Pterostilbene - Moligand™, ≥97% , Agonist of Peroxisome proliferator-activated receptor-α, CAS No.537-42-8, Agonist of Peroxisome proliferator-activated receptor-α

Name: Pterostilbene - Moligand™, ≥97% , Agonist of Peroxisome proliferator-activated receptor-α, CAS No.537-42-8, Agonist of Peroxisome proliferator-activated receptor-α
SKU: P108000
Availability: InStock

CAS: 537-42-8 Cat. No.: P108000 Formule: C₁₆H₁₆O₃ Poids moléculaire: 256.3 Beilstein Registry Number: 6(4)7592 Numéro CE: 611-041-4

12 Citations COA

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Pterostilbene - Moligand™, ≥97% CAS No(537-42-8) by Aladdin Scientific

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DISPONIBLE À COMMANDE

GRADE & PURITY Moligand™ ? ≥97%

Synonyms

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Vue d’ensemble Specifications Noms et identifiants Documentation Advanced Data Taxonomic Classification Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques FAQ et articles Citations of This Product Calculateurs de solution Avis

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Why this grade

Moligand™, ≥97% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 12 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Vue d’ensemble

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.

Specifications

Synonymes

Spécifications et pureté

Moligand™, ≥97%

Mécanismes biochimiques et physiologiques

Antioxidant and antiapoptotic agent; analog of resveratrol . Antineoplastic properties in vitro and in vivo .

Conditions de stockage de stockage

Store at 2-8°C,Argon charged

Expédié en

Wet ice

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Grade

Moligand™

Type d'action

AGONIST

Mécanisme d'action

Agonist of Peroxisome proliferator-activated receptor-α

Note

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 -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.

Pureté

≥97%

Noms et identifiants

Pubchem Sid

508815782

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508815782

Sourires canoniques

COC1=CC(=CC(=C1)C=CC2=CC=C(C=C2)O)OC

IUPAC Name

4-[(E)-2-(3,5-dimethoxyphenyl)ethenyl]phenol

InChIKey

VLEUZFDZJKSGMX-ONEGZZNKSA-N

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+

Isomères SMILES

COC1=CC(=CC(=C1)/C=C/C2=CC=C(C=C2)O)OC

WGK Allemagne

CAS alternatif

537-42-8

Numéro NSC

613735

Termes d'entrée MeSH

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

Poids moléculaire

256.3

Beilstein

6(4)7592

Reaxy-Rn

2278888

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2278888&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Phenylpropanoids and polyketides
  - Classe Stilbenes

Kingdom	Organic compounds
Superclass	Phenylpropanoids and polyketides
Classe	Stilbenes
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Stilbenes
Alternative Parents	Dimethoxybenzenes Styrenes Phenoxy compounds Anisoles Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Stilbene - Dimethoxybenzene - M-dimethoxybenzene - Anisole - Phenol ether - Phenoxy compound - Styrene - Methoxybenzene - Phenol - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Benzenoid - Ether - Organooxygen compound - Organic oxygen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.
External Descriptors	Diphenyl ethers, biphenyls, dibenzyls and stilbenes
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Structure 3D

Cibles associées (humaines)

CYP1B1 Tchem Cytochrome P450 1B1 (2 Activities)

Discover Target: CYP1B1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

PTGS1 Tclin Prostaglandin G/H synthase 1 (1 Activities)

Discover Target: PTGS1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

PTGS2 Tclin Prostaglandin G/H synthase 2 (1 Activities)

Discover Target: PTGS2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

ALOX5 Tclin Arachidonate 5-lipoxygenase (1 Activities)

Discover Target: ALOX5

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CYP1A1 Tchem Cytochrome P450 1A1 (2 Activities)

Discover Target: CYP1A1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

GFER Tchem FAD-linked sulfhydryl oxidase ALR (1 Activities)

Discover Target: GFER

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

PPARA Tclin Peroxisome proliferator-activated receptor alpha (0 Activities)

Discover Target: PPARA

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

ALOX5 Tclin Arachidonate 5-lipoxygenase (6568 Activities)

