-
1
-
-
0030799001
-
The prediction of human pharmacokinetic parameters from preclinical and in vitro metabolism data
-
Obach RS, Baxter JG, Liston TE, Silber BM, Jones BC, Maclntyre F, et al.: The prediction of human pharmacokinetic parameters from preclinical and in vitro metabolism data. J Pharmacol Exp Ther 1997;283:46-58.
-
(1997)
J Pharmacol Exp Ther
, vol.283
, pp. 46-58
-
-
Obach, R.S.1
Baxter, J.G.2
Liston, T.E.3
Silber, B.M.4
Jones, B.C.5
Maclntyre, F.6
-
2
-
-
0030022629
-
An overview of current cytochrome P450 technology for assessing the safety and efficacy of new materials
-
Parkinson A: An overview of current cytochrome P450 technology for assessing the safety and efficacy of new materials. Toxicol Pathol 1996;24:48-57.
-
(1996)
Toxicol Pathol
, vol.24
, pp. 48-57
-
-
Parkinson, A.1
-
3
-
-
34447563594
-
-
Remmel RP: Review of human UDP-glucuronosyl-transferases and their role in drug-drug interactions. In: Drugs and the Pharmaceutical Sciences, 116: Drug-Drug Interactions (Rodrigues AD, ed.), pp. 89-112. Marcel Dekker, New York, 2000.
-
Remmel RP: Review of human UDP-glucuronosyl-transferases and their role in drug-drug interactions. In: Drugs and the Pharmaceutical Sciences, Vol. 116: Drug-Drug Interactions (Rodrigues AD, ed.), pp. 89-112. Marcel Dekker, New York, 2000.
-
-
-
-
4
-
-
0028875109
-
Specificity of human UDP-glucuronosyltransferases and xenobiotic glucuronidation
-
Burchell B, Brierley CH, Rance D: Specificity of human UDP-glucuronosyltransferases and xenobiotic glucuronidation. Life Sci 1995;57:1819-1831.
-
(1995)
Life Sci
, vol.57
, pp. 1819-1831
-
-
Burchell, B.1
Brierley, C.H.2
Rance, D.3
-
5
-
-
8544224973
-
The UDP glycosyltransferase gene superfamily: Recommended nomenclature update based on evolutionary divergence
-
Mackenzie PI, Owens IS, Burchell B, Bock KW, Bairoch A, Belanger A, et al.: The UDP glycosyltransferase gene superfamily: recommended nomenclature update based on evolutionary divergence. Pharmacogenetics 1997;7:255-269.
-
(1997)
Pharmacogenetics
, vol.7
, pp. 255-269
-
-
Mackenzie, P.I.1
Owens, I.S.2
Burchell, B.3
Bock, K.W.4
Bairoch, A.5
Belanger, A.6
-
6
-
-
0034128936
-
Human UDP-glucuronosyltransferases: Metabolism, expression, and disease
-
Tukey RH, Strassburg CP: Human UDP-glucuronosyltransferases: metabolism, expression, and disease. Annu Rev Pharmacol Toxicol 2000;40:581-616.
-
(2000)
Annu Rev Pharmacol Toxicol
, vol.40
, pp. 581-616
-
-
Tukey, R.H.1
Strassburg, C.P.2
-
7
-
-
0034278984
-
-
King CD, Rios GR, Green MD, Tephly TR: UDP-glucuronosyltransferases. Curr Drug Metab 2000;1:143-161.
-
King CD, Rios GR, Green MD, Tephly TR: UDP-glucuronosyltransferases. Curr Drug Metab 2000;1:143-161.
-
-
-
-
8
-
-
15244342411
-
UDP-glucuronosyltransferases and clinical drug-drug interactions
-
Kiang TK, Ensom MH, Chang TK: UDP-glucuronosyltransferases and clinical drug-drug interactions. Pharmacol Ther 2005;106:97-132.
-
(2005)
Pharmacol Ther
, vol.106
, pp. 97-132
-
-
Kiang, T.K.1
Ensom, M.H.2
Chang, T.K.3
-
9
-
-
6344284951
-
Predicting pharmacokinetic herb-drug interactions
-
Zhou S, Chan E, Li SC, Huang M, Chen X, Li X, et al.: Predicting pharmacokinetic herb-drug interactions. Drug Metab Drug Interact 2004;20:143-158.
