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6-Shogaol
Clinical trialMechanism of Action
TRPV1 agonism (warming); anti-inflammatory via COX-2 and iNOS inhibition; more potent than gingerols after drying
Research Notes
6-Shogaol is formed from 6-gingerol during drying and is more pharmacologically potent. Clinical trials support anti-emetic and warming applications.
Found In 1 Herb
3D Molecular Structure
Phenylalkylketone
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6-Shogaol
PhenylalkylketoneBioactive phytochemical with therapeutic properties
Representative pattern: C₇H₆O₃
Atoms
Carbon
Oxygen
Hydrogen
Live Research
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