Aldose reductase inhibitors: 2013-present

Expert Opin Ther Pat. 2019 Mar;29(3):199-213. doi: 10.1080/13543776.2019.1582646. Epub 2019 Feb 27.

Abstract

Introduction: Aldose reductase (ALR2) is both the key enzyme of the polyol pathway, whose activation under hyperglycemic conditions leads to the development of chronic diabetic complications, and the crucial promoter of inflammatory and cytotoxic conditions, even under a normoglycemic status. Accordingly, it represents an excellent drug target and a huge effort is being done to disclose novel compounds able to inhibit it.

Areas covered: This literature survey summarizes patents and patent applications published over the last 5 years and filed for natural, semi-synthetic and synthetic ALR2 inhibitors. Compounds described have been discussed and analyzed from both chemical and functional angles.

Expert opinion: Several ALR2 inhibitors with a promising pre-clinical ability to address diabetic complications and inflammatory diseases are being developed during the observed timeframe. Natural compounds and plant extracts are the prevalent ones, thus confirming the use of phytopharmaceuticals as an increasingly pursued therapeutic trend also in the ALR2 inhibitors field. Intriguing hints may be taken from synthetic derivatives, the most significant ones being represented by the differential inhibitors ARDIs. Differently from classical ARIs, these compounds should fire up the therapeutic efficacy of the class while minimizing its side effects, thus overcoming the existing limits of this kind of inhibitors.

Keywords: Aldose reductase; aldose reductase differential inhibitors; aldose reductase inhibitor patents; aldose reductase inhibitors; phytoparmaceuticals; semi-synthetic inhibitors; synthetic inhibitors.

Publication types

  • Review

MeSH terms

  • Aldehyde Reductase / antagonists & inhibitors*
  • Aldehyde Reductase / metabolism
  • Animals
  • Diabetes Complications / drug therapy
  • Diabetes Complications / enzymology
  • Drug Design*
  • Enzyme Inhibitors / adverse effects
  • Enzyme Inhibitors / pharmacology*
  • Humans
  • Inflammation / drug therapy
  • Inflammation / enzymology
  • Patents as Topic

Substances

  • Enzyme Inhibitors
  • AKR1B1 protein, human
  • Aldehyde Reductase