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Novel derivatives of deoxycholic acid bearing aliphatic or cyclic diamine moieties at the C-3 position: Synthesis and evaluation of anti-proliferative activity Full article

Journal Bioorganic and Medicinal Chemistry Letters
ISSN: 0960-894X , E-ISSN: 1464-3405
Output data Year: 2017, Volume: 27, Number: 16, Pages: 3755-3759 Pages count : 5 DOI: 10.1016/j.bmcl.2017.06.072
Tags Deoxycholic acid derivatives; Epoxides; Diamines; Cytotoxicity; Anti-proliferative activity
Authors Popadyuk Irina I. 1 , Markov Andrey V. 2 , Babich Valeriya O. 2,3 , Salomatina Oksana V. 1 , Logashenko Evgeniya B. 2 , Zenkova Marina A. 2 , Salakhutdinov Nariman F. 1,3
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, 9 Lavrentev Ave, Novosibirsk 630090, Russia
2 (Данные Web of science) Russian Acad Sci, Siberian Branch, Inst Chem Biol & Fundamental Med, 8 Lavrentev Ave, Novosibirsk 630090, Russia
3 (Данные Web of science) Novosibirsk State Univ, 2 Pirogova Str, Novosibirsk 630090, Russia

Abstract: A new library of deoxycholic acid derivatives bearing nitrogen-containing moieties at the C-3 position was synthesised from epoxy derivative 1 via an epoxide ring-opening reaction promoted by aliphatic or cyclic diamines and fully characterised by NMR and mass-spectroscopy. The synthesised compounds were screened for cytotoxicity against four human tumour cell lines. The results showed that some of the novel diamine-bearing derivatives displayed improved anti-proliferative activities over the parent compound DCA. Among them, a 1-methylpiperazine containing compound (6) showed promising activity and the highest selectivity against tumour cells of enterohepatic origin (HepG2: IC50 = 3.6 mu M, SI = 9.0; HuTu-80: IC50 = 4.6 mu M, SI = 6.9) and was identified as a lead molecule. (C) 2017 Elsevier Ltd. All rights reserved.
Cite: Popadyuk I.I. , Markov A.V. , Babich V.O. , Salomatina O.V. , Logashenko E.B. , Zenkova M.A. , Salakhutdinov N.F.
Novel derivatives of deoxycholic acid bearing aliphatic or cyclic diamine moieties at the C-3 position: Synthesis and evaluation of anti-proliferative activity
Bioorganic and Medicinal Chemistry Letters. 2017. V.27. N16. P.3755-3759. DOI: 10.1016/j.bmcl.2017.06.072 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Aug 1, 2017
Identifiers:
Web of science: WOS:000407532900026
Scopus: 2-s2.0-85021831648
Elibrary: 31041308
OpenAlex: W2728830052
Citing:
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Web of science 4
Scopus 4
Elibrary 4
OpenAlex 4
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