9-hydroxy Stearic Acid

CAS No. 3384-24-5

9-hydroxy Stearic Acid( —— )

Catalog No. M34907 CAS No. 3384-24-5

9-hydroxy Stearic Acid is a hydroxy fatty acid that is the active metabolite of 9-PAHSA. 9-hydroxy Stearic Acid is formed from 9-PAHSA through carboxyl ester lipase in the liver and pancreas.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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25MG 467 In Stock
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Biological Information

  • Product Name
    9-hydroxy Stearic Acid
  • Note
    Research use only, not for human use.
  • Brief Description
    9-hydroxy Stearic Acid is a hydroxy fatty acid that is the active metabolite of 9-PAHSA. 9-hydroxy Stearic Acid is formed from 9-PAHSA through carboxyl ester lipase in the liver and pancreas.
  • Description
    9-Hydroxyoctadecanoic acid (9-HSA) is an HDAC1 inhibitor that inhibits ~66.4% HDAC1 enzymatic activity at 5 μM. 9-Hydroxyoctadecanoic acid shows anticancer activity.
  • In Vitro
    Cell Line:HT29 cell Concentration:100 μM Incubation Time:24 h Result:Decreased S-phase activity by 50.2% compared with untreated controls, and the growth inhibition was associated with a strong arrest in G0/G1.Cell Line:HT29 cell Concentration:100 μM Incubation Time:24 h Result:Increased the expression of p21WAF1。Cell Line:HT29 cell Concentration:100 μM Incubation Time:24 h Result:Induced p21WAF1 tanscript.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    HDAC
  • Recptor
    HDAC
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    3384-24-5
  • Formula Weight
    300.48
  • Molecular Formula
    C18H36O3
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : ≥ 100 mg/mL (332.80 mM)
  • SMILES
    C(C(CCCCCCCCC)O)CCCCCCC(O)=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Calonghi N, et al. Histone deacetylase 1: a target of 9-hydroxystearic acid in the inhibition of cell growth in human colon cancer. J Lipid Res. 2005 Aug;46(8):1596-603.?
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