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Results for "

Hook F.

" in MedChemExpress (MCE) Product Catalog:

10

Inhibitors & Agonists

9

Natural
Products

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-32736
    Triptonide
    2 Publications Verification

    NSC 165677; PG 492

    Wnt β-catenin Apoptosis Autophagy Inflammation/Immunology Cancer
    Triptonide (NSC 165677) is a natural product identified in Tripterygium wilfordii Hook F.. Triptonide is a Wnt signaling inhibitor with an IC50 of appropriately 0.3 nM. Triptonide has immunosuppression, anti-inflammatory, anti-fertility, neuroprotective and anti-lymphoma effects .
    Triptonide
  • HY-N10406

    Others Others
    Triptonoterpene is a natural product that can be isolated from the roots of Tripterygium wilfordii Hook. f. .
    Triptonoterpene
  • HY-N0476

    Regelide; Abruslactone A

    Others Inflammation/Immunology
    Wilforlide A is a bioactive triterpene isolated from Tripterygium wilfordii Hook f. Wilforlide A has anti-inflammatory and immune suppressive effects .
    Wilforlide A
  • HY-N12014

    Others Others
    Triptotriterpenic acid C is a ursolic-type acid that can be isolated from total glycosides extracted from the root of Tripterygium wilfordii Hook.f. .
    Triptotriterpenic acid C
  • HY-N3510

    HIV Infection Inflammation/Immunology
    Peritassine A, an alkaloid that could be isolated from Tripterygium wilfordii Hook. f., possesses anti-HIV activity .
    Peritassine A
  • HY-N3788

    Others Inflammation/Immunology
    Dulcioic acid (compound 19) is a product isolated from Tripterygium wilfordii Hook f. Dulcioic acid shows a significant inhibitory effect on cytokine production .
    Dulcioic acid
  • HY-N12212

    Others Others
    Triptonoterpene Me ether (compound 5) is a rosinane-type diterpenoid compound, which can be isolated from the traditional Chinese medicine Tripterygium wilfordii Hook. f .
    Triptonoterpene Me ether
  • HY-N1072

    Wilforgine is a bioactive sesquiterpene alkaloid in Tripterygium wilfordii Hook. F. Wilforgine can induce microstructural and ultrastructural changes in the muscles of Mythimna separata larvae, and the sites of action are proposed to be calcium receptors or channels in the muscular system .
    Wilforgine
  • HY-N0587
    Demethylzeylasteral
    2 Publications Verification

    Apoptosis Inflammation/Immunology Cancer
    Demethylzeylasteral is a triterpene compound isolated from Tripterygium wilfordii Hook F, with anti-inflammatory, immunosuppressive and anti-tumor activities . Demethylzeylasteral can significantly alleviates atherosclerosis (AS) . Demethylzeylasteral inhibits triple-negative breast cancer invasion by blocking the canonical and non-canonical TGF-β signaling pathways .
    Demethylzeylasteral
  • HY-N1638

    Monoamine Oxidase Neurological Disease
    1-Methyl-2-undecyl-4(1H)-quinolone is a potent, irreversible and selective inhibitor of type B monoamine oxidase (MAO-B). 1-Methyl-2-undecyl-4(1H)-quinolone shows a selective inhibition of MAO-B activity with the IC50 and Ki values of 15.3 μM and 9.91 μM, respectively, but did not inhibit type A MAO (MAO-A) activity. Methyl-2-undecyl-4(1H)-quinolone, as a quinolone alkaloid, is isolated from fresh leaves and fruits of Evodia rutaecarpa HOOK. f. et THOMS .
    1-Methyl-2-undecyl-4(1H)-quinolone

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