Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1373564 | Bioorganic & Medicinal Chemistry Letters | 2007 | 4 Pages |
Abstract
A series of N-(3-(4-hydroxyphenyl)-propenoyl)-amino acid tryptamides was based on a previously reported new SIRT2 inhibitor from our group, and it was designed to study if the molecular size of the compound could be reduced. The most potent compounds, N-(3-(4-hydroxyphenyl)-propenoyl)-2-aminoisobutyric acid tryptamide and N-(3-(4-hydroxyphenyl)-propenoyl)-l-alanine tryptamide, were equipotent, 30% smaller in molecular weight, and slightly more selective (SIRT2/SIRT1) than the parent compound.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Päivi H. Kiviranta, Jukka Leppänen, Valtteri M. Rinne, Tiina Suuronen, Olga Kyrylenko, Sergiy Kyrylenko, Erkki Kuusisto, Anu J. Tervo, Tomi Järvinen, Antero Salminen, Antti Poso, Erik A.A. Wallén,