BDBM50229661 (S)-pyrrolidin-2-ylmethyl 4-(hydroxycarbamoyl)-4-((4-o-tolylpiperidin-1-ylsulfonyl)methyl)piperidine-1-carboxylate::CHEMBL253019

SMILES: Cc1ccccc1C1CCN(CC1)S(=O)(=O)CC1(CCN(CC1)C(=O)OC[C@@H]1CCCN1)C(=O)NO

InChI Key: InChIKey=IKHATIJQVUIUCY-NRFANRHFSA-N

Data: 4 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50229661   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Disintegrin and metalloproteinase domain-containing protein 10 (ADAM10) (Homo sapiens (Human))	BDBM50229661 ((S)-pyrrolidin-2-ylmethyl 4-(hydroxycarbamoyl)-4-(...) Show SMILES Cc1ccccc1C1CCN(CC1)S(=O)(=O)CC1(CCN(CC1)C(=O)OC[C@@H]1CCCN1)C(=O)NO Show InChI InChI=1S/C25H38N4O6S/c1-19-5-2-3-7-22(19)20-8-13-29(14-9-20)36(33,34)18-25(23(30)27-32)10-15-28(16-11-25)24(31)35-17-21-6-4-12-26-21/h2-3,5,7,20-21,26,32H,4,6,8-18H2,1H3,(H,27,30)/t21-/m0/s1	PDB UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	34	n/a	n/a	n/a	n/a	n/a	n/a
Incyte Corporation Curated by ChEMBL					Assay Description Inhibition of ADAM10				Bioorg Med Chem Lett 18: 560-4 (2008) Article DOI: 10.1016/j.bmcl.2007.11.086 BindingDB Entry DOI: 10.7270/Q2CN73MJ
					More data for this Ligand-Target Pair
Disintegrin and metalloproteinase domain-containing protein 10 (ADAM10) (Homo sapiens (Human))	BDBM50229661 ((S)-pyrrolidin-2-ylmethyl 4-(hydroxycarbamoyl)-4-(...) Show SMILES Cc1ccccc1C1CCN(CC1)S(=O)(=O)CC1(CCN(CC1)C(=O)OC[C@@H]1CCCN1)C(=O)NO Show InChI InChI=1S/C25H38N4O6S/c1-19-5-2-3-7-22(19)20-8-13-29(14-9-20)36(33,34)18-25(23(30)27-32)10-15-28(16-11-25)24(31)35-17-21-6-4-12-26-21/h2-3,5,7,20-21,26,32H,4,6,8-18H2,1H3,(H,27,30)/t21-/m0/s1	PDB UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	23	n/a	n/a	n/a	n/a	n/a	n/a
Incyte Corporation Curated by ChEMBL					Assay Description Inhibition of HER2 sheddase in human BT474 cells				Bioorg Med Chem Lett 18: 560-4 (2008) Article DOI: 10.1016/j.bmcl.2007.11.086 BindingDB Entry DOI: 10.7270/Q2CN73MJ
					More data for this Ligand-Target Pair
Interstitial collagenase (Homo sapiens (Human))	BDBM50229661 ((S)-pyrrolidin-2-ylmethyl 4-(hydroxycarbamoyl)-4-(...) Show SMILES Cc1ccccc1C1CCN(CC1)S(=O)(=O)CC1(CCN(CC1)C(=O)OC[C@@H]1CCCN1)C(=O)NO Show InChI InChI=1S/C25H38N4O6S/c1-19-5-2-3-7-22(19)20-8-13-29(14-9-20)36(33,34)18-25(23(30)27-32)10-15-28(16-11-25)24(31)35-17-21-6-4-12-26-21/h2-3,5,7,20-21,26,32H,4,6,8-18H2,1H3,(H,27,30)/t21-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Incyte Corporation Curated by ChEMBL					Assay Description Inhibition of MMP1				Bioorg Med Chem Lett 18: 560-4 (2008) Article DOI: 10.1016/j.bmcl.2007.11.086 BindingDB Entry DOI: 10.7270/Q2CN73MJ
					More data for this Ligand-Target Pair
72 kDa type IV collagenase (Homo sapiens (Human))	BDBM50229661 ((S)-pyrrolidin-2-ylmethyl 4-(hydroxycarbamoyl)-4-(...) Show SMILES Cc1ccccc1C1CCN(CC1)S(=O)(=O)CC1(CCN(CC1)C(=O)OC[C@@H]1CCCN1)C(=O)NO Show InChI InChI=1S/C25H38N4O6S/c1-19-5-2-3-7-22(19)20-8-13-29(14-9-20)36(33,34)18-25(23(30)27-32)10-15-28(16-11-25)24(31)35-17-21-6-4-12-26-21/h2-3,5,7,20-21,26,32H,4,6,8-18H2,1H3,(H,27,30)/t21-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Incyte Corporation Curated by ChEMBL					Assay Description Inhibition of MMP2				Bioorg Med Chem Lett 18: 560-4 (2008) Article DOI: 10.1016/j.bmcl.2007.11.086 BindingDB Entry DOI: 10.7270/Q2CN73MJ
					More data for this Ligand-Target Pair