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5-hete

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    24
    TargetMol | All_Pathways
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    TargetMol | PROTAC
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    TargetMol | Standard_Products
5-HETE
(±)-5-HETE
T8456871030-39-2
5-HETE is a fatty acid metabolite and an oxidative derivative of arachidonic acid produced through lipoxygenase activity, existing as a racemic mixture of the 5(S)-HETE and 5(R)-HETE enantiomers, and it acts as a potent aggregating agent that induces the aggregation of human neutrophils with a IC50 value of approximately 200 nM.
  • $854
35 days
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Astragalus polyphenols
Astragalus polyphenols, 2,3,5,4'-Tetrahydroxystilbene-2-O-b-D-glucopyranoside, 2,3,5,4'-Tetrahydroxystilbene 2-O-β-D-glucoside, 2,3,4',5-Tetrahydroxystilbene 2-O-D-glucoside
T296482373-94-2
2,3,5,4'-Tetrahydroxystilbene 2-O-β-D-glucoside (Astragalus polyphenols) is a compound isolated from the roots of Polygonum species, which inhibits the formation of 5-HETE, HHT, and thromboxane B2.
  • $40
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Astragalus polyphenols (Standard)
2,3,5,4‘-Tetrahydroxystilbene 2-O-glucoside (Standard)
TMSM-147882373-94-2
Astragalus polyphenols (Standard) is a reference standard for research and analysis in studies involving Astragalus polyphenols. 2,3,5,4'-Tetrahydroxystilbene 2-O-β-D-glucoside (Astragalus polyphenols) is a compound isolated from the roots of Polygonum species, inhibits the formation of 5-HETE, HHT and thromboxane B2.
  • $116
7-10 days
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Magnolianin
TN4486147663-91-0
Magnolianin can inhibit strongly (IC50 = 0.45 uM) 5-HETE formation by die cytosol of guinea pig polymorphonuclear leukocytes.
  • $740
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Mulberrofuran A
TN458668978-04-1
Mulberrofuran A can inhibit the formations of 12-hydroxy-, 8, 10-heptadecatrienoic acid (HHT) and thromboxane B2, but it can increase the formation of 12-hydroxy-5, 8, 10, 14-eicosatetraenoic acid (12-HETE).
  • $440
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Hinokiol
8,11,13-Abietatriene-3,12-diol
TN7307564-73-8
Hinokiol exhibits anti-inflammatory activity by significantly inhibiting 5-hydroxy-eicosa-tetra-enoic acid (5-HETE) and leukotriene B(4) (LTB4) formations. Additionally, it demonstrates potent activity against clinical isolates of methicillin-resistant Staphylococcus aureus (MRSA).
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