-
(2004)
Drug Metab Drug Interact
, vol.20
, pp. 143-158
-
-
Zhou, S.1
Chan, E.2
Li, S.C.3
Huang, M.4
Chen, X.5
Li, X.6
-
10
-
-
0032456884
-
Clinically important pharmacokinetic drug-drug interactions: Role of cytochrome P450 enzymes
-
Tanaka E: Clinically important pharmacokinetic drug-drug interactions: role of cytochrome P450 enzymes. J Clin Pharmacol Ther 1998;23:403-416.
-
(1998)
J Clin Pharmacol Ther
, vol.23
, pp. 403-416
-
-
Tanaka, E.1
-
11
-
-
0030069046
-
Atovaquone inhibits the glucuronidation and increases the plasma concentrations of zidovudine
-
Lee BL, Tauber MG, Sadler B, Goldstein D, Chambers HF: Atovaquone inhibits the glucuronidation and increases the plasma concentrations of zidovudine. Clin Pharmacol Ther 1996;59:14-21.
-
(1996)
Clin Pharmacol Ther
, vol.59
, pp. 14-21
-
-
Lee, B.L.1
Tauber, M.G.2
Sadler, B.3
Goldstein, D.4
Chambers, H.F.5
-
12
-
-
6944221357
-
Drug-drug interactions for UDP-glucuronosyltransferase substrates: A pharmacokinetic explanation for typically observed low exposure (AUCi/AUC) ratios
-
Williams JA, Hyland R, Jones BC, Smith DA, Hurst S, Goosen TC, et al.: Drug-drug interactions for UDP-glucuronosyltransferase substrates: a pharmacokinetic explanation for typically observed low exposure (AUCi/AUC) ratios. Drug Metab Dispos 2004;32:1201-1208.
-
(2004)
Drug Metab Dispos
, vol.32
, pp. 1201-1208
-
-
Williams, J.A.1
Hyland, R.2
Jones, B.C.3
Smith, D.A.4
Hurst, S.5
Goosen, T.C.6
-
13
-
-
1842536833
-
Human UDP-glucuronosyltransferases: Isoform selectivity and kinetics of 4-methylumbelliferone and 1-naphthol glucuronidation, effects of organic solvents, and inhibition by diclofenac and probenecid
-
Uchaipichat V, Mackenzie PI, Guo XH, Gardner-Stephen D, Galetin A, Houston JB, et al.: Human UDP-glucuronosyltransferases: isoform selectivity and kinetics of 4-methylumbelliferone and 1-naphthol glucuronidation, effects of organic solvents, and inhibition by diclofenac and probenecid. Drug Metab Dispos 2004;32:413-423.
-
(2004)
Drug Metab Dispos
, vol.32
, pp. 413-423
-
-
Uchaipichat, V.1
Mackenzie, P.I.2
Guo, X.H.3
Gardner-Stephen, D.4
Galetin, A.5
Houston, J.B.6
-
14
-
-
30144436526
-
Isoform-selective probe substrates for in vitro studies of human UDP-glucuronosyltransferases
-
Court MH: Isoform-selective probe substrates for in vitro studies of human UDP-glucuronosyltransferases. Methods Enzymol 2005;400:104-116.
-
(2005)
Methods Enzymol
, vol.400
, pp. 104-116
-
-
Court, M.H.1
-
15
-
-
6044232040
-
Validation of model of cytochrome P450 2D6: An in silico tool for predicting metabolism and inhibition
-
Kemp CA, Flanagan JU, van Eldik AJ, Marechal JD, Wolf CR, Roberts GC, et al.: Validation of model of cytochrome P450 2D6: an in silico tool for predicting metabolism and inhibition. J Med Chem 2004;47:5340-5346.
-
(2004)
J Med Chem
, vol.47
, pp. 5340-5346
-
-
Kemp, C.A.1
Flanagan, J.U.2
van Eldik, A.J.3
Marechal, J.D.4
Wolf, C.R.5
Roberts, G.C.6
-
16
-
-
17444411955
-
Cytochrome p450 in silico: An integrative modeling approach
-
de Graaf C, Vermeulen NP, Feenstra KA: Cytochrome p450 in silico: an integrative modeling approach. J Med Chem 2005;48:2725-2755.
