Literature DB >> 30119995

Synthesis and bioactivities evaluation of l-pyroglutamic acid analogues from natural product lead.

Fang-Li Gang1, Feng Zhu1, Xiao-Ting Li1, Jie-Lu Wei1, Wen-Jun Wu2, Ji-Wen Zhang3.   

Abstract

A series of l-pyroglutamic acid analogues from natural product lead were designed and synthesized, as well as their antifungal activities against Phytophthora infestans, neuritogenic activities, antibacterial activities and anti-inflammatory activities are described. The bioassays and SAR study showed that the majority of l-pyroglutamic acid esters have a significant antifungal activity against P. infestans, especially 2d and 2j demonstrated the best activities with EC50 values of 1.44 and 1.21 μg mL-1, which were about seven times that of commercial azoxystrobin (7.85 μg mL-1). Moreover, compounds 2e, 2g and 4d displayed anti-inflammatory activity against LPS-induced NO production in BV-2 microglial cells; neuritogenic activity in NGF-induced PC-12 cells is the same activity. This study demonstrates that compounds 2d and 2j are potential drugs to control P. infestans.
Copyright © 2018. Published by Elsevier Ltd.

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Keywords:  Anti-inflammatory activity; Antifungal activity; Neuritogenic activity; Structure-activity-relationship; l-Pyroglutamic acid

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Year:  2018        PMID: 30119995     DOI: 10.1016/j.bmc.2018.07.041

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


  1 in total

1.  Base-Mediated Coupling Reactions of Benzenesulfonyl Azides with Proline: Synthesis of Proline-Derived Benzenesulfonamides.

Authors:  Hongyan Liu; Bin Zhang; Wei Zhao; Xiao Yu; Wenjing Zhu; Chengcai Xia; Yanmeng Zhou
Journal:  ACS Omega       Date:  2021-12-07
  1 in total

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