Sciact
  • EN
  • RU

Synthesis and Pro-Apoptotic Activity of Novel Glycyrrhetinic Acid Derivatives Full article

Journal ChemBioChem
ISSN: 1439-4227 , E-ISSN: 1439-7633
Output data Year: 2011, Volume: 12, Number: 5, Pages: 784-794 Pages count : 11 DOI: 10.1002/cbic.201000618
Tags antitumor agents; apoptosis; biological activity; glycyrrhetinic acid derivatives; medicinal chemistry
Authors Logashenko Evgeniya B. 1 , Salomatina Oksana V. 2 , Markov A.V. 1 , Korchagina Dina V. 2 , Salakhutdinov Nariman F. 2 , Tolstikov Genrikh A. 2 , Vlassov Valentin V. 1 , Zenkova Marina A. 1
Affiliations
1 (Данные Web of science) Russian Acad Sci, Inst Chem Biol & Fundamental Med, Siberian Branch, Novosibirsk 630090, Russia
2 (Данные Web of science) Russian Acad Sci, Siberian Branch, Vorozhtsov Inst Organ Chem, Novosibirsk 630090, Russia

Abstract: Triterpenoids are used for medicinal purposes in many countries. Some, such as oleanolic and glycyrrhetinic acids, are known to be anti-inflammatory and anticarcinogenic. However, the biological activities of these naturally occurring molecules against their particular targets are weak, so the synthesis of new synthetic analogues with enhanced potency is needed. By combining modifications to both the A and C rings of 18 beta H-glycyrrhetinic acid, the novel synthetic derivative methyl 2-cyano-3,12-dioxo-18bH-olean-9(11), 1(2)-dien-30-oate was obtained. This derivative displays high antiproliferative activity in cancer cells, including a cell line with a multidrug-resistance phenotype. It causes cell death by inducing the intrinsic caspase-dependent apoptotic pathway.
Cite: Logashenko E.B. , Salomatina O.V. , Markov A.V. , Korchagina D.V. , Salakhutdinov N.F. , Tolstikov G.A. , Vlassov V.V. , Zenkova M.A.
Synthesis and Pro-Apoptotic Activity of Novel Glycyrrhetinic Acid Derivatives
ChemBioChem. 2011. V.12. N5. P.784-794. DOI: 10.1002/cbic.201000618 WOS Scopus РИНЦ OpenAlex
Files: Full text from publisher
Dates:
Published online: Feb 15, 2011
Published print: Mar 21, 2011
Identifiers:
Web of science: WOS:000288563000019
Scopus: 2-s2.0-79952638583
Elibrary: 16663570
OpenAlex: W2053131185
Citing:
DB Citing
Web of science 53
Scopus 56
Elibrary 56
OpenAlex 50
Altmetrics: