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Home - Products - Others - Other Targets - (3β,4α,7β,15α)-3,7,15,28-Tetrahydroxy-11,23-dioxolanost-8-en-26-oic acid

(3β,4α,7β,15α)-3,7,15,28-Tetrahydroxy-11,23-dioxolanost-8-en-26-oic acid

CAS No. 1961358-03-1

(3β,4α,7β,15α)-3,7,15,28-Tetrahydroxy-11,23-dioxolanost-8-en-26-oic acid( ——— )

Catalog No. M38483 CAS No. 1961358-03-1

3β,7β,15α-Trihydroxy-4-(hydroxymethyl)-11,23-dioxo-lanost-8-en-26-oic acid is a triterpene compound that can be found in Ganoderma lucidum, and it inhibits nitric oxide (NO) production in BV-2 microglial cells induced by lipopolysaccharide (LPS), with an IC50 of 4.15 μM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    (3β,4α,7β,15α)-3,7,15,28-Tetrahydroxy-11,23-dioxolanost-8-en-26-oic acid
  • Note
    Research use only, not for human use.
  • Brief Description
    3β,7β,15α-Trihydroxy-4-(hydroxymethyl)-11,23-dioxo-lanost-8-en-26-oic acid is a triterpene compound that can be found in Ganoderma lucidum, and it inhibits nitric oxide (NO) production in BV-2 microglial cells induced by lipopolysaccharide (LPS), with an IC50 of 4.15 μM.
  • Description
    3β,7β,15α-Trihydroxy-4-(hydroxymethyl)-11,23-dioxo-lanost-8-en-26-oic acid is a triterpene compound that can be found in Ganoderma lucidum, and it inhibits nitric oxide (NO) production in BV-2 microglial cells induced by lipopolysaccharide (LPS), with an IC50 of 4.15 μM.
  • In Vitro
    ———
  • In Vivo
    ———
  • Synonyms
    ———
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ———
  • Research Area
    ———
  • Indication
    ———

Chemical Information

  • CAS Number
    1961358-03-1
  • Formula Weight
    534.68
  • Molecular Formula
    C30H46O8
  • Purity
    >98% (HPLC)
  • Solubility
    ———
  • SMILES
    ———
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Jiao Y, et al. Lanostane triterpenoids from Ganoderma curtisii and their NO production inhibitory activities of LPS-induced microgliaJ. Bioorganic & medicinal chemistry letters, 2016, 26(15): 3556-3561.
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