Literature DB >> 15080938

Synthesis and biological activity of novel alpha-substituted beta-phenylpropionic acids having pyridin-2-ylphenyl moiety as antihyperglycemic agents.

Makoto Takamura1, Mitsuya Sakurai, Eriko Yamada, Sachie Fujita, Makoto Yachi, Toshiyuki Takagi, Aya Isobe, Yuka Hagisawa, Toshihiko Fujiwara, Hiroaki Yanagisawa.   

Abstract

We previously reported the identification of novel oximes having 5-benzyl-2,4-thiazolidinedione with antihyperglycemic activity. We now report the synthesis and biological activity of a novel series of oximes and amides having alpha-substituted-beta-phenylpropionic acids. In this series, we obtained potent PPAR alpha/gamma dual agonist (S)-9d, with which activation of PPAR alpha and PPAR gamma was considerably more potent than that of the reference compounds GW9578 22 and rosiglitazone 3, respectively. This means (S)-9d is of the strongest class of PPAR alpha/gamma dual agonists. In the course of this study, we also obtained 8h, which indicated potent plasma glucose lowering effect in spite of weak PPAR alpha/gamma agonistic activity.

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Year:  2004        PMID: 15080938     DOI: 10.1016/j.bmc.2004.01.048

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  1 in total

1.  Efficient synthesis of Fmoc-protected phosphinic pseudodipeptides: Building blocks for the synthesis of matrix metalloproteinase inhibitors.

Authors:  Manishabrata Bhowmick; Ravinder R Sappidi; Gregg B Fields; Salvatore D Lepore
Journal:  Biopolymers       Date:  2011       Impact factor: 2.505

  1 in total

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