N-Arachidonoyl dopamine

N-Arachidonoyl dopamine
N-Arachidonoyl dopamine
Identifiers
CAS number 199875-69-9 YesY
PubChem 5282105
Jmol-3D images Image 1
Properties
Molecular formula C28H41NO3
Molar mass 439.63 g/mol
 YesY dopamine (verify) (what is: YesY/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

N-Arachidonoyl dopamine (NADA) is an endocannabinoid which acts as an agonist of the CB1 receptor[1] and the transient receptor potential V1 (TRPV1) ion channel. Its discovery was described in 2002 by an academic research group from Italy and the USA. It was found in the brain of rats, with especially high concentrations in the hippocampus, cerebellum and striatum. It activates the TRPV1 channel with an EC50 of approximately of 50nM. The high potency makes it the putative endogenous TRPV1 agonist.[2]

See also

  • Endocannabinoid

References

  1. ^ Ralevic V. (July 2003). "Cannabinoid modulation of peripheral autonomic and sensory neurotransmission.". European journal of pharmacology 472 (1-2): 1–21. doi:10.1016/S0014-2999(03)01813-2. PMID 12860468. 
  2. ^ Huang SM, Bisogno T, Trevisani M, et al. (June 2002). "An endogenous capsaicin-like substance with high potency at recombinant and native vanilloid VR1 receptors". Proceedings of the National Academy of Sciences of the United States of America 99 (12): 8400–5. doi:10.1073/pnas.122196999. PMC 123079. PMID 12060783. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=123079. 

External links


Wikimedia Foundation. 2010.

Игры ⚽ Нужно решить контрольную?

Look at other dictionaries:

  • N-arachidonoyl-dopamine — Chembox new ImageFile = NADA.png ImageSize = 275px IUPACName = (5Z,8Z,11Z,14Z) N [2 (3,4 dihydroxyphenyl)ethyl] icosa 5,8,11,14 tetraenamide OtherNames = NADA Section1 = Chembox Identifiers CASNo = 199875 69 9 PubChem = 5282105 SMILES =… …   Wikipedia

  • Cannabinoid receptor antagonist — The discovery of the endogenous cannabinoid system led to the development of CB1 receptor antagonists. The first cannabinoid receptor antagonist, rimonabant, was described in 1994. Rimonabant blocks the CB1 receptor selectively and it has been… …   Wikipedia

  • Tetrahydrocannabinol — THC redirects here. For other uses, see THC (disambiguation). Tetrahydrocannabinol (THC) …   Wikipedia

  • AM404 — Systematic (IUPAC) name (5Z,8Z,11Z,14Z) N (4 hydroxyphenyl)icosa 5,8,11,14 tetraenamide Clinical data Pregnancy cat …   Wikipedia

  • Anandamide — IUPAC name (5Z,8Z,11Z,14Z) N (2 hydroxyethyl)icosa 5,8,11,14 tetraenamide …   Wikipedia

  • Cannabinoids — (pron en|kəˈnæbɨˌnɔɪdz [cite book |title=The American Heritage Dictionary |year=2000 |publisher=Houghton Mifflin |edition=4th ed. |isbn=0395825172] ) are a group of terpenophenolic compounds present in Cannabis ( Cannabis sativa L). The broader… …   Wikipedia

  • Virodhamine — IUPAC name 2 aminoethyl (5Z,8Z,11Z,14Z) icosa 5,8,11,14 tetraenoate …   Wikipedia

  • Effects of cannabis — Short term effects of cannabis Classification and external resources ICD 10 F12.0 The effects of cannabis are caused by cannabinoids, most notably tetrahydrocannabinol (THC). Cannabis has both psychological and physiological effects on the human… …   Wikipedia

  • 2-Arachidonyl glyceryl ether — IUPAC name 2 [(5Z,8Z,11Z,14Z) 5,8,11,14 Icosatetraen 1 yloxy] 1,3 propanediol …   Wikipedia

  • Oleamide — Oleamide[1] IUPAC name (Z) Octa 9 decenami …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”