-
(2005)
J Med Chem
, vol.48
, pp. 2725-2755
-
-
de Graaf, C.1
Vermeulen, N.P.2
Feenstra, K.A.3
-
17
-
-
0033694566
-
Fluorometric high-throughput screening for inhibitors of cytochrome P450
-
Miller VP, Stresser DM, Blanchard AP, Turner S, Crespi CL: Fluorometric high-throughput screening for inhibitors of cytochrome P450. Ann N Y Acad Sci 2000;919:26-32.
-
(2000)
Ann N Y Acad Sci
, vol.919
, pp. 26-32
-
-
Miller, V.P.1
Stresser, D.M.2
Blanchard, A.P.3
Turner, S.4
Crespi, C.L.5
-
18
-
-
12244256555
-
High-throughput screening assays for the assessment of CYP2C9*1, CYP2C9*2, and CYP2C9*3 metabolism using fluorogenic Vivid substrates
-
Marks BD, Thompson DV, Goossens TA, Trubetskoy OV: High-throughput screening assays for the assessment of CYP2C9*1, CYP2C9*2, and CYP2C9*3 metabolism using fluorogenic Vivid substrates. J Biomol Screen 2004;9: 439-449.
-
(2004)
J Biomol Screen
, vol.9
, pp. 439-449
-
-
Marks, B.D.1
Thompson, D.V.2
Goossens, T.A.3
Trubetskoy, O.V.4
-
19
-
-
0026008487
-
Cloning of two human liver bilirubin UDP-glucuronosyltransferase cDNAs with expression in COS-1 cells
-
Ritter JK, Crawford JM, Owens IS: Cloning of two human liver bilirubin UDP-glucuronosyltransferase cDNAs with expression in COS-1 cells. J Biol Chem 1991;266: 1043-1047.
-
(1991)
J Biol Chem
, vol.266
, pp. 1043-1047
-
-
Ritter, J.K.1
Crawford, J.M.2
Owens, I.S.3
-
20
-
-
0842301047
-
Correlation between the UDP-glucuronosyltransferase (UGT1A1) TATAA box polymorphism and carcinogen detoxification phenotype: Significantly decreased glucuronidating activity against benzo(a)pyrene-7,8- dihydrodiol(-) in liver microsomes from subjects with the UGT1A1*28 variant
-
Fang JL, Lazarus P: Correlation between the UDP-glucuronosyltransferase (UGT1A1) TATAA box polymorphism and carcinogen detoxification phenotype: significantly decreased glucuronidating activity against benzo(a)pyrene-7,8- dihydrodiol(-) in liver microsomes from subjects with the UGT1A1*28 variant. Cancer Epidemiol Biomarkers Prev 2004;13:102-109.
-
(2004)
Cancer Epidemiol Biomarkers Prev
, vol.13
, pp. 102-109
-
-
Fang, J.L.1
Lazarus, P.2
-
21
-
-
27744567967
-
The impact of glucuronidation on the bioactivation and DNA adduction of the cooked-food carcinogen 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine in vivo
-
Malfatti MA, Ubick EA, Felton JS: The impact of glucuronidation on the bioactivation and DNA adduction of the cooked-food carcinogen 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine in vivo. Carcinogenesis 2005;26: 2019-2028.
-
(2005)
Carcinogenesis
, vol.26
, pp. 2019-2028
-
-
Malfatti, M.A.1
Ubick, E.A.2
Felton, J.S.3
-
22
-
-
18344383946
-
Cruciferae interact with the UGT1A1*28 polymorphism to determine serum bilirubin levels in humans
-
Peterson S, Bigler J, Horner NK, Potter JD, Lampe JW: Cruciferae interact with the UGT1A1*28 polymorphism to determine serum bilirubin levels in humans. J Nutr 2005;135:1051-1055.
