Tetradecenoic acid (cis-9)

For research use only. Not for therapeutic Use.

  • CAT Number: R067818
  • CAS Number: 544-64-9
  • Molecular Formula: C14H26O2
  • Molecular Weight: 226.36
  • Purity: ≥95%
Inquiry Now

Tetradecenoic acid (cis-9)(CAT: R067818) is a monounsaturated fatty acid with a cis double bond located at the ninth carbon atom from the carboxyl end of the molecule. Its mode of action involves participating in various biological processes as a component of cell membranes and as a precursor in the synthesis of lipid molecules. Pharmacologically, tetradecenoic acid (cis-9) is not used as a therapeutic drug. Instead, it is a naturally occurring fatty acid found in various plant and animal sources. It plays essential roles in cellular metabolism, energy storage, and signal transduction, and its presence in dietary fats contributes to overall health and nutrition.


Catalog Number R067818
CAS Number 544-64-9
Synonyms

Myristoleic acid; C14:1 (cis-9) Fatty acid

Molecular Formula C14H26O2
Purity ≥95%
Target Metabolic Enzyme/Protease
Solubility chloroform, hexane, ethyl ether
Storage Store at -20°C
IUPAC Name (Z)-tetradec-9-enoic acid
InChI InChI=1S/C14H26O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14(15)16/h5-6H,2-4,7-13H2,1H3,(H,15,16)/b6-5-
InChIKey YWWVWXASSLXJHU-WAYWQWQTSA-N
SMILES CCCCC=CCCCCCCCC(=O)O
Reference

<br>1. K. Hirano et al. “Myristoleic acid, a cytotoxic component in the extract from Serenoa repens, induces apoptosis and necrosis in human prostatic LNCaP cells” Prostate, vol. 47 pp. 59-64, 2001<br>2. R. Hiipakka et al. “Growth suppression of hamster flank organs by topical application of catechins, alizarin, curcumin, and myristoleic acid” Archives of Dermatological Research, vol. 293 pp. 200-205, 2001<br>3. P. Belhumeur et. al. “Whey-derived free fattyacids suppress the germination of Candida albicans invitro” FEMS Yeast Res, vol. 7 pp. 276-285, 2007<br>4. S. Sharma, P. Gao, and V. Steele “Quantitative Morphometry of Respiratory Tract Epithelial Cells as a Tool for Testing Chemopreventive Agent Efficacy” Anticancer Research, vol. 3 pp. 737-742, 2010</br></br></br></br>

Request a Quote