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Pinosylvin
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Product Name Pinosylvin
Price: $288 / 20mg
CAS No.: 22139-77-1
Catalog No.: CFN98203
Molecular Formula: C14H12O2
Molecular Weight: 212.3 g/mol
Purity: >=98%
Type of Compound: Phenols
Physical Desc.: Powder
Source: The herbs of Pinus yunnanensis
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF    Manual
Similar structural: Comparison (Web)  (SDF)
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Size /Price /Stock 10 mM * 1 mL in DMSO / $64.5 / In-stock
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: Pinosylvin is likely to act as a pro-angiogenic factor, it has anti-inflammatory activity, it may be utilized as a phytotherapic agent for the prevention of cardiovascular inflammatory diseases. Pinosylvin is an effective inhibitor of neutrophil activity, and is potentially useful as a complementary medicine in states associated with persistent inflammation. Pinosylvin has protection against oxidative stress through the induction of HO-1 in human RPE cells. Pinosylvin has inhibition against White-Rot and Brown-Rot Fungi.
Targets: AMPK | HO-1 | Caspase | MMP(e.g.TIMP) | COX | ERK | Akt | NOS | NO | IL Receptor | PKC | Antifection | Autophagy
In vitro:
Can J Physiol Pharmacol. 2014 Dec;92(12):993-9.
Pinosylvin at a high concentration induces AMPK-mediated autophagy for preventing necrosis in bovine aortic endothelial cells.[Pubmed: 25393712 ]
Pinosylvin is a known functional compound of the Pinus species. Pinosylvin at low concentrations (∼ pmol/L) was reported to promote cell proliferation in endothelial cells. However, this study found that Pinosylvin at a high concentration (100 μmol/L) induces cell death in bovine aortic endothelial cells. Therefore, we examined how Pinosylvin was associated with apoptosis, autophagy, and necrosis.
METHODS AND RESULTS:
Pinosylvin at a high concentration appeared to promote caspase-3 activation, nuclear condensation, and the "flip-flop" of phosphatidylserine, indicating that Pinosylvin induces apoptosis. However, based on flow cytometry data obtained from double-staining with annexin V and propidium iodide, Pinosylvin was shown to inhibit necrosis, a postapoptotic process. Pinosylvin induced LC3 conversion from LC3-I to LC3-II and p62 degradation, which are important indicators of autophagy. In addition, AMP-activated protein kinase (AMPK) appeared to be activated by Pinosylvin, and an AMPK inhibitor was markedly shown to reduce the LC3 conversion. The inhibitory effect of an AMPK inhibitor was reversed by Pinosylvin.
CONCLUSIONS:
These results suggest that Pinosylvin induces autophagy via AMPK activation. Further, necrosis was found to be promoted by an autophagy inhibitor and then restored by Pinosylvin, while the caspase-3 inhibitor had no effect on necrosis. These findings indicate that Pinosylvin-induced autophagy blocks necrotic progress in endothelial cells.
J Nutr Biochem. 2012 Aug;23(8):946-52.
Antimetastatic activity of pinosylvin, a natural stilbenoid, is associated with the suppression of matrix metalloproteinases.[Pubmed: 21937212 ]
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 cell lines via the regulation of cell cycle progression.
METHODS AND RESULTS:
In this study, we further evaluated the potential antimetastatic activity of Pinosylvin in in vitro and in vivo models. Pinosylvin suppressed the expression of matrix metalloproteinase (MMP)-2, MMP-9 and membrane type 1-MMP in cultured human fibrosarcoma HT1080 cells. We also found that Pinosylvin inhibited the migration of HT1080 cells in colony dispersion and wound healing assay systems. In in vivo spontaneous pulmonary metastasis model employing intravenously injected CT26 mouse colon cancer cells in Balb/c mice, Pinosylvin (10 mg/kg body weight, intraperitoneal administration) significantly inhibited the formation of tumor nodules and tumor weight in lung tissues. The analysis of tumor in lung tissues indicated that the antimetastatic effect of Pinosylvin coincided with the down-regulation of MMP-9 and cyclooxygenase-2 expression, and phosphorylation of ERK1/2 and Akt.
CONCLUSIONS:
These data suggest that Pinosylvin might be an effective inhibitor of tumor cell metastasis via modulation of MMPs.
Holzforschung, 1999, 53(5):491-7.
Efficacy of Pinosylvins against White-Rot and Brown-Rot Fungi.[Reference: WebLink]

METHODS AND RESULTS:
Three stilbenes, Pinosylvin (PS), Pinosylvin monomethyl ether (PSM) and Pinosylvin dimethyl ether (PSD), were extracted from white spruce (Picea glauca), jack pine (Pinus banksiana), and red pine (Pinus resinosa) pine cones, and their structures were confirmed by spectroscopic and chromatographic (HPLC, GC/MS, NMR and FTIR) analysis, PS, PSM, PSD or a 1:1:1 mixture of these stilbenes at concentrations of 0.1% and 1.0% were examined for their fungal inhibitory activity by two bioassay methods. Growth of white-tot fungi (Trametes versicolor and Phanerochaete chrysosporium), and brown-rot fungi (Neolentinus lepideus, Gloeophyllum trabeum and Postia placenta) on agar media in the presence of each of the stilbenes or a 1:1:1 mixture inhibited growth of white-rot fungi, but slightly stimulated growth of brown-rot fungi. Soil-block assays. conditions more representative of those found in nature did not correlate with those from the screening on agar media.
