Reaction Details |
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Target | Beta-lactamase |
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Ligand | BDBM50339869 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_740684 (CHEMBL1763746) |
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Ki | 20±n/a nM |
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Citation | Xia, Y; Cao, K; Zhou, Y; Alley, MR; Rock, F; Mohan, M; Meewan, M; Baker, SJ; Lux, S; Ding, CZ; Jia, G; Kully, M; Plattner, JJ Synthesis and SAR of novel benzoxaboroles as a new class of β-lactamase inhibitors. Bioorg Med Chem Lett21:2533-6 (2011) [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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BDBM50339869 |
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n/a |
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Name | BDBM50339869 |
Synonyms: | 5-(1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yloxy)pyrazine-2-carboxylic acid | CHEMBL1761275 |
Type | Small organic molecule |
Emp. Form. | C12H9BN2O5 |
Mol. Mass. | 272.021 |
SMILES | OB1OCc2ccc(Oc3cnc(cn3)C(O)=O)cc12 |
Structure |
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