Pterostilbene
- CAS No.
- 537-42-8
- Chemical Name:
- Pterostilbene
- Synonyms
- pterostibene;hydroxystilbene;AKOS 236-80;PTEROSTILBENE;(Z)-3,4’-aminostilbene;(E/Z)-3,4’POVIDONE USP(RG);Pterostilbene>PTEROSTILBENE(FG)
- CBNumber:
- CB8373368
- Molecular Formula:
- C16H16O3
- Molecular Weight:
- 256.3
- MDL Number:
- MFCD00238710
- MOL File:
- 537-42-8.mol
- MSDS File:
- SDS
| Melting point | 89-92 ºC |
|---|---|
| Boiling point | 420.4±35.0 °C(Predicted) |
| Density | 1.169±0.06 g/cm3(Predicted) |
| storage temp. | 2-8°C |
| solubility | DMSO: >20mg/mL |
| pka | 9.96±0.26(Predicted) |
| form | solid |
| color | White or off-white |
| Odor | Characteristic |
| λmax | 321nm(MeOH)(lit.) |
| Stability | Stable for 2 years from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 1 week. |
| InChI | InChI=1S/C16H16O3/c1-18-15-9-13(10-16(11-15)19-2)4-3-12-5-7-14(17)8-6-12/h3-11,17H,1-2H3/b4-3+ |
| InChIKey | VLEUZFDZJKSGMX-ONEGZZNKSA-N |
| SMILES | C1(O)=CC=C(/C=C/C2=CC(OC)=CC(OC)=C2)C=C1 |
| LogP | 4.056 (est) |
| EWG's Food Scores | 1 |
| FDA UNII | 26R60S6A5I |
| NCI Drug Dictionary | pterostilbene |
| UNSPSC Code | 41116107 |
| NACRES | NA.77 |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |   GHS05,GHS09 |
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Signal word | Danger | |||||||||
| Hazard statements | H318-H411 | |||||||||
| Precautionary statements | P273-P280-P305+P351+P338-P391-P501 | |||||||||
| Hazard Codes | Xi,N | |||||||||
| Risk Statements | 41-51/53 | |||||||||
| Safety Statements | 26-39-61 | |||||||||
| RIDADR | 3077 | |||||||||
| WGK Germany | 3 | |||||||||
| HazardClass | IRRITANT | |||||||||
| PackingGroup | Ⅲ | |||||||||
| HS Code | 29095000 | |||||||||
| NFPA 704 |
|
Pterostilbene price More Price(37)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Sigma-Aldrich | P1499 | Pterostilbene ≥97% (HPLC), solid | 537-42-8 | 10mg | $308 | 2024-03-01 | Buy |
| Sigma-Aldrich | 523310 | Pterostilbene | 537-42-8 | 10mg | $259 | 2024-03-01 | Buy |
| TCI Chemical | P1924 | Pterostilbene >98.0%(HPLC) | 537-42-8 | 100mg | $16 | 2024-03-01 | Buy |
| TCI Chemical | P1924 | Pterostilbene >98.0%(HPLC) | 537-42-8 | 1g | $35 | 2024-03-01 | Buy |
| Cayman Chemical | 13000 | Pterostilbene ≥98% | 537-42-8 | 50mg | $58 | 2024-03-01 | Buy |
Pterostilbene Chemical Properties,Uses,Production
Description
Pterostilbene (PTS) is a fragrant-smelling hydrocarbon called "styrene", which is a derivative of resveratrol. It is found in blueberries and Pterocarpus marsupium (PM) heartwood. Similar to resveratrol, PTS has anti-inflammatory, anti-thrombotic, anti-cancer, anti-cancer, anti-hyperlipidemia and antibacterial effects.
Chemical Properties
Pterostilbene is a white crystalline powder, sensitive to air, soluble in hot methanol, DMSO, insoluble in water. It is a stilbenoid chemically similar to resveratrol and from the leguminous plant Pterocarpus indicus.
Occurrence
Pterostilbene is a natural molecule found in fruits, vegetables and nuts. Blueberries are often quoted as one of the richest sources of pterostilbene. It is also found in almonds,various Vaccinium berries (including blueberries), grape leaves and vines,and Pterocarpus marsupium heartwood.
Uses
Substantial studies demonstrate that pterostilbene has diverse pharmacological activities for the prevention and treatment of diseases including inflammation, cancer, diabetes, and dyslipidemia.
Pterostilbene has been used:
to investigate its anti-oxidative stress activities and the involvement of the nuclear factor (erythroid-derived 2)-like 2 (Nrf2)-antioxidant response element (ARE) signaling pathway
to determine its effects on transcriptional activation of estrogen receptor-α (ERα) in hormone resistant breast cancer cells)
Preparation
Pterostilbene was synthesized from 3,5-dimethoxybenzyl bromide and p-nitrobenzaldehyde by Witting-Hornor reaction, reduction, diazotization and hydrolysis, with a total yield of 53.9%.
