PINOSYLVIN

Details

Stereochemistry	ACHIRAL
Molecular Formula	C14H12O2
Molecular Weight	212.2439
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	1
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

OC1=CC(\C=C\C2=CC=CC=C2)=CC(O)=C1

InChI

InChIKey=YCVPRTHEGLPYPB-VOTSOKGWSA-N

InChI=1S/C14H12O2/c15-13-8-12(9-14(16)10-13)7-6-11-4-2-1-3-5-11/h1-10,15-16H/b7-6+

HIDE SMILES / InChI

Molecular Formula	C14H12O2
Molecular Weight	212.2439
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	1
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
Suppression of Src/ERK and GSK-3/β-catenin signaling by pinosylvin inhibits the growth of human colorectal cancer cells.	2013-05	23333577
Interaction of stilbene compounds with human and rainbow trout estrogen receptors.	2008-02	18348622
Antibacterial and antifungal activity of pinosylvin, a constituent of pine.	2005-03	15752644

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:02:11 GMT 2025` Edited by `admin` on `Mon Mar 31 19:02:11 GMT 2025`
Record UNII	881R434AIB
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

PINOSYLVIN

Common Name

English

NSC-362430

Preferred Name

English

1,3-BENZENEDIOL, 5-(2-PHENYLETHENYL)-, (E)-

Common Name

English

1,3-BENZENEDIOL, 5-((1E)-2-PHENYLETHENYL)-

Systematic Name

English

PINOSYLVINE

Common Name

English

PINOSYLVIN [MI]

Common Name

English

3,5-DIHYDROXY-TRANS-STILBENE

Systematic Name

English

trans-pinosylvin

Common Name

English

3,5-STILBENEDIOL, (E)-

Systematic Name

English

TRANS-3,5-DIHYDROXYSTILBENE

Systematic Name

English

Code System Code Type Description

WIKIPEDIA

PINOSYLVIN