24-Nor-allobetulins possess strong α-glucosidase inhibitory activity
Author:
Affiliation:
1. Ufa Institute of Chemistry of the Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russian Federation
2. Institute of Chemistry, Vietnamese Academy of Science and Technology, Hanoi, Vietnam
Funder
Federal program
RFBR
Vietnam Academy of Science and Technology and Russian Foundation for Basic Research
Publisher
Informa UK Limited
Subject
Organic Chemistry,Plant Science,Biochemistry,Analytical Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/14786419.2022.2154347
Reference45 articles.
1. A general method for removal of a 4-methyl group from triterpenoids. Synthesis of 4β-demethylglycyrrhetinic acid
2. Synthesis and biological evaluation of antitumour-active betulin derivatives
3. Allobetulin and Its Derivatives: Synthesis and Biological Activity
4. Preparation and Conformational Study of 19β,28-Epoxy-18α-olean-5-ene Derivatives
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1. Ursolic acid-based 24-nor- and A- seco -24-oxy-triterpenoids;Natural Product Research;2024-08-21
2. A regiospecific fischer indole reaction with 3‐oxo‐24‐nor‐allobetulin;Journal of Heterocyclic Chemistry;2024-08-04
3. An unexpected conversion of 2E-furfurylidene-3-oxo-24-nor-allobetulin to 23-nor-allobetulins;Steroids;2024-03
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