Morusin

CAS No. 62596-29-6

Morusin ( Mulberrochromene )

Catalog No. M18920 CAS No. 62596-29-6

Morusin possesses antitumor effects of cell lines including HT-29, A549, MCF-7 and MDA-MB-231, through suppressing STAT3 and NFκB attenuation mediated apoptosis induction.

Purity : 98%

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 61 In Stock
10MG 97 In Stock
25MG 161 In Stock
50MG 239 In Stock
100MG 356 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Morusin
  • Note
    Research use only, not for human use.
  • Brief Description
    Morusin possesses antitumor effects of cell lines including HT-29, A549, MCF-7 and MDA-MB-231, through suppressing STAT3 and NFκB attenuation mediated apoptosis induction.
  • Description
    Morusin possesses antitumor effects of cell lines including HT-29, A549, MCF-7, and MDA-MB-231, through suppressing STAT3 and NFκB attenuation mediated apoptosis induction. Morusin possesses anti-oxidant and anti-inflammatory effects.
  • Synonyms
    Mulberrochromene
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    STAT3;NF-Κb
  • Research Area
    Others-Field
  • Indication
    ——

Chemical Information

  • CAS Number
    62596-29-6
  • Formula Weight
    420.46
  • Molecular Formula
    C25H24O6
  • Purity
    98%
  • Solubility
    DMSO : ≥ 125 mg/mL; 297.30 mM
  • SMILES
    CC(=CCC1=C(OC2=C3C=CC(OC3=CC(=C2C1=O)O)(C)C)C4=C(C=C(C=C4)O)O)C
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

molnova catalog
related products
  • Chelidonine hydrochl...

    Chelidonine hydrochloride?is one of the alkaloids of Chelidonium majus which has broad pharmacological activities.

  • Amphotericin B

    Amphotericin B is a Lipid-based Polyene Antifungal and Polyene Antifungal. The chemical classification of amphotericin b is Polyenes.

  • Ribostamycin sulfate

    Ribostamycin is a broad-spectrum antimicrobial, inhibits bacterial protein synthesis at the level of 30S and 50S ribosomal subunit binding, also inhibits the chaperone activity of protein disulfide isomerase (PDI), used in pharmacokinetic and nephrotoxicity studies.