-
1
-
-
0033800945
-
Rapid assessment of drug metabolism in the drug discovery process
-
Bertrand, M.; Jackson, P.; Walther, B. (2000). Rapid assessment of drug metabolism in the drug discovery process. Europ. J. of Pharm. Sci., 11 (suppl. 2), S61-S72.
-
(2000)
Europ. J. of Pharm. Sci.
, vol.11
, Issue.SUPPL. 2
-
-
Bertrand, M.1
Jackson, P.2
Walther, B.3
-
2
-
-
0034890106
-
Optimization of metabolic stability as a goal of modern drug design
-
Thompson, T. N. (2001). Optimization of metabolic stability as a goal of modern drug design. Med. Res. Rev., 21(5), 412-449.
-
(2001)
Med. Res. Rev.
, vol.21
, Issue.5
, pp. 412-449
-
-
Thompson, T.N.1
-
3
-
-
0035523337
-
Metabolism profiling, and cytochrome P450 inhibition & induction in drug discovery
-
Yan, Z.; Caldwell, G.W. (2001). Metabolism profiling, and cytochrome P450 inhibition & induction in drug discovery. Curr. Top. Med. Chem., 1(5), 403-425.
-
(2001)
Curr. Top. Med. Chem.
, vol.1
, Issue.5
, pp. 403-425
-
-
Yan, Z.1
Caldwell, G.W.2
-
4
-
-
0034770465
-
Human drug metabolism and the cytochromes P450: Application and relevance of in vitro models
-
Venkatakrishnan, K.; Von Moltke, L. L.; Greenblatt, D. J. (2001). Human drug metabolism and the cytochromes P450: application and relevance of in vitro models. J. of Clin. Pharmaco, 41(11), 1149-1179.
-
(2001)
J. of Clin. Pharmaco
, vol.41
, Issue.11
, pp. 1149-1179
-
-
Venkatakrishnan, K.1
Von Moltke, L.L.2
Greenblatt, D.J.3
-
5
-
-
0036890353
-
Complexities ofglucuronidation affecting in vitro-in vivo extrapolation
-
Lin, J. H.; Wong, B. K. (2002). Complexities ofglucuronidation affecting in vitro-in vivo extrapolation. Curr. Drug Met., 3(6), 623-646.
-
(2002)
Curr. Drug Met.
, vol.3
, Issue.6
, pp. 623-646
-
-
Lin, J.H.1
Wong, B.K.2
-
6
-
-
0035149349
-
Use of cloned and expressed human UDP-glucuronosyltransferases for the assessment of human drug conjugation and identification of potential drug interactions
-
Ethell, B.T.; Beaumont, K.; Rance, D.J.; Burchell, B. (2001). Use of cloned and expressed human UDP-glucuronosyltransferases for the assessment of human drug conjugation and identification of potential drug interactions. Drug Metab. Dispos., 29(1), 48-53.
-
(2001)
Drug Metab. Dispos.
, vol.29
, Issue.1
, pp. 48-53
-
-
Ethell, B.T.1
Beaumont, K.2
Rance, D.J.3
Burchell, B.4
-
7
-
-
0026699309
-
Topological disposition of UDP-glucuronyltransferase in rat liver microsomes
-
Yokota, H.; Yuasa, A.; Sato, R. (1992). Topological disposition of UDP-glucuronyltransferase in rat liver microsomes. J. of Biochem, 112(2), 192-196.
-
(1992)
J. of Biochem.
, vol.112
, Issue.2
, pp. 192-196
-
-
Yokota, H.1
Yuasa, A.2
Sato, R.3
-
8
-
-
0032147023
-
Determinants of UDP-glucuronosyltransferase membrane association and residency in the endoplasmic reticulum
-
Meech, R.; Mackenzie, P. I. (1998). Determinants of UDP-glucuronosyltransferase membrane association and residency in the endoplasmic reticulum. Arch. of Biochem. Biophy, 356(1), 77-85.
-
(1998)
Arch. of Biochem. Biophy.
