Tetrahydropiperine is an orally effective, selective inhibitor of NF-kappaB and MAPKs, and an activator of the PI3K/Akt/mTOR pathway. Tetrahydropiperine reduces the production of pro-inflammatory cytokines such as TNF-alpha, IL-6, and nitric oxide (NO) by inhibiting the nuclear translocation of NF-kappaB and the phosphorylation of MAPKs such as ERK, JNK, and p38. At the same time, Tetrahydropiperine inhibits excessive autophagy by activating the PI3K/Akt/mTOR pathway, protecting neurons from oxidative damage. Tetrahydropiperine has anti-inflammatory, anti-apoptotic, and neuroprotective effects, and is mainly used in the study of inflammatory diseases (such as endotoxemia, arthritis) and neurological diseases such as ischemic stroke[1][2][3].
Molekulargewicht:
289.37
Reinheit:
99.41
CAS Nummer:
[23434-88-0]
Formel:
C17H23NO3
Target-Kategorie:
Cytochrome P450
Anwendungsbeschreibung:
MCE Product type: Natural Products
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