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RPR107393 free base

Catalog No. T12765   CAS 197576-78-6

RPR107393 free base is a selective inhibitor of squalene synthase(rat liver microsomal squalene synthase, with an IC50 of 0.8 nM).

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RPR107393 free base Chemical Structure
RPR107393 free base, CAS 197576-78-6
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25 mg 6-8 weeks $ 1,520.00
50 mg 6-8 weeks $ 1,980.00
100 mg 6-8 weeks $ 2,500.00
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Biological Description
Chemical Properties
Storage & Solubility Information
Description RPR107393 free base is a selective inhibitor of squalene synthase(rat liver microsomal squalene synthase, with an IC50 of 0.8 nM).
Targets&IC50 Squalene synthase (rat liver microsomal):0.8±0.2 nM
In vitro RPR107393 is a selective inhibitor of squalene synthase with subnanomolar potency. Rat liver microsomal squalene synthase inhibited by RPR107393 (IC50 value of 0.8±0.2 nM (n=4))[1]. Cells are treated with ER-27856 (1 μM), RPR-107393 (10 μM), Atorvastatin (1 μM), or NB-598 (1 μM) for 2-24 h, and lipid biosynthesis during the last 2 h of the incubation is determined. RPR-107393 (10 μM) inhibits Cholesterol biosynthesis and reduces triglyceride biosynthesis. Similarly, 1 μM RPR-107393 inhibits Cholesterol and triglyceride biosynthesis by 82.4% and 70.0%, respectively[2].
In vivo Cholesterol biosynthesis is significantly reduced following administration of RPR107393, demonstrating a potent cholesterol-lowering effect in rats. Specifically, a 92% reduction in cholesterol biosynthesis is observed with a dose of 5 mg/kg, peaking one hour post-administration (10 mg/kg p.o.). This effect decreases to 74% six hours post-administration at the same dosage, with the half-life for 50% inhibition being approximately 7 hours. A more pronounced effect is seen 10 hours after administering a larger dose (25 mg/kg p.o.), achieving an 82% inhibition rate; however, this effect dissipates at 21 hours. Additionally, both Zaragozic acid and RPR107393 lead to an accumulation of radiolabeled diacid products in the liver, indicating a mechanism associated with the inhibition of cholesterol biosynthesis. Remarkably, repeated doses of RPR107393 (30 mg/kg p.o. b.i.d.) result in a substantial decrease in serum cholesterol, lowering it by 35% after two days and nearly 50% after three days of treatment.
Molecular Weight 330.42
Formula C22H22N2O
CAS No. 197576-78-6

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

TargetMolReferences and Literature

1. Amin D, et al. RPR107393, a potent squalene synthase inhibitor and orally effective Cholesterol-lowering agent: comparison with inhibitors of HMG-CoA reductase. J Pharmacol Exp Ther. 1997 May;281(2):746-52. 2. Hiyoshi H, et al. Squalene synthase inhibitors suppress triglyceride biosynthesis through the farnesol pathway in rat hepatocytes. J Lipid Res. 2003 Jan;44(1):128-35.

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Keywords

RPR107393 free base 197576-78-6 Others RPR107393 RPR 107393 RPR-107393 free base RPR-107393 inhibitor inhibit

 

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