82245-67-8Relevant articles and documents
Design, synthesis, and biological evaluation of 5-(4-(pyridin-4-yl)-1H-1,2,3-triazol-1-yl)benzonitrile derivatives as xanthine oxidase inhibitors
Zhang, Ting-Jian,Li, Song-Ye,Zhang, Yi,Wu, Qing-Xia,Meng, Fan-Hao
, p. 526 - 533 (2017/10/23)
A series of 5-(4-(pyridin-4-yl)-1H-1,2,3-triazol-1-yl)benzonitrile derivatives (1a–p) was designed, synthesized, and identified as xanthine oxidase inhibitors with micromolar level potencies. Among them, the most promising compounds 1j and 1k were obtained with IC50 values of 8.1 and 6.7?μm, respectively. The Lineweaver–Burk plot revealed that compound 1k acted as a mixed-type xanthine oxidase inhibitor. SAR analysis revealed that a carbon atom occupying the X3 position is not as effective as a nitrogen atom, and an iso-pentyloxy or a cyclopentyloxy at the 2-position of benzonitrile moiety will benefit the inhibitory potency. The basis of xanthine oxidase inhibition by 1k was rationalized by molecular modeling studies.
N-(3-cyano-4-alkoxyphenyl) pyridine carboxamide compound and application thereof
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, (2017/08/09)
The invention belongs to the field of medicines, and particularly relates to an N-(3-cyano-4-alkoxyphenyl) pyridine carboxamide compound and application thereof. The N-(3-cyano-4-alkoxyphenyl) pyridine carboxamide compound disclosed by the invention refle
