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SYNTHESIS AND CYTOTOXIC ACTIVITY OF AZA-MICHAEL REACTION PRODUCTS FROM ETHYL SORBATE AND HETEROCYCLIC AMINES Full article

Journal Chemistry of Natural Compounds
ISSN: 0009-3130 , E-ISSN: 1573-8388
Output data Year: 2015, Volume: 51, Number: 2, Pages: 296-301 Pages count : DOI: 10.1007/s10600-015-1264-1
Tags ethyl sorbate; aza-Michael reaction; cytotoxicity; heterocyclic amines; cancer
Authors Suslov E. V. 1 , Korchagina D. V. 1 , Pokrovskii M. A. 2 , Pokrovskii A. G. 2 , Volcho K. P. 1,2 , Salakhutdinov N. F. 1,2
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia

Abstract: The solvent-free reaction of ethyl sorbate and several heterocyclic amines at room temperature was shown to give aza-Michael 1,4-addition products. The newly formed double bond in the principal product had the E-configuration. It was found that the synthesized compounds exhibited cytotoxicity against cancer cell lines CEM-13, U-937, and MT-4. The piperazine derivative of ethyl sorbate exhibited the greatest activity against cancer cell line U-937, for which the concentration causing 50% death of the tumor cells (CTD50) was 10 mu g/mL.
Cite: Suslov E.V. , Korchagina D.V. , Pokrovskii M.A. , Pokrovskii A.G. , Volcho K.P. , Salakhutdinov N.F.
SYNTHESIS AND CYTOTOXIC ACTIVITY OF AZA-MICHAEL REACTION PRODUCTS FROM ETHYL SORBATE AND HETEROCYCLIC AMINES
Chemistry of Natural Compounds. 2015. V.51. N2. P.296-301. DOI: 10.1007/s10600-015-1264-1 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Mar 1, 2015
Published online: Mar 31, 2015
Identifiers:
Web of science: WOS:000352641900019
Scopus: 2-s2.0-84953361669
Elibrary: 26929361
OpenAlex: W2002656408
Citing:
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Web of science 3
Scopus 3
Elibrary 3
OpenAlex 3
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