双环分子
精氨酸酶
脯氨酸
立体化学
组合化学
化学
氨基酸
生物化学
精氨酸
作者
Derun Li,Hongjun Zhang,Thomas W. Lyons,Min Lu,Abdelghani Achab,Qinglin Pu,Matthew C. Childers,Matthew J. Mitcheltree,Jialiang Wang,Theodore A. Martinot,Spencer E. McMinn,David L. Sloman,Anandan Palani,Adam Beard,Lisa Nogle,Symon Gathiaka,Josep Saurí,Hai‐Young Kim,Donovon A. Adpressa,Peter Spacciapoli
标识
DOI:10.1021/acsmedchemlett.1c00258
摘要
Comprehensive synthetic strategies afforded a diverse set of structurally unique bicyclic proline-containing arginase inhibitors with a high degree of three-dimensionality. The analogs that favored the Cγ-exo conformation of the proline improved the arginase potency over the initial lead. The novel synthetic strategies reported here not only enable access to previously unknown stereochemically complex proline derivatives but also provide a foundation for the future synthesis of bicyclic proline analogs, which incorporate inherent three-dimensional character into building blocks, medicine, and catalysts and could have a profound impact on the conformation of proline-containing peptides and macrocycles.
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