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TargetBeta-lactamase
LigandBDBM50081057
Substrate/Competitorn/a
Meas. Tech.ChEBML_48696
IC50>1000000±n/a nM
Citation Greenlee, MLLaub, JBBalkovec, JMHammond, MLHammond, GGPompliano, DLEpstein-Toney, JH Synthesis and SAR of thioester and thiol inhibitors of IMP-1 metallo-beta-lactamase. Bioorg Med Chem Lett9:2549-54 (1999) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Beta-lactamase
Name:Beta-lactamase
Synonyms:AMPC_ECOLI | Beta-lactamase | Beta-lactamase (AmpC) | Beta-lactamase AmpC | Cephalosporinase | Escherichia coli K-12 | ampA | ampC
Type:Protien
Mol. Mass.:41561.62
Organism:Escherichia coli
Description:P00811
Residue:377
Sequence:
MFKTTLCALLITASCSTFAAPQQINDIVHRTITPLIEQQKIPGMAVAVIYQGKPYYFTWG
YADIAKKQPVTQQTLFELGSVSKTFTGVLGGDAIARGEIKLSDPTTKYWPELTAKQWNGI
TLLHLATYTAGGLPLQVPDEVKSSSDLLRFYQNWQPAWAPGTQRLYANSSIGLFGALAVK
PSGLSFEQAMQTRVFQPLKLNHTWINVPPAEEKNYAWGYREGKAVHVSPGALDAEAYGVK
STIEDMARWVQSNLKPLDINEKTLQQGIQLAQSRYWQTGDMYQGLGWEMLDWPVNPDSII
NGSDNKIALAARPVKAITPPTPAVRASWVHKTGATGGFGSYVAFIPEKELGIVMLANKNY
PNPARVDAAWQILNALQ
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  Blast E-value cutoff:
BDBM50081057
n/a
NameBDBM50081057
Synonyms:(R)-2-Benzoylsulfanyl-3-phenyl-propionic acid | CHEMBL315343
TypeSmall organic molecule
Emp. Form.C16H14O3S
Mol. Mass.286.346
SMILESOC(=O)[C@@H](Cc1ccccc1)SC(=O)c1ccccc1
Structure
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