Methanandamide
From Wikipedia, the free encyclopedia
Names | |
---|---|
IUPAC name
(5Z,8Z,11Z,14Z)-N-[(1R)-2-hydroxy-1-methylethyl]icosa-5,8,11,14-tetraenamide
|
|
Other names
AM-356; Arachidonyl-1'-hydroxy-2'-propylamide
|
|
Identifiers | |
157182-49-5 | |
3D model (Jmol) | Interactive image |
ChEMBL | ChEMBL120526 |
ChemSpider | 4881984 |
2506 | |
PubChem | 6321351 |
|
|
|
|
Properties | |
C23H39NO2 | |
Molar mass | 361.57 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
|
verify (what is ?) | |
Infobox references | |
Methanandamide (AM-356) is a synthetically created stable chiral analog of anandamide.[1] Its effects have been observed to act on the cannabinoid receptors (specifically on CB1 receptors, which are part of the central nervous system) found in different organisms such as mammals, fish, and certain invertebrates (e.g. Hydra).
References[edit]
- ^ Abadji, V.; et al. (1994). "(R)-methanandamide: A chiral novel anandamide possessing higher potency and metabolic stability". Journal of Medicinal Chemistry. 37 (12): 1889–93. doi:10.1021/jm00038a020. PMID 8021930.
This article about an alkene is a stub. You can help Wikipedia by expanding it. |
This cannabinoid related article is a stub. You can help Wikipedia by expanding it. |
This biochemistry article is a stub. You can help Wikipedia by expanding it. |
This article about an alcohol is a stub. You can help Wikipedia by expanding it. |