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Hybrid molecule from Farnesylthiosalicylic acid-diamine and phenylpropenoic acid as Ras-related signaling inhibitor with potent antitumor activities.

Abstract
Novel series of Farnesylthiosalicylic acid-diamine/phenylpropenoic acid hybrids were designed and synthesized. Their in vitro growth inhibitory assays showed that most compounds displayed strong antiproliferation activity against seven cancer cells. Especially, the new hybrid 12 f, by the conjugation of 10a with ferulic acid, could selectively suppress the proliferation of tumor cells and display significantly lower toxicities to normal cells than its intermediate 10a. Furthermore, 12 f dose-dependently induced SMMC-7721 cell apoptosis. Additionally, our observations demonstrated that 12 f inhibited both Ras-related signaling and phosphorylated NF-κB synergistically, which may be advantageous to the strong antitumor activities of 12 f. Our findings suggest that these novel hybrids may hold a great promise as therapeutic agents for the intervention of human cancers.
AuthorsYong Ling, Zhiqiang Wang, Xuemin Wang, Xianghua Li, Xinyang Wang, Wei Zhang, Hong Dai, Li Chen, Yihua Zhang
JournalChemical biology & drug design (Chem Biol Drug Des) Vol. 85 Issue 2 Pg. 145-52 (Feb 2015) ISSN: 1747-0285 [Electronic] England
PMID25043275 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2014 John Wiley & Sons A/S.
Chemical References
  • Antineoplastic Agents
  • Diamines
  • NF-kappa B
  • Phenylpropionates
  • Salicylates
  • farnesylthiosalicylic acid
  • Farnesol
  • ras Proteins
Topics
  • Antineoplastic Agents (chemistry, pharmacology)
  • Apoptosis (drug effects)
  • Cell Line, Tumor
  • Cell Proliferation (drug effects)
  • Diamines (chemistry, pharmacology)
  • Farnesol (analogs & derivatives, chemistry, pharmacology)
  • Humans
  • NF-kappa B (metabolism)
  • Neoplasms (drug therapy)
  • Phenylpropionates (chemistry, pharmacology)
  • Phosphorylation (drug effects)
  • Salicylates (chemistry, pharmacology)
  • Signal Transduction (drug effects)
  • ras Proteins (metabolism)

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