3'-Hydroxypterostilbene - ≥99% , CAS No.475231-21-1

CAS: 475231-21-1 Cat. No.: H413079 Formula: C16H16O4 Peso molecolare: 272.30
Disponibile su ordine
QUALITÀ & PUREZZA ≥99%
Synonyms
HY-N6002 | SCHEMBL17534875 | 4-[(1E)-2-(3,5-Dimethoxyphenyl)vinyl]benzene-1,2-diol | AMY22524 | CCG-267181 | AKOS015915121 | 3?-Hydroxypterostilbene | 3'-Hydroxypterostilbene | trans-4-[2-(3,5-dimethoxyphenyl)ethenyl]-1,2-benzenediol | C15837 | 4-((e)-2-(
Storage
Protected from light,Store at -20°C
Shipped In
Ice chest + Ice pads
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Dimensione
Germania (EU)
USA*
Prezzo
Qtà
5mg
H413079-5mg
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3 Disponibile

24,21€

36,36€
Salva 12,15 € (33.41%)
25mg
H413079-25mg
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3 Disponibile

79,75€

119,66€
Salva 39,92 € (33.36%)
100mg
H413079-100mg
—
1 Disponibile

255,90€

384,32€
Salva 128,43 € (33.42%)
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Perché questa qualità

≥99% per flussi di lavoro cromatografici e analitici sensibili che richiedono un'interferenza minima della linea di base.

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Stoccaggio e spedizione

Protected from light,Store at -20°C Spedizione Ice chest + Ice pads. Consultare il COA specifico del lotto per le specifiche esatte.

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Prova documentale

Citato in 0 pubblicazioni peer-reviewed su cromatografia, sintesi organica e reazioni di accoppiamento incrociato.

Panoramica

Information

3'-Hydroxypterostilbene 3'-Hydroxypterostilbene (3'-HPT) is one of the active constituents of Sphaerophysa salsula and Pterocarpus marsupium which may be useful in treating different types of haematological malignancies. 3'-Hydroxypterostilbene, a natural pterostilbene analogue, effectively inhibits the growth of human colon cancer cells (IC50s of 9.0, 40.2, and 70.9 µM for COLO 205, HCT-116, and HT-29 cells, respectively) by inducing apoptosis and autophagy. 3'-Hydroxypterostilbene inhibits the PI3K/Akt/mTOR/p70S6K, and p38MAPK pathways and activates the ERK1/2, JNK1/2 MAPK pathways.


Targets

p70S6K ; p38MAPK


In vitro

3\'-Hydroxypterostilbene decreases cell growth in cultured human colon cancer cells (COLO 205, HCT-116, and HT-29) in a dose-dependent manner, with IC50 values of 9.0, 40.2, and 70.9 µM, respectively. 3\'-Hydroxypterostilbene effectively inhibits the growth of human colon cancer cells by inducing apoptosis and autophagy. Treatment with HPSB causes reduction of mitochondrial membrane potential and induction of caspase-3 and caspage-9, which is associated with the degradation of DFF-45 and PARP, precedes the onset of apoptosis. It significantly down-regulates phosphatidylinositol 3-kinase (PI3K)/Akt and mitogen-activated protein kinases (MAPKs) signalings including decreased the phosphorylation of mammalian target of rapamycin (mTOR).


In vivo

3\'-Hydroxypterostilbene by i.p. injection has anti-tumor efficacy gainst colon cancer through the inhibition of inflammation, metastasis, and angiogenesis as well as through the induction of apoptosis.


Cell Research(from reference)

Cell lines:COLO 205 cells 

Concentrations:5-100 µM 

Incubation Time:24 h 

Specifiche

Sinonimi
HY-N6002 | SCHEMBL17534875 | 4-[(1E)-2-(3,5-Dimethoxyphenyl)vinyl]benzene-1,2-diol | AMY22524 | CCG-267181 | AKOS015915121 | 3?-Hydroxypterostilbene | 3'-Hydroxypterostilbene | trans-4-[2-(3,5-dimethoxyphenyl)ethenyl]-1,2-benzenediol | C15837 | 4-((e)-2-(
Specifiche e purezza
≥99%
Meccanismi biochimici e fisiologici
3'-Hydroxypterostilbene (3'-HPT) is one of the active constituents of Sphaerophysa salsula and Pterocarpus marsupium which may be useful in treating different types of haematological malignancies. 3'-Hydroxypterostilbene, a natural pterostilbene analogue,
Condizioni di conservazione di stoccaggio
Protected from light,Store at -20°C
Spedito in
Ice chest + Ice pads
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Purezza
≥99%
Nomi e identificatori
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504765210
Sorrisi canonici
COC1=CC(=CC(=C1)C=CC2=CC(=C(C=C2)O)O)OC
IUPAC Name
4-[(E)-2-(3,5-dimethoxyphenyl)ethenyl]benzene-1,2-diol
InChIKey
UQRBFXIUUDJHSN-ONEGZZNKSA-N
INCHI
1S/C16H16O4/c1-19-13-7-12(8-14(10-13)20-2)4-3-11-5-6-15(17)16(18)9-11/h3-10,17-18H,1-2H3/b4-3+
Isomeri SMILES
COC1=CC(=CC(=C1)/C=C/C2=CC(=C(C=C2)O)O)OC
Peso molecolare
272.30
Reaxy-Rn
52596319
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=52596319&ln=

Documentazione

📋 Scheda di dati di sicurezza (SDS)

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Dati avanzati

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassPhenylpropanoids and polyketides
ClasseStilbenes
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentStilbenes
Alternative Parents Dimethoxybenzenes  Styrenes  Phenoxy compounds  Catechols  Anisoles  Alkyl aryl ethers  1-hydroxy-4-unsubstituted benzenoids  1-hydroxy-2-unsubstituted benzenoids  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Stilbene - M-dimethoxybenzene - Dimethoxybenzene - Phenoxy compound - Anisole - Methoxybenzene - Styrene - Phenol ether - Catechol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Phenol - Benzenoid - Monocyclic benzene moiety - Ether - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Aromatic homomonocyclic compound
DescrizioneThis 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 Not available
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
ALOX5 Tclin Arachidonate 5-lipoxygenase (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ALOX5 Tclin Arachidonate 5-lipoxygenase (6568 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Obiettivi associati (non umani)
H9c2 (3506 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
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Analytical Chart:

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6 results found

Lot NumberCertificate TypeDataOggetto
J2517580J2517580Certificate of AnalysisSep 23, 2025 H413079
J2517581J2517581Certificate of AnalysisSep 23, 2025 H413079
J2517582J2517582Certificate of AnalysisSep 23, 2025 H413079
J2214402J2214402Certificate of AnalysisJul 21, 2025 H413079
J2214403J2214403Certificate of AnalysisJul 21, 2025 H413079
J2214404J2214404Certificate of AnalysisJul 21, 2025 H413079
Proprietà chimiche e fisiche
SolubilitàSolubility (25°C) In vitro DMSO: 54 mg/mL (198.31 mM); Ethanol: 54 mg/mL (198.31 mM); Water: Insoluble;
Sensibilità light sensitive
Peso molecolare272.290 g/mol
XLogP33.500
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count4
Exact Mass272.105 Da
Monoisotopic Mass272.105 Da
Topological Polar Surface Area58.900 Ų
Heavy Atom Count20
Formal Charge0
Complexity306.000
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
Calcolatori di soluzioni
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