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Target
Beta-lactamase
Ligand
BDBM40973
Substrate
n/a
Meas. Tech.
FRET-based counterscreen for selective VIM-2 inhibitors: dose response biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase.
IC50
59640±n/a nM
Citation
 PubChem, PC FRET-based counterscreen for selective VIM-2 inhibitors: dose response biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase. PubChem Bioassay (2009)[AID] 
Target
Name:
Beta-lactamase
Synonyms:
Beta-lactamase | metallo-beta-lactamase IMP-1
Type:
Enzyme Catalytic Domain
Mol. Mass.:
27125.88
Organism:
Pseudomonas aeruginosa
Description:
gi_27368096
Residue:
246
Sequence:
MSKLSVFFIFLFCSIATAAESLPDLKIEKLDEGVYVHTSFEEVNGWGVVPKHGLVVLVNAEAYLIDTPFTAKDTEKLVTWFVERGYKIKGSISSHFHSDSTGGIEWLNSRSIPTYASELTNELLKKDGKVQATNSFSGVNYWLVKNKIEVFYPGPGHTPDNVVVWLPERKILFGGCFIKPYGLGNLGDANIEAWPKSAKLLKSKYGKAKLVVPSHSEVGDASLLKLTLEQAVKGLNESKKPSKPSN
  
Inhibitor
Name:
BDBM40973
Synonyms:
2-{[5-(2-phosphonophenoxy)pentyl]oxy}phenylphosphonic acid | MLS000090074 | SMR000024692 | [2-[5-(2-phosphonophenoxy)pentoxy]phenyl]phosphonic acid | cid_3245548
Type:
Small organic molecule
Emp. Form.:
C17H22O8P2
Mol. Mass.:
416.2993
SMILES:
OP(O)(=O)c1ccccc1OCCCCCOc1ccccc1P(O)(O)=O
Structure:
Search PDB for entries with ligand similarity: