Free shipping on all orders over $ 500

Betulin

Cat. No. M3996

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

Betulin Structure
Synonym:

Trochol

Size Price Availability Quantity
50mg USD 60  USD60 In stock
100mg USD 95  USD95 In stock
200mg USD 125  USD125 In stock
Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation
Biological Activity

Betulin inhibited pro-inflammatory cytokines expression and NF-κB signaling activation through STAT3 signaling. Besides, betulin treatment also induced the expression of Bcl-xL, an anti-apoptotic downstream effector of STAT3.Betulin decreases lipid levels, enhances insulin sensitivity, and reduces the development of atherosclerotic plaques.Betulin can serve as a lead compound for pharmacological control of metabolic diseases.Betulin can effect intracellular signaling in ethanol-induced liver cells via inhibiting ROS, TNFα and TNFβ. In human cancer cells Betulin can induce mitochondrial cytochrome C release in human cancer cells, which results in apoptosis. Alternate studies on mice show that Betulin binds to melanocortin receptors and antagonizes the release of cAMP generation in mouse melanoma cells. Furthermore, Betulin has protective effects against cadmium induced apoptosis in human hepatoma cell lines.

Chemical Information
Molecular Weight 442.72
Formula C30H50O2
CAS Number 473-98-3
Form Solid
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Zhang SY, et al. Eur Rev Med Pharmacol Sci. Betulin inhibits pro-inflammatory cytokines expression through activation STAT3 signaling pathway in human cardiac cells.

[2] Li Y, et al. Mol Carcinog. Betulin induces mitochondrial cytochrome c release associated apoptosis in human cancer cells.

[3] Muceniece R, et al. Cell Biochem Funct. Betulin binds to melanocortin receptors and antagonizes alpha-melanocyte stimulating hormone induced cAMP generation in mouse melanoma cells.

[4] Oh SH, et al. Toxicology. Protection of betulin against cadmium-induced apoptosis in hepatoma cells.

Related FAS Products
Fasnall 

Fasnall is a selective fatty acid synthase (FASN) inhibitor with an IC50 of 3.71 μM.

Fasnall benzenesulfonate 

Fasnall benzenesulfonate is the benzenesulfonate salt form of Fasnall.

GSK837149A 

GSK837149A is a selective inhibitor of human Fatty Acid Synthase (FASN) targeting the KR domain. GSK837149A has reversible inhibition effect on FASN and selectivity for type I FASN (Ki=30 nM). GSK837149A is also a competitive inhibitor of NADPH and a non-competitive inhibitor of acetoacetyl-CoA. GSK837149A can be used for the research of obesity and breast cancer.

IPI-9119

IPI-9119 is an orally active, selective and irreversible Fatty Acid Synthase (FASN) inhibitor, with an IC50 of 0.3 nM.

Eicosapentaenoic acid ethyl ester

Eicosapentaenoic acid ethyl ester (AMR101, EPA ethyl ester, Ethyl eicosapentaenoate) is an omega-3 fatty acid agent that significantly reduces the triglyceride (TG) levels and improves other lipid parameters without significantly increasing the low-density lipoprotein (LDL) cholesterol levels.

  Catalog
Abmole Inhibitor Catalog




Keywords: Betulin, Trochol supplier, FAS, inhibitors, activators

All AbMole products are for research use only, cannot be used for human consumption or veterinary use. We do not provide products or services to individuals. Please comply with the intended use and do not use AbMole products for any other purpose.



Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2024 AbMole BioScience. All Rights Reserved.