Reaction Details |
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Target | Beta-lactamase |
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Ligand | BDBM50421220 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_839906 (CHEMBL2090107) |
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IC50 | >200000±n/a nM |
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Citation | Chen, P; Horton, LB; Mikulski, RL; Deng, L; Sundriyal, S; Palzkill, T; Song, Y 2-Substituted 4,5-dihydrothiazole-4-carboxylic acids are novel inhibitors of metallo-ß-lactamases. Bioorg Med Chem Lett22:6229-32 (2012) [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: | BAS3245 | Beta-lactamase (Bla2) | Beta-lactamase II | GBAA_3500 | bla2 |
Type: | Enzyme |
Mol. Mass.: | 28177.23 |
Organism: | Bacillus anthracis |
Description: | Q93T40 |
Residue: | 256 |
Sequence: | MKNTLLKLGVCVSLLGITPFVSTISSVQAERKVEHKVIKNETGTISISQLNKNVWVHTEL
GYFNGEAVPSNGLILNTSKGLVLVDSSWDDKLTKELIEMAEKKFKKSVTDVIITHAHADR
IGGIKTLKERGIKAHSTTLTAELAKKNGYEEPLGDLQAITKLKFGNMKVETFYPGKGHTE
DNIVVWLPQYNMLVGGCLVKSASAKDLGNITDAYVNEWSTSIENVLKRYENINFVVPGHG
EVGDKGLLLHTLDLLK
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BDBM50421220 |
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n/a |
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Name | BDBM50421220 |
Synonyms: | CHEMBL2087628 |
Type | Small organic molecule |
Emp. Form. | C10H9NO2S |
Mol. Mass. | 207.249 |
SMILES | OC(=O)[C@@H]1CSC(=N1)c1ccccc1 |r,c:6| |
Structure |
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