Pterostilbene

Pterostilbene Struktur
537-42-8
CAS-Nr.
537-42-8
Englisch Name:
Pterostilbene
Synonyma:
pterostibene;hydroxystilbene;PTEROCARPUS MARSUPIUM;nootropic blueberry extract Pterostilbene;AKOS 236-80;PTEROSTILBENE;(Z)-3,4’-aminostilbene;(E/Z)-3,4’POVIDONE USP(RG)
CBNumber:
CB8373368
Summenformel:
C16H16O3
Molgewicht:
256.3
MOL-Datei:
537-42-8.mol

Pterostilbene Eigenschaften

Schmelzpunkt:
89-92 ºC
Siedepunkt:
420.4±35.0 °C(Predicted)
Dichte
1.169±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
Löslichkeit
DMSO: >20mg/mL
pka
9.96±0.26(Predicted)
Aggregatzustand
solid
Farbe
White or off-white
Geruch (Odor)
Characteristic
maximale Wellenlänge (λmax)
321nm(MeOH)(lit.)
Stabilität:
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.
Kosmetik-Inhaltsstoffe Funktionen
SKIN CONDITIONING
ANTIOXIDANT
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)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xi,N
R-Sätze: 41-51/53
S-Sätze: 26-39-61
RIDADR  3077
WGK Germany  3
HazardClass  IRRITANT
PackingGroup 
HS Code  29095000
Speicherklasse 11 - Combustible Solids
Hazard Classifications Aquatic Chronic 2
Eye Dam. 1
Bildanzeige (GHS) Corrosion (GHS05)Environment (GHS09)
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H318 Verursacht schwere Augenschäden. Schwere Augenschädigung Kategorie 1 Achtung P280, P305+P351+P338, P310
H411 Giftig für Wasserorganismen, mit langfristiger Wirkung. Langfristig (chronisch) gewässergefährdend Kategorie 2
Sicherheit
P273 Freisetzung in die Umwelt vermeiden.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach Möglichkeit entfernen. Weiter spülen.
P391 Verschüttete Mengen aufnehmen.
P501 Inhalt/Behälter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

Pterostilbene Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R41:Gefahr ernster Augenschäden.
R51/53:Giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.

S-Sätze Betriebsanweisung:

S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S39:Schutzbrille/Gesichtsschutz tragen.
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.

Beschreibung

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.

Chemische Eigenschaften

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.

Verwenden

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)

synthetische

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%.
synthesis of Pterostilbene

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).

Nebenwirkungen

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.

Pterostilbene Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Pterostilbene Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 667)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Shenzhen Varror Biotech Co., Ltd
+undefined+86-15817492830
sales@varror.com China 103 58
Shaanxi Pioneer Biotech Co., Ltd .
029-84385017; +8613259417953
sales@pioneerbiotech.com China 1286 58
GIHI CHEMICALS CO.,LIMITED
+86-571-86217390; +8618058761490
info@gihichemicals.com China 49859 58
Hebei Chuanghai Biotechnology Co,.LTD
+86-86-13131129325
sales1@chuanghaibio.com China 5216 58
Shaanxi TNJONE Pharmaceutical Co., Ltd

sarah@tnjone.com China 1139 58
BINBOBIO CO., LTD.
+8618629063126
info@binbobiological.com China 480 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21533 55
career henan chemical co
+86-0371-86658258
sales@coreychem.com China 29766 58
Zhejiang ZETian Fine Chemicals Co. LTD
18957127338
stella@zetchem.com China 2993 58
SHANDONG ZHI SHANG CHEMICAL CO.LTD
0531-68652808 18953170293
sales@sdzschem.com China 2921 58

537-42-8()Verwandte Suche:


