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Polyamine derivatives of betulinic acid and beta-sitosterol: A comparative investigation

SYSNO ASEP	0447202
Document Type	J - Journal Article
R&D Document Type	Journal Article
Subsidiary J	Článek ve WOS
Title	Polyamine derivatives of betulinic acid and beta-sitosterol: A comparative investigation
Author(s)	Bildziukevich, Uladzimir (UEB-Q)_{RID, ORCID} Vida, N. (CZ) Rárová, Lucie (UEB-Q)_{RID, ORCID} Kolář, M. (CZ) Šaman, David (UOCHB-X)_{RID, ORCID} Havlíček, Libor (UEB-Q)_{RID, ORCID} Drašar, P. (CZ) Wimmer, Zdeněk (UEB-Q)_{RID, ORCID}
Source Title	Steroids. - : Elsevier - ISSN 0039-128X Roč. 100, AUG 2015 (2015), s. 27-35
Number of pages	9 s.
Language	eng - English
Country	US - United States
Keywords	Polyamine ; Betulinic acid ; beta-Sitosterol
Subject RIV	CC - Organic Chemistry
R&D Projects	LD13057 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
	TA03010877 GA TA ČR - Technology Agency of the Czech Republic (TA ČR)
Institutional support	UEB-Q - RVO:61389030 ; UOCHB-X - RVO:61388963
UT WOS	000357230300006
DOI	10.1016/j.steroids.2015.04.005
Annotation	beta-Sitosterol and betulinic acid were used in designing their conjugates with selected polyamines bearing either an amide bond, or an ester and an amide bond simultaneously in the target molecule. The synthesized compounds were subjected to basic cytotoxic and antimicrobial tests. The synthetic protocol is described separately for each of the three series of the target amides, because each series of compounds required a different synthetic approach. The cytotoxicity was tested on cells derived from human T-lymphoblastic leukemia, breast adenocarcinoma and cervical cancer, and compared with the tests on normal human fibroblasts. Most of the target compounds (5a-5c, 11a-11c and 16a-16c) showed medium to high cytotoxicity (0.7-7.8 mu M), however, in some cases the compounds showed high cytotoxicity even toward normal human fibroblasts (11a-11c). Two compounds of this series (11c and 16c) also displayed antimicrobial activity with high and selective microbe specificity. The compound 11c was potent against Escherichia coli (minimal inhibition concentration (MIC) 6.25 mu g mL(-1), i.e. 9.75 nM mL(-1)) and Staphylococcus aureus (MIC 12.5 mu g mL(-1), i.e. 19.5 nM mL(-1)), and showed medium activity against Pseudomonas aeruginosa. The compound 16c was highly active against Enterococcus faecalis and S. aureus (both, MIC 3.125 mu g mL(-1), i.e. 4.22 nM mL(-1)), both Gram-positive bacteria, however showed only weak activity against E. coli and no activity against P. aeruginosa, both Gram-negative bacteria, which indicates possible microbe specificity of 16c. Comparing beta-sitosterol-based series (5a-5c) and betulinic acid series (11a-11c and 16a-16c) of the target compounds, the latter one gave more promising structures. The compounds 11c and 16c showed effects which may be described as multifarious activity (pleiotropic effects).
Workplace	Institute of Experimental Botany
Contact	David Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469
Year of Publishing	2016

Number of the records: 1