Synthesis of 3-phenylpyrazolopyrimidine-1, 2, 3-triazole conjugates and evaluation of their Src kinase inhibitory and anticancer activities
…, I Ahmad, BS Chhikara, R Tiwari, D Mandal…
Index: Kumar, Anil; Ahmad, Israr; Chhikara, Bhupender S.; Tiwari, Rakesh; Mandal, Deendayal; Parang, Keykavous Bioorganic and Medicinal Chemistry Letters, 2011 , vol. 21, # 5 p. 1342 - 1346
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Citation Number: 54
Abstract
A series of two classes of 3-phenylpyrazolopyrimidine-1, 2, 3-triazole conjugates were synthesized using click chemistry approach. All compounds were evaluated for inhibition of Src kinase and human ovarian adenocarcinoma (SK-Ov-3), breast carcinoma (MDA-MB- 361), and colon adenocarcinoma (HT-29). Hexyl triazolyl-substituted 3- phenylpyrazolopyrimidine exhibited inhibition of Src kinase with an IC50 value of 5.6 μM. ...
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[Tominaga, Yoshinori; Matsuoka, Yoshiki; Oniyama, Yukio; Uchimura, Yoshimitsu; Komiya, Hirofumi; et al. Journal of Heterocyclic Chemistry, 1990 , vol. 27, # 3 p. 647 - 660]
[Tominaga, Yoshinori; Matsuoka, Yoshiki; Oniyama, Yukio; Uchimura, Yoshimitsu; Komiya, Hirofumi; et al. Journal of Heterocyclic Chemistry, 1990 , vol. 27, # 3 p. 647 - 660]