Leelamine is an orally active pyruvate dehydrogenase kinase (PDK) inhibitor with an IC50 value of 9.5 µM, showing a blood glucose lowering effect in the diabetic mouse. Leelamine is also a weak agonist of cannabinoid receptors CB1 and CB2. Leelamine decreases mitotic activity, prostate-specific antigen expression and induces Apoptosis to cell death in cancer cells[1][2][3].
Molekulargewicht:
285.48
Reinheit:
98.36
CAS Nummer:
[1446-61-3]
Formel:
C20H31N
Target-Kategorie:
Cannabinoid Receptor,PDK-1
Anwendungsbeschreibung:
MCE Product type: Reference compound
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