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Pterostilbene - 97%, high purity , CAS No.537-42-8, Agonist of Peroxisome proliferator-activated receptor-α

  • Moligand™
  • ≥97%
Item Number
P108000
Grouped product items
SKUSizeAvailabilityPrice Qty
P108000-1g
1g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$9.90
P108000-5g
5g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$24.90
P108000-25g
25g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$89.90
P108000-100g
100g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$249.90

Basic Description

SynonymsPterostilbene|537-42-8|trans-pterostilbene|4-(3,5-Dimethoxystyryl)phenol|(E)-4-(3,5-dimethoxystyryl)phenol|4-[(E)-2-(3,5-dimethoxyphenyl)ethenyl]phenol|18259-15-9|3',5'-Dimethoxy-4-stilbenol|pterostilbene, (E)-|4-[(E)-2-(3,5-dimethoxyphenyl)vinyl]phenol|3
Specifications & PurityMoligand™, ≥97%
Biochemical and Physiological MechanismsAntioxidant and antiapoptotic agent; analog of resveratrol . Antineoplastic properties in vitro and in vivo .
Storage TempStore at 2-8°C,Argon charged
Shipped InWet ice
GradeMoligand™
Action TypeAGONIST
Mechanism of actionAgonist of Peroxisome proliferator-activated receptor-α
NoteWherever 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 -20°C. Generally, these will be useable for up to one month. 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 visit our frequently asked questions (FAQ) page for more details.
Product Description

Pterostilbene (trans-3,5-dimethoxy-4-hydroxystilbene), an antioxidant is an analogue of resveratrol. It is present in blueberries, tree wood and some types of grapes.

Associated Targets

CYP1B1 Tchem Cytochrome P450 1B1 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GMNN Tbio Geminin 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RORC Tchem Nuclear receptor ROR-gamma 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ABCB1 Tchem Multidrug resistance protein 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KMT2A Tchem Histone-lysine N-methyltransferase 2A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HDAC6 Tclin Histone deacetylase 6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TRPV1 Tclin Transient receptor potential cation channel subfamily V member 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TRPA1 Tclin Transient receptor potential cation channel subfamily A member 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RAC1 Tbio Ras-related C3 botulinum toxin substrate 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PTGS1 Tclin Prostaglandin G/H synthase 1 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RAB9A Tbio Ras-related protein Rab-9A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PTGS2 Tclin Prostaglandin G/H synthase 2 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALOX5 Tclin Arachidonate 5-lipoxygenase 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GAA Tclin Lysosomal alpha-glucosidase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

BRCA1 Tchem Breast cancer type 1 susceptibility protein 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP19A1 Tclin Aromatase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP1A1 Tchem Cytochrome P450 1A1 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PLAU Tchem Urokinase-type plasminogen activator 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ACHE Tclin Acetylcholinesterase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ABL1 Tclin Tyrosine-protein kinase ABL1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GFER Tchem FAD-linked sulfhydryl oxidase ALR 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TARDBP Tchem TAR DNA-binding protein 43 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAPT Tclin Microtubule-associated protein tau 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GLP1R Tclin Glucagon-like peptide 1 receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PPARA Tclin Peroxisome proliferator-activated receptor alpha 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NQO2 Tchem Ribosyldihydronicotinamide dehydrogenase [quinone] 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NFE2L2 Tchem Nuclear factor erythroid 2-related factor 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KDM4E Tchem Lysine-specific demethylase 4E 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KEAP1 Tclin Kelch-like ECH-associated protein 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAPK1 Tchem Mitogen-activated protein kinase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NPC1 Tchem NPC intracellular cholesterol transporter 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NLRP3 Tchem NACHT, LRR and PYD domains-containing protein 3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 4-[(E)-2-(3,5-dimethoxyphenyl)ethenyl]phenol
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+
InChi Key VLEUZFDZJKSGMX-ONEGZZNKSA-N
Canonical SMILES COC1=CC(=CC(=C1)C=CC2=CC=C(C=C2)O)OC
Isomeric SMILES COC1=CC(=CC(=C1)/C=C/C2=CC=C(C=C2)O)OC
WGK Germany 3
Alternate CAS 537-42-8
PubChem CID 5281727
NSC Number 613735
MeSH Entry Terms 3',5'-dimethoxy-4E-stilbenol;3',5'-dimethoxy-4trans-stilbenol;3',5'-dimethoxy-resveratrol;3,5-dimethoxy-4'-hydroxy-trans-stilbene;4-((E)-2-(3,5-dimethoxyphenyl)ethenyl)phenol;4trans-(2-(3,5-dimethoxyphenyl)ethenyl)phenol;phenol, 4-((1E)-2-(3,5-dimethoxyph
Molecular Weight 256.3
Beilstein 6(4)7592
Reaxy-Rn 2054316

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

20 results found

Lot NumberCertificate TypeDateItem
D2017032Certificate of AnalysisFeb 23, 2024 P108000
A2419538Certificate of AnalysisJan 15, 2024 P108000
A2429350Certificate of AnalysisJan 15, 2024 P108000
A2419543Certificate of AnalysisJan 15, 2024 P108000
A2419541Certificate of AnalysisJan 15, 2024 P108000
A2419539Certificate of AnalysisJan 15, 2024 P108000
A2419537Certificate of AnalysisJan 15, 2024 P108000
K2309240Certificate of AnalysisNov 04, 2023 P108000
K2309241Certificate of AnalysisNov 04, 2023 P108000
D2312920Certificate of AnalysisJan 07, 2023 P108000
D2312936Certificate of AnalysisJan 07, 2023 P108000
D2312937Certificate of AnalysisJan 07, 2023 P108000
J22111366Certificate of AnalysisJul 22, 2022 P108000
J22111367Certificate of AnalysisJul 22, 2022 P108000
J22111369Certificate of AnalysisJul 22, 2022 P108000
J22111370Certificate of AnalysisJul 22, 2022 P108000
C2222568Certificate of AnalysisFeb 14, 2022 P108000
C2222570Certificate of AnalysisFeb 14, 2022 P108000
C2222602Certificate of AnalysisFeb 14, 2022 P108000
C1813145Certificate of AnalysisJan 25, 2022 P108000

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Chemical and Physical Properties

Sensitivitylight sensitive;Air sensitive;heat sensitive
Melt Point(°C)88°C

Safety and Hazards(GHS)

Pictogram(s) GHS09,   GHS05
Signal Danger
Hazard Statements

H411:Toxic to aquatic life with long lasting effects

H318:Causes serious eye damage

Precautionary Statements

P273:Avoid release to the environment.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P501:Dispose of contents/container to ...

P391:Collect spillage.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P305+P354+P338:IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing.

P317:Get emergency medical help.

WGK Germany 3
Reaxy-Rn 2054316

Related Documents

Solution Calculators