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Synthesis of selectively deuterated and tritiated lupane derivatives with cytotoxic activity
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SYSNO ASEP 0398914 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Synthesis of selectively deuterated and tritiated lupane derivatives with cytotoxic activity Author(s) Vlk, M. (CZ)
Urban, M. (CZ)
Elbert, Tomáš (UOCHB-X) RID, ORCID
Šarek, J. (CZ)Number of authors 4 Source Title Journal of Radioanalytical and Nuclear Chemistry. - : Springer - ISSN 0236-5731
Roč. 298, č. 2 (2013), s. 1149-1157Number of pages 9 s. Language eng - English Country HU - Hungary Keywords isotopic labelling ; tritium ; deuterium ; betulin ; betulinic acid ; cytotoxicity Subject RIV CB - Analytical Chemistry, Separation Institutional support UOCHB-X - RVO:61388963 UT WOS 000325624300049 EID SCOPUS 84885953073 DOI 10.1007/s10967-013-2533-8 Annotation The aim of this work was to synthesize deuterated and tritiated analogues of highly oxidized lupane derivatives known from our group. We selected compounds that previously showed very high cytotoxic activity on multiple cancer cell lines in order to further investigate the mechanism of their action. From starting material (compounds 1-4), we obtained benzyl platanate (5) and its reaction with deuteromethyltriphenylphosphonium iodide gave deuterated compound 6. Following benzyl deprotection gave free acid 7 and oxidation with SeO2 gave 30-oxo-[29-H-2(2)]lup-20(29)-en-28-oic acid (8), which is one of the most active compounds synthesized in our group to date (IC50 6 mu mol/L on CEM cell line). The alkylation of benzyl 2-hydroxy-3-oxolupa-1,20(29)-dien-28-oate (9) with methyliodide or deuteromethyliodide followed by a series of deprotection and hydrogenation steps gave compounds 10-14, where 2 beta-[31-H-2(3)]methoxy-3-oxolupan-20(29)-en-28-oic acid (13) is especially interesting, it showed lower activity on CEM cell line (IC50 10 mu mol/L) however, it was very active against Ph1-positive human leukemia BV-173 (IC50 0.91 mu mol/L) and against human myelogenous leukemia K562 (IC50 0.52 mu mol/L). Selectively labelled [3 alpha-H-2] and [3 alpha-H-3] methyl 3 beta-acetoxy-21,22-dioxolup-18-en-28-oates 24, 25 were prepared in three steps by reduction of corresponding 3-oxo derivatives and they showed moderate activity on CEM cell line (IC50 10 mu mol/L). In total, 11 labelled compounds (6-8, 11, 14, 18, 19, 21, 22, 24 and 25) have not been reported before. Workplace Institute of Organic Chemistry and Biochemistry Contact asep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Jana Procházková, Tel.: 220 183 418 Year of Publishing 2014
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