Intestinal absorption of acyclovir β-glucoside: Comparative study with acyclovir, guanosine, and kinetin β-glucoside

Pharmaceutical Research

Volumn 16, Issue 1, 1999, Pages 69-73

  Mizuma, Takashi ^a   Masubuchi, Satoshi ^a   Awazu, Shoji ^a  

^a TOKYO UNIVERSITY OF PHARMACY AND LIFE SCIENCES   (Japan)

Author keywords

glucoside; Acyclovir; Conformation; Intestinal absorption; Oil water partition; SGLT1

Indexed keywords

ACICLOVIR 9 [(2 HYDROXYETHOXY)METHYL]GUANINE; ACICLOVIR DERIVATIVE; ANTIVIRUS AGENT; CELLOBIOSE; CELLULASE; GLUCOSIDE; KINETIN; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ARTICLE; DRUG ABSORPTION; DRUG STABILITY; DRUG STRUCTURE; DRUG TRANSPORT; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; INTESTINE ABSORPTION; MALE; NONHUMAN; PARTITION COEFFICIENT; PRIORITY JOURNAL; RAT; SMALL INTESTINE;

ACYCLOVIR; ADENINE; ANIMALS; BIOLOGICAL TRANSPORT; GLUCOSE; GLUCOSIDES; GUANOSINE; INTESTINAL ABSORPTION; INTESTINE, SMALL; KINETIN; MAGNETIC RESONANCE SPECTROSCOPY; MALE; MEMBRANE GLYCOPROTEINS; MOLECULAR STRUCTURE; MONOSACCHARIDE TRANSPORT PROTEINS; OILS; RATS; RATS, WISTAR; SODIUM; SODIUM-GLUCOSE TRANSPORTER 1; WATER;

EID: 0032939194     PISSN: 07248741     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1018818728393     Document Type: Article

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