ChemicalBook--->CAS DataBase List--->1883528-69-5

1883528-69-5

1883528-69-5 Structure

1883528-69-5 Structure
IdentificationBack Directory
[Name]

Ly93
[CAS]

1883528-69-5
[Synonyms]

Ly93
SMS2-IN-Ly93
2-[(2-ethylphenyl)methoxy]-N-(pyridin-3-yl)benzamide
[Molecular Formula]

C21H20N2O2
[MDL Number]

MFCD32067900
[MOL File]

1883528-69-5.mol
[Molecular Weight]

332.4
Chemical PropertiesBack Directory
[Boiling point ]

450.6±35.0 °C(Predicted)
[density ]

1.191±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : 250 mg/mL (752.11 mM; Need ultrasonic)
[form ]

Solid
[pka]

12.67±0.70(Predicted)
[color ]

Off-white to light yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H315
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
Hazard InformationBack Directory
[Uses]

Ly93 is a selective and orally active sphingomyelin synthase 2 (SMS2) inhibitor, with an IC50 of 91 nM[1].
[Biological Activity]

Ly93 is a selective and orally active sphingomyelin synthase 2 (SMS2) inhibitor, with an IC50 of 91 nM[1]. Ly93 (100 mg/kg, i.g. once daily for 7 days) significantly decreases the plasma SM levels of C57BL/6J mice[1].Ly93 dose-dependently attenuates the atherosclerotic lesions in the root and the entire aorta as well as macrophage content in lesions, in apolipoprotein E gene knockout mice[1].
[in vivo]

Ly93 (100 mg/kg, i.g. once daily for 7 days) significantly decreases the plasma SM levels of C57BL/6J mice[1].
Ly93 dose-dependently attenuates the atherosclerotic lesions in the root and the entire aorta as well as macrophage content in lesions, in apolipoprotein E gene knockout mice[1].

Animal Model:C57BL/6J mice[1].
Dosage:100 mg/kg.
Administration:I.G. (gavage) once daily for 7 days.
Result:Significantly decreased the plasma SM levels compared with vehicle group.
Animal Model:ApoE KO mice (eight-week-old)[1].
Dosage:12.5 or 40 mg/kg.
Administration:I.G. (gavage) once daily.
Result:The levels of ALT and AST in the plasma of apoE KO mice did not show statistic changes when compared with the control group.
[References]

[1]. Li Y, et al. Discovery, synthesis and anti-atherosclerotic activities of a novel selective sphingomyelin synthase 2 inhibitor. Eur J Med Chem. 2019 Feb 1;163:864-882.
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