(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
Size Price / USD Stock Quantity
5MG 264 Get Quote
10MG 421 Get Quote
25MG 669 Get Quote
50MG 897 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
    (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.
molnova catalog
related products
  • Trk-IN-9

    Trk-IN-9 (Compound 12) is a potent inhibitor of TRK that inhibits the proliferation of Km-12 cell lines and induces apoptosis in a concentration-dependent manner.

  • SCH79797 dihydrochlo...

    SCH79797 dihydrochloride is an effective and selective antagonist of protease activated receptor 1 (PAR1) with an IC50 of 70 nM and a Ki of 35 nM.

  • ABT-510 acetate

    ABT-510 acetate is an endogenous anti-angiogenic TSP peptide inhibitor, a thrombospondin analog, with anti-inflammatory, anti-cancer and anti-angiogenic activity that induces apoptosis and inhibits ovarian tumor growth in an orthotopic, syngeneic model of epithelial ovarian cancer.