Mogroside I A1

CAS No. 88901-46-6

Mogroside I A1( —— )

Catalog No. M26301 CAS No. 88901-46-6

Mogroside I A1 is a triterpenoid glycoside isolated from the extracts of Luo Han Guo, exhibiting antioxidant, antidiabetic and anticancer activities.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 376 Get Quote
10MG 641 Get Quote
25MG 1098 Get Quote
50MG 1656 Get Quote
100MG Get Quote Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Mogroside I A1
  • Note
    Research use only, not for human use.
  • Brief Description
    Mogroside I A1 is a triterpenoid glycoside isolated from the extracts of Luo Han Guo, exhibiting antioxidant, antidiabetic and anticancer activities.
  • Description
    Mogroside I A1 is a triterpenoid glycoside isolated from the extracts of Luo Han Guo, exhibiting antioxidant, antidiabetic and anticancer activities.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    GLUT
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    88901-46-6
  • Formula Weight
    638.883
  • Molecular Formula
    C36H62O9
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (156.53 mM)
  • SMILES
    [H][C@@]1(CC[C@@]2(C)[C@]3([H])CC=C4[C@@]([H])(CC[C@H](O)C4(C)C)[C@]3(C)[C@H](O)C[C@]12C)[C@H](C)CC[C@@H](O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(C)(C)O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Olszewski K, et al. Inhibition of glucose transport synergizes with chemical or genetic disruption of mitochondrial metabolism and suppresses TCA cycle-deficient tumors. Cell Chem Biol. 2021 Oct 22:S2451-9456(21)00441-4.
molnova catalog
related products
  • Pep 2-8

    Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor. Potent inhibitor of PCSK9 binding to LDL receptor (IC50 = 0.8 μM). Restores LDL uptake in HepG2 cells treated with PCSK9.

  • Butyl chlorogenate

    Butylchlorogenate is a natural compound isolated from Lonicera japonica, Urceola rosea.

  • Synaptobrevin-2 (73-...

    Synaptobrevin-2 (73-79) (human, bovine, mouse, rat)