In vitro inhibition of OATP-mediated uptake of phalloidin using bile acid derivatives

Toxicology and Applied Pharmacology

Volumn 239, Issue 1, 2009, Pages 13-20

  Herraez, Elisa ^a   Macias, Rocio I R ^a   Vazquez Tato, Jose ^b   Vicens, Marta ^a   Monte, Maria J ^a   Marin, Jose J G ^a  

^a UNIVERSITY OF SALAMANCA   (Spain)

^b University of Santiago de Compastela   (Spain)

Author keywords

Amanita; Bioavailability; Hepatoprotection; Mushroom; Transport

Indexed keywords

BALU 1; BALU 2; BALU 3; BALU 4; BILE ACID; ORGANIC ANION TRANSPORTER; ORGANIC ANION TRANSPORTER 2; ORGANIC ANION TRANSPORTING POLYPEPTIDE 1A4; ORGANIC ANION TRANSPORTING POLYPEPTIDE 1B2; ORGANIC ANION TRANSPORTING POLYPEPTIDE 1B3; PEPTIDE DERIVATIVE; PHALLOIDIN; SODIUM; TAUROCHOLIC ACID; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CONTROLLED STUDY; DRUG MECHANISM; DRUG STRUCTURE; FEMALE; IN VITRO STUDY; KINETICS; NONHUMAN; OOCYTE; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN STABILITY;

ANIMALS; BILE ACIDS AND SALTS; BINDING, COMPETITIVE; BIOLOGICAL TRANSPORT; CHO CELLS; CRICETINAE; CRICETULUS; FEMALE; HUMANS; MUSHROOM POISONING; OOCYTES; ORGANIC ANION TRANSPORTERS; PHALLOIDINE; RATS; TAUROCHOLIC ACID; TRANSFECTION; XENOPUS LAEVIS;

AMANITA; BASIDIOMYCOTA; RATTUS; XENOPUS LAEVIS;

EID: 67650688077     PISSN: 0041008X     EISSN: 10960333     Source Type: Journal    
DOI: 10.1016/j.taap.2009.04.024     Document Type: Article

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