Amaryllidaceae alkaloids: Absolute configuration and biological activity

Chirality. 2017 Sep;29(9):486-499. doi: 10.1002/chir.22719. Epub 2017 Jun 26.

Abstract

Plants belonging to the Amaryllidaceae family are well known for their ornamental and medicinal use. Plant members of this group are distributed through both tropical and subtropical regions of the world and are dominant in Andean South America, the Mediterranean basin, and southern Africa. Amaryllidaceae plants have been demonstrated to be a good source of alkaloids with a large spectrum of biological activities, the latter being strictly related to the absolute stereochemistry of the alkaloid scaffold. Among them, great importance for practical applications in medicine has galanthamine, which has already spawned an Alzheimer's prescription drug as a potent and selective inhibitor of the enzyme acetylcholinesterase. Furthermore, lycorine as well as its related isocarbostyryl analogs narciclasine and pancratistatine have shown a strong anticancer activity in vitro against different solid tumors with malignant prognosis. This review addresses the assignment of the absolute configuration of several Amaryllidaceae alkaloids and its relationship with their biological activities.

Keywords: Amaryllidaceae; alkaloids; biological activity; relative and/or absolute configuration; structure-activity relationships.

Publication types

  • Review

MeSH terms

  • Amaryllidaceae Alkaloids / chemistry*
  • Amaryllidaceae Alkaloids / pharmacology*
  • Stereoisomerism
  • Structure-Activity Relationship

Substances

  • Amaryllidaceae Alkaloids