Abdelkhalek Ahmed S, Attia Mohamed S, Kamal Mohammad A
Department of Medicinal Chemistry, Faculty of Pharmacy, Zagazig University, Zagazig, 44519, Egypt.
Department of Pharmaceutics, Faculty of Pharmacy, Zagazig University, Zagazig, 44519, Egypt.
Curr Med Chem. 2024;31(14):1896-1919. doi: 10.2174/0929867330666230228120416.
Molecules containing triazolopyrimidine core showed diverse biological activities, including anti-Alzheimer's, anti-diabetes, anti-cancer, anti-microbial, anti-tuberculosis, anti-viral, anti-malarial, anti-inflammatory, anti-parkinsonism, and anti-glaucoma activities. Triazolopyrimidines have 8 isomeric structures, including the most stable 1,2,4-triazolo[1,5- a] pyrimidine ones. Triazolopyrimidines were obtained by using various chemical reactions, including a) 1,2,4-triazole nucleus annulation to pyrimidine, b) pyrimidines annulation to 1,2,4-triazole structure, c) 1,2,4-triazolo[l,5-a] pyrimidines rearrangement, and d) pyrimidotetrazine rearrangement. This review discusses synthetic methods, recent pharmacological actions and drug delivery perspectives of triazolopyrimidines.
含有三唑并嘧啶核心的分子具有多种生物活性,包括抗阿尔茨海默病、抗糖尿病、抗癌、抗微生物、抗结核、抗病毒、抗疟疾、抗炎、抗帕金森病和抗青光眼活性。三唑并嘧啶有8种异构体结构,包括最稳定的1,2,4-三唑并[1,5-a]嘧啶结构。三唑并嘧啶可通过各种化学反应获得,包括:a)嘧啶的1,2,4-三唑环化;b)1,2,4-三唑结构的嘧啶环化;c)1,2,4-三唑并[1,5-a]嘧啶重排;d)嘧啶并四嗪重排。本文综述了三唑并嘧啶的合成方法、近期药理作用和药物递送前景。