Summary

IMPPAT Phytochemical identifier: IMPHY000827

Phytochemical name: Resveratrol

Synonymous chemical names:
(e)-resveratrol, (z)-1-(3,4-dihydroxyphenyl)-2-(4-hydroxyphenyl)ethylene, 3,5,4'-trihydroxystilbene, 3,5,4-trihydroxystilbene, e-resveratrol, resveratrol, resveratrol ( 3,4',5-trihydroxystilbene), trans-resveratrol

External chemical identifiers:
CID:445154, ChEMBL:CHEMBL165, ChEBI:45713, ZINC:ZINC000000006787, FDASRS:Q369O8926L, SureChEMBL:SCHEMBL19425, MolPort-002-499-801

---

Chemical structure information

SMILES:
Oc1ccc(cc1)/C=C/c1cc(O)cc(c1)O

InChI:
InChI=1S/C14H12O3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h1-9,15-17H/b2-1+

InChIKey:
LUKBXSAWLPMMSZ-OWOJBTEDSA-N

DeepSMILES:
Occcccc6))/C=C/cccO)ccc6)O

Functional groups:
c/C=C/c, cO

---

Molecular scaffolds

Scaffold Graph/Node/Bond level:
C(=Cc1ccccc1)c1ccccc1

Scaffold Graph/Node level:
C1CCC(CCC2CCCCC2)CC1

Scaffold Graph level:
C1CCC(CCC2CCCCC2)CC1

---

Chemical classification

ClassyFire Kingdom: Organic compounds

ClassyFire Superclass: Phenylpropanoids and polyketides

ClassyFire Class: Stilbenes

NP Classifier Biosynthetic pathway: Shikimates and Phenylpropanoids

NP Classifier Superclass: Stilbenoids

NP Classifier Class: Monomeric stilbenes

NP-Likeness score: 0.754

---

Chemical structure download