, vol.356
, Issue.1
, pp. 77-85
-
-
Meech, R.1
Mackenzie, P.I.2
-
9
-
-
0031974584
-
A universal radiochemical high-performance liquid chromatographic assay for the determination of UDP-glucuronosyltransferase activity
-
Ethell, B.T.; Anderson, G.D.; Beaumont, K.; Rance, D.J.; Burchell, B. (1998). A universal radiochemical high-performance liquid chromatographic assay for the determination of UDP-glucuronosyltransferase activity. Anal. Biochem, 255(1), 142-147.
-
(1998)
Anal. Biochem.
, vol.255
, Issue.1
, pp. 142-147
-
-
Ethell, B.T.1
Anderson, G.D.2
Beaumont, K.3
Rance, D.J.4
Burchell, B.5
-
10
-
-
0028223564
-
Evidence for the intraluminal positioning of p-nitrophenol UDP-glucuronosyltransferase activity in rat liver microsomal vesicles
-
Fulceri R; Banhegyi G; Gamberucci A; Giunti R; Mandl J; Benedetti A. (1994). Evidence for the intraluminal positioning of p-nitrophenol UDP-glucuronosyltransferase activity in rat liver microsomal vesicles. Arch. of Biochem. Biophy, 309(1), 43-46.
-
(1994)
Arch. of Biochem. Biophy.
, vol.309
, Issue.1
, pp. 43-46
-
-
Fulceri, R.1
Banhegyi, G.2
Gamberucci, A.3
Giunti, R.4
Mandl, J.5
Benedetti, A.6
-
11
-
-
0031808472
-
Glucuronidation of 3′-azido-3′-deoxythymidine (zidovadine) by human liver microsomes: Relevance to clinical pharmacokinetic interactions with atovaquone, fluconazole, methadone, and valproic acid
-
Trapnell, C. B.; Klecker, R. W.; Jamis-Dow, C.; Collins, J. M. (1998). Glucuronidation of 3′-azido-3′-deoxythymidine (zidovadine) by human liver microsomes: Relevance to clinical pharmacokinetic interactions with atovaquone, fluconazole, methadone, and valproic acid. Antimicrobial Agents Chemother, 42(7), 1592-1596.
-
(1998)
Antimicrobial Agents Chemother.
, vol.42
, Issue.7
, pp. 1592-1596
-
-
Trapnell, C.B.1
Klecker, R.W.2
Jamis-Dow, C.3
Collins, J.M.4
-
12
-
-
0034009448
-
In vitro glucuronidation using human liver microsomes and the pore-forming peptide alamethicin
-
Fisher, M. B.; Campanale, K.; Ackermann, B. L.; Vandenbranden, M.; Wrighton, S. A. (2000). In vitro glucuronidation using human liver microsomes and the pore-forming peptide alamethicin. Drug Metab. Dispos., 28(5), 560-566.
-
(2000)
Drug Metab. Dispos.
, vol.28
, Issue.5
, pp. 560-566
-
-
Fisher, M.B.1
Campanale, K.2
Ackermann, B.L.3
Vandenbranden, M.4
Wrighton, S.A.5
-
13
-
-
0036850028
-
In vitro identification of metabolic pathways and cytochrome P450 enzymes involved in the metabolism of etoperidone
-
Yan, Z.; Caldwell, G. W.; Wu, W. N.; McKown, L. A.; Rafferty, B.; Jones, W.; Masucci, J. A. (2002). In vitro identification of metabolic pathways and cytochrome P450 enzymes involved in the metabolism of etoperidone. Xenobiotica, 32(11), 949-962.
-
(2002)
Xenobiotica
, vol.32
, Issue.11
, pp. 949-962
-
-
Yan, Z.1
Caldwell, G.W.2
Wu, W.N.3
McKown, L.A.4
Rafferty, B.5
Jones, W.6
Masucci, J.A.7
-
14
-
-
0036893593
-
Evaluation of cytochrome P450 probe substrates commonly used by the pharmaceutical industry to study in vitro drug interactions
-
Yuan, R.; Madani, S.; Wei, X. X.; Reynolds, K.; Huang, S. M. (2002). Evaluation of cytochrome P450 probe substrates commonly used by the pharmaceutical industry to study in vitro drug interactions. Drug Metab. Dispos., 30(12), 1311-1319.