Discover Target: ALOX5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP19A1 Tclin Cytochrome P450 19A1 (6099 Activities)

Discover Target: CYP19A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ACHE Tclin Acetylcholinesterase (18204 Activities)

Discover Target: ACHE

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

Discover Target: PTGS1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

Discover Target: PTGS2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP1B1 Tchem Cytochrome P450 1B1 (1148 Activities)

Discover Target: CYP1B1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NQO2 Tchem Quinone reductase 2 (885 Activities)

Discover Target: NQO2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TRPV1 Tclin Vanilloid receptor (8273 Activities)

Discover Target: TRPV1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GAA Tclin Lysosomal alpha-glucosidase (35701 Activities)

Discover Target: GAA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP1A1 Tchem Cytochrome P450 1A1 (1169 Activities)

Discover Target: CYP1A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)

Discover Target: GLP1R

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PLAU Tchem Urokinase-type plasminogen activator (2016 Activities)

Discover Target: PLAU

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

A-375 (9258 Activities)

Lot Number	Certificate Type	Date	Article
J2610792	Certificate of Analysis	Sep 22, 2026	P108000
J2610773	Certificate of Analysis	Sep 22, 2026	P108000
J2610772	Certificate of Analysis	Sep 22, 2026	P108000
J2610771	Certificate of Analysis	Sep 22, 2026	P108000
J22111370	Certificate of Analysis	Jul 03, 2026	P108000
J22111369	Certificate of Analysis	Jul 03, 2026	P108000
K2504530	Certificate of Analysis	Oct 20, 2025	P108000
K2504512	Certificate of Analysis	Oct 20, 2025	P108000
K2504511	Certificate of Analysis	Oct 20, 2025	P108000
K2504510	Certificate of Analysis	Oct 20, 2025	P108000
E2612026	Certificate of Analysis	Oct 20, 2025	P108000
C1813145	Certificate of Analysis	Oct 14, 2025	P108000
K2504531	Certificate of Analysis	Jul 13, 2024	P108000
D2017032	Certificate of Analysis	Feb 23, 2024	P108000
I2614160	Certificate of Analysis	Jan 15, 2024	P108000
A2419537	Certificate of Analysis	Jan 15, 2024	P108000
A2429350	Certificate of Analysis	Jan 15, 2024	P108000
A2419543	Certificate of Analysis	Jan 15, 2024	P108000
A2419541	Certificate of Analysis	Jan 15, 2024	P108000
A2419539	Certificate of Analysis	Jan 15, 2024	P108000
A2419538	Certificate of Analysis	Jan 15, 2024	P108000
K2309240	Certificate of Analysis	Nov 04, 2023	P108000
K2309241	Certificate of Analysis	Nov 04, 2023	P108000
D2312937	Certificate of Analysis	Jan 07, 2023	P108000
D2312936	Certificate of Analysis	Jan 07, 2023	P108000
D2312920	Certificate of Analysis	Jan 07, 2023	P108000
J22111366	Certificate of Analysis	Jul 22, 2022	P108000
J22111367	Certificate of Analysis	Jul 22, 2022	P108000
C2222602	Certificate of Analysis	Feb 14, 2022	P108000
C2222570	Certificate of Analysis	Feb 14, 2022	P108000
C2222568	Certificate of Analysis	Feb 14, 2022	P108000

Sensibilité	light sensitive；Air sensitive；heat sensitive
Point de fusion (°C)	88°C
Poids moléculaire	256.300 g/mol
XLogP3	3.800
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	4
Exact Mass	256.11 Da
Monoisotopic Mass	256.11 Da
Topological Polar Surface Area	38.700 Å²
Heavy Atom Count	19
Formal Charge	0
Complexity	270.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	1
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	1
Covalently-Bonded Unit Count	1

Pterostilbene - Moligand™, ≥97% , Agonist of Peroxisome proliferator-activated receptor-α, CAS No.537-42-8, Agonist of Peroxisome proliferator-activated receptor-α

Storage & shipping

Quality documents

Literature proof

Vue d’ensemble

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Avis des clients

📚 Citations by Application

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