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

CAS: 475231-21-1 Cat. No.: H424135 Fórmula: C16H16O4 Peso molecular: 272.30
Disponível para encomenda
GRAU & PUREZA 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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Tamanho
Alemanha (EU)
USA*
Preço
Qtd
1ml
H424135-1ml
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2 Em stock

58,92€

69,33€
Gravar 10,41 € (15.02%)
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Por que este grau

10mM in DMSO para fluxos de trabalho cromatográficos e analíticos sensíveis que exigem interferência mínima da linha de base.

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Armazenamento e envio

Protected from light,Store at -80°C Envio Dry ice packs + Cold packs. Consulte o COA específico do lote para obter as especificações exatas.

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Comprovação documental

Citado em 0 publicações revisadas por pares nas áreas de cromatografia, síntese orgânica e reações de acoplamento cruzado.

Visão geral

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 

Especificações

Sinónimos
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-(
Especificações e pureza
10mM in DMSO
Mecanismos bioquímicos e fisiológicos
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,
Condições de armazenamento de armazenamento
Protected from light,Store at -80°C
Enviado em
Dry ice packs + Cold packs
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Nomes e identificadores
Pubchem Sid
Sorrisos canónicos
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+
SMILES isoméricas
COC1=CC(=CC(=C1)/C=C/C2=CC(=C(C=C2)O)O)OC
Peso molecular
272.30
Reaxy-Rn
52596319
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=52596319&ln=

Documentação

📋 Ficha de dados de segurança (FDS)

Documento abrangente sobre perigos, manuseamento, armazenamento e conformidade regulamentar.

<<<<<<< HEAD Baixar SDS → ======= Baixar SDS → >>>>>>> release248-p3

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Dados avançados

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
DescriçãoThis 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
Estrutura 3D
Modelo de Estrutura Química Interativa





Alvos associados (humanos)
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
Alvos associados (não humanos)
H9c2 (3506 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
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Analytical Chart:

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Lot NumberCertificate TypeDataItem
K2405601K2405601Certificate of AnalysisSep 20, 2026 H424135
Propriedades químicas e físicas
Sensibilidade light sensitive
Peso molecular272.290 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
Calculadoras de soluções
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