Borapetoside B

CAS No. 104901-05-5

Borapetoside B( —— )

Catalog No. M31489 CAS No. 104901-05-5

Borapetoside B is a natural product of Tinospora, Menispermaceae. Borapetoside B can be used as a reference standard.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 603 In Stock
50MG Get Quote In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Borapetoside B
  • Note
    Research use only, not for human use.
  • Brief Description
    Borapetoside B is a natural product of Tinospora, Menispermaceae. Borapetoside B can be used as a reference standard.
  • Description
    Borapetoside B is a natural product of Tinospora, Menispermaceae. Borapetoside B can be used as a reference standard.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    104901-05-5
  • Formula Weight
    552.6
  • Molecular Formula
    C27H36O12
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    ——
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • Phenibut (hydrochlor...

    Phenibut (hydrochloride)?is a GABA mimetic that acts as an agonist at GABAB receptors, blocks α2δ subunit-containing voltage-gated calcium channels, stimulates dopamine receptors, and inhibits the actions of β-phenethylamine.

  • Chrysin 6-C-arabinos...

    Chrysin 6-C-arabinoside 8-C-glucoside and chrysin-6-C-glucosyl-8-C-arabinoside are α±-glucosidase inhibitors, α±-glucosidase inhibitors are widely used in the treatment of type 2 diabetes.

  • Tenuifoliside A

    Tenuifoliside A has anti-apoptotic, neuroprotective activity. And tenuifoliside A has anti-inflammatory effect, which is mediated by the inhibition of the NF-κB and MAPK pathways.