Reaction Details |
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Target | Mycothiol S-conjugate amidase |
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Ligand | BDBM50117080 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_321414 (CHEMBL881945) |
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IC50 | 2720000±n/a nM |
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Citation | Nicolaou, KC Joys of molecules. 2. Endeavors in chemical biology and medicinal chemistry. J Med Chem48:5613-38 (2005) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Mycothiol S-conjugate amidase |
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Name: | Mycothiol S-conjugate amidase |
Synonyms: | MCA_MYCTU | mca |
Type: | PROTEIN |
Mol. Mass.: | 32719.79 |
Organism: | Mycobacterium tuberculosis |
Description: | ChEMBL_626858 |
Residue: | 288 |
Sequence: | MSELRLMAVHAHPDDESSKGAATLARYADEGHRVLVVTLTGGERGEILNPAMDLPDVHGR
IAEIRRDEMTKAAEILGVEHTWLGFVDSGLPKGDLPPPLPDDCFARVPLEVSTEALVRVV
REFRPHVMTTYDENGGYPHPDHIRCHQVSVAAYEAAGDFCRFPDAGEPWTVSKLYYVHGF
LRERMQMLQDEFARHGQRGPFEQWLAYWDPDHDFLTSRVTTRVECSKYFSQRDDALRAHA
TQIDPNAEFFAAPLAWQERLWPTEEFELARSRIPARPPETELFAGIEP
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BDBM50117080 |
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n/a |
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Name | BDBM50117080 |
Synonyms: | 3-(3,5-Difluoro-phenyl)-N-[2-(4-fluoro-phenyldisulfanyl)-ethyl]-2-[(Z)-hydroxyimino]-propionamide | CHEMBL194921 | CHEMBL314490 |
Type | Small organic molecule |
Emp. Form. | C17H15F3N2O2S2 |
Mol. Mass. | 400.438 |
SMILES | Fc1ccc(SSCCNC(=O)C(Cc2cc(F)cc(F)c2)N=O)cc1 |
Structure |
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