Synthesis and evaluation of some novel isochroman carboxylic acid derivatives as potential anti-diabetic agents

Eur J Med Chem. 2009 Aug;44(8):3147-57. doi: 10.1016/j.ejmech.2009.03.009. Epub 2009 Mar 24.

Abstract

A series of novel isochroman mono-carboxylic acid derivatives were synthesized, characterized and evaluated for their ability to inhibit protein tyrosine phosphatase 1B (PTP1B) in vitro in order to use them as potential anti-diabetic agents. Analysis of structure-activity relationships led to the identification of potent compound 4n which inhibited PTP1B with IC(50) value of 51.63+/-0.91 nM. In general, high potency was associated with a dithiolane ring with a spacer of five carbons to the isochroman ring. Compound 4n has been selected for in vivo evaluation as drug candidate for anti-diabetic activity.

MeSH terms

  • Animals
  • Carboxylic Acids / chemical synthesis*
  • Carboxylic Acids / chemistry
  • Carboxylic Acids / pharmacology*
  • Drug Design*
  • Hypoglycemic Agents / chemical synthesis*
  • Hypoglycemic Agents / chemistry
  • Hypoglycemic Agents / pharmacology*
  • Inhibitory Concentration 50
  • Male
  • Mice
  • Protein Tyrosine Phosphatases / antagonists & inhibitors
  • Stereoisomerism
  • Structure-Activity Relationship

Substances

  • Carboxylic Acids
  • Hypoglycemic Agents
  • Protein Tyrosine Phosphatases