-
(2005)
J Nutr
, vol.135
, pp. 1051-1055
-
-
Peterson, S.1
Bigler, J.2
Horner, N.K.3
Potter, J.D.4
Lampe, J.W.5
-
23
-
-
0036843701
-
Differential modulation of UDP-glucuronosyltransferase 1A1 (UGT1A1)-catalyzed estradiol-3-glucuronidation by the addition of UGT1A1 substrates and other compounds to human liver microsomes
-
Williams JA, Ring BJ, Cantrell VE, Campanale K, Jones DR, Hall SD, et al.: Differential modulation of UDP-glucuronosyltransferase 1A1 (UGT1A1)-catalyzed estradiol-3-glucuronidation by the addition of UGT1A1 substrates and other compounds to human liver microsomes. Drug Metab Dispos 2002;30:1266-1273.
-
(2002)
Drug Metab Dispos
, vol.30
, pp. 1266-1273
-
-
Williams, J.A.1
Ring, B.J.2
Cantrell, V.E.3
Campanale, K.4
Jones, D.R.5
Hall, S.D.6
-
24
-
-
15444367186
-
Polymorphism of UDP-glucuronosyltransferase and drug metabolism
-
Maruo Y, Iwai M, Mori A, Sato H, Takeuchi Y: Polymorphism of UDP-glucuronosyltransferase and drug metabolism. Curr Drug Metab 2005;6:91-99.
-
(2005)
Curr Drug Metab
, vol.6
, pp. 91-99
-
-
Maruo, Y.1
Iwai, M.2
Mori, A.3
Sato, H.4
Takeuchi, Y.5
-
25
-
-
0344223485
-
A fluorescent assay amenable to measuring production of beta-D-glucuronides produced from recombinant UDP-glycosyl transferase enzymes
-
Trubetskoy OV, Shaw PM: A fluorescent assay amenable to measuring production of beta-D-glucuronides produced from recombinant UDP-glycosyl transferase enzymes. Drug Metab Dispos 1999;27:555-557.
-
(1999)
Drug Metab Dispos
, vol.27
, pp. 555-557
-
-
Trubetskoy, O.V.1
Shaw, P.M.2
-
26
-
-
33745619265
-
Engineered polymeric nanoparticles for receptor-targeted blockage of oxidized low density lipoprotein uptake and atherogenesis in macrophages
-
Chnari E, Nikitczuk JS, Wang J, Uhrich KE, Moghe PV: Engineered polymeric nanoparticles for receptor-targeted blockage of oxidized low density lipoprotein uptake and atherogenesis in macrophages. Biomacromolecules 2006; 7:1796-1805.
-
(2006)
Biomacromolecules
, vol.7
, pp. 1796-1805
-
-
Chnari, E.1
Nikitczuk, J.S.2
Wang, J.3
Uhrich, K.E.4
Moghe, P.V.5
-
27
-
-
33947524042
-
Evaluation of synthetic polymeric micelles as a stabilization medium for the handling of membrane proteins in pharmaceutical drug discovery
-
Trubetskoy OV, Finel M, Burke TJ, Trubetskoy VS: Evaluation of synthetic polymeric micelles as a stabilization medium for the handling of membrane proteins in pharmaceutical drug discovery. J Pharm Pharmaceut Sci 2006;9:271-280.
-
(2006)
J Pharm Pharmaceut Sci
, vol.9
, pp. 271-280
-
-
Trubetskoy, O.V.1
Finel, M.2
Burke, T.J.3
Trubetskoy, V.S.4
-
28
-
-
0037423299
-
Expression and characterization of recombinant human UDP-glucuronosyltransferases (UGTs). UGT1A9 is more resistant to detergent inhibition than other UGTs and was purified as an active dimeric enzyme
-
Kurkela M, Garcia-Horsman JA, Luukkanen L, Morsky S, Taskinen J, Baumann M, et al.: Expression and characterization of recombinant human UDP-glucuronosyltransferases (UGTs). UGT1A9 is more resistant to detergent inhibition than other UGTs and was purified as an active dimeric enzyme. J Biol Chem 2003;278:3536-3544.
-
(2003)
J Biol Chem
, vol.278
, pp. 3536-3544
-
-
Kurkela, M.1
Garcia-Horsman, J.A.2
Luukkanen, L.3
Morsky, S.4
Taskinen, J.5
Baumann, M.6
-
29
-
-
0033003760
-
A simple statistical parameter for use in evaluation and validation of high throughput screening assays
-
Zhang JH, Chung TD, Oldenburg KR: A simple statistical parameter for use in evaluation and validation of high throughput screening assays. J Biomol Screen 1999; 4:67-73.
