Pharmacokinetics and metabolism of UK-383,367 in rats and dogs: A rationale for long-lived plasma radioactivity

被引:14
作者
Allan, G. A. [1 ]
Gedge, J. I. [1 ]
Nedderman, A. N. R. [1 ]
Roffey, S. J. [1 ]
Small, H. F. [1 ]
Webster, R. [1 ]
机构
[1] Pfizer Global Res & Dev, Dept Pharmacokinet Dynam & Metab, Sandwich CT13 9NJ, Kent, England
关键词
oxadiazole cleavage; oxamide; unretained radioactivity; long-lived plasma radioactivity;
D O I
10.1080/00498250600618177
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
UK-383,367(5-{(1R)-4-cyclohexyl-1-[2-(hydroxyamino)-2-oxoethyl]butyl}-1,2,4-oxadiazole-3- carboxamide) is a novel procollagen C-proteinase inhibitor evaluated for the treatment of post-surgical dermal scarring. It is extensively metabolized in rat and dog absorption, distribution, metabolism and excretion studies, and a metabolic pathway for UK- 383,367 was determined. A long-lived metabolite was identified in dog plasma. Data indicate that this metabolite results from the oxadiazole ring-cleavage- producing oxamic acid, oxamide and oxalic acid. Ion exclusion chromatography was used to identify these polar metabolites, which were unretained on a standard reversed-phase high-performance liquid chromatography system. The oxamide metabolite was identified as the long-lived radioactivity, which was observed in dog plasma.
引用
收藏
页码:399 / 418
页数:20
相关论文
共 26 条
[1]   Comparative pharmacokinetics and metabolism of levetiracetam, a new anti-epileptic agent, in mouse, rat, rabbit and dog [J].
Benedetti, MS ;
Coupez, R ;
Whomsley, R ;
Nicolas, JM ;
Collart, P ;
Baltes, E .
XENOBIOTICA, 2004, 34 (03) :281-300
[2]   Functional characterization of two novel mammalian electrogenic proton-dependent amino acid cotransporters [J].
Boll, M ;
Foltz, MT ;
Rubio-Aliaga, I ;
Kottra, G ;
Daniel, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (25) :22966-22973
[3]   Molecular cloning of mouse amino acid transport system B0, a neutral amino acid transporter related to Hartnup disorder [J].
Bröer, A ;
Klingel, K ;
Kowalczuk, S ;
Rasko, JEJ ;
Cavanaugh, J ;
Bröer, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (23) :24467-24476
[4]   Identification of urinary metabolites of clemastine after oral administration to man [J].
Choi, MH ;
Jung, BH ;
Chung, BC .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1999, 51 (01) :53-59
[5]  
FISHBEIN WN, 1973, J PHARMACOL EXP THER, V186, P173
[6]   COMPARISON OF THE DISPOSITION OF 2 NOVEL COMBINED THROMBOXANE SYNTHASE INHIBITORS THROMBAXANE-A(2) RECEPTOR ANTAGONISTS IN THE ISOLATED-PERFUSED RAT-LIVER [J].
GARDNER, IB ;
WALKER, DK ;
LENNARD, MS ;
SMITH, DA ;
TUCKER, GT .
XENOBIOTICA, 1995, 25 (02) :185-197
[7]   Na+-independent transporters, LAT-2 and b0,+, exchange L-DOPA with neutral and basic amino acids in two clonal renal cell lines [J].
Gomes, P ;
Soares-Da-Silva, P .
JOURNAL OF MEMBRANE BIOLOGY, 2002, 186 (02) :63-80
[8]  
GYARMATI L, 1976, PHARMAZIE, V31, P246
[9]   HYDROLYSIS OF AN ORALLY ACTIVE PLATELET INHIBITORY PROSTANOID AMIDE IN THE PLASMA OF SEVERAL SPECIES [J].
HONOHAN, T ;
FITZPATRICK, FA ;
BOOTH, DG ;
MCGRATH, JP ;
MORTON, DR ;
NISHIZAWA, EE .
PROSTAGLANDINS, 1980, 19 (01) :123-136
[10]   A comprehensive listing of bioactivation pathways of organic functional groups [J].
Kalgutkar, AS ;
Gardner, I ;
Obach, RS ;
Shaffer, CL ;
Callegari, E ;
Henne, KR ;
Mutlib, AE ;
Dalvie, DK ;
Lee, JS ;
Nakai, Y ;
O'Donnell, JP ;
Boer, J ;
Harriman, SP .
CURRENT DRUG METABOLISM, 2005, 6 (03) :161-225