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Journal Abstract Search

757 related items for PubMed ID: 8894513

  • 21. Interaction with indinavir to enhance systemic exposure of an investigational HIV protease inhibitor in rats, dogs and monkeys.
    Jin L, Chen IW, Chiba M, Lin JH.
    Xenobiotica; 2003 Jun; 33(6):643-54. PubMed ID: 12851040
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  • 22. Preclinical assessment of the absorption, distribution, metabolism and excretion of GDC-0449 (2-chloro-N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-(methylsulfonyl)benzamide), an orally bioavailable systemic Hedgehog signalling pathway inhibitor.
    Wong H, Chen JZ, Chou B, Halladay JS, Kenny JR, La H, Marsters JC, Plise E, Rudewicz PJ, Robarge K, Shin Y, Wong S, Zhang C, Khojasteh SC.
    Xenobiotica; 2009 Nov; 39(11):850-61. PubMed ID: 19845436
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  • 23. Disposition of the dipeptidyl peptidase 4 inhibitor sitagliptin in rats and dogs.
    Beconi MG, Reed JR, Teffera Y, Xia YQ, Kochansky CJ, Liu DQ, Xu S, Elmore CS, Ciccotto S, Hora DF, Stearns RA, Vincent SH.
    Drug Metab Dispos; 2007 Apr; 35(4):525-32. PubMed ID: 17220241
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  • 25. Pharmacokinetics and interactions of a novel antagonist of chemokine receptor 5 (CCR5) with ritonavir in rats and monkeys: role of CYP3A and P-glycoprotein.
    Kumar S, Kwei GY, Poon GK, Iliff SA, Wang Y, Chen Q, Franklin RB, Didolkar V, Wang RW, Yamazaki M, Chiu SH, Lin JH, Pearson PG, Baillie TA.
    J Pharmacol Exp Ther; 2003 Mar; 304(3):1161-71. PubMed ID: 12604693
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  • 27. NTP technical report on the toxicity and metabolism studies of chloral hydrate (CAS No. 302-17-0). Administered by gavage to F344/N rats and B6C3F1 mice.
    Beland FA.
    Toxic Rep Ser; 1999 Aug; (59):1-66, A1-E7. PubMed ID: 11803702
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  • 30. Pharmacokinetic properties of TDP4815 after single intravenous and oral administrations to rat, rabbit, monkey, dog and in vitro drug metabolism.
    Chen Y, Cheng D, Tio C, Kagan N, Eisennagel S, Dasgupta M, Tomczuk B, Bone R, Huebert N.
    Biopharm Drug Dispos; 2008 Apr; 29(3):127-38. PubMed ID: 18186144
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  • 32. Orally active inhibitors of human leukocyte elastase. II. Disposition of L-694,458 in rats and rhesus monkeys.
    Vincent SH, Painter SK, Luffer-Atlas D, Karanam BV, McGowan E, Cioffe C, Doss G, Chiu SH.
    Drug Metab Dispos; 1997 Aug; 25(8):932-9. PubMed ID: 9280401
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  • 34. Metabolism distribution and excretion of a matrix metalloproteinase-13 inhibitor, 4-[4-(4-fluorophenoxy)-benzenesulfonylamino]tetrahydropyran-4-carboxylic acid hydroxyamide (CP-544439), in rats and dogs: assessment of the metabolic profile of CP-544439 in plasma and urine of humans.
    Dalvie D, Cosker T, Boyden T, Zhou S, Schroeder C, Potchoiba MJ.
    Drug Metab Dispos; 2008 Sep; 36(9):1869-83. PubMed ID: 18566038
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  • 36. Disposition of remoxipride in different species. Species differences in metabolism.
    Widman M, Nilsson LB, Bryske B, Lundström J.
    Arzneimittelforschung; 1993 Mar; 43(3):287-97. PubMed ID: 8489555
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  • 38. Stereoselective metabolism of felodipine in liver microsomes from rat, dog, and human.
    Eriksson UG, Lundahl J, Bäärnhielm C, Regårdh CG.
    Drug Metab Dispos; 1991 Mar; 19(5):889-94. PubMed ID: 1686232
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