期刊
MEDICINAL CHEMISTRY RESEARCH
卷 32, 期 4, 页码 659-681出版社
SPRINGER BIRKHAUSER
DOI: 10.1007/s00044-023-03040-y
关键词
Thienopyrimidine; Synthesis; Anticancer agents; Enzyme inhibition
Thienopyrimidine derivatives occupy a special place in fused pyrimidine compounds due to their structural analogs of purines. They have significant biological activities and are widely used in medicinal chemistry. This review discusses various synthetic methods for preparing heterocyclic thienopyrimidine derivatives and highlights recent research on their anticancer effects through enzyme and pathway inhibition in the past 9 years.
Thienopyrimidine derivatives hold a unique place between fused pyrimidine compounds. They are important and widely represented in medicinal chemistry as they are structural analogs of purines. Thienopyrimidine derivatives have various biological activities. The current review discusses different synthetic methods for the preparation of heterocyclic thienopyrimidine derivatives. It also highlights the most recent research on the anticancer effects of thienopyrimidines through the inhibition of various enzymes and pathways, which was published within the last 9 years. [GRAPHICS] .
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