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 In stock
100mg USD 95 In stock
200mg USD 125 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
C75

C75 is a novel, potent synthetic inhibitor of fatty acid synthase (FAS). C75 inhibits prostate cancer cells PC3 with an IC50 of 35 μM. C75 is a potent CPT1A activator.

Orlistat

Orlistat is an irreversible inhibitor of pancreatic and gastric lipases with IC50 of 122 ng/ml for PL from human duodenal juice.

Pseudoprotodioscin

Pseudoprotodioscin, a furan glucoside, inhibits sREBP1/2 and microRNA 33A/B levels and reduces the expression of genes associated with cholesterol and triglyceride synthesis.

Albaspidin-AP

Albaspidin AP inhibited fatty acid synthase (FAS) with IC50 value of 71.7 μM. Fatty acid synthase is emerging as a potential therapeutic target for cancer and obesity.

Pedunculoside

Pedunculoside plays a lipid-lowering role by regulating lipid formation and fatty acid β -oxidation.

  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 2010-2026 AbMole BioScience. All Rights Reserved.