Literature DB >> 26974375

Chroman-4-one and chromone based somatostatin β-turn mimetics.

Maria Fridén-Saxin1, Tina Seifert1, Marcus Malo1, Krystle da Silva Andersson1, Nils Pemberton1, Christine Dyrager1, Annika Friberg1, Kristian Dahlén1, Erik A A Wallén2, Morten Grøtli1, Kristina Luthman3.   

Abstract

A scaffold approach has been used to develop somatostatin β-turn mimetics based on chroman-4-one and chromone ring systems. Such derivatives could adopt conformations resembling type II or type II' β-turns. Side chain equivalents of the crucial Trp8 and Lys9 in somatostatin were introduced in the 2- and 8-positions of the scaffolds using efficient reactions. Interestingly, this proof-of-concept study shows that 4 and 9 have Ki-values in the low μM range when evaluated for their affinity for the sst2 and sst4 receptors.
Copyright © 2016 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Chroman-4-one; Chromone; Peptidomimetics; Somatostatin

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Substances:

Year:  2016        PMID: 26974375     DOI: 10.1016/j.ejmech.2016.02.046

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  1 in total

1.  Asymmetric synthesis of polysubstituted chiral chromans via an organocatalytic oxa-Michael-nitro-Michael domino reaction.

Authors:  Cheng-Ke Tang; Kai-Xiang Feng; Ai-Bao Xia; Chen Li; Ya-Yun Zheng; Zhen-Yuan Xu; Dan-Qian Xu
Journal:  RSC Adv       Date:  2018-01-17       Impact factor: 3.361

  1 in total

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