Reaction Details |
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Target | Beta-lactamase |
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Ligand | BDBM50021959 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_41049 |
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IC50 | 80±n/a nM |
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Citation | Micetich, RG; Maiti, SN; Spevak, P; Hall, TW; Yamabe, S; Ishida, N; Tanaka, M; Yamazaki, T; Nakai, A; Ogawa, K Synthesis and beta-lactamase inhibitory properties of 2 beta-[(1,2,3-triazol-1-yl)methyl]-2 alpha-methylpenam-3 alpha-carboxylic acid 1,1-dioxide and related triazolyl derivatives. J Med Chem30:1469-74 (1987) [PubMed] |
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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: | BLAC_STAAU | Beta-lactamase TEM | Penicillinase | blaZ |
Type: | PROTEIN |
Mol. Mass.: | 31367.53 |
Organism: | Staphylococcus aureus |
Description: | ChEMBL_41052 |
Residue: | 281 |
Sequence: | MKKLIFLIVIALVLSACNSNSSHAKELNDLEKKYNAHIGVYALDTKSGKEVKFNSDKRFA
YASTSKAINSAILLEQVPYNKLNKKVHINKDDIVAYSPILEKYVGKDITLKALIEASMTY
SDNTANNKIIKEIGGIKKVKQRLKELGDKVTNPVRYEIELNYYSPKSKKDTSTPAAFGKT
LNKLIANGKLSKENKKFLLDLMLNNKSGDTLIKDGVPKDYKVADKSGQAITYASRNDVAF
VYPKGQSEPIVLVIFTNKDNKSDKPNDKLISETAKSVMKEF
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BDBM50021959 |
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n/a |
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Name | BDBM50021959 |
Synonyms: | CHEMBL777 | MM 14151 | US9120808, Clavulanic acid potassium salt | antibiotic MM 14151 | clavulanic acid |
Type | Small organic molecule |
Emp. Form. | C8H9NO5 |
Mol. Mass. | 199.1608 |
SMILES | OC\C=C1/O[C@@H]2CC(=O)N2[C@H]1C(O)=O |r| |
Structure |
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