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TargetBeta-lactamase
LigandBDBM51953
Substrate/Competitorn/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]
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
Beta-lactamase
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:
MSKLSVFFIFLFCSIATAAESLPDLKIEKLDEGVYVHTSFEEVNGWGVVPKHGLVVLVNA
EAYLIDTPFTAKDTEKLVTWFVERGYKIKGSISSHFHSDSTGGIEWLNSRSIPTYASELT
NELLKKDGKVQATNSFSGVNYWLVKNKIEVFYPGPGHTPDNVVVWLPERKILFGGCFIKP
YGLGNLGDANIEAWPKSAKLLKSKYGKAKLVVPSHSEVGDASLLKLTLEQAVKGLNESKK
PSKPSN
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BDBM51953
n/a
NameBDBM51953
Synonyms:4-(4-methoxyphenyl)-2-(4-methyl-1-piperazinyl)-6-(trifluoromethyl)pyrimidine | 4-(4-methoxyphenyl)-2-(4-methylpiperazin-1-yl)-6-(trifluoromethyl)pyrimidine | 4-(4-methoxyphenyl)-2-(4-methylpiperazino)-6-(trifluoromethyl)pyrimidine | MLS000044538 | SMR000022315 | cid_2985091
TypeSmall organic molecule
Emp. Form.C17H19F3N4O
Mol. Mass.352.3542
SMILESCOc1ccc(cc1)-c1cc(nc(n1)N1CCN(C)CC1)C(F)(F)F
Structure
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