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ChemicalBook--->CAS DataBase List--->2641484-61-7

2641484-61-7

2641484-61-7 Structure

2641484-61-7 Structure
IdentificationBack Directory
[Name]

MK-0159
[CAS]

2641484-61-7
[Synonyms]

MK-0159
[Molecular Formula]

C20H24N4O3S
[MOL File]

2641484-61-7.mol
[Molecular Weight]

400.49
Chemical PropertiesBack Directory
[density ]

1.33±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO: 2mg/mL, clear
[form ]

Solid
[pka]

12.17±0.40(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Description]

MK-0159 is a CD38 enzymatic inhibitor. Mice treated with MK-0159 show strong protection from myocardial damage upon cardiac I/R injury compared to those treated with NAD+ precursors (nicotinamide riboside) or another CD38 inhibitor.
[Uses]

MK-0159 is an orally active, potent and selective CD38 inhibitor, with IC50 values of 22, 3, and 70 nM for human, mouse and rat CD38, respectively. MK-0159 also shows good microsomal stability for human and rodent liver microsomes. MK-0159 increases NAD+ (nicotinamide adenine dinucleotide) and reduces ADPR (adenosine diphosphate ribose) in whole blood and heart[1].
[in vivo]

MK-0159 (3-30 mg/kg, p.o., a single dose) increases systemic NAD+ and decreases ADPR levels (the product and substrate of CD38 enzymatic activity) in blood and heart of mice[1].
MK-0159 (30 mg/kg, p.o.) reduces infarct size in cardiac I/R injury mice[2].
MK-0159 (30 mg/kg, oral gavage, twice a day for 9 days) reverses mitochondrial defect, restores CD8+ T cell function and inhibits virally induced organ inflammation in BXD2 lupus-prone mice with LCMV infection[2].

Animal Model:Cardiac I/R injury mice[1]
Dosage:30 mg/kg
Administration:p.o.
Result:Reduced infarct size, and the combination of MK-0159 and NAD+ precursor significantly reduced the infarct size compared to MK-0159 alone.
Increased whole heart NAD+ levels and decreased ADPR in the heart.
[References]

[1] Lagu B, et al. Orally Bioavailable Enzymatic Inhibitor of CD38, MK-0159, Protects against Ischemia/Reperfusion Injury in the Murine Heart. J Med Chem. 2022 Jun 28. DOI:10.1021/acs.jmedchem.2c00688
[2] Chen PM, et al. CD38 reduces mitochondrial fitness and cytotoxic T cell response against viral infection in lupus patients by suppressing mitophagy. Sci Adv. 2022 Jun 17;8(24):eabo4271. DOI:10.1126/sciadv.abo4271
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