Poster presentation
227
SYNTHESIS OF N-(R-PHENYL)-(4,5-DIPHENYL-1,2,4-TRIAZOL-3-
YLTHIO)ACETOHYDRAZONES AND THEIR CYTOTOXIC
ACTIVITY
A.A. Ziyaev
1
, E.O. Terenteva
1
, B.N. Babaev
2
, T.T. Toshmurodov
1
1) S.Yu. Yunusov Institute of the Chemistry of Plant Substances, Academy of Sciences of
the Republic of Uzbekistan, Mirzo Ulugbek Str. 77, 100170, Tashkent, Uzbekistan
e-mail: aziyaev05@rambler.ru
2) National University of Uzbekistan
Recently, derivatives of 1,2,4-triazoles and their thio-analogues - 1,2,4-triazole-3-
thiones have received much attention due to their chemical and different biological
activity. Drugs containing a 1,2,4-triazole cycle such as fluconazole, itraconazole,
voriconazole, triazolam, alprazolam, etizolam, etc. are widely used in medical practice
[2]. In order to search for new biologically active derivatives of 1,2,4-triazole, we have
synthesized N-(R-phenyl)-(4,5-diphenyl-1,2,4-triazol-3-ylthio)acetohydrazones (3-6)
and their cytotoxic activity was studied:
By reacting equimolar amounts of ethyl ester[(4,5-diphenyl)-1,2,4-triazol-3-
ylthio]acetic acid (1) with hydrazine hydrate in ethanol, hydrazide[(4,5-diphenyl)-1,2,4-
triazol-3-ylthio]acetic acid (2) was synthesized in high yield (89%). Further, by
condensation of 2 with aromatic aldehydes at a molar ratio of reagents of 1:1.2 with
boiling in an alcoholic solution, the corresponding acetohydrazones (3–6) were obtained
in 79–87% yields. The cytotoxic properties of the compounds were determined by the in
vitro MTT method [2] on cell cultures of cervical
epithelial carcinoma HeLa, breast
adenocarcinoma HBL-100, laryngeal adenocarcinoma HEp-2, and T-lymphoblastic
leukemia
CCRF-CEM; Cytostatic Cisplatin-Naprod (India) was used as a positive
control. According to the test results, the inhibition of
cell growth of the studied
compounds in relation to the HEP-2 and HBL-100 lines varied within 47-59%, while
their activity was minimal on other cells.
Referenses
1. P. Kaur et al. 1,2,4-Triazole: a revive of pharmacological activities Int. Res. J.
Pharm. 2017, 8(7), p. 10-29.
2. Niks M., Otto M. Towards an optimized MTT assay// Journal of Immunological
Methods, 1990, 130, p.149-151.