trans-3-Hexenoic acid (CAS 1577-18-0)
QUICK LINKS
trans-3-Hexenoic acid is a monocarboxylic acid abundantly present in numerous plants. This unsaturated fatty acid serves as a significant dietary component. Furthermore, it finds applications as a food preservative and in the manufacturing of various chemicals. In the realm of scientific research, trans-3-Hexenoic acid holds promise across diverse domains, encompassing synthesis, investigation, and elucidation of mechanisms. In scientific research, trans-3-Hexenoic acid has proven valuable as a substrate for synthesizing a range of compounds, such as 3-Hexenoic acid esters and 3-Hexenoic acid amides. While the precise mechanism of action for trans-3-Hexenoic acid is not yet entirely understood, it is thought to exert its effects through the inhibition of fatty acid biosynthesis. Notably, it has demonstrated inhibitory activity against fatty acid synthase, an enzyme vital in fatty acid synthesis. Moreover, trans-3-Hexenoic acid has been observed to impede the activity of acetyl-CoA carboxylase, another key enzyme involved in fatty acid synthesis.
trans-3-Hexenoic acid (CAS 1577-18-0) References
- A broadly tuned mouse odorant receptor that detects nitrotoluenes. | Li, J., et al. 2012. J Neurochem. 121: 881-90. PMID: 22443178
- Characterization of the antibacterial activity and the chemical components of the volatile oil of the leaves of Rubus parvifolius L. | Cai, Y., et al. 2012. Molecules. 17: 7758-68. PMID: 22732887
- Simple Synthesis of Amides and Weinreb Amides via Use of PPh3 or Polymer-Supported PPh3 and Iodine. | Kumar, A., et al. 2010. European J Org Chem. 2010: PMID: 24223494
- Characterization of an epoxide hydrolase from the Florida red tide dinoflagellate, Karenia brevis. | Sun, P., et al. 2016. Phytochemistry. 122: 11-21. PMID: 26626160
- Functional and Nonfunctional Forms of CquiOR91, an Odorant Selectivity Subunit of Culex quinquefasciatus. | Hughes, DT., et al. 2017. Chem Senses. 42: 333-341. PMID: 28334229
- Comprehensive 2D Gas Chromatography with TOF-MS Detection Confirms the Matchless Discriminatory Power of Monoterpenes and Provides In-Depth Volatile Profile Information for Highly Efficient White Wine Varietal Differentiation. | Lukić, I., et al. 2020. Foods. 9: PMID: 33276447
- Changes of microbial and metabolome of the equine hindgut during oligofructose-induced laminitis. | Tuniyazi, M., et al. 2021. BMC Vet Res. 17: 11. PMID: 33407409
- Influence of ceramide on lipid domain stability studied with small-angle neutron scattering: The role of acyl chain length and unsaturation. | DiPasquale, M., et al. 2022. Chem Phys Lipids. 245: 105205. PMID: 35483419
- Effects of turning over intensity on fatty acid metabolites in postharvest leaves of Tieguanyin oolong tea (Camellia sinensis). | Ni, Z., et al. 2022. PeerJ. 10: e13453. PMID: 35722255
- A Targeted and an Untargeted Metabolomics Approach to the Volatile Aroma Profile of Young 'Maraština' Wines. | Boban, A., et al. 2022. Metabolites. 12: PMID: 36557333
- Comprehensive Volatilome Signature of Various Brassicaceae Species. | Lukić, I., et al. 2023. Plants (Basel). 12: PMID: 36616312
- Heracleum persicum Desf. ex Fisch., C.A.Mey. & Avé-Lall. fruit essential oil: content, antimicrobial activity and cytotoxicity against ovarian cancer cell line. | Ghavam, M. 2023. BMC Complement Med Ther. 23: 87. PMID: 36944973
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
trans-3-Hexenoic acid, 10 g | sc-229508 | 10 g | $49.00 |