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Merck

SML0067

Sigma-Aldrich

IOX1

≥97% (HPLC)

Sinónimos:

5-Carboxy-8-hydroxyquinoline, 8-Hydroxy-5-quinolinecarboxylic acid

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5 MG
116,00 €
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About This Item

Fórmula empírica (notación de Hill):
C10H7NO3
Número de CAS:
Peso molecular:
189.17
Número MDL:
Código UNSPSC:
51111800
ID de la sustancia en PubChem:
NACRES:
NA.77

116,00 €


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Análisis

≥97% (HPLC)

formulario

powder

color

white to brown

solubilidad

DMSO: 10 mg/mL, clear

temp. de almacenamiento

2-8°C

cadena SMILES

OC(=O)c1ccc(O)c2ncccc12

InChI

1S/C10H7NO3/c12-8-4-3-7(10(13)14)6-2-1-5-11-9(6)8/h1-5,12H,(H,13,14)

Clave InChI

JGRPKOGHYBAVMW-UHFFFAOYSA-N

Aplicación

IOX1 has been used:
  • To eliminate viral latency in latent viruses in order to sensitize the viral infections to antiviral therapy.[1]
  • In histone lysine demethylase 4A (KDM4A) inhibition, to serve as a unique strategy to decrease hypoxia-inducible factors signalling.[2]
  • to restore oncogene-induced senescence in wild-type mouse embryo fibroblasts.[3]

Acciones bioquímicas o fisiológicas

IOX1 (5-Carboxy-8-hydroxyquinoline) is a broad spectrum inhibitor of 2-oxoglutarate (2OG) oxygenases, including Jumonji C domain (JmjC) demethylases. It is useful for the study of histone demethylation and hypoxic sensing and results in translocation of active site iron on the 2OG oxygenases. For full characterization details, please visit the IOX1 probe summary on the Structural Genomics Consortium (SGC) website.

To learn about other SGC chemical probes for epigenetic targets, visit sigma.com/sgc
IOX1 has an IC50 value as 200nM.[4] IOX1 might be used in the treatment of β-thalassemia by α-globin downregulation.[5]

Características y beneficios

IOX1 is an epigenetic chemical probe available through a partnership with the Structural Genomics Consortium (SGC). To learn more and view other SGC epigenetic probes, visit sigma.com/SGC.
This compound is a featured product for Gene Regulation research. Click here to discover more featured Gene Regulation products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

Producto relacionado

Referencia del producto
Descripción
Precios

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Acetylation of intragenic histones on HPV16 correlates with enhanced HPV16 gene expression
Johansson C, et al.
Virology, 482(3), 244-259 (2015)
Epigenetic Cancer Therapy, 453-453 (2015)
Wenyu Yu et al.
Analytical biochemistry, 463, 54-60 (2014-07-11)
Covalent modifications, such as methylation and demethylation of lysine residues in histones, play important roles in chromatin dynamics and the regulation of gene expression. The lysine demethylases (KDMs) catalyze the demethylation of lysine residues on histone tails and are associated
Selective silencing of alpha-globin by the histone demethylase inhibitor IOX1: a potentially new pathway for treatment of beta-thalassemia
Mettananda S, et al.
Haematologica, 102(3), e80-e84 (2017)
Tian Tian et al.
Experimental and therapeutic medicine, 21(3), 180-180 (2021-01-26)
The aim of the present study was to investigate the effect of the histone H3K9 demethylase inhibitor, IOX1, on the mechanism of hepatic fibrosis in TGF-β-induced human hepatic stellate LX-2 cells. Cellular proliferation, apoptosis, histone H3K9 dimethylation (H3K9me2), protein expression

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We offer a variety of small molecule research tools, such as transcription factor modulators, inhibitors of chromatin modifying enzymes, and agonists/antagonists for target identification and validation in gene regulation research; a selection of these research tools is shown below.

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