3'-Hydroxypterostilbene - 10mM in DMSO , CAS No.475231-21-1

CAS: 475231-21-1 Cat. No.: H424135 Formule: C16H16O4 Poids moléculaire: 272.30
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ 10mM in DMSO
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 -80°C
Shipped In
Dry ice packs + Cold packs
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Taille
Allemagne (EU)
USA*
Prix
Qté
1ml
H424135-1ml
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58,92€

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Pourquoi cette qualité

10mM in DMSO pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

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Stockage & expédition

Protected from light,Store at -80°C Expédition Dry ice packs + Cold packs. Consultez le COA spécifique au lot pour les spécifications exactes.

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Documents qualité

SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

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Preuve documentaire

Cité dans 0 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

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 

Spécifications

Synonymes
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-(
Spécifications et pureté
10mM in DMSO
Mécanismes biochimiques et physiologiques
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,
Conditions de stockage de stockage
Protected from light,Store at -80°C
Expédié en
Dry ice packs + Cold packs
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Noms et identifiants
Pubchem Sid
Sourires canoniques
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+
Isomères SMILES
COC1=CC(=CC(=C1)/C=C/C2=CC(=C(C=C2)O)O)OC
Poids moléculaire
272.30
Reaxy-Rn
52596319
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=52596319&ln=

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

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📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

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🔬 Fiche de spécifications

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Données avancées

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
DescriptionThis 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
Structure 3D
Modèle de structure chimique interactif





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Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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Lot NumberCertificate TypeDateArticle
K2405601K2405601Certificate of AnalysisSep 20, 2026 H424135
Propriétés chimiques et physiques
Sensibilité light sensitive
Poids moléculaire272.290 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
Calculateurs de solution
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