Dehydrocrenatidine, a natural alkaloid, is a specific JAK inhibitor. Dehydrocrenatidine inhibits voltage-gated sodium channels and ameliorates mechanic allodia in a rat model of neuropathic pain[1][2].
Molecular Weight:
254.28
Purity:
98
CAS Number:
[65236-62-6]
Formula:
C15H14N2O2
Target:
Apoptosis,JAK
Application Notes:
MCE Product type: Natural Products
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