(Rac)-Idroxioleic acid

CAS No. 56472-29-8

(Rac)-Idroxioleic acid( Minerval | 2-Hydroxyoleic acid | 2-OHOA | (Rac)-Idroxioleic acid )

Catalog No. M26756 CAS No. 56472-29-8

Minerval is a fatty acid amide hydrolase inhibitor with anti-tumor effect.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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10MG 421 Get Quote
25MG 669 Get Quote
50MG 897 Get Quote
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Biological Information

  • Product Name
    (Rac)-Idroxioleic acid
  • Note
    Research use only, not for human use.
  • Brief Description
    Minerval is a fatty acid amide hydrolase inhibitor with anti-tumor effect.
  • Description
    Minerval is a fatty acid amide hydrolase inhibitor with anti-tumor effect. It binds to the plasma membrane and alters lipid organization.(In Vitro):Minerval (25-50 μM; 72 hours) causes a marked and concentration-dependent increase in the proteolytic cleavage of PARP, a molecular marker of apoptosis. Minerval (25-75 μM; 72 hours) impairs Jurkat cell growth in a time- and concentration-dependent manner (IC50: 40 μM).(In Vivo): In nude mice infected with Jurkat cells, Minerval significantly inhibits tumour growth.
  • In Vitro
    (Rac)-Idroxioleic acid (25-75 μM; 72 hours) impairs Jurkat cell growth in a time- and concentration-dependent manner, with an IC50 of ~40 μM.(Rac)-Idroxioleic acid (25-50 μM; 72 hours) also induces a marked and concentration-dependent increase in the proteolytic cleavage of PARP, a molecular marker of apoptosis.Cell Viability Assay Cell Line:Jurkat cells Concentration:25 μM, 50 μM, 75 μM Incubation Time:24 hours, 48 hours, 72 hours Result:Impaired Jurkat cell growth in a time- and concentration-dependent manner.Western Blot Analysis Cell Line:Jurkat cells Concentration:25 μM, 50 μM Incubation Time:72 hours Result:Induced a marked and concentration-dependent increase in the proteolytic cleavage of PARP.
  • In Vivo
    (Rac)-Idroxioleic acid markedly and significantly inhibits tumour growth in nude mice infected with Jurkat cells. Animal Model:6-week-old nude male mice (Jurkat cells xenograft model)Dosage:600 mg/kg Administration:Oral administration; daily; for 21 days Result:Markedly and significantly inhibited tumour growth.
  • Synonyms
    Minerval | 2-Hydroxyoleic acid | 2-OHOA | (Rac)-Idroxioleic acid
  • Pathway
    Apoptosis
  • Target
    Apoptosis
  • Recptor
    Human Endogenous Metabolite
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    56472-29-8
  • Formula Weight
    298.467
  • Molecular Formula
    C18H34O3
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (335.05 mM)
  • SMILES
    CCCCCCCC\C=C/CCCCCCC(O)C(O)=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Jones KH, Langley PF, Lees LJ. Bioavailability and metabolism of talampicillin. Chemotherapy. 1978;24(4):217-26.
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