Reaction Details |
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Target | HTH-type transcriptional regulator EthR |
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Ligand | BDBM50395186 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_859798 (CHEMBL2169626) |
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IC50 | 2900±n/a nM |
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Citation | Flipo, M; Willand, N; Lecat-Guillet, N; Hounsou, C; Desroses, M; Leroux, F; Lens, Z; Villeret, V; Wohlkönig, A; Wintjens, R; Christophe, T; Kyoung Jeon, H; Locht, C; Brodin, P; Baulard, AR; Déprez, B Discovery of novel N-phenylphenoxyacetamide derivatives as EthR inhibitors and ethionamide boosters by combining high-throughput screening and synthesis. J Med Chem55:6391-402 (2012) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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HTH-type transcriptional regulator EthR |
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Name: | HTH-type transcriptional regulator EthR |
Synonyms: | ETHR_MYCS2 | MSMEI_6273 | ethR |
Type: | PROTEIN |
Mol. Mass.: | 23512.52 |
Organism: | Mycobacterium smegmatis (strain ATCC 700084 / mc(2)155) |
Description: | ChEMBL_859798 |
Residue: | 217 |
Sequence: | MTTASQTRTPRGRRSARPSGDDREAAILATAQRLLETKKFAEISVDDLAKGAGISRPTFY
FYFPSKEAVLLSLIDPLIKRADSGFDNAVESMPADPQRAIRRGIEIFFNSFGSHPATARA
GTEALKSSPEFKEFWSGLMQKWIAATAALITAERERGAAPDTIPALDLATSLNLMNERTM
MAALADEQPGVAPEKVVATLTHIWLNSIYGTLPVGTA
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BDBM50395186 |
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n/a |
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Name | BDBM50395186 |
Synonyms: | CHEMBL1612418 |
Type | Small organic molecule |
Emp. Form. | C22H20N4O2 |
Mol. Mass. | 372.4198 |
SMILES | Cc1ccc(cc1)-n1nc2ccc(NC(=O)COc3ccccc3C)cc2n1 |
Structure |
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