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Merck
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56297

Sigma-Aldrich

Pinosylvin

≥97.0% (HPLC)

Synonyme(s) :

(E)-3,5-Stilbenediol, (E)-5-(2-Phenylethenyl)-1,3-benzenediol, 5-Styrylresorcinol, trans-3,5-Dihydroxystilbene, Pinosylvine

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About This Item

Formule empirique (notation de Hill) :
C14H12O2
Numéro CAS:
22139-77-1
Poids moléculaire :
212.24
Beilstein:
1870942
Numéro MDL:
MFCD00210544
Code UNSPSC :
41116107
ID de substance PubChem :
329758200
Nomenclature NACRES :
NA.25

Niveau de qualité

100

Essai

≥97.0% (HPLC)

Forme

solid

Conditions de stockage

protect from light

Pf

153-157 °C

Conditions d'expédition

wet ice

Température de stockage

2-8°C

Chaîne SMILES 

Oc1cc(O)cc(\C=C\c2ccccc2)c1

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+

Clé InChI

YCVPRTHEGLPYPB-VOTSOKGWSA-N

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Application

Pinosylvin, a pre-infectious stilbenoid toxin, is used to study its properties as a fungitoxin and therapeutic agent. Pinosylvin is used as a representative stilbene to study its biological actions and therapeutic value in processes such as cell survival, apoptosis and cell mobility.

Conditionnement

Bottomless glass bottle. Contents are inside inserted fused cone.

Attention

sensitive to oxidation

Pictogrammes

Exclamation markEnvironment
GHS07,GHS09

Mention d'avertissement

Warning

Mentions de danger

H315,H319,H335,H400

Classification des risques

Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Faites votre choix parmi les versions les plus récentes :

Certificats d'analyse (COA)

Lot/Batch Number
BCCG9175
BCCF3980
BCCC9375
BCCC5171
BCBS1031V

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Consulter la Bibliothèque de documents

Kathryn A Roupe et al.
The Journal of pharmacy and pharmacology, 58(11), 1443-1450 (2006-11-30)
The pharmacokinetics of piceatannol, pinosylvin and rhapontigenin were characterized in male Sprague-Dawley rats after single intravenous doses of 10 mg kg(-1) of each stilbene. Serial blood samples were collected via a catheter inserted into the right jugular vein and plasma
Ferenc Billes et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 68(3), 669-679 (2007-04-10)
In this article the authors deal with the experimental and theoretical interpretation of the vibrational spectra of trans-resveratrol (3,5,4'-trihydroxy-trans-stilbene) of diverse beneficial biological activity. Infrared and Raman spectra of the compound were recorded; density functional calculations were carried out resulting
Eun-Jung Park et al.
The Journal of nutritional biochemistry, 23(8), 946-952 (2011-09-23)
Metastasis is a major cause of death in cancer patients. Our previous studies showed that pinosylvin, a naturally occurring trans-stilbenoid mainly found in Pinus species, exhibited a potential cancer chemopreventive activity and also inhibited the growth of various human cancer
S K Lee et al.
Fitoterapia, 76(2), 258-260 (2005-03-09)
The antibacterial and antifungal activities of pinosylvin (3,5-dihydroxy-trans-stilbene), a constituent of pine, were studied and compared with those of resveratrol (3,5,4'-trihydroxy-trans-stilbene). Pinosylvin exhibited more potent growth inhibitory activity against Candida albicans and Saccharomyces cerevisiae.
Eunsil Jeong et al.
Phytotherapy research : PTR, 27(4), 610-617 (2012-06-28)
Pinosylvin is a phenolic compound mainly found in the Pinus species. To determine the vascular functions of pinosylvin, we first examined both proliferation and apoptosis of bovine aortic endothelial cells (BAECs) in the presence of pinosylvin. When BAECs were treated
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