Home / Publications / A comparative evaluation of monomethoxy substituted o-diarylazoles as antiproliferative microtubule destabilizing agents

A comparative evaluation of monomethoxy substituted o-diarylazoles as antiproliferative microtubule destabilizing agents

Eugenia A Silyanova 1
Eugenia A Silyanova
Vladimir Igorevich Ushkarov 1
Vladimir Igorevich Ushkarov
Alexander Viktorovich Samet 1
Alexander Viktorovich Samet
Anna Sergeevna Maksimenko 1
Anna Sergeevna Maksimenko
Ivan Aleksandrovich Koblov 1, 2
Ivan Aleksandrovich Koblov
Victor Petrovich Kislyi 1
Victor Petrovich Kislyi
Marina Nikolaevna Semenova 3
Marina Nikolaevna Semenova
Victor Vladimirovich Semenov 1
Victor Vladimirovich Semenov
Published 2022-01-03
CommunicationVolume 32, Issue 1, 120-122
11
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Silyanova E. A. et al. A comparative evaluation of monomethoxy substituted o-diarylazoles as antiproliferative microtubule destabilizing agents // Mendeleev Communications. 2022. Vol. 32. No. 1. pp. 120-122.
GOST all authors (up to 50) Copy
Silyanova E. A., Ushkarov V. I., Samet A. V., Maksimenko A. S., Koblov I. A., Kislyi V. P., Semenova M. N., Semenov V. V. A comparative evaluation of monomethoxy substituted o-diarylazoles as antiproliferative microtubule destabilizing agents // Mendeleev Communications. 2022. Vol. 32. No. 1. pp. 120-122.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.mencom.2022.01.039
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2022.01.039
TI - A comparative evaluation of monomethoxy substituted o-diarylazoles as antiproliferative microtubule destabilizing agents
T2 - Mendeleev Communications
AU - Silyanova, Eugenia A
AU - Ushkarov, Vladimir Igorevich
AU - Samet, Alexander Viktorovich
AU - Maksimenko, Anna Sergeevna
AU - Koblov, Ivan Aleksandrovich
AU - Kislyi, Victor Petrovich
AU - Semenova, Marina Nikolaevna
AU - Semenov, Victor Vladimirovich
PY - 2022
DA - 2022/01/03
PB - Mendeleev Communications
SP - 120-122
IS - 1
VL - 32
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2022_Silyanova,
author = {Eugenia A Silyanova and Vladimir Igorevich Ushkarov and Alexander Viktorovich Samet and Anna Sergeevna Maksimenko and Ivan Aleksandrovich Koblov and Victor Petrovich Kislyi and Marina Nikolaevna Semenova and Victor Vladimirovich Semenov},
title = {A comparative evaluation of monomethoxy substituted o-diarylazoles as antiproliferative microtubule destabilizing agents},
journal = {Mendeleev Communications},
year = {2022},
volume = {32},
publisher = {Mendeleev Communications},
month = {Jan},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2022.01.039},
number = {1},
pages = {120--122},
doi = {10.1016/j.mencom.2022.01.039}
}
MLA
Cite this
MLA Copy
Silyanova, Eugenia A., et al. “A comparative evaluation of monomethoxy substituted o-diarylazoles as antiproliferative microtubule destabilizing agents.” Mendeleev Communications, vol. 32, no. 1, Jan. 2022, pp. 120-122. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2022.01.039.

Keywords

o-diarylazoles
antimitotic activity
isoxazoles
microtubule destabilization
nitrostilbenes
pyrazoles
pyrroles
sea urchin embryo
triazoles

Abstract

Monomethoxy substituted o-diarylazoles with isoxazole, triazole, pyrazole, or pyrrole linkers were synthesized and evaluated for antimitotic antitubulin activity in a sea urchin embryo model. Structure–activity relationship study revealed that only isoxazole heterocycle together with the unsubstituted phenyl ring next to the heteroatom endowed the molecule with appropriate configuration to exhibit antiproliferative effect by microtubule destabilizing mode of action.

