BDBM50284625 (3R,4S)-3-Benzyl-4-bromomethyl-oxetan-2-one::CHEMBL26280

SMILES: BrC[C@H]1OC(=O)[C@@H]1Cc1ccccc1

InChI Key: InChIKey=GGEUYQPTWGLJLG-NXEZZACHSA-N

Data: 1 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 1 hit for monomerid = 50284625   

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
Chymotrypsinogen B (Homo sapiens (Human))	BDBM50284625 ((3R,4S)-3-Benzyl-4-bromomethyl-oxetan-2-one | CHEM...) Show SMILES BrC[C@H]1OC(=O)[C@@H]1Cc1ccccc1 Show InChI InChI=1S/C11H11BrO2/c12-7-10-9(11(13)14-10)6-8-4-2-1-3-5-8/h1-5,9-10H,6-7H2/t9-,10-/m1/s1	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article	2.55E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of Alpha-chymotrypsin was determined by competitive substrate assay method				Bioorg Med Chem Lett 5: 1287-1292 (1995) Article DOI: 10.1016/0960-894X(95)00216-G BindingDB Entry DOI: 10.7270/Q2H70FRX
					More data for this Ligand-Target Pair