| 词条 | Ro10-5824 |
| 释义 |
| verifiedrevid = 449585803 | IUPAC_name = 2-methyl-5-[(4-phenyl-3,6-dihydro-2H-pyridin-1-yl)methyl]pyrimidin-4-amine | image = Ro10-5824_structure.png | tradename = | licence_EU = | pregnancy_category = | legal_UK = | routes_of_administration = | bioavailability = | metabolism = | elimination_half-life = | excretion = | CAS_number = 189744-46-5 | ATC_suffix = | PubChem = 16759175 | ChEMBL = 1616116 | DrugBank_Ref = {{drugbankcite|correct|drugbank}} | ChemSpiderID = 14016802 | C=17 | H=20 | N=4 | molecular_weight = 280.367 g/mol | smiles = c3ccccc3C(=CC2)CCN2Cc1cnc(C)nc1N | StdInChI = 1S/C17H20N4/c1-13-19-11-16(17(18)20-13)12-21-9-7-15(8-10-21)14-5-3-2-4-6-14/h2-7,11H,8-10,12H2,1H3,(H2,18,19,20) | StdInChIKey = KABDATZAOUSYES-UHFFFAOYSA-N }}Ro10-5824 is a drug which acts as a dopamine receptor partial agonist selective for the D4 subtype, and has nootropic effects in animal studies.[1][2] References1. ^{{cite journal |vauthors=Powell SB, Paulus MP, Hartman DS, Godel T, Geyer MA |title=RO-10-5824 is a selective dopamine D4 receptor agonist that increases novel object exploration in C57 mice |journal=Neuropharmacology |volume=44 |issue=4 |pages=473–81 |date=March 2003 |pmid=12646284 |doi= 10.1016/S0028-3908(02)00412-4|url=}} {{Dopaminergics}}{{nervous-system-drug-stub}}2. ^{{cite journal |vauthors=Newman-Tancredi A, Heusler P, Martel JC, Ormière AM, Leduc N, Cussac D |title=Agonist and antagonist properties of antipsychotics at human dopamine D4.4 receptors: G-protein activation and K+ channel modulation in transfected cells |journal=The International Journal of Neuropsychopharmacology |volume=11 |issue=3 |pages=293–307 |date=May 2008 |pmid=17897483 |doi=10.1017/S1461145707008061 |url=}} 4 : Dopamine agonists|Hoffmann-La Roche|Tetrahydropyridines|Pyrimidines |
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