4.5 Article

Synthesis and Cytotoxicity of Semisynthetic Withalongolide A Analogues

Journal

ACS MEDICINAL CHEMISTRY LETTERS
Volume 4, Issue 11, Pages 1069-1073

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ml400267q

Keywords

Withalongolide A; withaferin A; triacetate; jaborosalactone; macrocycle; DRO81-1

Funding

  1. Office of Research and Graduate Studies, University of Kansas
  2. Mitscher Fellowship, University of Kansas
  3. Kansas Bioscience Authority (KBA) [IND 0061464]
  4. Center for Heartland Plant Innovations (HPI)
  5. Institute for Advancing Medical Innovation (IAMI) [NFP0066367]
  6. Department of Surgery at the University of Kansas Medical Center
  7. Department of Surgery at the University of Michigan
  8. University of Kansas Center for Cancer Experimental Therapeutics NIH-COBRE [P20 RR015563]

Ask authors/readers for more resources

The natural product withaferin A exhibits potent antitumor activity and other diverse pharmacological activities. The recently discovered withalongolide A, a C-19 hydroxylated congener of withaferin A, was recently reported to possess cytotoxic activity against head and neck squamous cell carcinomas. Semisynthetic acetylated analogues of withalongolide A were shown to be considerably more cytotoxic than the parent compound. To further explore the structure activity relationships, 20 new semisynthetic analogues of withalongolide A were synthesized and evaluated for cytotoxic activity against four different cancer cell lines. A number of derivatives were found to be more potent than the parent compound and withaferin A.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available