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Details

Stereochemistry ACHIRAL
Molecular Formula C15H14O3
Molecular Weight 242.2699
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of PINOSTILBENE

SMILES

COC1=CC(O)=CC(\C=C\C2=CC=C(O)C=C2)=C1

InChI

InChIKey=KUWZXOMQXYWKBS-NSCUHMNNSA-N
InChI=1S/C15H14O3/c1-18-15-9-12(8-14(17)10-15)3-2-11-4-6-13(16)7-5-11/h2-10,16-17H,1H3/b3-2+

HIDE SMILES / InChI

Molecular Formula C15H14O3
Molecular Weight 242.2699
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
594.0 µM [IC50]
Target ID: Alpha-glucosidase, Saccharomyces cerevisiae
PubMed

PubMed

TitleDatePubMed
Determination of pinostilbene in rat plasma by LC-MS/MS: Application to a pharmacokinetic study.
2016 Feb 20
Resveratrol and pinostilbene confer neuroprotection against aging-related deficits through an ERK1/2-dependent mechanism.
2018 Apr
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:30:07 GMT 2023
Edited
by admin
on Sat Dec 16 17:30:07 GMT 2023
Record UNII
4PAK325BEM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PINOSTILBENE
Common Name English
3-[2-(4-Hydroxyphenyl)ethenyl]-5-methoxyphenol
Systematic Name English
3-((1E)-2-(4-HYDROXYPHENYL)ETHENYL)-5-METHOXYPHENOL
Systematic Name English
PHENOL, 3-(2-(4-HYDROXYPHENYL)ETHENYL)-5-METHOXY-, (E)-
Systematic Name English
TRANS-PINOSTILBENE
Common Name English
PHENOL, 3-((1E)-2-(4-HYDROXYPHENYL)ETHENYL)-5-METHOXY-
Systematic Name English
PINOSTILBENE, TRANS-
Common Name English
Phenol, 3-[2-(4-hydroxyphenyl)ethenyl]-5-methoxy-
Systematic Name English
3,4-DIHYDROXY-5-METHOXY-TRANS-STILBENE
Systematic Name English
Code System Code Type Description
CAS
871504-87-9
Created by admin on Sat Dec 16 17:30:07 GMT 2023 , Edited by admin on Sat Dec 16 17:30:07 GMT 2023
NON-SPECIFIC STEREOCHEMISTRY
FDA UNII
4PAK325BEM
Created by admin on Sat Dec 16 17:30:07 GMT 2023 , Edited by admin on Sat Dec 16 17:30:07 GMT 2023
PRIMARY
CAS
42438-89-1
Created by admin on Sat Dec 16 17:30:07 GMT 2023 , Edited by admin on Sat Dec 16 17:30:07 GMT 2023
PRIMARY
EPA CompTox
DTXSID50420234
Created by admin on Sat Dec 16 17:30:07 GMT 2023 , Edited by admin on Sat Dec 16 17:30:07 GMT 2023
PRIMARY
WIKIPEDIA
Pinostilbene
Created by admin on Sat Dec 16 17:30:07 GMT 2023 , Edited by admin on Sat Dec 16 17:30:07 GMT 2023
PRIMARY
PUBCHEM
5473050
Created by admin on Sat Dec 16 17:30:07 GMT 2023 , Edited by admin on Sat Dec 16 17:30:07 GMT 2023
PRIMARY