info@targetmol.com    Tel: (857) 239-0968 / (617) 419-7131
Home > Stem Cells > TGF/beta/Smad > Hydroxysafflor yellow A
Hydroxysafflor yellow A  
Catalog No. T3674    CAS 78281-02-4
Pack Size
Availability
Price/USD
Quantity
10mg
9 days
68.00
25mg
9 days
126.00
50mg
9 days
221.00
1g
Get quote
0.00
5g
Get quote
0.00
10mM * 1mL (in DMSO)
9 days
75.00
Bulk Size: Please Quote for Discount
Documents and Quality Management
Purity:97.00% COA Datasheet HNMR
Biological Activity:

Product Description:

Hydroxysafflor yellow A inhibited adipogenesis by increasing HSL promoter activities. Hydroxysafflor yellow A can effectively protect the liver from long-term alcohol injury by enhancing antioxidant capacity and inhibiting the expression of TGF-β. It prevents steroid-induced avascular necrosis of femoral head by inhibiting primary bone marrow-derived mesenchymal stromal cells. Also, Hydroxysafflor yellow A has anti-tumor effects.

Target:
TGF-β;
Research Area:
Others
Chemical Information:
Molecular Weight 612.53
Formula C27H32O16
CAS Number 78281-02-4
Solubility DMSO: ≥ 34 mg/mL
Storage 3 years -20°C powder;
2 years -80°C in solvent;
Remark For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20 ℃ for several month.
Technical Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store Products, and issues that need special attention for cell-based assays and animal experiments.

Product Recommendations
  • GNE-617, GNE-617 is a specific NAMPT inhibitor that inhibits the biochemical activity of NAMPT with an IC50 o...
  • IPTG, IPTG is a molecular mimic of allolactose, a lactose metabolite that triggers transcription of the la...
  • Quinine dihydrochloride, Quinine Dihydrochloride is a primary alkaloid of various species of Cinchona (Rubiaceae). It is also...
  • CaCCinh-A01, CaCCinh-A01 is an inhibitor of both TMEM16A and calcium-activated chloride channel (CaCC) with IC50s...
  • CP 376395, CP 376395 is a potent and selective Corticotropin releasing factor 1 (CRF1) receptor antagonist.

 

Reference

If you have additional questions, Please send us a message. * Required