Structure via PubChem · Public domain (PubChem)
تروستیلبن
Sign in to saveAlso known as 4-[(E)-2-(3,5-dimethoxyphenyl)vinyl]phenol, 3,5-dimethoxy-4'-hydroxy-trans-stilbene, trans-pterostilbene, (E)-1-hydroxy-4-(3,5-dimethoxy)styrylbenzene, (E)-4'-hydroxy-3,5-dimethoxystilbene, (E)-3',5'-dimethoxy-4-stilbenol, 3',5'-dimethoxy-4-stilbenol, 4-(2-(3,5-Dimethoxyphenyl)ethenyl)phenol
Pterostilbene () (trans-3,5-dimethoxy-4-hydroxystilbene) is a stilbenoid chemically related to resveratrol. In plants, it serves a defensive phytoalexin role.
Chemical data
- Formula
- C16H16O3
- Molecular weight
- 256.3 g/mol
- IUPAC name
- 4-[(E)-2-(3,5-dimethoxyphenyl)ethenyl]phenol
- SMILES
- COC1=CC(=CC(=C1)/C=C/C2=CC=C(C=C2)O)OC
- InChIKey
- VLEUZFDZJKSGMX-ONEGZZNKSA-N
- XLogP
- 3.8
- Polar surface area
- 38.7 Ų
- H-bond donors
- 1
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
- Indications
- endometrial carcinoma, Acute kidney injury
via ChEMBL · EBI
Wikidata facts
- Has part
- hydrogen
- Mass
- 256.11
Show 5 more facts
- found in taxon
- Vitis vinifera
- chemical formula
- C₁₆H₁₆O₃
- canonical SMILES
- COC1=CC(=CC(=C1)C=CC2=CC=C(C=C2)O)OC
- isomeric SMILES
- COC1=CC(=CC(=C1)/C=C/C2=CC=C(C=C2)O)OC
- subject has role
- phytoalexin
via Wikidata · CC0