-
(2002)
Drug Metab. Dispos.
, vol.30
, Issue.12
, pp. 1311-1319
-
-
Yuan, R.1
Madani, S.2
Wei, X.X.3
Reynolds, K.4
Huang, S.M.5
-
15
-
-
0026649268
-
The metabolism of tramadol by human liver microsomes
-
Paar, W. D.; Frankus, P.; Dengler, H. J. (1992). The metabolism of tramadol by human liver microsomes. Clin. Investig., 70(8), 708-710.
-
(1992)
Clin. Investig.
, vol.70
, Issue.8
, pp. 708-710
-
-
Paar, W.D.1
Frankus, P.2
Dengler, H.J.3
-
16
-
-
0036276786
-
Metabolism of the analgesic drug ULTRAM (tramadol hydrochloride) in humans: API-MS and MS/MS characterization of metabolites
-
Wu, W. N.; McKown, L. A.; Liao, S. (2002). Metabolism of the analgesic drug ULTRAM (tramadol hydrochloride) in humans: API-MS and MS/MS characterization of metabolites. Xenobiotica, 32(5), 411-425.
-
(2002)
Xenobiotica
, vol.32
, Issue.5
, pp. 411-425
-
-
Wu, W.N.1
McKown, L.A.2
Liao, S.3
-
17
-
-
0034885572
-
Metabolism of the analgesic drug, tramadol hydrochloride, in rat and dog
-
Wu, W. N.; McKown, L. A.; Gauthier, A. D.; Jones, W. J.; Raffa, R. B. (2001). Metabolism of the analgesic drug, tramadol hydrochloride, in rat and dog. Xenobiotica, 31(7), 423-441.
-
(2001)
Xenobiotica
, vol.31
, Issue.7
, pp. 423-441
-
-
Wu, W.N.1
McKown, L.A.2
Gauthier, A.D.3
Jones, W.J.4
Raffa, R.B.5
-
18
-
-
0030911863
-
The use of human hepatocytes to select compounds based on their expected hepatic extraction ratios in humans
-
Lave, T.; Dupin, S.; Schmitt, C.; Valles, B.; Ubeaud, G.; Chou, R. C.; Jaeck, D.; Coassolo, P. (1997). The use of human hepatocytes to select compounds based on their expected hepatic extraction ratios in humans. Pharm. Res., 14(2), 152-155.
-
(1997)
Pharm. Res.
, vol.14
, Issue.2
, pp. 152-155
-
-
Lave, T.1
Dupin, S.2
Schmitt, C.3
Valles, B.4
Ubeaud, G.5
Chou, R.C.6
Jaeck, D.7
Coassolo, P.8
-
19
-
-
0032733974
-
Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: An examination of in vitro half-life approach and nonspecific binding to microsomes
-
Obach, R. S. (1999). Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: an examination of in vitro half-life approach and nonspecific binding to microsomes. Drug Metab. Dispos. 27(11), 1350-1359.
-
(1999)
Drug Metab. Dispos.
, vol.27
, Issue.11
, pp. 1350-1359
-
-
Obach, R.S.1
-
20
-
-
0036746856
-
Characterization of mixtures of recombinant human cytochrome p450s as a screening model for metabolic stability in drug discovery
-
Hagen N.; Olsen A. K.; Andersen J. V.; Tjornelund J.; Hansen S. H. (2002). Characterization of mixtures of recombinant human cytochrome p450s as a screening model for metabolic stability in drug discovery. Xenobiotica, 32(9), 749-759.
