Reaction Details |
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Target | Peptide deformylase |
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Ligand | BDBM50201878 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_423229 (CHEMBL913367) |
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IC50 | 30±n/a nM |
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Citation | Boularot, A; Giglione, C; Petit, S; Duroc, Y; Alves de Sousa, R; Larue, V; Cresteil, T; Dardel, F; Artaud, I; Meinnel, T Discovery and refinement of a new structural class of potent peptide deformylase inhibitors. J Med Chem50:10-20 (2007) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Peptide deformylase |
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Name: | Peptide deformylase |
Synonyms: | 3.5.1.88 | BON69_24600 | BON94_18585 | D9G11_24945 | D9G11_25760 | D9J60_20755 | FORC82_p394 | PDF | Polypeptide deformylase | SAMEA3472033_04733 | def | def_2 |
Type: | n/a |
Mol. Mass.: | 16901.39 |
Organism: | Escherichia coli |
Description: | n/a |
Residue: | 150 |
Sequence: | MSVLQVLHIPDERLRKVAKPVEEVNAEIQRIVDDMFETMYAEKGIGLAATQVDIHQRIIV
IDVSENRDERLVLINPELLEKSGETGIEEGCLSIPEQRALVPRAEKVKIRALDRDGKPFE
LEADGLLAICIGLRLGNGKYCTLRLFFNQV
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BDBM50201878 |
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n/a |
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Name | BDBM50201878 |
Synonyms: | CHEMBL220027 | N-(1-benzenesulfonyl-5-bromo-2-methyl-1H-indol-3-ylmethyl)-N-hydroxyformamide |
Type | Small organic molecule |
Emp. Form. | C17H15BrN2O4S |
Mol. Mass. | 423.281 |
SMILES | Cc1c(CN(O)C=O)c2cc(Br)ccc2n1S(=O)(=O)c1ccccc1 |
Structure |
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