CONCLUSIONS:
PS, PSM, PSD or a 1:1:1 mixture of the three compound\ at concentrations of 0.1 % and 1.0% did not impart any significant decay resistance to white-rot fungi inoculated on a hardwood (Red maple). However under the same conditions, decay reststance was observed against brown-rot fungi on a softwood (Southern yellow pine). It appears that stilbenes at least partially contribute to wood decay resistance against brown-rot fungi.
In vivo:
J Agric Food Chem. 2015 Apr 8;63(13):3445-53.
Pinosylvin and Monomethylpinosylvin, Constituents of an Extract from the Knot of Pinus sylvestris, Reduce Inflammatory Gene Expression and Inflammatory Responses in Vivo.[Pubmed: 25763469]
Scots pine (Pinus sylvestris) is known to be rich in phenolic compounds, which may have anti-inflammatory properties.
METHODS AND RESULTS:
The present study investigated the anti-inflammatory effects of a knot extract from P. sylvestris and two stilbenes, Pinosylvin and monomethylPinosylvin, isolated from the extract. Inflammation is characterized by increased release of pro-inflammatory and regulatory mediators including nitric oxide (NO) produced by the inducible nitric oxide synthase (iNOS) pathway. The knot extract (EC50 values of 3 and 3 μg/mL) as well as two of its constituents, Pinosylvin (EC50 values of 13 and 15 μM) and monomethylPinosylvin (EC50 values of 8 and 12 μM), reduced NO production and iNOS expression in activated macrophages. They also inhibited the production of inflammatory cytokines IL-6 and MCP-1. More importantly, Pinosylvin and monomethylPinosylvin exerted a clear anti-inflammatory effect (80% inhibition at the dose of 100 mg/kg) in the standard in vivo model, carrageenan-induced paw inflammation in the mouse, with the effect being comparable to that of a known iNOS inhibitor L-NIL.
CONCLUSIONS:
The results reveal that the Scots pine stilbenes Pinosylvin and monomethylPinosylvin are potential anti-inflammatory compounds.
Pinosylvin Description
Source: The herbs of Pinus yunnanensis
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12.
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Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.7103 mL 23.5516 mL 47.1032 mL 94.2063 mL 117.7579 mL
5 mM 0.9421 mL 4.7103 mL 9.4206 mL 18.8413 mL 23.5516 mL
10 mM 0.471 mL 2.3552 mL 4.7103 mL 9.4206 mL 11.7758 mL
50 mM 0.0942 mL 0.471 mL 0.9421 mL 1.8841 mL 2.3552 mL
100 mM 0.0471 mL 0.2355 mL 0.471 mL 0.9421 mL 1.1776 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Kinase Assay:
Phytother Res. 2013 Apr;27(4):610-7.
Pinosylvin induces cell survival, migration and anti-adhesiveness of endothelial cells via nitric oxide production.[Pubmed: 22736379]
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.
METHODS AND RESULTS:
When BAECs were treated with Pinosylvin, etoposide- or starvation-induced apoptosis was shown to be significantly reduced. The anti-apoptotic effect of Pinosylvin was mediated by inhibition of caspase-3. Moreover, Pinosylvin was shown to activate endothelial nitric oxide synthetase (eNOS). At 1 pM, Pinosylvin appeared to have a cell-proliferative effect in the endothelial cell. The Pinosylvin-induced cell proliferation was declined by treatment with L-NAME, an eNOS inhibitor. Then, we found that Pinosylvin had a stimulatory effect on cell migration and tube formation. These stimulatory effects suggest that Pinosylvin is likely to act as a pro-angiogenic factor. Yet another effect of Pinosylvin was inhibition of lipopolysaccharide-induced THP-1 cell adhesion to endothelial cells.
CONCLUSIONS:
Altogether, we propose that Pinosylvin may be utilized as a phytotherapic agent for the prevention of cardiovascular inflammatory diseases.
Animal Research:
Acta Pharmacol Sin. 2012 Oct;33(10):1285-92.
The natural stilbenoid pinosylvin and activated neutrophils: effects on oxidative burst, protein kinase C, apoptosis and efficiency in adjuvant arthritis.[Pubmed: 22842731 ]
To investigate the effects of the naturally occurring stilbenoid Pinosylvin on neutrophil activity in vitro and in experimental arthritis, and to examine whether protein kinase C (PKC) activation served as an assumed target of Pinosylvin action.
METHODS AND RESULTS:
Fresh human blood neutrophils were isolated. The oxidative burst of neutrophils was evaluated on the basis of enhanced chemiluminescence. Neutrophil viability was evaluated with flow cytometry, and PKC phosphorylation was assessed by Western blotting analysis. Adjuvant arthritis was induced in Lewis rats with heat-killed Mycobacterium butyricum, and the animals were administered with Pinosylvin (30 mg/kg, po) daily for 21 d after arthritis induction. In isolated human neutrophils, Pinosylvin (10 and 100 μmol/L) significantly decreased the formation of oxidants, both extra- and intracellularly, and effectively inhibited PKC activation stimulated by phorbol myristate acetate (0.05 μmol/L). The inhibition was not due to neutrophil damage or increased apoptosis. In arthritic rats, the number of neutrophils in blood was dramatically increased, and whole blood chemiluminescence (spontaneous and PMA-stimulated) was markedly enhanced. Pinosylvin administration decreased the number of neutrophils (from 69 671 ± 5588/μL to 51 293 ± 3947/μL, P=0.0198) and significantly reduced the amount of reactive oxygen species in blood.
CONCLUSIONS:
Pinosylvin is an effective inhibitor of neutrophil activity, and is potentially useful as a complementary medicine in states associated with persistent inflammation.
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