Antihyperglycemic activities of cryptolepine analogues: an ethnobotanical lead structure isolated from Cryptolepis sanguinolenta

J Med Chem. 1998 Jul 16;41(15):2754-64. doi: 10.1021/jm970735n.

Abstract

Cryptolepine (1) is a rare example of a natural product whose synthesis was reported prior to its isolation from nature. In the previous paper we reported the discovery of cryptolepine's antihyperglycemic properties. As part of a medicinal chemistry program designed to optimize natural product lead structures originating from our ethnobotanical and ethnomedical field research, a series of substituted and heterosubstituted cryptolepine analogues was synthesized. Antihyperglycemic activity was measured in vitro and in an NIDDM mouse model to generate the first structure-bioactivity study about the cryptolepine nucleus.

MeSH terms

  • 3T3 Cells
  • Adipose Tissue / cytology
  • Adipose Tissue / drug effects
  • Adipose Tissue / metabolism
  • Alkaloids / chemical synthesis
  • Alkaloids / chemistry
  • Alkaloids / pharmacology*
  • Animals
  • Biological Transport / drug effects
  • Blood Glucose / metabolism
  • Diabetes Mellitus, Experimental / blood
  • Glucose / metabolism
  • Hypoglycemic Agents / chemical synthesis
  • Hypoglycemic Agents / chemistry
  • Hypoglycemic Agents / pharmacology*
  • Indole Alkaloids
  • Indoles*
  • Mice
  • Mice, Obese
  • Plants, Medicinal / chemistry*
  • Quinolines*
  • Structure-Activity Relationship

Substances

  • Alkaloids
  • Blood Glucose
  • Hypoglycemic Agents
  • Indole Alkaloids
  • Indoles
  • Quinolines
  • cryptolepine
  • Glucose