Year: 2025
Type: article
Abstract: Diversifying the sp 3 -rich triquinazine core, we prepared four new chiral scaffolds and 26 analogues that reveal how subtle structural changes modulate Janus Kinase activity, yielding a potent JAK1 inhibitor comparable to FDA-approved drugs.
Source: RSC Medicinal Chemistry
DOI: 10.1039/d5md00921a
Institution: University of Bern
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
OpenAlex ID: W4416164725
