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Volumn 1236, Issue 1, 1995, Pages 31-38
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Molecular mechanism for the relative binding affinity to the intestinal peptide carrier. Comparison of three ACE-inhibitors: enalapril, enalaprilat, and lisinopril
a
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Author keywords
Computational chemistry; Intestinal transport Peptide transporter; Structure transport relation
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Indexed keywords
CEFALEXIN;
DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR;
ENALAPRIL;
ENALAPRILAT;
LISINOPRIL;
TUMOR PROTEIN;
ANIMAL TISSUE;
ARTICLE;
COMPUTER SIMULATION;
CONTROLLED STUDY;
DRUG PROTEIN BINDING;
DRUG TRANSPORT;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
INTESTINE;
MALE;
MATHEMATICS;
NONHUMAN;
PRIORITY JOURNAL;
PROTEIN STRUCTURE;
RAT;
STRUCTURE ACTIVITY RELATION;
ULTRAVIOLET SPECTROPHOTOMETRY;
ANGIOTENSIN-CONVERTING ENZYME INHIBITORS;
ANIMAL;
BIOLOGICAL TRANSPORT, ACTIVE;
CARRIER PROTEINS;
CEPHALEXIN;
COMPARATIVE STUDY;
ENALAPRIL;
ENALAPRILAT;
INTESTINES;
LISINOPRIL;
MALE;
RATS;
RATS, WISTAR;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 0029013867
PISSN: 00052736
EISSN: None
Source Type: Journal
DOI: 10.1016/0005-2736(95)00030-7 Document Type: Article |
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Times cited : (82)
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References (29)
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