:Ro10-5824

{{Short description|Chemical compound}}

{{Drugbox

| verifiedrevid = 449585803

| IUPAC_name = 2-methyl-5-[(4-phenyl-3,6-dihydro-2H-pyridin-1-yl)methyl]pyrimidin-4-amine

| image = Ro10-5824 Structure.svg

| tradename =

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| legal_UK =

| routes_of_administration =

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| CAS_number_Ref = {{cascite|correct|CAS}}

| CAS_number = 189744-46-5

| UNII_Ref = {{fdacite|correct|FDA}}

| UNII = 8X35VUU4YY

| ATC_suffix =

| PubChem = 16759175

| ChEMBL = 1616116

| DrugBank_Ref = {{drugbankcite|correct|drugbank}}

| ChemSpiderID = 14016802

| C=17 | H=20 | N=4

| 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.{{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|s2cid=16594644 }}{{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 |doi-access= }}

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