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Synthesis of Natural Product-Inspired Inhibitors of Mycobacterium tuberculosis Mycothiol-Associated Enzymes: The First Inhibitors of GlcNAc-Ins Deacetylase
- Source :
- Journal of Medicinal Chemistry. 50:6326-6336
- Publication Year :
- 2007
- Publisher :
- American Chemical Society (ACS), 2007.
-
Abstract
- Synthesis and evaluation of a chemical library of inhibitors of the mycothiol biosynthesis enzyme GlcNAc-Ins deacetylase (MshB) and the mycothiol-dependent detoxification enzyme mycothiol- S-conjugate amidase (MCA) from Mycobacterium tuberculosis are reported. The library was biased to include structural features of a group of natural products previously shown to competitively inhibit MCA. Molecular docking studies that reproducibly placed the inhibitors in the active site of the enzyme MshB reveal the mode of binding and are consistent with observed biological activity.
- Subjects :
- Models, Molecular
Stereochemistry
Amidohydrolases
Chemical library
Amidase
chemistry.chemical_compound
Bacterial Proteins
Oxazines
Drug Discovery
Cysteine
Furans
Oxazoles
Pyrans
Antibacterial agent
chemistry.chemical_classification
Sulfonamides
Binding Sites
Natural product
biology
Glycopeptides
Active site
Stereoisomerism
Isoxazoles
Mycobacterium tuberculosis
Mycothiol
Enzyme
chemistry
Biochemistry
Thioglycosides
Enzyme inhibitor
biology.protein
Molecular Medicine
Inositol
Protein Binding
Subjects
Details
- ISSN :
- 15204804 and 00222623
- Volume :
- 50
- Database :
- OpenAIRE
- Journal :
- Journal of Medicinal Chemistry
- Accession number :
- edsair.doi.dedup.....062160ab261c71b044f945cf58f7ebde
- Full Text :
- https://doi.org/10.1021/jm070669h