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Volumn 54, Issue 7, 2014, Pages 800-808

Pharmacokinetic and pharmacodynamic drug-drug interaction assessment between pradigastat and digoxin or warfarin

Author keywords

digoxin; interaction; pharmacodynamics; pharmacokinetics; warfarin

Indexed keywords

CHYLOMICRON; CYTOCHROME P450 2C9; DIACYLGLYCEROL ACYLTRANSFERASE 1; DIGOXIN; PLASMA PROTEIN; PRADIGASTAT; TRIACYLGLYCEROL; WARFARIN; ACETIC ACID DERIVATIVE; AMINOPYRIDINE DERIVATIVE; ANTILIPEMIC AGENT; CARDIOTONIC AGENT; DGAT1 PROTEIN, HUMAN; DIACYLGLYCEROL ACYLTRANSFERASE; ENZYME INHIBITOR;

EID: 84902001376     PISSN: 00912700     EISSN: 15524604     Source Type: Journal    
DOI: 10.1002/jcph.285     Document Type: Article
Times cited : (18)

References (13)
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  • 3
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    • The DGAT1 inhibitor Pradigastat decreases chylomicron secretion and prevents postprandial triglyceride elevation in humans
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    • Meyers, C.D.1    Serran-Wu, M.2    Amer, A.3
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    • Lapham K, Bauman JN, Walsky RL, et al. Digoxin and tranilast identified as novel isoform-selective inhibitors of human UDP-glucuronosyltransferase 1A9 (UGT1A9) activity. Conference: 18th North American Regional ISSX Meeting Dallas, TX, United States. Conference Poster. Drug Metab Rev. 2012; 44 (S1): 82.
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    • Maddison, J.1    Somogyi, A.A.2    Jensen, B.P.3
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.