Date published: 2025-12-5

1-800-457-3801

SCBT Portrait Logo
Seach Input

Ro 48-8071 fumarate (CAS 189197-69-1)

0.0(0)
Write a reviewAsk a question

Alternate Names:
[4′-[6-(Allylmethylamino)hexyloxy]-4-bromo-2′-fluorobenzophenone fumarate (1:1)
Application:
Ro 48-8071 fumarate is an orally active OSC (2,3-oxidosqualene lanosterol cyclase) inhibitor
CAS Number:
189197-69-1
Molecular Weight:
564.44
Molecular Formula:
C23H27NO2BrF•C4H4O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Ro 48-8071 fumarate, a selective inhibitor of microsomal triglyceride transfer protein (MTP), has emerged as a valuable tool in elucidating the role of lipid metabolism in various physiological processes. By inhibiting MTP, Ro 48-8071 fumarate disrupts the assembly and secretion of very low-density lipoprotein (VLDL) particles in the liver, consequently leading to reduced plasma levels of triglycerides and cholesterol. This mechanism of action has been extensively studied in the context of dyslipidemia and cardiovascular diseases, providing insights into the regulation of lipid homeostasis and the development of novel strategies. Additionally, Ro 48-8071 fumarate has been utilized in research to investigate the pathophysiology of lipid-related disorders, such as non-alcoholic fatty liver disease (NAFLD), hyperlipidemia, and atherosclerosis. Furthermore, its inhibitory effect on MTP has been leveraged to explore its potential as a pharmacological intervention for the treatment of obesity and metabolic syndrome. Through mechanistic studies and experimental models, Ro 48-8071 fumarate continues to contribute to our understanding of lipid metabolism and its implications for human health, offering promising avenues for further research and development.


Ro 48-8071 fumarate (CAS 189197-69-1) References

  1. Induction of CYP3A by 2,3-oxidosqualene:lanosterol cyclase inhibitors is mediated by an endogenous squalene metabolite in primary cultured rat hepatocytes.  |  Shenoy, SD., et al. 2004. Mol Pharmacol. 65: 1302-12. PMID: 15102959
  2. Oxidosqualene cyclase from Saccharomyces cerevisiae, Trypanosoma cruzi, Pneumocystis carinii and Arabidopsis thaliana expressed in yeast: a model for the development of novel antiparasitic agents.  |  Balliano, G., et al. 2009. Bioorg Med Chem Lett. 19: 718-23. PMID: 19119009
  3. Human pregnane X receptor activation and CYP3A4/CYP2B6 induction by 2,3-oxidosqualene:lanosterol cyclase inhibition.  |  Duniec-Dmuchowski, Z., et al. 2009. Drug Metab Dispos. 37: 900-8. PMID: 19158313
  4. Novel pyrrole- and 1,2,3-triazole-based 2,3-oxidosqualene cyclase inhibitors.  |  Watanabe, T., et al. 2010. Bioorg Med Chem Lett. 20: 5807-10. PMID: 20728352
  5. Sustained and selective suppression of intestinal cholesterol synthesis by Ro 48-8071, an inhibitor of 2,3-oxidosqualene:lanosterol cyclase, in the BALB/c mouse.  |  Chuang, JC., et al. 2014. Biochem Pharmacol. 88: 351-63. PMID: 24486573
  6. Cholesterol biosynthesis inhibitor RO 48-8071 suppresses growth of hormone-dependent and castration-resistant prostate cancer cells.  |  Liang, Y., et al. 2016. Onco Targets Ther. 9: 3223-32. PMID: 27313468
  7. Activation of WNT signaling restores the facial deficits in a zebrafish with defects in cholesterol metabolism.  |  Castro, VL., et al. 2020. Genesis. 58: e23397. PMID: 33197123
  8. The estrogen receptor beta agonist liquiritigenin enhances the inhibitory effects of the cholesterol biosynthesis inhibitor RO 48-8071 on hormone-dependent breast-cancer growth.  |  Liang, Y., et al. 2022. Breast Cancer Res Treat. 192: 53-63. PMID: 35037188
  9. Cholesterol Biosynthesis Inhibitor RO 48-8071 Suppresses Growth of Epithelial Ovarian Cancer Cells in Vitro and In Vivo.  |  Liang, Y., et al. 2023. J Cancer Sci Clin Ther. 7: 1-8. PMID: 38105923

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ro 48-8071 fumarate, 10 mg

sc-215817
10 mg
$92.00

Ro 48-8071 fumarate, 50 mg

sc-215817A
50 mg
$403.00