volume 19 issue 9 pages 1172-1183

Synthesis of new dihydroquinopimaric acid analogs with nitrile groups as apoptosis-inducing anticancer agents

Publication typeJournal Article
Publication date2019-10-23
scimago Q3
wos Q2
SJR0.562
CiteScore5.8
Impact factor3.0
ISSN18715206, 18755992
Cancer Research
Pharmacology
Molecular Medicine
Abstract
Background:

Cyan-containing compounds are of great interest as potential anticancer agents. Terpenoids can severe as a natural matrix for the development of promising derivatives with antitumor activity.

Methods:

The 2-cyanoethoxy methyl dihydroquinopimarate derivatives (5-9) were synthesized by the reaction of the intermediates (1-4) with acrylonitrile in the presence of alkali (30% KOH solution) using triethylbenzylammonium chloride. The cytotoxicity evaluation was carried out according to the National Cancer Institute (NCI) Protocol, while apoptosis was studied by flow cytometric analysis of Annexin V and 7-aminoactinomycin D staining and cell cycle was analyzed using the method of propidium iodide staining.

Results:

Synthesis of new dihydroquinopimaric acid derivatives with nitrile groups was carried out. The obtained cyanoethyl derivatives were converted into tetrazole, amine, oxadiazole and amidoxime analogs. The primary screening for antitumor activity showed the highest cytotoxic potency of the cyanoethyl-substituted compounds. The introduction of cyanoethyl groups at C-1, C-4 and C-1, C-4, C-20 positions of dihydroquinopimaric acid methyl ester provided antiproliferative effect towards the Jurkat, K562, U937, and HeLa tumor cell cultures (CC50=0.045-0.154µM). These nitrile derivatives are effective inducers of tumor cell apoptosis affecting the S and G2 phases of the cell cycle in a dose-dependent manner.

Conclusion:

The cyanoethyl analogs of dihydroquinopimaric acid reported herein are apoptosis inducers and cytotoxic agents. These findings will be useful for the further design of more potent cytotoxic agents based on natural terpenes.

Found 
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Tretyakova E. V. et al. Synthesis of new dihydroquinopimaric acid analogs with nitrile groups as apoptosis-inducing anticancer agents // Anti-Cancer Agents in Medicinal Chemistry. 2019. Vol. 19. No. 9. pp. 1172-1183.
GOST all authors (up to 50) Copy
Tretyakova E. V., Salimova E. V., Parfenova L. V., Yunusbaeva M. M., Dzhemileva L. U., D'yakonov V. A., Dzhemilev U. M. Synthesis of new dihydroquinopimaric acid analogs with nitrile groups as apoptosis-inducing anticancer agents // Anti-Cancer Agents in Medicinal Chemistry. 2019. Vol. 19. No. 9. pp. 1172-1183.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.2174/1871520619666190404100846
UR - https://doi.org/10.2174/1871520619666190404100846
TI - Synthesis of new dihydroquinopimaric acid analogs with nitrile groups as apoptosis-inducing anticancer agents
T2 - Anti-Cancer Agents in Medicinal Chemistry
AU - Tretyakova, Elena V.
AU - Salimova, Elena V.
AU - Parfenova, Lyudmila V.
AU - Yunusbaeva, Milyausha M.
AU - Dzhemileva, Lilya U.
AU - D'yakonov, Vladimir A.
AU - Dzhemilev, Usein M.
PY - 2019
DA - 2019/10/23
PB - Bentham Science Publishers Ltd.
SP - 1172-1183
IS - 9
VL - 19
PMID - 30947679
SN - 1871-5206
SN - 1875-5992
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2019_Tretyakova,
author = {Elena V. Tretyakova and Elena V. Salimova and Lyudmila V. Parfenova and Milyausha M. Yunusbaeva and Lilya U. Dzhemileva and Vladimir A. D'yakonov and Usein M. Dzhemilev},
title = {Synthesis of new dihydroquinopimaric acid analogs with nitrile groups as apoptosis-inducing anticancer agents},
journal = {Anti-Cancer Agents in Medicinal Chemistry},
year = {2019},
volume = {19},
publisher = {Bentham Science Publishers Ltd.},
month = {oct},
url = {https://doi.org/10.2174/1871520619666190404100846},
number = {9},
pages = {1172--1183},
doi = {10.2174/1871520619666190404100846}
}
MLA
Cite this
MLA Copy
Tretyakova, Elena V., et al. “Synthesis of new dihydroquinopimaric acid analogs with nitrile groups as apoptosis-inducing anticancer agents.” Anti-Cancer Agents in Medicinal Chemistry, vol. 19, no. 9, Oct. 2019, pp. 1172-1183. https://doi.org/10.2174/1871520619666190404100846.