Compile Data Set for Download or QSAR

Found 4 hits of ki for monomerid = 50285572   

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
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50285572 ((R)-2-((S)-4-(4-isopropylphenyl)-1-((S)-4-methyl-1...) Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCc1ccc(cc1)C(C)C)N[C@H](C)C(O)=O)C(=O)Nc1ccccc1 Show InChI InChI=1S/C28H39N3O4/c1-18(2)17-25(27(33)30-23-9-7-6-8-10-23)31-26(32)24(29-20(5)28(34)35)16-13-21-11-14-22(15-12-21)19(3)4/h6-12,14-15,18-20,24-25,29H,13,16-17H2,1-5H3,(H,30,33)(H,31,32)(H,34,35)/t20-,24+,25+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	130	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against human gelatinase-A (MMP-2)				Bioorg Med Chem Lett 5: 2441-2446 (1995) Article DOI: 10.1016/0960-894X(95)00425-S BindingDB Entry DOI: 10.7270/Q2D21XK6
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50285572 ((R)-2-((S)-4-(4-isopropylphenyl)-1-((S)-4-methyl-1...) Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCc1ccc(cc1)C(C)C)N[C@H](C)C(O)=O)C(=O)Nc1ccccc1 Show InChI InChI=1S/C28H39N3O4/c1-18(2)17-25(27(33)30-23-9-7-6-8-10-23)31-26(32)24(29-20(5)28(34)35)16-13-21-11-14-22(15-12-21)19(3)4/h6-12,14-15,18-20,24-25,29H,13,16-17H2,1-5H3,(H,30,33)(H,31,32)(H,34,35)/t20-,24+,25+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	178	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Pomona College Curated by ChEMBL					Assay Description Inhibition of MMP3				Bioorg Med Chem 15: 2223-68 (2007) Article DOI: 10.1016/j.bmc.2007.01.011 BindingDB Entry DOI: 10.7270/Q2571DBD
					More data for this Ligand-Target Pair
Stromelysin-1 (Homo sapiens (Human))	BDBM50285572 ((R)-2-((S)-4-(4-isopropylphenyl)-1-((S)-4-methyl-1...) Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCc1ccc(cc1)C(C)C)N[C@H](C)C(O)=O)C(=O)Nc1ccccc1 Show InChI InChI=1S/C28H39N3O4/c1-18(2)17-25(27(33)30-23-9-7-6-8-10-23)31-26(32)24(29-20(5)28(34)35)16-13-21-11-14-22(15-12-21)19(3)4/h6-12,14-15,18-20,24-25,29H,13,16-17H2,1-5H3,(H,30,33)(H,31,32)(H,34,35)/t20-,24+,25+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	180	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against human stromelysin-3 (MMP-3)				Bioorg Med Chem Lett 5: 2441-2446 (1995) Article DOI: 10.1016/0960-894X(95)00425-S BindingDB Entry DOI: 10.7270/Q2D21XK6
					More data for this Ligand-Target Pair
Interstitial collagenase (Homo sapiens (Human))	BDBM50285572 ((R)-2-((S)-4-(4-isopropylphenyl)-1-((S)-4-methyl-1...) Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCc1ccc(cc1)C(C)C)N[C@H](C)C(O)=O)C(=O)Nc1ccccc1 Show InChI InChI=1S/C28H39N3O4/c1-18(2)17-25(27(33)30-23-9-7-6-8-10-23)31-26(32)24(29-20(5)28(34)35)16-13-21-11-14-22(15-12-21)19(3)4/h6-12,14-15,18-20,24-25,29H,13,16-17H2,1-5H3,(H,30,33)(H,31,32)(H,34,35)/t20-,24+,25+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory activity against human collagenase (MMP-1)				Bioorg Med Chem Lett 5: 2441-2446 (1995) Article DOI: 10.1016/0960-894X(95)00425-S BindingDB Entry DOI: 10.7270/Q2D21XK6
					More data for this Ligand-Target Pair