Gitogenin

CAS No. 511-96-6

Gitogenin ( AI3-62266, Digin, Gitogenin )

Catalog No. M18692 CAS No. 511-96-6

Gitogenin, tigogenin, and solasodine are novel selective inhibitors of UGT1A4, and do not inhibit the activities of major human CYP isoforms.

Purity : 98%

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 174 In Stock
10MG 300 In Stock
25MG 509 In Stock
50MG 731 In Stock
100MG 1017 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Gitogenin
  • Note
    Research use only, not for human use.
  • Brief Description
    Gitogenin, tigogenin, and solasodine are novel selective inhibitors of UGT1A4, and do not inhibit the activities of major human CYP isoforms.
  • Description
    Gitogenin, tigogenin, and solasodine are novel selective inhibitors of UGT1A4, and do not inhibit the activities of major human CYP isoforms. Gitogenin and (25S)-5α-furastan-3β, 22, 26-triol are the inhibitors of enzyme α-glucosidase with IC50 values of 37.2±0.18 and 33.5±0.22 uM, respectively.3. Gitogenin shows moderate stimulation of release activity on growth hormone from rat pituitary cells.
  • Synonyms
    AI3-62266, Digin, Gitogenin
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    UGT1A4
  • Research Area
    Others-Field
  • Indication
    ——

Chemical Information

  • CAS Number
    511-96-6
  • Formula Weight
    432.64
  • Molecular Formula
    C27H44O4
  • Purity
    98%
  • Solubility
    ——
  • SMILES
    CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1
  • Chemical Name
    5alpha,22alpha-Spirostane-2alpha,3beta-diol

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • Acevaltrate

    Acevaltrate displays high cytotoxicity against GLC(4), a human small-cell lung cancer cell line, and against COLO 320, a human colorectal cancer cell line, with IC50 values of 1-6 uM.

  • PS 48

    PS 48 has been shown to be a PKB Kinase (PDK1) activator (Kd: 10.3 μM). This compound selectively binds to the PIF-binding pocket of PKB Kinase (PDK1).

  • Spathulenol

    Spathulenol has immunomodulatory effect. Spathulenol shows the capacity to inhibit proliferation in the lymphocytes and to induce apoptosis in these cells possibly through a caspase-3 independent pathway.