Synthesis, Electronic Structure and Anti-Cancer Activity of the Phenyl Substituted Pyrazolo[1,5-a][1,3,5]triazines

Title:Synthesis, Electronic Structure and Anti-Cancer Activity of the Phenyl Substituted Pyrazolo[1,5-a][1,3,5]triazines

Volume: 25 Issue: 12

Author(s): Evgenia S. Velihina, Nataliya V. Obernikhina*, Stepan G. Pilyo, Oleksiy D. Kachkovsky and Volodymyr S. Brovarets

Affiliation:

• Department of Bioorganic and Biological Chemistry, O.O. Bogomolets National Medical University, 13 T. Shevchenko boul., 01601, Kyiv,Ukraine

Keywords: Pyrazolo[1, 5-a][1, 3, 5]triazines, anti-cancer activity, barriers of rotation, parameter Φ₀, quantum-chemical, spectral methods.

Abstract:

Background: Synthesis of a series of 2-(dichloromethyl)pyrazolo[1,5- a][1,3,5]triazines was carried out and evaluated in vitro for their anticancer activity against a panel of 60 cell lines derived from nine cancer types.

Methods: The joint quantum-chemical and experimental study of the influence of the extended πconjugated phenyl substituents on the electron structure of the pyrazolo[1,5- a][1,3,5]triazines as Pharmacophores were performed. It is shown that the decrease in the barriers to the rotation of phenyl substituents in compounds 1-7 possibly leads to an increase in the anti-cancer activity, which is in agreement with the change in the parameter biological affinity Φ₀. Analysis of the S₀ → S₁ electronic transitions (π→π*) of the pyrazolo[1,5- a][1,3,5]triazines shows that an increase in their intensity correlates with anti-cancer activity.

Results: Thus, the introduction of phenyl substituents increases the likelihood of investigated pyrazolo[1,5-a][1,3,5]triazines interacting with protein molecules (Biomolecule) by the π-stacking mechanism. In both methyl and phenyl derivatives of pyrazolo[1,5-a][1,3,5]triazines, the second electronic transition includes the n- MO (the level of the lone electron pair in two-coordinated nitrogen atoms). The highest intensity of the η→π* electronic transition is observed in pyrazolo[1,5-a][1,3,5]triazine with pyridine residue, which does not exhibit anticancer activity, but exhibits antiviral activity [13].

Conclusion: It can be assumed that the possibility of the formation of [Pharmacophore-Biomolecule] complex by hydrogen bonding ([H-B]) mechanism with protein molecules increases.

Cite this article as:

Velihina S. Evgenia , Obernikhina V. Nataliya *, Pilyo G. Stepan , Kachkovsky D. Oleksiy and Brovarets S. Volodymyr, Synthesis, Electronic Structure and Anti-Cancer Activity of the Phenyl Substituted Pyrazolo[1,5-a][1,3,5]triazines, Current Organic Chemistry 2021; 25 (12) . https://dx.doi.org/10.2174/1385272825666210607004536