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Results for "

15(S)-HETE

" in MedChemExpress (MCE) Product Catalog:

5

Inhibitors & Agonists

1

Natural
Products

1

Isotope-Labeled Compounds

Targets Recommended:
Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-113336
    15(S)-HETE

    		Endogenous Metabolite Inflammation/Immunology
    15(S)-HETE is an endogenous metabolite present in Urine that can be used for the research of Zellweger Syndrome .
    <em>15(S)-HETE</em>
  • HY-134132
    15(S)-HETE methyl ester

    Methyl 15(S)-HETE

    		 Others Others
    15(S)-HETE methyl ester (Methyl 15(S)-HETE) (compound 1) is a derivative of 15(S)-HETE (HY-113336), a endogenous metabolite presenting in Urine that can be used for the research of Zellweger Syndrome. 15(S)-HETE methyl ester is commonly used in formations of nutritional supplements .
    <em>15(S)-HETE</em> methyl ester
  • HY-145473
    1-Stearoyl-2-15(S)-HETE-sn-glycero-3-PE

    15(S)-HETE-SAPE; 15(S)-Hydroxyeicosatetraenoic acid-SAPE; 1-Stearoyl-2-15(S)-HETE-sn-glycero-3-Phosphatidylethanolamine

    		 Others Metabolic Disease
    1-Stearoyl-2-15(S)-HETE-sn-glycero-3-PE is a phospholipid that contains stearic acid (HY-B2219) at the sn-1 position and 15(S)-HETE at the sn-2 position. It is formed in human peripheral monocytes activated by the calcium ionophore A23187 (HY-N6687) by direct oxidation of 1-stearoyl-2-arachidonoyl-sn-glycero-3-PE (SAPE) by 15-LO. Phosphoethanolamine (PE) HETEs (PE-HETEs), including 1-stearoyl-2-15(S)-HETE-sn-glycero-3-PE, are the main source of esterified HETE in ionophore-activated monocytes.
    1-Stearoyl-2-<em>15(S)-HETE</em>-sn-glycero-3-PE
  • HY-113336S
    15(S)-HETE-d8

    		Endogenous Metabolite Isotope-Labeled Compounds Others
    15(S)-HETE-d8 is the deuterium labeled 15(S)-HETE[1].
    <em>15(S)-HETE</em>-d8
  • HY-113438
    15(S)-HPETE

    		Others Inflammation/Immunology
    15(S)-HpETE is a monohydroperoxy polyunsaturated fatty acid (PUFA) produced by the action of 15-lipoxygenase (15-LO) on arachidonic acid. It is either metabolized to 14,15-leukotriene A41 or reduced to 15(S)-HETE by peroxidases.2,1 15(S)-HpETE mediates a number of biological functions including the induction of c-fos and c-jun, and activation of AP-1.3 15(S)-HpETE inhibits prostacyclin synthesis in porcine aortic microsomes and bovine endothelial cells, and can cause the suicide inactivation of porcine 12-LO.
    <em>15</em>(S)-HPETE

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