E3330 - ≥97% , DNA-(apurinic or apyrimidinic site) lyase inhibitor, CAS No.136164-66-4, DNA-(apurinic or apyrimidinic site) lyase inhibitor

CAS: 136164-66-4 Cat. No.: E413754 Fórmula: C21H30O6 Peso molecular: 378.46 Número CE: 693-030-4
Disponível para encomenda
GRAU & PUREZA ≥97%
Synonyms
E3330 | E-3330 | EX-A2212 | Undecanoic acid, 2-((4,5-dimethoxy-2-methyl-3,6-dioxo-1,4-cyclohexadien-1-yl)methylene)-, (E)- | (2E)-2-[(4,5-Dimethoxy-2-methyl-3,6-dioxo-1,4-cyclohexadien-1-yl)methylene]undecanoic acid | (2E)-2-[(4,5-Dimethoxy-2-methyl-3,6-d
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
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Tamanho
Alemanha (EU)
USA*
Preço
Qtd
5mg
E413754-5mg
—
4 Em stock
110,98€
25mg
E413754-25mg
—
2 Em stock
332,26€
50mg
E413754-50mg
—
1 Em stock
604,73€
100mg
E413754-100mg
—
1 Em stock
1057,69€
250mg
E413754-250mg
—
1 Em stock
1735,39€
Enter a quantity for the sizes you want to add.
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Por que este grau

≥97% para fluxos de trabalho cromatográficos e analíticos sensíveis que exigem interferência mínima da linha de base.

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Armazenamento e envio

Store at -20°C Envio Ice chest + Ice pads. Consulte o COA específico do lote para obter as especificações exatas.

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Documentos de qualidade

SDS, COA, ficha técnica e folha de especificações disponíveis para download. COA específico do lote acessível por meio de pesquisa por número de lote.

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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

Product Describtion:

E3330 (APX-3330) is a direct, orally active and selective inhibitor of Ape-1 (apurinic/apyrimidinic endonuclease 1)/Ref-1 (redox factor-1) redox. E3330 is able to impair tumor growth and blocks the activity of NF-κB, AP-1, and HIF-1α in pancreatic cancer. E3330 shows anticancer activities.


Information

E3330 E3330 (APX-3330) is a potent and selective APE1(Ref-1) inhibitor, which suppressed NF-kappa B DNA-binding activity.


Targets

NF-κB ; APE1(Ref-1)


In vitro

E3330 affects hemangioblast development in vitro via inhibition of Ape1 redox activity. E3330 inhibits the growth of human pancreatic cancer cell line PANC1, XPA1, MIAPACA, BxPC3, and PK9. E3330 also promotes exit of cell cycle in PANC1 cells, inhibits the DNA-Binding activity of HIF-1α and migration of pancreatic cancer cells. In JHH6 cells, E3330 prevents the functional activation of NF-κB via the alteration of APE1 subcellular trafficking and reduces IL-6 and IL-8 expression induced by TNF-α and FAs accumulation through blockage of the redox-mediated activation of NF-κB.


In vivo

In mice with endotoxin-mediated hepatitis, E3330 (300 mg/kg, p.o.) attenuates the elevation of plasma tumor necrosis factor activity and protectes mice from liver injury. In Rat model, E3330 (100 mg/kg, p.o.) also protectes rats from severe liver injury induced with endotoxin plus galactosamine.


Cell Research(from reference)

