Thieno[2,3-d] pyrimidine as a promising scaffold in medicinal chemistry: Recent advances

被引:94
|
作者
Ali, Eslam M. H. [1 ,2 ]
Abdel-Maksoud, Mohammed S. [3 ]
Oh, Chang-Hyun [1 ,2 ]
机构
[1] KIST, Ctr Biomat, Seoul 02792, South Korea
[2] UST, Dept Biomol Sci, Daejeon 34113, South Korea
[3] NRC, Pharmaceut & Drug Ind Res Div, Med & Pharmaceut Chem Dept, Giza 12622, Egypt
关键词
Thienopyrimidine; Anti-inflammatory; Anticancer; Antimicrobial; Antiviral; CNS protective agents; RECEPTOR TYROSINE KINASE; INITIATION-FACTOR; 4E; BIOLOGICAL EVALUATION; DERIVATIVES BEARING; ANTICANCER ACTIVITY; 3-D PYRIMIDINE; THIENO; SUBSTITUTED THIENOPYRIMIDINES; STRUCTURAL MODIFICATIONS; ANTIBACTERIAL AGENTS;
D O I
10.1016/j.bmc.2019.02.044
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
Thienopyrimidine scaffold is a fused heterocyclic ring system that structurally can be considered as adenine, the purine base that is found in both DNA and RNA-bioisosteres. Thienopyrimidines exist in three distinct isomeric forms. The current review discusses thieno[2,3-d] pyrimidine as a one of the opulent heterocycles in drug discovery. Its broad range of medical applications such as anticancer, anti-inflammatory, anti-microbial, and CNS protective agents has inspired us to study its structure-activity relationship (SAR), along with its relevant synthetic strategies. The present review briefly summarizes synthetic approaches for the preparation of thieno[2,3-d] pyrimidine derivatives. In addition, the promising biological activities of this scaffold are also illustrated with explanatory diagrams for their SAR studies.
引用
收藏
页码:1159 / 1194
页数:36
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