Highly potent binding and inverse agonist activity of bisphenol A derivatives for retinoid-related orphan nuclear receptor RORγ

Toxicology Letters

Volumn 212, Issue 2, 2012, Pages 205-211

  Nishigori, Mitsuhiro ^a   Nose, Takeru ^a   Shimohigashi, Yasuyuki ^a  

^a KYUSHU UNIVERSITY   (Japan)

Author keywords

Bisphenols; Endocrine disruptor; Nuclear receptor; ROR

Indexed keywords

2,2 BIS(3 SEC BUTYL 4 HYDROXYPHENYL)PROPANE; 2,2 BIS(4 HYDROXY 3 ISOPROPYLPHENYL)PROPANE; 4,4' ISOPROPYLIDENEDIPHENOL; BISPHENOL AF; DI ISOPROPYLBISPHENOL(DIISOPROPYL BISPHENOL A); DI SEC BUTYLBISPHENOL; HYDROXYL GROUP; RETINOID RELATED ORPHAN RECEPTOR ALPHA; RETINOID RELATED ORPHAN RECEPTOR BETA; RETINOID RELATED ORPHAN RECEPTOR GAMMA; UNCLASSIFIED DRUG;

ALKYLATION; ANIMAL CELL; ARTICLE; BINDING AFFINITY; BINDING ASSAY; CHEMICAL STRUCTURE; GENETIC ANALYSIS; HYDROPHOBICITY; IC 50; NONHUMAN; PRIORITY JOURNAL; RECEPTOR BINDING;

ANIMALS; CERCOPITHECUS AETHIOPS; COS CELLS; DRUG INVERSE AGONISM; NUCLEAR RECEPTOR SUBFAMILY 1, GROUP F, MEMBER 3; PHENOLS; TRITIUM;

EID: 84862289170     PISSN: 03784274     EISSN: 18793169     Source Type: Journal    
DOI: 10.1016/j.toxlet.2012.05.020     Document Type: Article

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