Spiradoline

Spiradoline

Drugbox
IUPAC_name = 2-(3,4-dichlorophenyl)-N-methyl-N- [(5R,7S,8S)-7-pyrrolidin-1-yl-1-oxaspiro [4.5] decan-8-yl] acetamide



width = 200
CAS_number = 87151-85-7
smiles = CN( [C@H] 1CC [C@@] 2(CCCO2)C [C@@H] 1N3CCCC3)C(=O)CC4=CC(=C(C=C4)Cl)Cl
ATC_prefix =
ATC_suffix =
PubChem = 55652
DrugBank =
C=22|H=30|Cl=2|N=2|O=2
molecular_weight = 425.392 g/mol
bioavailability =
protein_bound =
metabolism =
elimination_half-life =
excretion =
pregnancy_AU =
pregnancy_US =
pregnancy_category=
legal_AU =
legal_CA =
legal_UK =
legal_US =
legal_status =
routes_of_administration =

Spiradoline (U-62066) is a drug which acts as a highly selective κ-opioid agonist. [Vonvoigtlander PF, Lewis RA. Analgesic and mechanistic evaluation of spiradoline, a potent kappa opioid. "Journal of Pharmacology and Experimental Therapeutics". 1988 Jul;246(1):259-62. PMID 2839665] It has analgesic, [Kunihara M, Ohyama M, Nakano M, Hayashi S. Analgesic activity of spiradoline mesylate (U-62,066E), a kappa opioid agonist in mice. "Life Sciences". 1989;45(13):1191-8. PMID 2796604] diuretic [Yamada K, Imai M, Yoshida S. Mechanism of diuretic action of U-62,066E, a kappa opioid receptor agonist. "European Journal of Pharmacology". 1989 Jan 31;160(2):229-37. PMID 2547626] and antitussive effects, [Kamei J, Tanihara H, Kasuya Y. Antitussive effects of two specific kappa-opioid agonists, U-50,488H and U-62,066E, in rats. "European Journal of Pharmacology". 1990 Oct 9;187(2):281-6. PMID 2272363] and produces subjective effects in animals similar to those of ketocyclazocine and allylnormetazocine. [Holtzman SG. Further characterization of the discriminative stimulus effects of spiradoline. "Pharmacology, Biochemistry and Behaviour". 2000 Jul;66(3):517-22. PMID 10899364] The main effect in humans is sedation, along with analgesic and diuretic effects, but significant side effects such as dysphoria and hallucinations have stopped it from being used clinically. [Wadenberg ML. A review of the properties of spiradoline: a potent and selective kappa-opioid receptor agonist. "CNS Drug Reviews". 2003 Summer;9(2):187-98. PMID 12847558]

References


Wikimedia Foundation. 2010.

Игры ⚽ Нужен реферат?

Look at other dictionaries:

  • Dissociative — See dissociation for the dissociative state in psychology. For the Australian band, see The Dissociatives. Dissociatives are a class of psychoactive drugs which are said to reduce or block signals to the conscious mind from other parts of the… …   Wikipedia

  • Ayahuasca — This entry focuses on the Ayahuasca brew; for information on the vine of the same name, see Banisteriopsis caapi Ayahuasca cooking in the Napo region of Ecuador Ayahuasca (ayawaska pronounced [ajaˈwaska] in the Quechua language) is any of various …   Wikipedia

  • Dimethyltryptamine — Systematic (IUPAC) name 2 (1H indol 3 yl) N …   Wikipedia

  • Datura — This article is about the plant genus. For the Italian dance group, see Datura (band). For the former town in California, see Datura, California. For The Tori Amos song, see Datura (song). Datura Datura stramonium …   Wikipedia

  • Lysergic acid diethylamide — LSD redirects here. For other uses, see LSD (disambiguation). LSD 25 redirects here. For the dock landing ship, see USS San Marcos (LSD 25). For the Fringe episode, see Lysergic Acid Diethylamide (Fringe). Lysergic acid diethylamide …   Wikipedia

  • Mandrake (plant) — Mandrake root redirects here. For the Deep Purple song, see Mandrake Root. Mandragora redirects here. For other uses, see Mandragora (disambiguation). Mandrake Scientific classification Kingdom …   Wikipedia

  • Phencyclidine — Systematic (IUPAC) name …   Wikipedia

  • Solanaceae — Nightshade redirects here. For other uses, see Nightshade (disambiguation). Solanaceae A flowering Brugmansia suaveolens from the US Botanic Garden Scientific classification …   Wikipedia

  • Scopolamine — Systematic (IUPAC) name (–) (S) 3 hydroxy 2 pheny …   Wikipedia

  • Toluene — IUPAC name …   Wikipedia

Share the article and excerpts

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