Synthesis and initial structure--activity relationships of modified salicylihalamides

Org Lett. 2000 Dec 28;2(26):4241-4. doi: 10.1021/ol0068086.

Abstract

[reaction:see text] The first stereoselective total synthesis of the potent antitumor compound (-)-salicylihalamide A is presented. The practicality of our approach provides for high material throughput and is highlighted by the rapid construction of a variety of modified congeners. Initial structure-activity relationships are derived from growth inhibition experiments with a human melanoma cancer cell line.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / chemical synthesis*
  • Amides / chemistry
  • Amides / pharmacology
  • Cell Division / drug effects
  • Humans
  • Melanoma / pathology
  • Salicylic Acid / chemistry*
  • Structure-Activity Relationship
  • Tumor Cells, Cultured

Substances

  • Amides
  • Salicylic Acid