References

1.
Microtubule-binding agents: a dynamic field of cancer therapeutics
Dumontet C., Jordan M.A.
Nature Reviews Drug Discovery, 2010
3.
Anti-tubulin agents of natural origin: Targeting taxol, vinca, and colchicine binding domains.
Naaz F., Haider M.R., Shafi S., Yar M.S.
European Journal of Medicinal Chemistry, 2019
5.
Natural antitubulin agents: Importance of 3,4,5-trimethoxyphenyl fragment
Negi A.S., Gautam Y., Alam S., Chanda D., Luqman S., Sarkar J., Khan F., Konwar R.
Bioorganic and Medicinal Chemistry, 2015
7.
Recent advances in trimethoxyphenyl (TMP) based tubulin inhibitors targeting the colchicine binding site
Li L., Jiang S., Li X., Liu Y., Su J., Chen J.
European Journal of Medicinal Chemistry, 2018
8.
SYNTHESIS AND BIOLOGICAL EVALUATION OF CIS-COMBRETASTATIN ANALOGS AND THEIR NOVEL 1,2,3-TRIAZOLE DERIVATIVES
Pati H.N., Wicks M., Holt Jr. H.L., LeBlanc R., Weisbruch P., Forrest L., Lee M.
Heterocyclic Communications, 2005
9.
Solution-Phase Parallel Synthesis and Biological Evaluation of Combretatriazoles
Cafici L., Pirali T., Condorelli F., Del Grosso E., Massarotti A., Sorba G., Canonico P.L., Tron G.C., Genazzani A.A.
Journal of Combinatorial Chemistry, 2008
10.
Synthesis and biological evaluation of 3,4-diaryl-5-aminoisoxazole derivatives
Liu T., Dong X., Xue N., Wu R., He Q., Yang B., Hu Y.
Bioorganic and Medicinal Chemistry, 2009
11.
Pyrazolone-fused combretastatins and their precursors: synthesis, cytotoxicity, antitubulin activity and molecular modeling studies
Burja B., Čimbora-Zovko T., Tomić S., Jelušić T., Kočevar M., Polanc S., Osmak M.
Bioorganic and Medicinal Chemistry, 2010
12.
Sea Urchin Embryo Model As a Reliable in Vivo Phenotypic Screen to Characterize Selective Antimitotic Molecules. Comparative evaluation of Combretapyrazoles, -isoxazoles, -1,2,3-triazoles, and -pyrroles as Tubulin-Binding Agents.
Semenova M.N., Demchuk D.V., Tsyganov D.V., Chernysheva N.B., Samet A.V., Silyanova E.A., Kislyi V.P., Maksimenko A.S., Varakutin A.E., Konyushkin L.D., Raihstat M.M., Kiselyov A.S., Semenov V.V.
ACS Combinatorial Science, 2018
13.
Structural requirements for the interaction of combretastatins with tubulin: how important is the trimethoxy unit?
Gaukroger K., Hadfield J.A., Lawrence N.J., Nolan S., McGown A.T.
Organic and Biomolecular Chemistry, 2003
14.
In vivo Evaluation of Indolyl Glyoxamides in the Phenotypic Sea Urchin Embryo Assay
Semenova M.N., Kiselyov A.S., Titov I.Y., Raihstat M.M., Molodtsov M., Grishchuk E., Spiridonov I., Semenov V.V.
Chemical Biology and Drug Design, 2007
15.
Polyalkoxybenzenes from Plants. 5. Parsley Seed Extract in Synthesis of Azapodophyllotoxins Featuring Strong Tubulin Destabilizing Activity in the Sea Urchin Embryo and Cell Culture Assays
Semenova M.N., Kiselyov A.S., Tsyganov D.V., Konyushkin L.D., Firgang S.I., Semenov R.V., Malyshev O.R., Raihstat M.M., Fuchs F., Stielow A., Lantow M., Philchenkov A.A., Zavelevich M.P., Zefirov N.S., Kuznetsov S.A., et. al.
Journal of Medicinal Chemistry, 2011
16.
Polyalkoxy Substituted 4H-Chromenes: Synthesis by Domino Reaction and Anticancer Activity
Shestopalov A.M., Litvinov Y.M., Rodinovskaya L.A., Malyshev O.R., Semenova M.N., Semenov V.V.
ACS Combinatorial Science, 2012
17.
Comparative in vivo evaluation of polyalkoxy substituted 4H-chromenes and oxa-podophyllotoxins as microtubule destabilizing agents in the phenotypic sea urchin embryo assay
Semenova M.N., Tsyganov D.V., Malyshev O.R., Ershov O.V., Bardasov I.N., Semenov R.V., Kiselyov A.S., Semenov V.V.
Bioorganic and Medicinal Chemistry Letters, 2014
18.
Synthesis and anti-mitotic activity of 6,7-dihydro-4H-isothiazolo[4,5-b]pyridin-5-ones: In vivo and cell-based studies
Semenov V.V., Lichitsky B.V., Komogortsev A.N., Dudinov A.A., Krayushkin M.M., Konyushkin L.D., Atamanenko O.P., Karmanova I.B., Strelenko Y.A., Shor B., Semenova M.N., Kiselyov A.S.
European Journal of Medicinal Chemistry, 2017
19.
Computational modeling and target synthesis of monomethoxy-substituted o-diphenylisoxazoles with unexpectedly high antimitotic microtubule destabilizing activity
Stroylov V.S., Svitanko I.V., Maksimenko A.S., Kislyi V.P., Semenova M.N., Semenov V.V.
Bioorganic and Medicinal Chemistry Letters, 2020
20.
Regioselective synthesis of 3,4-diaryl-5-unsubstituted isoxazoles, analogues of natural cytostatic combretastatin A4.
Chernysheva N.B., Maksimenko A.S., Andreyanov F.A., Kislyi V.P., Strelenko Y.A., Khrustalev V.N., Semenova M.N., Semenov V.V.
European Journal of Medicinal Chemistry, 2018