Novel Natural Product- and Privileged Scaffold-Based Tubulin Inhibitors Targeting the Colchicine Binding Site

Molecules. 2016 Oct 15;21(10):1375. doi: 10.3390/molecules21101375.

Abstract

Tubulin inhibitors are effective anticancer agents, however, there are many limitations to the use of available tubulin inhibitors in the clinic, such as multidrug resistance, severe side-effects, and generally poor bioavailability. Thus, there is a constant need to search for novel tubulin inhibitors that can overcome these limitations. Natural product and privileged structures targeting tubulin have promoted the discovery and optimization of tubulin inhibitors. This review will focus on novel tubulin inhibitors derived from natural products and privileged structures targeting the colchicine binding site on tubulin.

Keywords: antimitotic; microtubule dynamics; multidrug resistance; tubulin inhibitors.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacokinetics
  • Antineoplastic Agents / pharmacology
  • Binding Sites / drug effects
  • Biological Availability
  • Biological Products / chemistry
  • Biological Products / pharmacokinetics
  • Biological Products / pharmacology*
  • Colchicine / analogs & derivatives
  • Colchicine / chemistry*
  • Molecular Structure
  • Protein Binding
  • Structure-Activity Relationship
  • Tubulin Modulators / chemistry
  • Tubulin Modulators / pharmacokinetics
  • Tubulin Modulators / pharmacology*

Substances

  • Antineoplastic Agents
  • Biological Products
  • Tubulin Modulators
  • Colchicine