Online Purchasing Account You are logged on as Guest. LoginRegister a New AccountShopping cart (Empty)
United States 

U-18666A

Oxido-squalene cyclase inhibitor
 
BML-S200-0010 10 mg 129.00 USD
 
BML-S200-0050 50 mg 509.00 USD
Do you need bulk/larger quantities?
 
A useful tool for inhibition of cholesterol transport from late endosomes/lysosomes to the endoplasmic reticulum. Inhibits cholesterol transport in a variety of cell types such as macrophages and sympathetic neurons. May be used to induce a Neimann-Pick disease type C (NPC)or NPC-like phenotype in a variety of cell types. Inhibits cholesterol biosynthesis at the level of oxido-squalene cyclase (OSC). Induction of cataracts is a common toxic feature of OSC inhibitors such as U18666A.

Product Details

Alternative Name:3β-(2-Diethylaminoethoxy)-Androstenone . HCl
 
Formula:C25H41NO2 . HCl
 
MW:424.1
 
CAS:3039-71-2
 
Purity:≥99% (TLC)
 
Appearance:White solid.
 
Shipping:Ambient Temperature
 
Long Term Storage:Ambient
 
Regulatory Status:RUO - Research Use Only
 
BML-S200 structure
Please mouse over
BML-S200 structure

Product Literature References

Genistein Activates Transcription Factor EB and Corrects Niemann–Pick C Phenotype: G. Argüello, et al.; Int. J. Mol. Sci. 22, 4220 (2021), Abstract;
Synthesis and Biological Evaluation of Cationic Top-Fluor Cholesterol Analogues: M. Jurášek, et al.; Bioorg. Chem. 117, 105410 (2021), Abstract;
Cooperative binding promotes demand-driven recruitment of AnxA8 to cholesterol-containing membranes: N. Heitzig, et al.; Biochim. Biophys. Acta. 1863, 349 (2018), Abstract;

Product Toolbox

PRODUCT RESOURCES

Datasheet
SDS
Certificate of Analysis

RELATED PRODUCTS

By target:
Oxido-squalene cyclase
By biological activity:
Oxido-squalene cyclase Inhibitor
By catalog section:

PRODUCT SUPPORT

FAQs
Technical Service
Customer Service