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RO 48-8071 fumarate

Cat. No. M4883

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

RO 48-8071 fumarate Structure
Synonym:

4012AH

Size Price Availability Quantity
10mM*1mL in DMSO USD 65  USD65 In stock
5mg USD 55  USD55 In stock
10mg USD 85  USD85 In stock
50mg USD 165  USD165 In stock
100mg USD 275  USD275 In stock
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Quality Control & Documentation
Biological Activity

Ro 48-8071 blocked human liver OSC and cholesterol synthesis in HepG2 cells in the nanomolar range; in cells it triggered the production of monooxidosqualene, dioxidosqualene, and epoxycholesterol. Administration of Ro 48-8071 to mice with BT-474 tumor xenografts prevented tumor growth, with no apparent toxicity. Ro 48-8071 degraded ERα while concomitantly inducing the anti-proliferative protein ERβ.

Chemical Information
Molecular Weight 564.44
Formula C27H31BrFNO6
CAS Number 189197-69-1
Solubility (25°C) DMSO 55 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Yayun Liang, et al. The estrogen receptor beta agonist liquiritigenin enhances the inhibitory effects of the cholesterol biosynthesis inhibitor RO 48-8071 on hormone-dependent breast-cancer growth

[2] Yayun Liang, et al. Cholesterol biosynthesis inhibitor RO 48-8071 suppresses growth of hormone-dependent and castration-resistant prostate cancer cells

[3] Yayun Liang, et al. Cholesterol biosynthesis inhibitors as potent novel anti-cancer agents: suppression of hormone-dependent breast cancer by the oxidosqualene cyclase inhibitor RO 48-8071

[4] Zofia Duniec-Dmuchowski, et al. Human pregnane X receptor activation and CYP3A4/CYP2B6 induction by 2,3-oxidosqualene:lanosterol cyclase inhibition

[5] Sarita D Shenoy, et al. Induction of CYP3A by 2,3-oxidosqualene:lanosterol cyclase inhibitors is mediated by an endogenous squalene metabolite in primary cultured rat hepatocytes

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Keywords: RO 48-8071 fumarate, 4012AH supplier, inhibitors, activators

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