  • AKOS 236-80
  • 3,5-DIMETHOXY-4'-HYDROXYSTILBENE
  • 3',5'-DIMETHOXY-4-STILBENOL
  • 4-[(1E)-2-(3,5-DIMETHOXYPHENYL)ETHENYL]PHENOL
  • PTEROSTILBENE
  • TRANS-3,5-DIMETHOXY-4'-HYDROXYSTILBENE
  • (E)-3,5-Dimethoxy-4'-hydroxystilbene
  • (E)-3',5'-Dimethoxystilbene-4-ol
  • 4-[(E)-2-(3,5-Dimethoxyphenyl)vinyl]phenol
  • 4-[(E)-3,5-Dimethoxystyryl]phenol
  • trans- Pterostilbene
  • Pterostilbene IN STOCK
  • Pterostilbene Factory
  • Pterostilbene COA
  • Pterostilbene, Pterocarpus marsupium - CAS 537-42-8 - Calbiochem
  • NanoLiposomal Pterostilbene
  • nootropic blueberry extract Pterostilbene powder
  • (Z)-3,4&rsquo
  • 5-Trimethoxy-3&rsquo
  • Pterostilbene CAS 537-42-8 Phenol,4-[(1E)-2-(3,5-diMethoxyphenyl)ethenyl]- 3,5-DiMethoxy-4'-hydroxy-trans-stilbene
  • Phenol,4-[(1E)-2-(3,5-diMethoxyphenyl)ethenyl]-
  • Pterostilbene 3',5'-Dimethoxy-4-stilbenol
  • 3,5-Dimethoxy-4'-hydroxy-trans-stilbene
  • 4-(2-(3,5-Dimethoxyphenyl)
  • 4-[2-(3,5-dimethoxyphenyl)ethenyl]phenol
  • 4-[2-(3,5-dimethoxyphenyl)vinyl]phenol
  • 4-Stilbenol, 3',5'-dimethoxy-, (E)-
  • Pterostilbene 99.8%
  • BioaActive Pterostilbene
  • Nanoactive Pterostilbene
  • Soluble Pterostilbene
  • (E/Z)-3,4&rsquo
  • -aminostilbene
  • -(tert-butyldimethylsilyloxy)stilbene
  • Liposomal PTEROSTILBENE, PTEROSTILBENE NanoEmulsion, NanoActive PTEROSTILBENE,Water/Oil-Soluble PTEROSTILBENE
  • hydroxystilbene
  • Phenol, 4-(2-(3,5-dimethoxyphenyl)ethenyl)-, (E)-
  • Pterostilbene, Pterocarpus marsupium
  • trans-3,5-Dimethoxy-4&prime
  • Pterostilbene, Pterocarpus marsupium
  • 4-[(1E)-2-(3,5-Dimethoxyphenyl)ethenyl]phenol, Pterocarpus marsupium
  • (E)-4-[2-(3,5-dimethoxyphenyl)ethenyl]-Phenol
  • -4-(3,5-Dimethoxystyryl)
  • phenol, 4-[(E)-2-(3,5-dimethoxyphenyl)ethenyl]-
  • POVIDONE USP(RG)
  • PTEROSTILBENE(FG)
  • PTEROSTILBENE(DS)
  • 4-(3,5-DiMethoxystyryl)phenol
  • 4'-Hydroxy-3,5-dimethoxy-trans-stilbene trans-1-(3,5-Dimethoxyphenyl)-2-(4-hydroxyphenyl)ethylene
  • 4'-Hydroxy-3,5-diMethoxystilbene
  • PTEROSTILBENE(FG)(REQUEST QUOTE)
  • Pterostilbene>
  • Pterostilbene powder
  • 4'-Hydroxy-3,5-dimethoxy-trans-stilbene
  • trans-1-(3,5-Dimethoxyphenyl)-2-(4-hydroxyphenyl)ethylene
  • Pterostilbene Powder CAS No 537-42-8 Pterostilbene 98%
  • 3,5-Dimethoxy-4-hydroxystilbene, 4-[(1E)-2-(3,5-Dimethoxyphenyl)ethenyl]phenol,
  • Pteris tatarinowii
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