Literature DB >> 8868006

Plasma and urinary metabolites of efonidipine hydrochloride in man.

H Nakabeppu1, M Asada, T Oda, Y Shinozaki, T Yajima.   

Abstract

1. The plasma and urinary metabolite profiles of efonidipine hydrochloride, a new dihydropyridine calcium antagonist, have been examined in six healthy male volunteers after oral dosing. 2. Unchanged drug in plasma was determined by hplc-ms. Five metabolites in plasma and five metabolites and unchanged drug in urine were identified by hplc. 3. The main plasma metabolites were N-dephenylated-efonidipine and deaminated-efonidipine. 4. No significant amount of unchanged drug was excreted in urine. In the urine collected for 24 h after a oral dosing, 1.1% of the dose was excreted as deaminated-efonidipine, and 0.5% as a pyridine analogue of deaminated-efonidipine.

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Year:  1996        PMID: 8868006     DOI: 10.3109/00498259609046703

Source DB:  PubMed          Journal:  Xenobiotica        ISSN: 0049-8254            Impact factor:   1.908


  3 in total

1.  Effects of efonidipine on the pharmacokinetics and pharmacodynamics of repaglinide: possible role of CYP3A4 and P-glycoprotein inhibition by efonidipine.

Authors:  Cheng Li; Dong-Hyun Choi; Jun-Shik Choi
Journal:  J Pharmacokinet Pharmacodyn       Date:  2012-01-01       Impact factor: 2.745

2.  Structure-activity relationships and molecular modeling of 3, 5-diacyl-2,4-dialkylpyridine derivatives as selective A3 adenosine receptor antagonists.

Authors:  A H Li; S Moro; N Melman; X D Ji; K A Jacobson
Journal:  J Med Chem       Date:  1998-08-13       Impact factor: 7.446

3.  Effect of an L- and T-type calcium channel blocker on 24-hour systolic blood pressure and heart rate in hypertensive patients.

Authors:  Masae Komukai; Takeshi Tsutsumi; Mio Ebado; Youichi Takeyama
Journal:  Korean Circ J       Date:  2012-04-26       Impact factor: 3.243

  3 in total

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