Notholaenic acid
From Wikipedia, the free encyclopedia
| Notholaenic acid | ||
|---|---|---|
 | ||
| IUPAC name 2-hydroxy-4-methoxy-6-[2-(4-methoxyphenyl)ethyl]benzoic acid | ||
| Identifiers | ||
| CAS number | 72578-97-3 | |
| PubChem | 3085829 | |
| Jmol-3D images | Image 1 | |
| ||
| ||
| Properties | ||
| Molecular formula | C17H18O5 | |
| Molar mass | 302.32 g mol−1 | |
| Melting point | 149–150 °C | |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | ||
| Infobox references | ||
Notholaenic acid is a dihydrostilbenoid found in the farina of some ferns of the genus Notholaena.[1] It has been shown to have anti-HSV-1 activity at high concentrations in vitro.[2] It was artificially synthesized, starting from 3-benzyloxy-5-methoxybenzyl alcohol, in 1985.[3]
References
- ↑ Wollenweber, Eckhard; Favre-Bonvin, Jean (1979). "Novel dihydrostilbene from fronds of Notholaena dealbata and Notholaena limitanea". Phytochemistry 18 (7): 1243–1244. doi:10.1016/0031-9422(79)80153-3.
- ↑ Rinehart, Kenneth L.; Tom G. Holt, Nancy L. Fregeau, Paul A. Keifer, George Robert Wilson, Thomas J. Perun Jr., Ryuichi Sakai, Anthony G. Thompson, Justin G. Stroh, Lois S. Shield, David S. Seigler, Li H. Li, David G. Martin, Cornelis J. P. Grimmelikhuijzen, Gerd Gäde (July–Aug 1990). "Bioactive Compounds from Aquatic and Terrestrial Sources". Journal of Natural Products 53: 771–792. doi:10.1021/np50070a001. Retrieved 29 April 2012.
- ↑ El-Feraly, Farouk S.; Cheatham, Steve F.; McChesney, James D. (1985). "Total Synthesis of Notholaenic Acid". Journal of Natural Products 48 (2): 293–298. doi:10.1021/np50038a015.
| ||||||||
This article is issued from Wikipedia. The text is available under the Creative Commons Attribution/Share Alike; additional terms may apply for the media files.