Synthesis, Molecular Docking Study, and Effect on the Methylation of Tumor DNA of Benzo[4′,5′]imidazo[2′,1′:6,1]pyrido[2,3-d]pyrimidines Functionalized by Aromatic Groups and Azines

6-Benzyl-4-styrylbenzo[4′,5′]imidazo[2′,1′:6,1]pyrido[2,3-d]pyrimidines and their conjugates with uracil, 5-fluorouracil, and 6-azauracile were synthesized. In addition to the previous findings, it was found that the reaction of 4-methyl-2-phenyl-5,6-dihydrobenzo[4′,5′]imidazo[2′,1′:6,1]pyrido[2,3-d]pyrimidine with aromatic aldehydes in acetic anhydride, depending on the nucleophilicity of the aldehyde carbonyl group, involved both C6H2 methylene group at the α-position with respect to the benzimidazole fragment and the 4-methyl group. The results of molecular docking study of the synthesized compounds and their effect on the methylation of tumor DNA are presented.

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Journal
Russian Journal of Organic Chemistry
Published
2024-10-01
DOI
https://doi.org/10.1134/s1070428024100051
Primary Topic
Synthesis and Characterization of Heterocyclic Compounds
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article
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article

Synthesis, Molecular Docking Study, and Effect on the Methylation of Tumor DNA of Benzo[4′,5′]imidazo[2′,1′:6,1]pyrido[2,3-d]pyrimidines Functionalized by Aromatic Groups and Azines

H. А. Panosyan, M. S. Safaryan, S. G. Israelyan, Artur A. Hambardzumyan et al.
Russian Journal of Organic Chemistry
Synthesis and Characterization of Heterocyclic Compounds
article

Synthesis, Molecular Docking Study, and Effect on the Methylation of Tumor DNA of Benzo[4′,5′]imidazo[2′,1′:6,1]pyrido[2,3-d]pyrimidines Functionalized by Aromatic Groups and Azines

H. А. Panosyan, M. S. Safaryan, S. G. Israelyan, Artur A. Hambardzumyan, A. S. Sargsyan, R. E. Muradyan, I. S. Danielyan, A. S. Aharonyan, А. А. Harutyunyan, L. E. Nersesyan, A. S. Sumbatyan
article en

Abstract

6-Benzyl-4-styrylbenzo[4′,5′]imidazo[2′,1′:6,1]pyrido[2,3-d]pyrimidines and their conjugates with uracil, 5-fluorouracil, and 6-azauracile were synthesized. In addition to the previous findings, it was found that the reaction of 4-methyl-2-phenyl-5,6-dihydrobenzo[4′,5′]imidazo[2′,1′:6,1]pyrido[2,3-d]pyrimidine with aromatic aldehydes in acetic anhydride, depending on the nucleophilicity of the aldehyde carbonyl group, involved both C6H2 methylene group at the α-position with respect to the benzimidazole fragment and the 4-methyl group. The results of molecular docking study of the synthesized compounds and their effect on the methylation of tumor DNA are presented.

Russian Journal of Organic ChemistryVol. 60(10)
Institute of Fine Organic Chemistry of Scientific - Technological Center of Organic and Pharmaceutical Chemistry (AM), National Academy of Sciences of Armenia (AM)
Openalex Percentile: Top 83%
Synthesis and Characterization of Heterocyclic Compounds
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Synthesis, Molecular Docking Study, and Effect on the Methylation of Tumor DNA of Benzo[4′,5′]imidazo[2′,1′:6,1]pyrido[2,3-d]pyrimidines Functionalized by Aromatic Groups and Azines — H. А. Panosyan, M. S. Safaryan, et al. · Russian Journal of Organic Chemistry (2024) | TGRS Research Map | TGRS