8-Dehydroxy shanzhiside

CAS No. 1008532-71-5

8-Dehydroxy shanzhiside( ——— )

Catalog No. M38694 CAS No. 1008532-71-5

8-Dehydroxyshanzhiside is an iridoid glycoside that can be isolated from Lamiophlomis rotata.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG Get Quote Get Quote
50MG Get Quote 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
    8-Dehydroxy shanzhiside
  • Note
    Research use only, not for human use.
  • Brief Description
    8-Dehydroxyshanzhiside is an iridoid glycoside that can be isolated from Lamiophlomis rotata.
  • Description
    8-Dehydroxyshanzhiside is an iridoid glycoside that can be isolated from Lamiophlomis rotata.
  • In Vitro
    ———
  • In Vivo
    ———
  • Synonyms
    ———
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ———
  • Research Area
    ———
  • Indication
    ———

Chemical Information

  • CAS Number
    1008532-71-5
  • Formula Weight
    376.36
  • Molecular Formula
    C16H24O10
  • Purity
    >98% (HPLC)
  • Solubility
    ———
  • SMILES
    ———
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Li M, et al. The structure of an iridoid glycoside, 8-deoxyshanzhiside, from Lamiophlomis rotata. Carbohydr Res. 2008 Feb 25;343(3):561-5.?
molnova catalog
related products
  • FEN1 Inhibitor C2

    FEN1-IN-4 is an inhibitor of human flap endonuclease-1 (hFEN1)FEN1 Inhibitor C2 inhibition selectively impairs proliferation of colon cancer cells deficient in Cdc4 and Mre11a, both frequently mutated in colorectal cancers.?

  • Bucladesine sodium s...

    Bucladesine, PKA activator, is a cyclic nucleotide derivative that mimics the action of endogenous cAMP and is capable of permeating the cell membrane.

  • Boc-Gly-Gly-Phe-Gly-...

    Boc-Gly-Gly-Phe-Gly-OH TFA is a self-assembly of N-protected and C-protected tetrapeptides and is a protease cleaved connector for antibody-drug binding (ADC).