ChemicalBook--->CAS DataBase List--->2837993-05-0

2837993-05-0

2837993-05-0 Structure

2837993-05-0 Structure
IdentificationBack Directory
[Name]

JNT-517
[CAS]

2837993-05-0
[Synonyms]

JNT-517
[Molecular Formula]

C18H22F4N4O3
[MOL File]

2837993-05-0.mol
[Molecular Weight]

418.39
Chemical PropertiesBack Directory
[density ]

1.424±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
[form ]

Solid
[pka]

13.022±0.46(predicted)
[color ]

White to off-white
[InChIKey]

FNRHWODWSBDOOY-CYBMUJFWSA-N
[SMILES]

N(C1CC1)([C@@H]1CCCN(C1)C(=O)N)C(=O)NCC1C=CC(=CC=1F)OC(F)(F)F
Hazard InformationBack Directory
[Uses]

JNT-517 is an orally active, selective SLC6A19 allosteric inhibitor with an IC50 of 47 nM for human SLC6A19. JNT-517 can be used for the study of phenylketonuria (PKU)[1].
[in vivo]

JN-170 (precursor of JN-517) (50-250 mg/kg, po, single dose) increases the excretion of amino acids in urine in mouse models[2].

Animal Model:C57Bl/6J wild-type mouse[2]
Dosage:50-200 mg/kg
Administration:po, single dose
Result:Increaesed the excretion of glutamine, histidine, and threonine i urine.
[References]

[1] Dean G Brown, et al. Small molecule inhibitors of mammalian slc6a19 function. Patent WO2022192370A1.
[2] Wobst HJ, et al., SLC6A19 inhibition facilitates urinary neutral amino acid excretion and lowers plasma phenylalanine. JCI Insight. 2024 Nov 8;9(21):e182876. DOI:10.1172/jci.insight.182876
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