Triazolopyrimidine Derivatives: An Updated Review on Recent Advances in Synthesis, Biological Activities and Drug Delivery Aspects

被引:7
|
作者
Abdelkhalek, Ahmed S. [1 ]
Attia, Mohamed S. [2 ]
Kamal, Mohammad A. [3 ,4 ,5 ,6 ]
机构
[1] Zagazig Univ, Fac Pharm, Dept Med Chem, Zagazig 44519, Egypt
[2] Zagazig Univ, Fac Pharm, Dept Pharmaceut, Zagazig 44519, Egypt
[3] Sichuan Univ, West China Hosp, Inst Syst Genet, Frontiers Sci Ctr Dis Related Mol Network, Chengdu, Peoples R China
[4] King Abdulaziz Univ, King Fahd Med Res Ctr, Jeddah, Saudi Arabia
[5] Daffodil Int Univ, Fac Allied Hlth Sci, Dept Pharm, Birulia, Bangladesh
[6] Enzymoics, Novel Global Community Educ Fdn, 7 Peterlee Pl, Hebersham, NSW 2770, Australia
关键词
Alzheimer's; triazolopyrimidine; pharmacological actions; biology; drug delivery; tetrazines; ALZHEIMERS-DISEASE; DIHYDROOROTATE DEHYDROGENASE; SUSTAINED-RELEASE; DESIGN; POTENT; INHIBITORS; AGENTS; ZINC; PHARMACOKINETICS; TRIAZOLOTRIAZINE;
D O I
10.2174/0929867330666230228120416
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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) pyrimido-tetrazine rearrangement. This review discusses synthetic methods, recent pharmacological actions and drug delivery perspectives of triazolopyrimidines.
引用
收藏
页码:1896 / 1919
页数:24
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