Quinelorane

Quinelorane
Systematic (IUPAC) name
(5aR,9aR)-6-propyl-5a,7,8,9,9a,10-hexahydro-5H-pyrido[2,3-g]quinazolin-2-amine
Clinical data
Pregnancy cat.  ?
Legal status  ?
Identifiers
CAS number 97548-97-5 Y
ATC code  ?
PubChem CID 57242
UNII Z0X4VT3Y1Q N
KEGG D05677 Y
ChEMBL CHEMBL155731 N
Chemical data
Formula C14H22N4 
Mol. mass 246.350 g/mol
SMILES eMolecules & PubChem
 N(what is this?)  (verify)

Quinelorane is a drug which acts as a dopamine agonist selective for the D2 subtype.[1][2][3]

See also

References

  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. 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. 
  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. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2000917.