BDBM50129070 Acetic acid (2S,3S)-3-((S)-2-benzyloxycarbonylamino-4-methyl-1-oxo-pentylamino)-4-oxo-azetidin-2-yl ester::Acetic acid (2S,3S)-3-((S)-2-benzyloxycarbonylamino-4-methyl-pentanoylamino)-4-oxo-azetidin-2-yl ester::CHEMBL292513

SMILES: CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@H]1[C@@H](NC1=O)OC(C)=O

InChI Key: InChIKey=BPWLNYHXMVOMFP-DAYGRLMNSA-N

Data: 4 KI

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 = 50129070   

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
Cathepsin K (Homo sapiens (Human))	BDBM50129070 (Acetic acid (2S,3S)-3-((S)-2-benzyloxycarbonylamin...) Show SMILES CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@H]1[C@@H](NC1=O)OC(C)=O Show InChI InChI=1S/C19H25N3O6/c1-11(2)9-14(20-19(26)27-10-13-7-5-4-6-8-13)16(24)21-15-17(25)22-18(15)28-12(3)23/h4-8,11,14-15,18H,9-10H2,1-3H3,(H,20,26)(H,21,24)(H,22,25)/t14-,15+,18-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	2.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description Inhibitory activity of the compound was measured against Cathepsin K				Bioorg Med Chem Lett 13: 2051-3 (2003) BindingDB Entry DOI: 10.7270/Q2BG2NDJ
					More data for this Ligand-Target Pair
Cathepsin S (Homo sapiens (Human))	BDBM50129070 (Acetic acid (2S,3S)-3-((S)-2-benzyloxycarbonylamin...) Show SMILES CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@H]1[C@@H](NC1=O)OC(C)=O Show InChI InChI=1S/C19H25N3O6/c1-11(2)9-14(20-19(26)27-10-13-7-5-4-6-8-13)16(24)21-15-17(25)22-18(15)28-12(3)23/h4-8,11,14-15,18H,9-10H2,1-3H3,(H,20,26)(H,21,24)(H,22,25)/t14-,15+,18-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	9.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description Inhibitory activity of the compound was measured against Cathepsin S				Bioorg Med Chem Lett 13: 2051-3 (2003) BindingDB Entry DOI: 10.7270/Q2BG2NDJ
					More data for this Ligand-Target Pair
Procathepsin L (Homo sapiens (Human))	BDBM50129070 (Acetic acid (2S,3S)-3-((S)-2-benzyloxycarbonylamin...) Show SMILES CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@H]1[C@@H](NC1=O)OC(C)=O Show InChI InChI=1S/C19H25N3O6/c1-11(2)9-14(20-19(26)27-10-13-7-5-4-6-8-13)16(24)21-15-17(25)22-18(15)28-12(3)23/h4-8,11,14-15,18H,9-10H2,1-3H3,(H,20,26)(H,21,24)(H,22,25)/t14-,15+,18-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	88	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description Inhibitory activity of the compound was measured against Cathepsin L				Bioorg Med Chem Lett 13: 2051-3 (2003) BindingDB Entry DOI: 10.7270/Q2BG2NDJ
					More data for this Ligand-Target Pair
Cathepsin B (Homo sapiens (Human))	BDBM50129070 (Acetic acid (2S,3S)-3-((S)-2-benzyloxycarbonylamin...) Show SMILES CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@H]1[C@@H](NC1=O)OC(C)=O Show InChI InChI=1S/C19H25N3O6/c1-11(2)9-14(20-19(26)27-10-13-7-5-4-6-8-13)16(24)21-15-17(25)22-18(15)28-12(3)23/h4-8,11,14-15,18H,9-10H2,1-3H3,(H,20,26)(H,21,24)(H,22,25)/t14-,15+,18-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	2.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description Inhibitory activity of the compound was measured against Cathepsin B				Bioorg Med Chem Lett 13: 2051-3 (2003) BindingDB Entry DOI: 10.7270/Q2BG2NDJ
					More data for this Ligand-Target Pair