Resveratrol

DB02709InvestigationalSmall molecule

Resveratrol (3,5,4'-trihydroxystilbene) is a polyphenolic phytoalexin. It is a stilbenoid, a derivate of stilbene, and is produced in plants with the help of the enzyme stilbene synthase. It exists as... It exists as cis-(Z) and trans-(E) isomers.

Chemical structure of Resveratrol
Mechanism
Curator reviewed
Primary indication
Being investigated for the treatment of Herpes labialis infections (cold sores).Curator reviewed
Formula / weight
C14H12O3 · 228.2433 g/mol (avg)
Also known as
(E)-resveratrol · 3,4',5-trihydroxystilbene · 5-[(1E)-2-(4-hydroxyphenyl)ethenyl]benzene-1,3-diol · 5-[(E)-2-(4-Hydroxyphenyl)-Ethenyl] Benzene-1,3 Diol · 5-[(E)-2-(4-hydroxyphenyl)ethenyl]benzene-1,3-diol
Code names
SRT-501

Resolves to

Structure
InChIKeyLUKBXSAWLPMMSZ-OWOJBTEDSA-NSMILESOC1=CC=C(\C=C\C2=CC(O)=CC(O)=C2)C=C1

What you can answer from here — as of August 31, 2026

26Protein targetsEach mapped to UniProt, with action and pharmacological action
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436Drug interactionsStructured to mechanism, not free text
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76Clinical trialsPhase, status and sponsor resolved per trial
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19Marketed productsAcross 1 country and 11 labellers
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90+ReferencesStructured and connected to the statements they support
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