)29-41/h7-14,16-23,28-29,32-34,44-45,47,56H,15,24-27,30-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47-,51-,52-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.04E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP8 (Phe21 to Gly467 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456773 (CHEMBL4211258) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@H](Cc1ccccc1)C(=O)Nc1cccc(OC)c1)S(=O)(=O)N[C@H](Cc1ccccc1)C(=O)Nc1cccc(OC)c1 |r| Show InChI InChI=1S/C52H60N4O7S/c1-34(2)42-30-37-24-25-47-51(3,26-15-27-52(47,4)50(59)55-44(28-35-16-9-7-10-17-35)48(57)53-38-20-13-22-40(31-38)62-5)43(37)33-46(42)64(60,61)56-45(29-36-18-11-8-12-19-36)49(58)54-39-21-14-23-41(32-39)63-6/h7-14,16-23,30-34,44-45,47,56H,15,24-29H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47-,51-,52-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.08E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Neutrophil collagenase (Homo sapiens (Human))	BDBM50456789 (CHEMBL4203206) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1F)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1F |r| Show InChI InChI=1S/C50H54F2N4O5S/c1-32(2)36-30-35-24-25-45-49(3,26-15-27-50(45,4)48(59)55-42(28-33-16-7-5-8-17-33)46(57)53-40-22-13-11-20-38(40)51)37(35)31-44(36)62(60,61)56-43(29-34-18-9-6-10-19-34)47(58)54-41-23-14-12-21-39(41)52/h5-14,16-23,30-32,42-43,45,56H,15,24-29H2,1-4H3,(H,53,57)(H,54,58)(H,55,59)/t42-,43-,45+,49+,50+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.15E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP8 (Phe21 to Gly467 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Neutrophil collagenase (Homo sapiens (Human))	BDBM50456790 (CHEMBL4214436) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1OC)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1OC |r| Show InChI InChI=1S/C52H60N4O7S/c1-34(2)38-32-37-26-27-47-51(3,28-17-29-52(47,4)50(59)55-42(30-35-18-9-7-10-19-35)48(57)53-40-22-13-15-24-44(40)62-5)39(37)33-46(38)64(60,61)56-43(31-36-20-11-8-12-21-36)49(58)54-41-23-14-16-25-45(41)63-6/h7-16,18-25,32-34,42-43,47,56H,17,26-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t42-,43-,47+,51+,52+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP8 (Phe21 to Gly467 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50456790 (CHEMBL4214436) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1OC)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1OC |r| Show InChI InChI=1S/C52H60N4O7S/c1-34(2)38-32-37-26-27-47-51(3,28-17-29-52(47,4)50(59)55-42(30-35-18-9-7-10-19-35)48(57)53-40-22-13-15-24-44(40)62-5)39(37)33-46(38)64(60,61)56-43(31-36-20-11-8-12-21-36)49(58)54-41-23-14-16-25-45(41)63-6/h7-16,18-25,32-34,42-43,47,56H,17,26-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t42-,43-,47+,51+,52+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.39E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP9 (Ala20 to Asp707 residues) expressed in CHO cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrate preincub...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Neutrophil collagenase (Homo sapiens (Human))	BDBM50456795 (CHEMBL4215930) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccc(C)cc1)S(=O)(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccc(C)cc1 |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)42-32-39-22-27-47-51(5,28-13-29-52(47,6)50(59)55-44(30-37-14-9-7-10-15-37)48(57)53-40-23-18-35(3)19-24-40)43(39)33-46(42)62(60,61)56-45(31-38-16-11-8-12-17-38)49(58)54-41-25-20-36(4)21-26-41/h7-12,14-21,23-26,32-34,44-45,47,56H,13,22,27-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47-,51-,52-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.67E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP8 (Phe21 to Gly467 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50456774 (CHEMBL4211189) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1cccc(F)c1)S(O)(=O)=O |r| Show InChI InChI=1S/C35H41FN2O5S/c1-22(2)27-19-24-14-15-31-34(3,28(24)21-30(27)44(41,42)43)16-9-17-35(31,4)33(40)38-29(18-23-10-6-5-7-11-23)32(39)37-26-13-8-12-25(36)20-26/h5-8,10-13,19-22,29,31H,9,14-18H2,1-4H3,(H,37,39)(H,38,40)(H,41,42,43)/t29-,31+,34+,35+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.72E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP3 (Tyr18 to Cys477 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 1 (Homo sapiens (Human))	BDBM50479040 (Hydroxybutenolide) Show SMILES C[C@@H]1CC=CC(=C)[C@]1(C)CCC1=CC(O)OC1=O |r,c:3,t:12| Show InChI InChI=1S/C15H20O3/c1-10-5-4-6-11(2)15(10,3)8-7-12-9-13(16)18-14(12)17/h4-5,9,11,13,16H,1,6-8H2,2-3H3/t11-,13?,15+/m1/s1	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	4.83E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of human recombinant PTP1B catalytic domain				J Nat Prod 71: 1399-403 (2008) Article DOI: 10.1021/np8002035 BindingDB Entry DOI: 10.7270/Q2VT1VW1
