Reaction Details |
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Target | Mycothiol S-conjugate amidase |
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Ligand | BDBM50227095 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_452330 (CHEMBL902567) |
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IC50 | 145000±n/a nM |
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Citation | Metaferia, BB; Fetterolf, BJ; Shazad-Ul-Hussan, S; Moravec, M; Smith, JA; Ray, S; Gutierrez-Lugo, MT; Bewley, CA Synthesis of natural product-inspired inhibitors of Mycobacterium tuberculosis mycothiol-associated enzymes: the first inhibitors of GlcNAc-Ins deacetylase. J Med Chem50:6326-36 (2007) [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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BDBM50227095 |
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n/a |
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Name | BDBM50227095 |
Synonyms: | CHEMBL238991 | tert-butyl 1-((2R,3R,4R,5S,6R)-2-(cyclohexylthio)-4,5-dihydroxy-6-(hydroxymethyl)-tetrahydro-2H-pyran-3-ylamino)-1-oxo-4-phenylbutan-2-ylcarbamate |
Type | Small organic molecule |
Emp. Form. | C27H42N2O7S |
Mol. Mass. | 538.697 |
SMILES | CC(C)(C)C(=O)ON[C@@H](CCc1ccccc1)C(=O)N[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1SC1CCCCC1 |
Structure |
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