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2499962-58-0

2499962-58-0 Structure

2499962-58-0 Structure
IdentificationBack Directory
[Name]

7H-Pyrrolo[2,3-d]pyrimidin-4-amine, N-[(1R)-1,2,3,4-tetrahydro-1-naphthalenyl]-6-(trifluoromethyl)-
[CAS]

2499962-58-0
[Synonyms]

Mitophagy activator 1
MTK458 EP-0035985
7H-Pyrrolo[2,3-d]pyrimidin-4-amine, N-[(1R)-1,2,3,4-tetrahydro-1-naphthalenyl]-6-(trifluoromethyl)-
[Molecular Formula]

C17H15F3N4
[MOL File]

2499962-58-0.mol
[Molecular Weight]

332.32
Chemical PropertiesBack Directory
[density ]

1.422±0.06 g/cm3(Predicted)
[form ]

Solid
[pka]

10.59±0.50(Predicted)
[color ]

White to yellow
Hazard InformationBack Directory
[Uses]

MTK458 is an orally active brain penetrant PINK1 activator. MTK458 binds to PINK1 and stabilizes an active heterocomplex, thereby increasing mitophagy. MTK458 can be used for research on Parkinson's disease[1].
[in vivo]

MTK458 (50 mg/kg, p.o., daily, 6 months) drives clearance of pathologic α-synuclein in a dose-dependent manner in the stratum of mice injected with α-synuclein preformed fibrils (PFFs)[1].
MTK458 (50 mg/kg, p.o., 6 doses, 5 days) decreases plasma pS65-Ubiquitin (pUb) in wild-type Sprague-Dawley rats[1].

Animal Model:Stratum of mice injected with α-synuclein preformed fibrils (PFFs)[1]
Dosage:50 mg/kg
Administration:Oral gavage (p.o.), daily, 6 months
Result:Rescued an activity deficit in freely moving PFF mice.
Reduced the levels of inflammatory markers (TREM2, IL-6, and CXCL1).
Animal Model:C57BL6J wildtype mice injected with PFF [1]
Dosage:50 mg/kg
Administration:Oral gavage (p.o.); 7 days, 3 weeks
Result:Decreased pUb in the brain and plasma of PFF seeded mice.
[References]

[1] Chin RM, et al. Pharmacological PINK1 activation ameliorates Pathology in Parkinson's Disease models. bioRxiv [Preprint]. 2023 Feb 15:2023.02.14.528378. DOI:10.1101/2023.02.14.528378
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