Reaction Details |
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Target | Beta-lactamase |
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Ligand | BDBM50284789 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_40414 (CHEMBL652629) |
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IC50 | 45±n/a nM |
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Citation | Buynak, JD; Geng, B; Bachmann, B; Ling, Hua The synthesis and lactamase inhibitory activity of 6-(carboxymethylene)penicillins and 7-(carboxymethylene)cephalosporins Bioorg Med Chem Lett5:1513-1518 (1995) 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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BDBM50284789 |
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n/a |
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Name | BDBM50284789 |
Synonyms: | (2S,5R,6Z)-6-(carboxymethylene)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide;sodium salt | CHEMBL287095 |
Type | Small organic molecule |
Emp. Form. | C10H9NO7S |
Mol. Mass. | 287.247 |
SMILES | CC1(C)[C@@H](N2[C@@H](\C(=C/C([O-])=O)C2=O)S1(=O)=O)C([O-])=O |
Structure |
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