Reaction Details |
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Target | Beta-lactamase |
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Ligand | BDBM50142711 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_41188 |
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Ki | 29000±n/a nM |
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Citation | Tsang, WY; Dhanda, A; Schofield, CJ; Frère, JM; Galleni, M; Page, MI The inhibition of metallo-beta-lactamase by thioxo-cephalosporin derivatives. Bioorg Med Chem Lett14:1737-9 (2004) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Beta-lactamase |
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Name: | Beta-lactamase |
Synonyms: | AMPC_ENTCL | ampC |
Type: | PROTEIN |
Mol. Mass.: | 41306.67 |
Organism: | Enterobacter cloacae |
Description: | ChEMBL_40258 |
Residue: | 381 |
Sequence: | MMRKSLCCALLLGISCSALATPVSEKQLAEVVANTITPLMKAQSVPGMAVAVIYQGKPHY
YTFGKADIAANKPVTPQTLFELGSISKTFTGVLGGDAIARGEISLDDAVTRYWPQLTGKQ
WQGIRMLDLATYTAGGLPLQVPDEVTDNASLLRFYQNWQPQWKPGTTRLYANASIGLFGA
LAVKPSGMPYEQAMTTRVLKPLKLDHTWINVPKAEEAHYAWGYRDGKAVRVSPGMLDAQA
YGVKTNVQDMANWVMANMAPENVADASLKQGIALAQSRYWRIGSMYQGLGWEMLNWPVEA
NTVVEGSDSKVALAPLPVAEVNPPAPPVKASWVHKTGSTGGFGSYVAFIPEKQIGIVMLA
NTSYPNPARVEAAYHILEALQ
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BDBM50142711 |
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n/a |
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Name | BDBM50142711 |
Synonyms: | (R)-5-Methyl-2-(6-oxo-5-phenyl-3-thioxo-piperazin-2-yl)-3,6-dihydro-2H-[1,3]thiazine-4-carboxylic acid anion |
Type | Small organic molecule |
Emp. Form. | C16H16N3O3S2 |
Mol. Mass. | 362.447 |
SMILES | CC1CS[C@@H](NC1C([O-])=O)c1nc(O)c([nH]c1=S)-c1ccccc1 |
Structure |
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