134834-73-4Relevant academic research and scientific papers
Design, synthesis, biological assessment, and in-Silico studies of 1,2,4-triazolo[1,5-a]pyrimidine derivatives as tubulin polymerization inhibitors
Abdel-Rahman, Hamdy M.,Amin, Noha H.,El-Saadi, Mohammed T.,Mohamed, Heba S.
, (2022/02/22)
A series of 1,2,4-triazolo[1,5-a]pyrimidine derivatives have been designed and synthesized as combretastatin CA-4 analogs. They were screened for anticancer and tubulin polymerization inhibition activities. The trimethoxyphenyl 1,2,4-triazolo[1,5-a]pyrimidine derivative 4c showed significant antiproliferative activity in which it exhibited IC50 = 0.53 μM against HCT-116 cancer cell line. It was further tested as a tubulin polymerization inhibitor showing an IC50 = 3.84 μM if compared to combretastatin IC50 = 1.10 μM. Further mechanism studies revealed that compound 4c could obviously inhibit the proliferation of HCT-116 cancer cells by inducing apoptosis and arresting the cell cycle at the G2/M phase. Furthermore, docking studies showed that compound 4c illustrated good fitting to the colchicine binding site of tubulin. Thus, it is considered an anticancer lead compound worthy of further development as a tubulin polymerization inhibitor.
Improved synthesis of 2-amino-1,2,4-triazolo[1,5-a]pyrimidines
Chernyshev,Sokolov,Taranushich
, p. 1134 - 1137 (2008/02/05)
An improved procedure is suggested for preparing 2-amino-1,2,4-triazolo[1, 5-a]pyrimidines from 3,5-diamino-1,2,4-triazole and unsaturated aromatic ketones, with acetyl protection of the amino group in the step of oxidation of 2-amino-4,7-dihydro-1,2,4-tr
CYCLOCONDENSATION OF CHALCONES WITH DI- AND TRIAMINO-1,2,4-TRIAZOLES
Desenko, S. M.,Kolos, N. N.,Tueni, M.,Orlov, V. D.
, p. 782 - 784 (2007/10/02)
We have carried out the synthesis of 2-amino-5,7-diaryl-1,2,4-triazolopyrimidines from chalcones and 3,4,5-triamino-1,2,4-triazole and synthesized them independently via the 4,7-dihydro derivatives.The course and mechanism of the cyclocondensation
