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Quinelorane

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Quinelorane
Identifiers
  • (5aR,9aR)-6-propyl-5a,7,8,9,9a,10-hexahydro-5H-pyrido[2,3-g]quinazolin-2-amine
CAS Number
PubChemCID
IUPHAR/BPS
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC14H22N4
Molar mass246.358 g·mol−1
3D model (JSmol)
  • CCCN1CCC[C@H]2[C@H]1CC3=CN=C(N=C3C2)N
  • InChI=1S/C14H22N4/c1-2-5-18-6-3-4-10-7-12-11(8-13(10)18)9-16-14(15)17-12/h9-10,13H,2-8H2,1H3,(H2,15,16,17)/t10-,13-/m1/s1 ☒N
  • Key:TUFADSGTJUOBEH-ZWNOBZJWSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Quinelorane is a drug which acts as adopamine agonist for theD2[1][2][3] andD3 receptor.

See also

[edit]

References

[edit]
  1. ^Caine SB, Negus SS, Mello NK, Patel S, Bristow L, Kulagowski J, Vallone D, Saiardi A, Borrelli E (April 2002)."Role of dopamine D2-like receptors in cocaine self-administration: studies with D2 receptor mutant mice and novel D2 receptor antagonists".Journal of Neuroscience.22 (7):2977–88.doi:10.1523/JNEUROSCI.22-07-02977.2002.PMC 6758322.PMID 11923462.
  2. ^Gasior M, Paronis CA, Bergman J (January 2004). "Modification by dopaminergic drugs of choice behavior under concurrent schedules of intravenous saline and food delivery in monkeys".The Journal of Pharmacology and Experimental Therapeutics.308 (1):249–59.doi:10.1124/jpet.103.052795.PMID 14563783.S2CID 5879400.
  3. ^Brooks JM, Sarter M, Bruno JP (September 2007)."D2-like receptors in nucleus accumbens negatively modulate acetylcholine release in prefrontal cortex".Neuropharmacology.53 (3):455–63.doi:10.1016/j.neuropharm.2007.06.006.PMC 2000917.PMID 17681559.
D1-like
Agonists
PAMs
Antagonists
D2-like
Agonists
Antagonists


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