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Synthesis and cytotoxic activity of substituted hexahydro-2H-4,6-(epoxymethano)chromen-8(5H)-ones obtained from (-)-verbenone Full article

Journal Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171
Output data Year: 2015, Volume: 64, Number: 9, Pages: 2257-2260 Pages count : DOI: 10.1007/s11172-015-1148-3
Tags monoterpene; cytotoxicity; verbenone; clay; heterocyclic compounds
Authors Il'ina I. V. 1,2 , Pokrovsky M. A. 2 , Mikhalchenko O. S. 1 , Korchagina D. V. 1 , Volcho K. P. 1,2 , Pokrovsky A. G. 2 , Salakhutdinov N. F. 1,2
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, 9 Prosp Akad Lavrenteva, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia

Abstract: A number of compounds with a substituted hexahydro-2H-4,6-(epoxymethano)chromen-8(5H)-one framework was synthesized starting from monoterpenoid (-)-verbenone and aromatic aldehydes containing methoxy and hydroxy groups. Cytotoxic activity of these compounds on human tumor cell lines was studied for the first time. Compounds containing three methoxy groups in each aromatic ring were found to be the most promising for further studies.
Cite: Il'ina I.V. , Pokrovsky M.A. , Mikhalchenko O.S. , Korchagina D.V. , Volcho K.P. , Pokrovsky A.G. , Salakhutdinov N.F.
Synthesis and cytotoxic activity of substituted hexahydro-2H-4,6-(epoxymethano)chromen-8(5H)-ones obtained from (-)-verbenone
Russian Chemical Bulletin. 2015. V.64. N9. P.2257-2260. DOI: 10.1007/s11172-015-1148-3 WOS Scopus РИНЦ OpenAlex
Original: Ильина И.В. , Покровский М.А. , Патрушева О.С. , Корчагина Д.В. , Волчо К.П. , Покровский А.Г. , Салахутдинов Н.Ф.
Синтез и цитотоксическая активность замещенных гексагидро-2 н-4,6-(эпоксиметано)хромен-8(5 н)-онов, получаемых из (-)-вербенона
Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2015. №9. С.2257. РИНЦ
Dates:
Published print: Sep 1, 2015
Published online: Sep 27, 2016
Identifiers:
Web of science: WOS:000383958300038
Scopus: 2-s2.0-84988719637
Elibrary: 27567848
OpenAlex: W2525390355
Citing:
DB Citing
Web of science 2
Scopus 2
Elibrary 2
OpenAlex 2
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