PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
12948398-2	2003	The high basal activity of mCAR can be modulated by inhibitory steroids related to androstenol and by activating xenobiotic chemicals such as 1,4-bis-[2-(3,5-dichloropyridyloxy)]benzene and chlorpromazine.	Androstenols	83-94	coxsackie virus and adenovirus receptor	Mus musculus	27-31	
14561088-2	2003	Uniquely among nuclear receptors, mouse CAR (mCAR) can be suppressed by androstenol and activated by structurally diverse drugs, pesticides, and environmental pollutants.	Androstenols	72-83	coxsackie virus and adenovirus receptor	Mus musculus	45-49	
14561088-6	2003	Analysis of chimeric and mutant mCAR constructs suggested that androstenol sensitivity is controlled by residues between amino acids 201-263 (helices 5-7) and it does not depend on the residue 350 within helix 12, as previously suggested.	Androstenols	63-74	coxsackie virus and adenovirus receptor	Mus musculus	32-36	
12869636-8	2003	Androstenol repressed the mCAR-mediated constitutive activation of the CYP2C19 promoter in HepG2 cells, whereas the potent mCAR ligand 1,4-bis[2-3,5-dichloropyridyloxyl)] benzene derepressed this response.	Androstenols	0-11	coxsackie virus and adenovirus receptor	Mus musculus	26-30