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Dokumente

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Sigma-Aldrich

Pinosylvin

≥97.0% (HPLC)

Synonym(e):

(E)-3,5-Stilbendiol, (E)-5-(2-Phenylethenyl)-1,3-benzoldiol, 5-Styrylresorcin, trans-3,5-Dihydroxy-stilben

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About This Item

Empirische Formel (Hill-System):
C14H12O2
CAS-Nummer:
22139-77-1
Molekulargewicht:
212.24
Beilstein:
1870942
MDL-Nummer:
MFCD00210544
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329758200
NACRES:
NA.25

Assay

≥97.0% (HPLC)

Form

solid

Lagerbedingungen

protect from light

mp (Schmelzpunkt)

153-157 °C

Versandbedingung

wet ice

Lagertemp.

2-8°C

SMILES String

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+

InChIKey

YCVPRTHEGLPYPB-VOTSOKGWSA-N

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Anwendung

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.

Verpackung

Bottomless glass bottle. Contents are inside inserted fused cone.

Vorsicht

sensitive to oxidation

Piktogramme

Exclamation markEnvironment
GHS07,GHS09

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Analysenzertifikate (COA)

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José Manuel López-Nicolás et al.
Journal of agricultural and food chemistry, 57(21), 10175-10180 (2009-10-10)
The complexation of pinosylvin, a potent antimicrobial and antifungal stilbenoid, by cyclodextrins (CDs) is described for first time in this work. Steady-state fluorescence was used to demonstrate that natural (alpha-, beta-, and gamma-CD) and modified (HP-beta-CD, methyl-beta-CD, and ethyl-beta-CD) CDs
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
Andrea Ganthaler et al.
Plant molecular biology, 94(3), 229-251 (2017-02-13)
Accumulation of phenolic needle metabolites in Norway spruce is regulated by many genes with small and additive effects and is correlated with the susceptibility against fungal attack. Norway spruce accumulates high foliar concentrations of secondary phenolic metabolites, with important functions
Mirka Laavola et al.
Molecules (Basel, Switzerland), 24(1) (2019-01-02)
Interleukin-6 (IL-6) is involved in the pathogenesis of various inflammatory diseases, like rheumatoid arthritis (RA). In the present study, we investigated the role of IL-6 in osteoarthritis (OA) patients and the effects of the stilbenoids monomethyl pinosylvin and pinosylvin on
Takao Koeduka et al.
Journal of bioscience and bioengineering, 127(5), 539-543 (2018-11-26)
Resveratrol and its methyl ethers, which belong to a class of natural polyphenol stilbenes, play important roles as biologically active compounds in plant defense as well as in human health. Although the biosynthetic pathway of resveratrol has been fully elucidated
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