(Q33236675)

English

Novel compound 2-methyl-2H-pyrazole-3-carboxylic acid (2-methyl-4-o-tolylazo-phenyl)-amide (CH-223191) prevents 2,3,7,8-TCDD-induced toxicity by antagonizing the aryl hydrocarbon receptor

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Europe PubMed Central

PubMed publication ID

24 July 2017

Novel compound 2-methyl-2H-pyrazole-3-carboxylic acid (2-methyl-4-o-tolylazo-phenyl)-amide (CH-223191) prevents 2,3,7,8-TCDD-induced toxicity by antagonizing the aryl hydrocarbon receptor (English)

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Europe PubMed Central

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24 July 2017

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object named as

Sung Ho Ryu

10

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11

object named as

Pann-Ghill Suh

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24 July 2017

7

object named as

Taehoon G Lee

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24 July 2017

5

object named as

Kum Joo Shin

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24 July 2017

Myoung Sook Han

6

object named as

Myoung Sook Han

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24 July 2017

author name string

Sun-Hee Kim

1

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24 July 2017

Ellen C Henry

2

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24 July 2017

Dong-Kyu Kim

3

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24 July 2017

Yun-Hee Kim

4

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24 July 2017

Jong-Ku Kang

8

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24 July 2017

Thomas A Gasiewicz

9

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24 July 2017

publication date

15 March 2006

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24 July 2017

Molecular Pharmacology

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24 July 2017

69

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24 July 2017

6

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Europe PubMed Central

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24 July 2017

1871-1878

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24 July 2017

The aryl hydrocarbon receptor antagonist, 3'methoxy-4'nitroflavone, attenuates 2,3,7,8-tetrachlorodibenzo-p-dioxin-dependent regulation of growth factor signaling and apoptosis in the MCF-10A cell line.

1 reference

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3'-methoxy-4'-nitroflavone, a reported aryl hydrocarbon receptor antagonist, enhances Cyp1a1 transcription by a dioxin responsive element-dependent mechanism

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Synthesis and biological properties of new stilbene derivatives of resveratrol as new selective aryl hydrocarbon modulators.

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A critical review of the developmental toxicity and teratogenicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin: recent advances toward understanding the mechanism.

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Indole-3-carbinol and diindolylmethane as aryl hydrocarbon (Ah) receptor agonists and antagonists in T47D human breast cancer cells

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1 reference

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Resveratrol inhibits TCDD-induced expression of CYP1A1 and CYP1B1 and catechol estrogen-mediated oxidative DNA damage in cultured human mammary epithelial cells

1 reference

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The examination and quantitation of tissue cytosolic receptors for 2,3,7,8-tetrachlorodibenzo-p-dioxin using hydroxylapatite

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Analysis of structural requirements for Ah receptor antagonist activity: ellipticines, flavones, and related compounds

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Overexpression of cytochrome P450 1A1 and its novel spliced variant in ovarian cancer cells: alternative subcellular enzyme compartmentation may contribute to carcinogenesis.

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1 reference

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Substituted flavones as aryl hydrocarbon (Ah) receptor agonists and antagonists

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On the significance of the role of cellular stress response reactions in the toxic actions of dioxin

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Protein kinase Ctheta activity is involved in the 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced signal transduction pathway leading to apoptosis in L-MAT, a human lymphoblastic T-cell line.

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Does disruption of immune and endocrine systems by environmental toxins contribute to development of endometriosis?

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Mechanisms of TCDD-induced abnormalities and embryo lethality in white leghorn chickens

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Quercetin-induced lipid peroxidation and DNA damage in isolated rat-liver nuclei

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Protection of the Cyp1a2(-/-) null mouse against uroporphyria and hepatic injury following exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin

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Dioxin and cancer: a critical review

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Aryl-hydrocarbon receptor-deficient mice are resistant to 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced toxicity.

1 reference

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Why are glycoproteins modified by poly-N-acetyllactosamine glyco-conjugates?

1 reference

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Identifiers

10.1124/MOL.105.021832

1 reference

Europe PubMed Central

PubMed publication ID

24 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 July 2017

ResearchGate publication ID

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