
(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)






Size | Price / USD | Stock | Quantity |
5MG | 264 | Get Quote |
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10MG | 421 | Get Quote |
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25MG | 669 | Get Quote |
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50MG | 897 | Get Quote |
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100MG | Get Quote | Get Quote |
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200MG | Get Quote | Get Quote |
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500MG | Get Quote | Get Quote |
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Biological Information
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Product Name(Rac)-Idroxioleic acid
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NoteResearch use only, not for human use.
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Brief DescriptionMinerval is a fatty acid amide hydrolase inhibitor with anti-tumor effect.
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DescriptionMinerval 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.
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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.
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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.
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SynonymsMinerval | 2-Hydroxyoleic acid | 2-OHOA | (Rac)-Idroxioleic acid
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PathwayApoptosis
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TargetApoptosis
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RecptorHuman Endogenous Metabolite
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Research Area——
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Indication——
Chemical Information
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CAS Number56472-29-8
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Formula Weight298.467
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Molecular FormulaC18H34O3
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (335.05 mM)
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SMILESCCCCCCCC\C=C/CCCCCCC(O)C(O)=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Jones KH, Langley PF, Lees LJ. Bioavailability and metabolism of talampicillin. Chemotherapy. 1978;24(4):217-26.
molnova catalog



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