Reaction Details |
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Target | Oxa40 |
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Ligand | BDBM50347181 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_754356 (CHEMBL1799222) |
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IC50 | >12500±n/a nM |
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Citation | Tan, Q; Ogawa, AM; Raghoobar, SL; Wisniewski, D; Colwell, L; Park, YW; Young, K; Hermes, JD; Dininno, FP; Hammond, ML Thiophenyl oxime-derived phosphonates as nano-molar class C beta-lactamase inhibitors reducing MIC of imipenem against Pseudomonas aeruginosa and Acinetobacter baumannii. Bioorg Med Chem Lett21:4363-5 (2011) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Oxa40 |
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Name: | Oxa40 |
Synonyms: | Beta-lactamase | Class D β-lactamase (OXA-24) |
Type: | Enzyme |
Mol. Mass.: | 30946.50 |
Organism: | Acinetobacter baumannii |
Description: | Q8RLA6 |
Residue: | 275 |
Sequence: | MKKFILPIFSISILVSLSACSSIKTKSEDNFHISSQQHEKAIKSYFDEAQTQGVIIIKEG
KNLSTYGNALARANKEYVPASTFKMLNALIGLENHKATTNEIFKWDGKKRTYPMWEKDMT
LGEAMALSAVPVYQELARRTGLELMQKEVKRVNFGNTNIGTQVDNFWLVGPLKITPVQEV
NFADDLAHNRLPFKLETQEEVKKMLLIKEVNGSKIYAKSGWGMGVTPQVGWLTGWVEQAN
GKKIPFSLNLEMKEGMSGSIRNEITYKSLENLGII
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BDBM50347181 |
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n/a |
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Name | BDBM50347181 |
Synonyms: | CHEMBL1795564 |
Type | Small organic molecule |
Emp. Form. | C16H12Cl3FN5O6PS |
Mol. Mass. | 558.693 |
SMILES | CO\N=C(/C(=O)NCP(O)(=O)Oc1ccc(C#N)c(F)c1)c1cnc(NC(=O)C(Cl)(Cl)Cl)s1 |
Structure |
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