YM-53601 – 1 mg

Brand:
Cayman
CAS:
182959-33-7
Storage:
-20
UN-No:
Non-Hazardous - /

YM-53601 is a squalene synthase inhibitor (IC50s = 79 and 90 nM in HepG2 cells and rat liver microsomes, respectively).{16636} It inhibits cholesterol biosynthesis in rats (ED50 = 32 mg/kg).{16636} YM-53601 dose-dependently reduces plasma triglyceride and non-HDL cholesterol levels in hamsters fed both normal and high-fat diets. It also reduces viral RNA, core and NS3 protein production, and secreted viral particles in Huh7.5.1-8 cells infected with the hepatitis C virus (HCV) strain JFH-1 without affecting cell viability at concentrations ranging from 0.5 to 1.5 μM.{36948} YM-53601 (1-10 μM) confers protection against cytotoxicity induced by the bacterial pore-forming toxin pneumolysin in HBE1 and normal human bronchial epithelial (NHBE) cells.{36949}  

 

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Description

A squalene synthase inhibitor (IC50s = 79 and 90 nM in HepG2 cells and rat liver microsomes, respectively); inhibits cholesterol biosynthesis in rats (ED50 = 32 mg/kg); dose-dependently reduces plasma triglyceride and non-HDL cholesterol levels in hamsters fed both normal and high-fat diets; reduces viral RNA, core and NS3 protein production, and secreted viral particles in Huh-7.5.1-8 cells infected with HCV strain JFH-1 without affecting cell viability at 0.5-1.5 μM; confers protection against cytotoxicity induced by the bacterial pore-forming toxin pneumolysin in HBE1 and NHBE cells at 1-10 μM


Formal name: 2-[(2E)-2-(1-azabicyclo[2.2.2]oct-3-ylidene)-2-fluoroethoxy]-9H-carbazole, monohydrochloride

Synonyms: 

Molecular weight: 372.9

CAS: 182959-33-7

Purity: ≥98%

Formulation: A crystalline solid


Product Type|Biochemicals|Antivirals||Product Type|Biochemicals|Small Molecule Inhibitors||Research Area|Immunology & Inflammation||Research Area|Infectious Disease|Viral Diseases|Hepatitis