首页 | 本学科首页   官方微博 | 高级检索  
     


Synthesis of Dimeric Quinazolin‐2‐one, 1,4‐Benzodiazepin‐2‐one,and Isoalloxazine Compounds as Inhibitors of Amyloid Peptides Association
Authors:Alexander Barthel  Lothar Trieschmann  Dieter Ströhl  Ralph Kluge  Gerald Böhm  René Csuk
Affiliation:1. Martin‐Luther‐Universit?t Halle‐Wittenberg, Organische Chemie, Halle (Saale), Germany. Fax: +49 345 552‐7030;2. Scil Proteins Production GmbH, Halle (Saale), Germany;3. IGZ BioMed/ZmK Würzburg, Würzburg, Germany
Abstract:The synthesis of dimeric compounds derived from quinazolin‐2‐one and 1,4‐benzodiazepin‐2‐one possessing a piperazine or homopiperazine spacer was investigated. In addition, a piperazine spacered bis‐isoalloxazine and a bis‐riboflavin compound were prepared and their ability to interrupt the association of prion proteins and Alzheimer‐specific Aβ peptides was investigated using a fast screening system based on flow cytometry. The bis‐isoalloxazine 14 was identified as a new lead structure.
Keywords:Anti‐Alzheimer  Antiprion  1,4‐Benzodiazepin‐2‐one  Isoalloxazine  Quinazolin‐2‐one
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号