Synthesis of an Immunologically Active Heptamannoside of <i>Mycobacterium tuberculosis</i> by the [Au]/[Ag]-Catalyzed Activation of Ethynylcyclohexyl Glycosyl Carbonate Donor
Ganesh P. Shinde, Yogesh Sutar, Niteshlal Kasdekar, Pooja Joshi, Omid Rasool, Lech Ignatowicz, Beston Hamasur, Srinivas Hotha
Organic Letters · 2024-03
Abstract
(MTb) is the causative agent for TB and has a thick and waxy cell wall, making it an attractive target for immunological studies. In this study, a heptamannopyranoside containing 1 → 2 and 1 → 6 α-mannopyranosidic linkages has been explored for the immunological evaluations. The conjugation-ready heptamannopyranoside was synthesized by exploiting the salient features of recently discovered [Au]/[Ag]-glycosidation of ethynylcyclohexyl glycosyl carbonate donors. The glycan was conjugated to the ESAT6, an early secreted protein of MTb for further characterization as a potential subunit vaccine candidate.
MeSH terms
- Chemistry
- Mycobacterium tuberculosis
- Glycan
- Glycosyl
- Tuberculosis
- Protein subunit
- Combinatorial chemistry
- Microbiology
- Stereochemistry