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50456789 (CHEMBL4203206) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1F)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccccc1F |r| Show InChI InChI=1S/C50H54F2N4O5S/c1-32(2)36-30-35-24-25-45-49(3,26-15-27-50(45,4)48(59)55-42(28-33-16-7-5-8-17-33)46(57)53-40-22-13-11-20-38(40)51)37(35)31-44(36)62(60,61)56-43(29-34-18-9-6-10-19-34)47(58)54-41-23-14-12-21-39(41)52/h5-14,16-23,30-32,42-43,45,56H,15,24-29H2,1-4H3,(H,53,57)(H,54,58)(H,55,59)/t42-,43-,45+,49+,50+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.83E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP9 (Ala20 to Asp707 residues) expressed in CHO cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrate preincub...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50456795 (CHEMBL4215930) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccc(C)cc1)S(=O)(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccc(C)cc1 |r| Show InChI InChI=1S/C52H60N4O5S/c1-34(2)42-32-39-22-27-47-51(5,28-13-29-52(47,6)50(59)55-44(30-37-14-9-7-10-15-37)48(57)53-40-23-18-35(3)19-24-40)43(39)33-46(42)62(60,61)56-45(31-38-16-11-8-12-17-38)49(58)54-41-25-20-36(4)21-26-41/h7-12,14-21,23-26,32-34,44-45,47,56H,13,22,27-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47-,51-,52-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.16E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP9 (Ala20 to Asp707 residues) expressed in CHO cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrate preincub...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Matrix metalloproteinase-9 (Homo sapiens (Human))	BDBM50456797 (CHEMBL4218730) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1cccc(OC)c1)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1cccc(OC)c1 |r| Show InChI InChI=1S/C52H60N4O7S/c1-34(2)42-30-37-24-25-47-51(3,26-15-27-52(47,4)50(59)55-44(28-35-16-9-7-10-17-35)48(57)53-38-20-13-22-40(31-38)62-5)43(37)33-46(42)64(60,61)56-45(29-36-18-11-8-12-19-36)49(58)54-39-21-14-23-41(32-39)63-6/h7-14,16-23,30-34,44-45,47,56H,15,24-29H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47+,51+,52+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.19E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP9 (Ala20 to Asp707 residues) expressed in CHO cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrate preincub...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Neutrophil collagenase (Homo sapiens (Human))	BDBM50456781 (CHEMBL4210975) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccc(OC)cc1)S(=O)(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccc(OC)cc1 |r| Show InChI InChI=1S/C52H60N4O7S/c1-34(2)42-32-37-18-27-47-51(3,28-13-29-52(47,4)50(59)55-44(30-35-14-9-7-10-15-35)48(57)53-38-19-23-40(62-5)24-20-38)43(37)33-46(42)64(60,61)56-45(31-36-16-11-8-12-17-36)49(58)54-39-21-25-41(63-6)26-22-39/h7-12,14-17,19-26,32-34,44-45,47,56H,13,18,27-31H2,1-6H3,(H,53,57)(H,54,58)(H,55,59)/t44-,45-,47+,51+,52+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.21E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP8 (Phe21 to Gly467 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair
Neutrophil collagenase (Homo sapiens (Human))	BDBM50456777 (CHEMBL4206886) Show SMILES [H][C@@]12CCc3cc(C(C)C)c(cc3[C@@]1(C)CCC[C@@]2(C)C(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccccc1)S(=O)(=O)N[C@H](Cc1ccccc1)C(=O)Nc1ccccc1 |r| Show InChI InChI=1S/C50H56N4O5S/c1-34(2)40-32-37-26-27-45-49(3,28-17-29-50(45,4)48(57)53-42(30-35-18-9-5-10-19-35)46(55)51-38-22-13-7-14-23-38)41(37)33-44(40)60(58,59)54-43(31-36-20-11-6-12-21-36)47(56)52-39-24-15-8-16-25-39/h5-16,18-25,32-34,42-43,45,54H,17,26-31H2,1-4H3,(H,51,55)(H,52,56)(H,53,57)/t42-,43-,45-,49-,50-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.25E+4	n/a	n/a	n/a	n/a	n/a	n/a
Southeast University Curated by ChEMBL					Assay Description Inhibition of recombinant human MMP8 (Phe21 to Gly467 residues) expressed in mouse myeloma cells using Mca-Pro-LeuGly-Leu-Dpa-Ala-Arg-NH2 as substrat...				Eur J Med Chem 138: 979-992 (2017) Article DOI: 10.1016/j.ejmech.2017.07.020 BindingDB Entry DOI: 10.7270/Q2R49TBN
					More data for this Ligand-Target Pair

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