Synthesis of Dimeric Quinazolin‐2‐one, 1,4‐Benzodiazepin‐2‐one,and Isoalloxazine Compounds as Inhibitors of Amyloid Peptides Association |
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Authors: | Alexander Barthel Lothar Trieschmann Dieter Ströhl Ralph Kluge Gerald Böhm René Csuk |
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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 |
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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. |
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Keywords: | Anti‐Alzheimer Antiprion 1,4‐Benzodiazepin‐2‐one Isoalloxazine Quinazolin‐2‐one |
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