Phenolic marine natural products as aldose reductase inhibitors

J Nat Prod. 2006 Oct;69(10):1485-7. doi: 10.1021/np0503698.

Abstract

Four different types of marine natural compounds isolated from tunicates were found to inhibit human aldose reductase. They all are characterized by a heterocyclic system, and at least two phenolic groups are present in the structure. Two of the compounds tested showed an inhibitory potency 5/6-fold higher than that of the known AR inhibitor sorbinil. One notable structural feature of these active compounds is the lack of either the carboxylic acid or the spiro-hydantoin commonly present in the principal classes of currently used inhibitors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehyde Reductase / antagonists & inhibitors*
  • Animals
  • Biological Products / chemistry
  • Biological Products / isolation & purification*
  • Biological Products / pharmacology
  • Humans
  • Imidazolidines / chemistry
  • Imidazolidines / isolation & purification*
  • Imidazolidines / pharmacology
  • Marine Biology
  • Naphthalenes / chemistry
  • Naphthalenes / isolation & purification*
  • Naphthalenes / pharmacology
  • Quinazolines / chemistry
  • Quinazolines / isolation & purification*
  • Quinazolines / pharmacology
  • Rhodanine / analogs & derivatives*
  • Rhodanine / chemistry
  • Rhodanine / isolation & purification
  • Rhodanine / pharmacology
  • Thiazolidines / chemistry
  • Thiazolidines / isolation & purification*
  • Thiazolidines / pharmacology
  • Urochordata / chemistry

Substances

  • Biological Products
  • Imidazolidines
  • Naphthalenes
  • Quinazolines
  • Thiazolidines
  • tolrestat
  • FR 74366
  • epalrestat
  • Rhodanine
  • AKR1B1 protein, human
  • Aldehyde Reductase
  • sorbinil