DESIGN AND SYNTHESIS OF 4,6-DISUBSTITUTED QUINAZOLINE DERIVATIVES AS JANUS KINASE INHIBITORS

Sh. Gaybullaev, Y. Takhirov, K. Zohidov, Chao Niu, Kh. Bozorov

Samarqand davlat universiteti ilmiy tadqiqotlar axborotnomasi · 2026-yil

Annotatsiya

Janus kinases (JAKs) are recognized as important molecular targets in targeted therapy, and their inhibitors are widely used for the treatment of various autoimmune and inflammatory diseases. Although several JAK inhibitors have been approved by the U.S. Food and Drug Administration (FDA), the development of new compounds with improved selectivity and reduced toxicity remains highly relevant. In this study, a series of novel 4,6-disubstituted quinazoline derivatives were designed using a scaffold-hopping approach, and their targeted synthesis was successfully accomplished, providing a promising basis for the development of more effective JAK inhibitors.

Maqola ma’lumotlari
MualliflarSh. Gaybullaev, Y. Takhirov, K. Zohidov, Chao Niu, Kh. Bozorov
JurnalSamarqand davlat universiteti ilmiy tadqiqotlar axborotnomasi
Nashr sanasi2026-01-01
Jild1
Son1
Betlar37-43
DOI10.59251/2181-3973.2025.v1.138.1.3745

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