Regaloside H

CAS No. 126239-77-8

Regaloside H( —— )

Catalog No. M29431 CAS No. 126239-77-8

Regaloside H, a glyceryl phenylpropionate glycoside, is a gluconeogenesis inhibitor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 291 Get Quote
10MG 432 Get Quote
25MG 707 Get Quote
50MG 963 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
    Regaloside H
  • Note
    Research use only, not for human use.
  • Brief Description
    Regaloside H, a glyceryl phenylpropionate glycoside, is a gluconeogenesis inhibitor.
  • Description
    Regaloside H, a glyceryl phenylpropionate glycoside, is a gluconeogenesis inhibitor.(In Vitro):Administration of Regaloside H inhibited glucose production in H4IIE rat hepatoma cells by 36.8% .
  • In Vitro
    Regaloside H (10 μM) suppresses the glucose production by 36.8% in H4IIE rat hepatoma cells.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    126239-77-8
  • Formula Weight
    400.38
  • Molecular Formula
    C18H24O10
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (249.76 mM)
  • SMILES
    OC[C@H](CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)OC(=O)\C=C\c1ccc(O)cc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • MDL-28170

    Calpain Inhibitor III is a potent, cell-permeable inhibitor of calpain I and II (Ki = 8 nM)., The Calpain Inhibitor III, also referenced under CAS 88191-84-8, controls the biological activity of Calpain.

  • Salvianolic acid E

    Salvianolic acid E is a natural product from Salvia miltiorrhiza Bge.

  • Fmoc-Gly-Gly-Phe-OtB...

    Fmoc-Gly-Gly-Phe-OtBu is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).