Pinosylvin - ≥97%(HPLC) , CAS No.22139-77-1

CAS: 22139-77-1 Cat. No.: P168709 Peso molecular: 212.24 Número EC: 683-184-0 PubChem CID: 5280457
Disponible para pedir
GRADE & PURITY ≥97%(HPLC)
Synonyms
5-(2-phenylethenyl)-1,3-benzenediol | Stilbene, 3,5-dihydroxy-, trans- | BCP18617 | Stilbene, 1f | 5-[(1E)-2-phenylethenyl]-1,3-benzenediol | PINOSYLVIN [MI] | Q7196412 | AS-76520 | DTXSID00895857 | 1,3-Benzenediol, 5-(2-phenylethenyl)-, (E)- | NSC 36243
Storage
Protected from light,Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5mg
P168709-5mg
3
35,90US$
10mg
P168709-10mg
3
49,90US$
25mg
P168709-25mg
3
83,90US$
50mg
P168709-50mg
2
122,90US$
100mg
P168709-100mg
1
179,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥97%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Store at -20°C,Argon charged Ships Ice chest + Ice pads 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.

📚

Literature proof

Cited in 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

application:

Pinosylvin, a pre-infectious stilbenoid toxin, is used to study its properties as a fungitoxin and therapeutic agent. Pinosylvin is used as a representative stilbene to study its biological actions and therapeutic value in processes such as cell survival, apoptosis and cell mobility.

Specifications

Sinónimos
5-(2-phenylethenyl)-1, 3-benzenediol | Stilbene, 3, 5-dihydroxy-, trans- | BCP18617 | Stilbene, 1f | 5-[(1E)-2-phenylethenyl]-1, 3-benzenediol | PINOSYLVIN [MI] | Q7196412 | AS-76520 | DTXSID00895857 | 1, 3-Benzenediol, 5-(2-phenylethenyl)-, (E)- | NSC 36243
Especificaciones y pureza
≥97%(HPLC)
Condiciones de almacenamiento de almacenamiento
Protected from light, Store at -20°C, Argon charged
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Tipo de acción
INHIBITOR
Pureza
≥97%(HPLC)
Nombres e identificadores
Pubchem Sid504763302
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504763302
Sonrisas canónicasC1=CC=C(C=C1)C=CC2=CC(=CC(=C2)O)O
IUPAC Name5-[(E)-2-phenylethenyl]benzene-1,3-diol
InChIKeyYCVPRTHEGLPYPB-VOTSOKGWSA-N
INCHI1S/C14H12O2/c15-13-8-12(9-14(16)10-13)7-6-11-4-2-1-3-5-11/h1-10,15-16H/b7-6+
Isómeros SMILES C1=CC=C(C=C1)/C=C/C2=CC(=CC(=C2)O)O
PubChem CID 5280457
Peso molecular 212.24

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

KingdomOrganic compounds
SuperclassPhenylpropanoids and polyketides
ClaseStilbenes
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentStilbenes
Alternative Parents Styrenes  Resorcinols  1-hydroxy-4-unsubstituted benzenoids  1-hydroxy-2-unsubstituted benzenoids  Organooxygen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Stilbene - Styrene - Resorcinol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Benzenoid - Monocyclic benzene moiety - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
LCK Tclin Tyrosine-protein kinase LCK (9212 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TRPV1 Tclin Vanilloid receptor (8273 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HL-60 (67320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Botrytis cinerea (4183 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RAW264.7 (28094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
J774 (3120 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
B16-F10 (4610 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nqo1 NAD(P)H dehydrogenase [quinone] 1 (1058 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trpa1 Transient receptor potential cation channel subfamily A member 1 (1003 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cladosporium herbarum (157 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Diaporthe ampelina (88 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

10 results found

Lot NumberCertificate TypeFechaArticulo
C2609591Certificate of AnalysisFeb 26, 2026 P168709
C2609592Certificate of AnalysisFeb 26, 2026 P168709
C2609601Certificate of AnalysisFeb 26, 2026 P168709
C2609602Certificate of AnalysisFeb 26, 2026 P168709
C2609603Certificate of AnalysisFeb 26, 2026 P168709
C2226581Certificate of AnalysisJan 14, 2025 P168709
C2226593Certificate of AnalysisJan 14, 2025 P168709
C2226642Certificate of AnalysisJan 14, 2025 P168709
C2226664Certificate of AnalysisJan 14, 2025 P168709
C2226665Certificate of AnalysisJan 14, 2025 P168709
Propiedades químicas y físicas
SolubilidadDMSO (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
Sensibilidadlight & air sensitive
Punto de inflamación (°C)154-155ºC
Peso molecular212.240 g/mol
XLogP33.500
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Exact Mass212.084 Da
Monoisotopic Mass212.084 Da
Topological Polar Surface Area40.500 Ų
Heavy Atom Count16
Formal Charge0
Complexity221.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Ming Su, Lei Ye, Yunbing Tang, Shaowei Wang, Zhiyan Hu, Huitao Li, Yiyan Wang, Xiaoheng Li, Yi Liu, Ren-Shan Ge.  (2023)  Inhibition of Resveratrol Analogs on Human and Rat 3β-Hydroxysteroid Dehydrogenases: Structure–Activity Relationship and Docking Analysis.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:37129992] [10.1021/acs.jafc.3c01919]
2. C. Hu, Y. Zhai, H. Lin, H. Lu, J. Zheng, C. Wen, X. Li, R.S. Ge, Y. Liu, Q. Zhu.  (2024)  Resveratrol analogues and metabolites selectively inhibit human and rat 11β-hydroxysteroid dehydrogenase 1 as the therapeutic drugs: structure–activity relationship and molecular dynamics analysis.  SAR AND QSAR IN ENVIRONMENTAL RESEARCH,      [PMID:39139138] [10.1080/1062936X.2024.2389817]
3. Yaxuan Yue, Jing Liu, Chen Li, Fengfeng Chen, Cheng Yang, Bingtian Zhao.  (2025)  Pinosylvin and Sanguinarine Combination to Enhance Antifungal Activity against Candida albicans.  JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY,      [PMID:40374536] [10.4014/jmb.2412.12055]
4. Wei Zhang, Xiangbing Wu, Wenming Li, Haifeng Zhang, Yijun Wang, Jing Xu, Wenhao Li, Yi Qin, Zebin Wu, Gaoran Ge, Shujun Lv, Lu Mao, Liangliang Wang, Dechun Geng.  (2025)  Pinosylvin Inhibits Inflammatory and Osteoclastogenesis via NLRP3 Inflammasome.  Advanced Science,      [PMID:40492417] [10.1002/advs.202501532]
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