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YM-53601 hydrochloride

Cat. No. M28936

All AbMole products are for research use only, cannot be used for human consumption.

YM-53601 hydrochloride Structure
Size Price Availability Quantity
1mg USD 160  USD160 In stock
5mg USD 320  USD320 In stock
10mg USD 440  USD440 In stock
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Quality Control & Documentation
Biological Activity

YM-53601 hydrochloride is a squalene synthase inhibitor, reduces plasma cholesterol and triglyceride levels in vivo. YM-53601 hydrochloride inhibits squalene synthase derived from human hepatoma cells with an IC50 of 79 nM. YM-53601 hydrochloride is also an inhibitor of farnesyl-diphosphate farnesyltransferase 1 (FDFT1) enzyme activity and abrogates HCV propagation.

Chemical Information
Molecular Weight 372.86
Formula C21H22ClFN2O
CAS Number 182959-33-7
Form Solid
Solubility (25°C) DMSO 80 mg/mL (ultrasonic and warming)
Storage 4°C, dry, sealed
References

[1] Yasushi Takemoto, et al. J Am Chem Soc. Discovery of a Small-Molecule-Dependent Photolytic Peptide

[2] Tohru Ugawa, et al. Br J Pharmacol. YM-53601, a novel squalene synthase inhibitor, suppresses lipogenic biosynthesis and lipid secretion in rodents

[3] Tohru Ugawa, et al. Br J Pharmacol. Effect of YM-53601, a novel squalene synthase inhibitor, on the clearance rate of plasma LDL and VLDL in hamsters

[4] Tohru Ugawa, et al. Br J Pharmacol. Experimental model of escape phenomenon in hamsters and the effectiveness of YM-53601 in the model

[5] T Ugawa, et al. Br J Pharmacol. YM-53601, a novel squalene synthase inhibitor, reduces plasma cholesterol and triglyceride levels in several animal species

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YM-53601

YM-53601 is a squalene synthase inhibitor, reduces plasma cholesterol and triglyceride levels in vivo. YM-53601 inhibits squalene synthase derived from human hepatoma cells with an IC50 of 79 nM. YM-53601 is also an inhibitor of farnesyl-diphosphate farnesyltransferase 1 (FDFT1) enzyme activity and abrogates HCV propagation.

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Keywords: YM-53601 hydrochloride supplier, Farnesyl Transferase, inhibitors, activators

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