Literature DB >> 28392277

N-(Aroyl)-N-(arylmethyloxy)-α-alanines: Selective inhibitors of aldose reductase.

Susanna Nencetti1, Concettina La Motta2, Armando Rossello2, Stefania Sartini2, Elisa Nuti2, Lidia Ciccone3, Elisabetta Orlandini4.   

Abstract

Aldose reductase (ALR2), a NADPH-dependent reductase, is the first and rate-limiting enzyme of the polyol pathway of glucose metabolism and is implicated in the pathogenesis of secondary diabetic complications. In the last decades, this enzyme has been targeted for inhibition but despite the numerous efforts made to identify potent and safe ALR2 inhibitors, many clinical candidates have been a failure. For this reason the research of new ALR2 inhibitors highly effective, selective and with suitable pharmacokinetic properties is still of great interest. In this paper some new N-(aroyl)-N-(arylmethyloxy)alanines have been synthesized and tested for their ability to inhibit ALR2. Some of the synthesized compounds exhibit IC50 in the low micromolar range and all have proved to be highly selective towards ALR2. The N-(aroyl)-N-(arylmethyloxy)-α-alanines are a promising starting point for the development of new ALR2 selective drugs with the aim of delaying the onset of diabetic complications.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Aldose reductase (ALR2); Aldose reductase selective inhibitors; Diabetes mellitus; α-Alanines

Mesh:

Substances:

Year:  2017        PMID: 28392277     DOI: 10.1016/j.bmc.2017.03.056

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


  4 in total

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Authors:  Xiaoqing Chen; Cheng Chen; Jie Hao; Rongqing Qin; Baiyu Qian; Kai Yang; Jiyun Zhang; Feng Zhang
Journal:  Neurochem Res       Date:  2018-06-12       Impact factor: 3.996

2.  Comparative transcriptome analysis reveals significant metabolic alterations in eri-silkworm (Samia cynthia ricini) haemolymph in response to 1-deoxynojirimycin.

Authors:  Shang-Zhi Zhang; Hai-Zhong Yu; Ming-Jie Deng; Yan Ma; Dong-Qiong Fei; Jie Wang; Zhen Li; Yan Meng; Jia-Ping Xu
Journal:  PLoS One       Date:  2018-01-11       Impact factor: 3.240

3.  Oxy-imino saccharidic derivatives as a new structural class of aldose reductase inhibitors endowed with anti-oxidant activity.

Authors:  Felicia D'Andrea; Stefania Sartini; Ilaria Piano; Matteo Franceschi; Luca Quattrini; Lorenzo Guazzelli; Lidia Ciccone; Elisabetta Orlandini; Claudia Gargini; Concettina La Motta; Susanna Nencetti
Journal:  J Enzyme Inhib Med Chem       Date:  2020-12       Impact factor: 5.051

4.  Nature-Inspired O-Benzyl Oxime-Based Derivatives as New Dual-Acting Agents Targeting Aldose Reductase and Oxidative Stress.

Authors:  Lidia Ciccone; Giovanni Petrarolo; Francesca Barsuglia; Carole Fruchart-Gaillard; Evelyne Cassar Lajeunesse; Adeniyi T Adewumi; Mahmoud E S Soliman; Concettina La Motta; Elisabetta Orlandini; Susanna Nencetti
Journal:  Biomolecules       Date:  2022-03-14
  4 in total

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