Tavapadon

Chemical compound From Wikipedia, the free encyclopedia

Tavapadon (developmental code names CVL-751, PF-06649751) is a dopamine receptor agonist which is under development for the treatment of Parkinson's disease.[2][3][4] It is under development by Cerevel Therapeutics, which acquired tavapadon from Pfizer in 2018.[2] It is taken by mouth.[1]

Other namesCVL-751; PF-6649751; PF-06649751
CAS Number
Quick facts Clinical data, Other names ...
Tavapadon
Clinical data
Other namesCVL-751; PF-6649751; PF-06649751
Routes of
administration
By mouth[1]
Drug classDopamine receptor agonist
Identifiers
  • (−)-(6Ξ)-1,5-dimethyl-6-(2-methyl-4-[(3-[trifluoromethyl]pyridin-2-yl)oxy]phenyl)pyrimidine-2,4(1H,3H)-dione
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC19H16F3N3O3
Molar mass391.350 g·mol−1
3D model (JSmol)
  • CC1=C(C=CC(=C1)OC2=C(C=CC=N2)C(F)(F)F)C3=C(C(=O)NC(=O)N3C)C
  • InChI=1S/C19H16F3N3O3/c1-10-9-12(28-17-14(19(20,21)22)5-4-8-23-17)6-7-13(10)15-11(2)16(26)24-18(27)25(15)3/h4-9H,1-3H3,(H,24,26,27)
  • Key:AKQXQLUNFKDZBN-UHFFFAOYSA-N
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Tavapadon acts as a highly selective partial agonist of the dopamine D1 receptor (Ki = 9 nM; IATooltip Intrinsic activity = 65%) and the dopamine D5 receptor (Ki = 13 nM; IA = 81%).[3][4][1] It has no significant affinity or functional activity at the D2-like receptors (D2, D3, D4) (Ki ≥ 4,870 to 6,720 nM).[1] Tavapadon also shows biased agonism for Gs-coupled signaling at the D1-like receptors.[1][3]

As of December 2024, tavapadon has completed phase 3 clinical trials for Parkinson's disease.[2]

See also

References

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