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تروستیلبن

Structure via PubChem · Public domain (PubChem)

EntityQ2908011· pop 16· linked from 60 articles

تروستیلبن

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Also 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
Sources (4)

via Wikidata · CC0