Similar articles for PMID: 17939741

Year	Number of Results
1958	1
1961	1
1969	2
1978	2
1981	1
1984	2
1988	1
1989	1
1993	2
1994	3
1995	4
1996	2
1997	5
1998	3
1999	7
2000	1
2001	1
2003	3
2004	4
2005	10
2006	10
2007	21
2008	33
2009	25
2010	7
2011	4
2012	1
2013	2
2014	4
2015	4
2016	5
2017	1
2018	4
2019	4
2020	1
2021	1
2022	1
2024	0

1

Species-specific, P450- and sulfotransferase-mediated novel ring contraction of a naphthyridine-N-oxide compound in cynomolgus monkey.

Daniels JS, Espina R, Cao K, Yuan H, Lin J, Diamond S, Johnson B, Rodgers J, Prakash S, Unger S, Christ D, Miwa G, Gan LS, Mutlib A. Daniels JS, et al. Chem Res Toxicol. 2007 Nov;20(11):1709-17. doi: 10.1021/tx700170q. Epub 2007 Oct 17. Chem Res Toxicol. 2007. PMID: 17939741

2

Bioactivation of isothiazoles: minimizing the risk of potential toxicity in drug discovery.

Teffera Y, Choquette D, Liu J, Colletti AE, Hollis LS, Lin MH, Zhao Z. Teffera Y, et al. Chem Res Toxicol. 2010 Nov 15;23(11):1743-52. doi: 10.1021/tx100208k. Epub 2010 Sep 8. Chem Res Toxicol. 2010. PMID: 20825217

3

Preclinical pharmacokinetics and metabolism of 6-(4-(2,5-difluorophenyl)oxazol-5-yl)-3-isopropyl-[1,2,4]-triazolo[4,3-a]pyridine, a novel and selective p38alpha inhibitor: identification of an active metabolite in preclinical species and human liver microsomes.

Kalgutkar AS, Hatch HL, Kosea F, Nguyen HT, Choo EF, McClure KF, Taylor TJ, Henne KR, Kuperman AV, Dombroski MA, Letavic MA. Kalgutkar AS, et al. Biopharm Drug Dispos. 2006 Nov;27(8):371-86. doi: 10.1002/bdd.520. Biopharm Drug Dispos. 2006. PMID: 16944451

4

Metabolism of 5-isopropyl-6-(5-methyl-1,3,4-oxadiazol-2-yl)-N-(2-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)pyrrolo[2,1-f][1,2,4]triazin-4-amine (BMS-645737): identification of an unusual N-acetylglucosamine conjugate in the cynomolgus monkey.

Johnson BM, Kamath AV, Leet JE, Liu X, Bhide RS, Tejwani RW, Zhang Y, Qian L, Wei DD, Lombardo LJ, Shu YZ. Johnson BM, et al. Drug Metab Dispos. 2008 Dec;36(12):2475-83. doi: 10.1124/dmd.108.022624. Epub 2008 Sep 11. Drug Metab Dispos. 2008. PMID: 18787055

5

In vitro studies on the metabolic activation of the furanopyridine L-754,394, a highly potent and selective mechanism-based inhibitor of cytochrome P450 3A4.

Sahali-Sahly Y, Balani SK, Lin JH, Baillie TA. Sahali-Sahly Y, et al. Chem Res Toxicol. 1996 Sep;9(6):1007-12. doi: 10.1021/tx960060b. Chem Res Toxicol. 1996. PMID: 8870989

6

Metabolism of mofarotene in hepatocytes and liver microsomes from different species. Comparison with in vivo data and evaluation of the cytochrome P450 isoenzymes involved in human biotransformation.

Valles B, Schiller CD, Coassolo P, De Sousa G, Wyss R, Jaeck D, Viger-Chougnet A, Rahmani R. Valles B, et al. Drug Metab Dispos. 1995 Oct;23(10):1051-7. Drug Metab Dispos. 1995. PMID: 8654192

7

Comparisons of phase I and phase II in vitro hepatic enzyme activities of human, dog, rhesus monkey, and cynomolgus monkey.

Sharer JE, Shipley LA, Vandenbranden MR, Binkley SN, Wrighton SA. Sharer JE, et al. Drug Metab Dispos. 1995 Nov;23(11):1231-41. Drug Metab Dispos. 1995. PMID: 8591724

8

Preclinical pharmacokinetics of a novel HIV-1 attachment inhibitor BMS-378806 and prediction of its human pharmacokinetics.

Yang Z, Zadjura L, D'Arienzo C, Marino A, Santone K, Klunk L, Greene D, Lin PF, Colonno R, Wang T, Meanwell N, Hansel S. Yang Z, et al. Biopharm Drug Dispos. 2005 Dec;26(9):387-402. doi: 10.1002/bdd.471. Biopharm Drug Dispos. 2005. PMID: 16142720

9

Identification of the metabolites of the HIV-1 reverse transcriptase inhibitor delavirdine in monkeys.

Chang M, Sood VK, Kloosterman DA, Hauer MJ, Fagerness PE, Sanders PE, Vrbanac JJ. Chang M, et al. Drug Metab Dispos. 1997 Jul;25(7):814-27. Drug Metab Dispos. 1997. PMID: 9224776

10

Biotransformation of nevirapine, a non-nucleoside HIV-1 reverse transcriptase inhibitor, in mice, rats, rabbits, dogs, monkeys, and chimpanzees.

Riska PS, Joseph DP, Dinallo RM, Davidson WC, Keirns JJ, Hattox SE. Riska PS, et al. Drug Metab Dispos. 1999 Dec;27(12):1434-47. Drug Metab Dispos. 1999. PMID: 10570025

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