Leelamine
From Wikipedia, the free encyclopedia
![]() |
|
Names | |
---|---|
IUPAC name
[(1R,4aS,10aR)-1,4a-Dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]methanamine
|
|
Systematic IUPAC name
Abieta-8,11,13-trien-18-amine
|
|
Other names
(+)-Dehydroabietylamine; Amine D
|
|
Identifiers | |
1446-61-3 | |
ChemSpider | 55878 |
ECHA InfoCard | 100.014.454 |
Jmol 3D model | Interactive image |
PubChem | 62034 |
|
|
|
|
Properties | |
C20H31N | |
Molar mass | 285.48 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
|
Infobox references | |
Leelamine (dehydroabietylamine) is a diterpene amine that has weak affinity for the cannabinoid receptors CB1 and CB2, as well as being an inhibitor of pyruvate dehydrogenase kinase.[1] Optically active leelamine is also used as a chiral resolving agent for carboxylic acids.[2][3]
See also[edit]
References[edit]
- ^ "Leelamine - Dehydroabietylamine - Cayman Chemical". Retrieved May 20, 2013.
- ^ US patent 3454626
- ^ US patent 4559178
![]() |
This cannabinoid related article is a stub. You can help Wikipedia by expanding it. |