Definition
ChEBI: Pterostilbene is a stilbenol that consists of trans-stilbene bearing a hydroxy group at position 4 as well as two methoxy substituents at positions 3' and 5'. It has a role as an antioxidant, an antineoplastic agent, a neurotransmitter, a plant metabolite, an apoptosis inducer, a neuroprotective agent, an anti-inflammatory agent, a radical scavenger and a hypoglycemic agent. It is a stilbenol, a member of methoxybenzenes and a diether. It derives from a hydride of a trans-stilbene.
benefits
Pterostilbene is a naturally-derived stilbenoid structurally related to resveratrol, with potential antioxidant, anti-inflammatory, pro-apoptotic, antineoplastic and cytoprotective activities. Pterostilbene is known to have many pharmacological benefits for the prevention and treatment of a wide variety of diseases, including ( cancer (McCormack and McFadden 2012), dyslipidaemia (Rimando et al. 2005), diabetes (Amarnath Satheesh and Pari 2006), cardiovascular degeneration (Amarnath Satheesh and Pari 2008) and pain (Hougee et al. 2005).
Biological Activity
A cell-permeable methoxylated analog of Resveratrol that displays antioxidant, anti-proliferative, and hypoglycemic properties. Appears to be a better free radical scavenger than Trolox. Moderately inhibits COX-1 & COX-2 activities (IC50 = 19.8 μM & 83.9 μM, respectively) and induces apoptosis in HL60 cells (IC50 = 70 μM). Also prevents DMBA-induced pre-neoplastic lesions (ED50 = 4.8 μM). Reported to decrease plasma glucose levels in streptozotocin-induced diabetic rats comparable to that of Metformin.
Side effects
The side effects of pterostilbene are relatively minor, but you still need to pay attention to the dosage. Low-dose pterostilbene supplementation improves cholesterol metabolism and reduces triglyceride levels. Side effects include mild weight loss and muscle pain, but dose adjustment is usually not necessary.
References
[1] ESTRELAJOSé M. Pterostilbene: Biomedical applications.[J]. Critical reviews in clinical laboratory sciences, 2013. DOI:10.3109/10408363.2013.805182.
[2] HYUNSOOK KIM Wallace Y Kun Ho Seo. Chemistry of Pterostilbene and Its Metabolic Effects[J]. Journal of Agricultural and Food Chemistry, 2020. DOI:10.1021/acs.jafc.0c00070.
[3] MACICKOVATATIANA. In vivo effect of pinosylvin and pterostilbene in the animal model of adjuvant arthritis.[J]. Neuro endocrinology letters, 2010.
[4] WASAMON NUTAKUL. Inhibitory Effects of Resveratrol and Pterostilbene on Human Colon Cancer Cells: A Side-by-Side Comparison[J]. Journal of Agricultural and Food Chemistry, 2011. DOI:10.1021/jf202846b.
Pterostilbene Preparation Products And Raw materials
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| Shaanxi Pioneer Biotech Co., Ltd . | +8613259417953 | sales@pioneerbiotech.com | China | 1287 | 58 |
| PNP Biotech Co. Ltd | +8618516098983 | sales@pnpbiotech.com | China | 1001 | 58 |
| Shaanxi Haibo Biotechnology Co., Ltd | +undefined18602966907 | qinhe02@xaltbio.com | China | 997 | 58 |
| Beri Pharma Co., Ltd. | +8613417710166 | sales@zhberi.com | China | 227 | 58 |
| Hengshui Haoye Co.,Ltd. | +86-2102300 +86-18632882519 | hy@haoyecom.cn | China | 307 | 58 |
| Hebei Shengyang Water Conservancy Engineering Co., Ltd. | +8615373025980 | clara@hbshengyang.com | China | 822 | 58 |
| GIHI CHEMICALS CO.,LIMITED | +8618058761490 | info@gihichemicals.com | China | 49984 | 58 |
| Hebei Chuanghai Biotechnology Co., Ltd | +8615531157085 | abby@chuanghaibio.com | China | 8808 | 58 |
| Hebei Chuanghai Biotechnology Co,.LTD | +86-13131129325 | sales1@chuanghaibio.com | China | 5868 | 58 |
| Henan Bao Enluo International TradeCo.，LTD | +86-17331933971 +86-17331933971 | deasea125996@gmail.com | China | 2472 | 58 |
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Related Qustion
- Q:Is pterostilbene better than resveratrol?
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View Lastest Price from Pterostilbene manufacturers
| Image | Update time | Product | Price | Min. Order | Purity | Supply Ability | Manufacturer | |
|---|---|---|---|---|---|---|---|---|
 |
2025-04-29 | Pterostibene
537-42-8
|
US $0.00 / KG | 2KG | 99% up | 20 tons | Sinoway Industrial co., ltd. | |
 |
2025-04-29 | Pterostilbene
537-42-8
|
US $40.00 / mg | 99.71% | 10g | TargetMol Chemicals Inc. | ||
 |
2025-04-29 | Pterostilbene
537-42-8
|
US $0.00-0.00 / kg | 1kg | 98% | 1000 | Changsha Staherb Natural Ingredients Co., Ltd. |
-
- Pterostibene
537-42-8
- US $0.00 / KG
- 99% up
- Sinoway Industrial co., ltd.
-
- Pterostilbene
537-42-8
- US $40.00 / mg
- 99.71%
- TargetMol Chemicals Inc.
-
- Pterostilbene
537-42-8
- US $0.00-0.00 / kg
- 98%
- Changsha Staherb Natural Ingredients Co., Ltd.