Saquinavir, an HIV protease inhibitor, is transported by P-Glycoprotein

Journal of Pharmacology and Experimental Therapeutics

Volumn 286, Issue 3, 1998, Pages 1439-1445

  Kim, Annice E ^a   Dintaman, Jay M ^a   Waddell, David S ^a   Silverman, Jeffrey A ^a  

^a AvMax Inc   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOSPORIN; DOXORUBICIN; GLYCOPROTEIN P; MULTIDRUG RESISTANCE PROTEIN; PROTEINASE INHIBITOR; RHODAMINE 123; SAQUINAVIR; VERAPAMIL; VINBLASTINE; ZALCITABINE; ZIDOVUDINE; ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; RHODAMINE;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; CYTOTOXICITY; DRUG BLOOD LEVEL; DRUG STRUCTURE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HUMAN CELL; HUMAN IMMUNODEFICIENCY VIRUS INFECTION; IMMUNOBLOTTING; MORTALITY; MULTIDRUG RESISTANCE; NONHUMAN; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; PROTEIN TRANSPORT; VIRUS LOAD; ANIMAL; CELL STRAIN 3T3; CELL SURVIVAL; DRUG EFFECT; MOUSE; PHYSIOLOGY;

3T3 CELLS; ANIMALS; ANTI-HIV AGENTS; CELL SURVIVAL; CYCLOSPORINE; HIV PROTEASE INHIBITORS; MICE; P-GLYCOPROTEIN; RHODAMINE 123; RHODAMINES; SAQUINAVIR;

EID: 0032159263     PISSN: 00223565     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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