-
(2002)
Xenobiotica
, vol.32
, Issue.9
, pp. 749-759
-
-
Hagen, N.1
Olsen, A.K.2
Andersen, J.V.3
Tjornelund, J.4
Hansen, S.H.5
-
21
-
-
0034824439
-
Utility of metabolic stability screening: Comparison of a vitro and in vivo clearance
-
Clarke, S. E.; Jeffrey, P. (2001). Utility of metabolic stability screening: comparison of a vitro and in vivo clearance. Xenobiotica, 31(8/9), 591-598.
-
(2001)
Xenobiotica
, vol.31
, Issue.8-9
, pp. 591-598
-
-
Clarke, S.E.1
Jeffrey, P.2
-
22
-
-
0036846773
-
The use of in vitro metabolic stability for rapid selection of compounds in early discovery based on their expected hepatic extraction ratios
-
Lau, Y. Y.; Krishna, G.; Yumibe, N. P.; Grotz, D. E.; Sapidou, E.; Norton, L.; Chu, I.; Chen, C.; Soares, A. D.; Lin, C. C. (2002). The use of in vitro metabolic stability for rapid selection of compounds in early discovery based on their expected hepatic extraction ratios. Pharm. Res., 19(11), 1606-1610.
-
(2002)
Pharm. Res.
, vol.19
, Issue.11
, pp. 1606-1610
-
-
Lau, Y.Y.1
Krishna, G.2
Yumibe, N.P.3
Grotz, D.E.4
Sapidou, E.5
Norton, L.6
Chu, I.7
Chen, C.8
Soares, A.D.9
Lin, C.C.10
-
23
-
-
0035147471
-
The prediction of human clearance from hepatic microsomal metabolism data
-
Obach, R. S. (2001). The prediction of human clearance from hepatic microsomal metabolism data. Curr. Opin. in Drug Disc. & Develop., 4(1), 36-44.
-
(2001)
Curr. Opin. in Drug Disc. & Develop.
, vol.4
, Issue.1
, pp. 36-44
-
-
Obach, R.S.1
-
24
-
-
0034835463
-
Prediction of human hepatic clearance from in vivo animal experiments and in vitro metabolic studies with liver microsomes from animals and humans
-
Naritomi, Y.; Terashita, S.; Kimura, S.; Suzuki, A.; Kagayama, A. (2001) ; Sugiyama, Y. Prediction of human hepatic clearance from in vivo animal experiments and in vitro metabolic studies with liver microsomes from animals and humans. Drug Metab. Dispos., 29(10), 1316-1324.
-
(2001)
Drug Metab. Dispos.
, vol.29
, Issue.10
, pp. 1316-1324
-
-
Naritomi, Y.1
Terashita, S.2
Kimura, S.3
Suzuki, A.4
Kagayama, A.5
Sugiyama, Y.6
-
25
-
-
0030918716
-
Integration of in vitro data into allometric scaling to predict hepatic metabolic clearance in man: Application to 10 extensively metabolized drugs
-
Lave, T.; Dupin, S.; Schmitt, C.; Chou, R. C.; Jaeck, D.; Coassolo, P. (1997). Integration of in vitro data into allometric scaling to predict hepatic metabolic clearance in man: application to 10 extensively metabolized drugs. J. of Pharm. Sci., 86(5), 584-590.
-
(1997)
J. of Pharm. Sci.
, vol.86
, Issue.5
, pp. 584-590
-
-
Lave, T.1
Dupin, S.2
Schmitt, C.3
Chou, R.C.4
Jaeck, D.5
Coassolo, P.6
-
26
-
-
0036194124
-
In vitro analysis of human drug glucuronidation and prediction of in vivo metabolic clearance
-
Soars, M.G.; Burchell, B.; Riley, R.J. (2002). In vitro analysis of human drug glucuronidation and prediction of in vivo metabolic clearance. J. of Pharm. Experi. Thera., 301(1), 382-390.
-
(2002)
J. of Pharm. Experi. Thera.
, vol.301
, Issue.1
, pp. 382-390
-
-
Soars, M.G.1
Burchell, B.2
Riley, R.J.3
|