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Synthesis and Peptidyl-Prolyl Isomerase Inhibitory Activity of Quinoxalines as Ligands of Cyclophilin A.

✍ Scribed by Feng Wang; Jing Chen; Xuejun Liu; Xu Shen; Xuchang He; Hualiang Jiang; Donglu Bai


Publisher
John Wiley and Sons
Year
2006
Weight
19 KB
Volume
37
Category
Article
ISSN
0931-7597

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Substituted 4-[Chloropyrazolyl][1,2,4]triazolo[4,3-a]quinoxalines: Synthesis and Structure-Activity Relationships of a New Class of Benzodiazepine and Adenosine Receptor Ligands. -A series of substituted triazoloquinoxaline derivatives (VI) (6 examples) is synthesized starting from quinoxalinone (I)