Home - Products - Others - Other Targets - 11(α)-hydroxyNepasaikosaponin k

11(α)-hydroxyNepasaikosaponin k

CAS No. 1152168-63-2

11(α)-hydroxyNepasaikosaponin k( ——— )

Catalog No. M38130 CAS No. 1152168-63-2

11(α)-Hydroxynepasaikosaponin k (compound HOSSc) is a saikosaponin that can be found in B. scorzonerifolium Willd.

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
    11(α)-hydroxyNepasaikosaponin k
  • Note
    Research use only, not for human use.
  • Brief Description
    11(α)-Hydroxynepasaikosaponin k (compound HOSSc) is a saikosaponin that can be found in B. scorzonerifolium Willd.
  • Description
    11(α)-Hydroxynepasaikosaponin k (compound HOSSc) is a saikosaponin that can be found in B. scorzonerifolium Willd.
  • In Vitro
    ———
  • In Vivo
    ———
  • Synonyms
    ———
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ———
  • Research Area
    ———
  • Indication
    ———

Chemical Information

  • CAS Number
    1152168-63-2
  • Formula Weight
    961.14
  • Molecular Formula
    C48H80O19
  • Purity
    >98% (HPLC)
  • Solubility
    ———
  • SMILES
    ———
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Huang HQ, et, al. Characterization and identification of saikosaponins in crude extracts from three Bupleurum species using LC-ESI-MS. J Sep Sci. 2008 Oct;31(18):3190-201.?
molnova catalog
related products
  • Testosterone decanoa...

    Subcutaneous etonogestrel can be used for birth control.

  • 3,5-Di-tert-butylben...

    3,5-Di-tert-butylbenzaldehyde may be used in the synthesis of the following:5-p-pyridyl-15-(3,5-di-tert-butylphenyl)porphyrin via condensation reaction with 4-pyridinecarboxaldehyde and 2,2′-dipyrrylmethane.3,5-di-tert-butylphenyl-dipyrromethane via reaction with pyrrole in the presence of trifluoroacetic acid.3,5-di-tert-butyl-2-nitrobenzaldehyde via nitration reaction.

  • Menisperine

    Anti-inflammatory effects (potential NF-κB inhibitors).