Cell lines:PANC1 cells 

Concentrations:~30 μM 

Incubation Time:72 hours 

Especificações

Sinónimos
E3330 | E-3330 | EX-A2212 | Undecanoic acid, 2-((4,5-dimethoxy-2-methyl-3,6-dioxo-1,4-cyclohexadien-1-yl)methylene)-, (E)- | (2E)-2-[(4,5-Dimethoxy-2-methyl-3,6-dioxo-1,4-cyclohexadien-1-yl)methylene]undecanoic acid | (2E)-2-[(4,5-Dimethoxy-2-methyl-3,6-d
Especificações e pureza
≥97%
Mecanismos bioquímicos e fisiológicos
E3330 (APX-3330) is a potent and selective APE1(Ref-1) inhibitor, which suppressed NF-kappa B DNA-binding activity.
Condições de armazenamento de armazenamento
Store at -20°C
Enviado em
Ice chest + Ice pads
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Tipo de ação
INHIBITOR
Mecanismo de ação
DNA-(apurinic or apyrimidinic site) lyase inhibitor
Pureza
≥97%
Propriedades do produto
ALogP
5.3
Nomes e identificadores
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504764185
Sorrisos canónicos
CCCCCCCCCC(=CC1=C(C(=O)C(=C(C1=O)OC)OC)C)C(=O)O
IUPAC Name
(2E)-2-[(4,5-dimethoxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl)methylidene]undecanoic acid
InChIKey
AALSSIXXBDPENJ-FYWRMAATSA-N
INCHI
1S/C21H30O6/c1-5-6-7-8-9-10-11-12-15(21(24)25)13-16-14(2)17(22)19(26-3)20(27-4)18(16)23/h13H,5-12H2,1-4H3,(H,24,25)/b15-13+
SMILES isoméricas
CCCCCCCCC/C(=C\C1=C(C(=O)C(=C(C1=O)OC)OC)C)/C(=O)O
Peso molecular
378.46
Reaxy-Rn
24609616
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=24609616&ln=

Documentação

📋 Ficha de dados de segurança (FDS)

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

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

✅ Certificado de análise (COA)

Dados de qualidade específicos do lote. Introduza o número de lote para obter o COA exato.

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📊 Ficha técnica

Resumo de referência rápida das especificações e aplicações do produto.

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🔬 Folha de especificações

Atributos de qualidade completos e critérios de aceitação para este grau.

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Dados avançados

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClassePrenol lipids
SubclassQuinone and hydroquinone lipids
Intermediate Tree Nodes Prenylquinones
Direct ParentUbiquinones
Alternative Parents P-benzoquinones  Medium-chain fatty acids  Methyl-branched fatty acids  Unsaturated fatty acids  Vinylogous esters  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic homomonocyclic compounds
Substituents Ubiquinone skeleton - P-benzoquinone - Quinone - Medium-chain fatty acid - Branched fatty acid - Methyl-branched fatty acid - Fatty acyl - Fatty acid - Unsaturated fatty acid - Vinylogous ester - Ketone - Cyclic ketone - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Carbonyl group - Organic oxygen compound - Aliphatic homomonocyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as ubiquinones. These are coenzyme Q derivatives containing a 5, 6-dimethoxy-3-methyl(1,4-benzoquinone) moiety to which an isoprenyl group is attached at ring position 2(or 6).
External Descriptors Not available
Estrutura 3D
Modelo de Estrutura Química Interativa





Alvos associados (humanos)
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Mecanismos de ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
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.

11 results found

Lot NumberCertificate TypeDataItem
G23121170G23121170Certificate of AnalysisJun 14, 2023 E413754
G23121173G23121173Certificate of AnalysisJun 14, 2023 E413754
G23121174G23121174Certificate of AnalysisJun 14, 2023 E413754
G23121176G23121176Certificate of AnalysisJun 14, 2023 E413754
G23121178G23121178Certificate of AnalysisJun 14, 2023 E413754
G23121200G23121200Certificate of AnalysisJun 14, 2023 E413754
G23121211G23121211Certificate of AnalysisJun 14, 2023 E413754
G23121212G23121212Certificate of AnalysisJun 14, 2023 E413754
G23121216G23121216Certificate of AnalysisJun 14, 2023 E413754
G23121222G23121222Certificate of AnalysisJun 14, 2023 E413754
H2504045H2504045Certificate of AnalysisJun 14, 2023 E413754
Propriedades químicas e físicas
SolubilidadeSolubility (25°C) In vitro DMSO: 100 mg/mL (264.22 mM); Ethanol: 75 mg/mL (198.17 mM); Water: Insoluble;
Peso molecular378.500 g/mol
XLogP35.300
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count6
Rotatable Bond Count12
Exact Mass378.204 Da
Monoisotopic Mass378.204 Da
Topological Polar Surface Area89.900 Ų
Heavy Atom Count27
Formal Charge0
Complexity666.000
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
Revisões

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