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Acylation of Azepanoglycyrrhetol Full article

Journal Chemistry of Natural Compounds
ISSN: 0009-3130 , E-ISSN: 1573-8388
Output data Year: 2024, Volume: 60, Number: 6, Pages: 1066-1071 Pages count : 6 DOI: 10.1007/s10600-024-04521-1
Tags glycyrrhetinic acid synthesis azepanotriterpenoids cytotoxicity
Authors Terekhova A.V. 1 , Petrova A.V. 1 , Kazakova O.B. 1 , Vakhitova Yu.V. 2 , Polovyanenko D.N. 3 , Bagryanskaya I.Yu. 3
Affiliations
1 Ufa Institute of Chemistry, Ufa Federal Research Center, Russian Academy of Sciences
2 Institute of Biochemistry and Genetics, Ufa Federal Research Center, Russian Academy of Sciences
3 N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences

Abstract: Acylation of azepano-11-deoxoglycyrrhetol synthesized N-acetyl- and N,O-bis-acetyl derivatives. The structure of azepano-11-deoxoglycyrrhetol was confirmed by an XSA. Data for its influence on cell cycle progression suggested that suppression of cell survival was due primarily to a cytostatic effect that was related to arrest of the S or G1 phase, depending on the cell line.
Cite: Terekhova A.V. , Petrova A.V. , Kazakova O.B. , Vakhitova Y.V. , Polovyanenko D.N. , Bagryanskaya I.Y.
Acylation of Azepanoglycyrrhetol
Chemistry of Natural Compounds. 2024. V.60. N6. P.1066-1071. DOI: 10.1007/s10600-024-04521-1 WOS Scopus OpenAlex
Dates:
Submitted: Mar 10, 2024
Published online: Nov 8, 2024
Identifiers:
Web of science: WOS:001351186100009
Scopus: 2-s2.0-85208783404
OpenAlex: W4404196893
Citing: Пока нет цитирований
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