-
(1999)
J Biomol Screen
, vol.4
, pp. 67-73
-
-
Zhang, J.H.1
Chung, T.D.2
Oldenburg, K.R.3
-
31
-
-
27544468948
-
In vitro inhibition of UDP glucuronosyltransferases by atazanavir and other HIV protease inhibitors and the relationship of this property to in vivo bilirubin glucuronidation
-
Zhang D, Chando TJ, Everett DW, Patten CJ, Dehal SS, Humphreys WG: In vitro inhibition of UDP glucuronosyltransferases by atazanavir and other HIV protease inhibitors and the relationship of this property to in vivo bilirubin glucuronidation. Drug Metab Dispos 2005;33:1729-1739.
-
(2005)
Drug Metab Dispos
, vol.33
, pp. 1729-1739
-
-
Zhang, D.1
Chando, T.J.2
Everett, D.W.3
Patten, C.J.4
Dehal, S.S.5
Humphreys, W.G.6
-
32
-
-
0037404036
-
Glucuronidation of etoposide in human liver microsomes is specifically catalyzed by UDP-glucuronosyltransferase 1A1
-
Watanabe Y, Nakajima M, Ohashi N, Kume T, Yokoi T: Glucuronidation of etoposide in human liver microsomes is specifically catalyzed by UDP-glucuronosyltransferase 1A1. Drug Metab Dispos 2003;31:589-595.
-
(2003)
Drug Metab Dispos
, vol.31
, pp. 589-595
-
-
Watanabe, Y.1
Nakajima, M.2
Ohashi, N.3
Kume, T.4
Yokoi, T.5
-
33
-
-
0043027104
-
In vitro drug interactions of cytochrome p450: An evaluation of fluorogenic to conventional substrates
-
Cohen LH, Remley MJ, Raunig D, Vaz AD: In vitro drug interactions of cytochrome p450: an evaluation of fluorogenic to conventional substrates. Drug Metab Dispos 2003;31:1005-1015.
-
(2003)
Drug Metab Dispos
, vol.31
, pp. 1005-1015
-
-
Cohen, L.H.1
Remley, M.J.2
Raunig, D.3
Vaz, A.D.4
-
34
-
-
0036092999
-
Regioselectivity of phase II metabolism of luteolin and quercetin by UDP-glucuronosyl transferases
-
Boersma MG, van der Woude H, Bogaards J, Boeren S, Vervoort J, Cnubben NH, et al.: Regioselectivity of phase II metabolism of luteolin and quercetin by UDP-glucuronosyl transferases. Chem Res Toxicol 2002;15: 662-670.
-
(2002)
Chem Res Toxicol
, vol.15
, pp. 662-670
-
-
Boersma, M.G.1
van der Woude, H.2
Bogaards, J.3
Boeren, S.4
Vervoort, J.5
Cnubben, N.H.6
-
35
-
-
33745652497
-
Drug-drug interactions of anti-infective drugs: Utility of fluorescence CYP inhibition assays in drug discovery
-
Friden M, Vanaja K, Nandi VN: Drug-drug interactions of anti-infective drugs: utility of fluorescence CYP inhibition assays in drug discovery. Drug Metab Drug Interact 2006;21:163-185.
-
(2006)
Drug Metab Drug Interact
, vol.21
, pp. 163-185
-
-
Friden, M.1
Vanaja, K.2
Nandi, V.N.3
-
36
-
-
17044381648
-
Highly miniaturized formats for in vitro drug metabolism assays using vivid fluorescent substrates and recombinant human cytochrome P450 enzymes
-
Trubetskoy OV, Gibson JR, Marks BD: Highly miniaturized formats for in vitro drug metabolism assays using vivid fluorescent substrates and recombinant human cytochrome P450 enzymes. J Biomol Screen 2005;10:56-66.
-
(2005)
J Biomol Screen
, vol.10
, pp. 56-66
-
-
Trubetskoy, O.V.1
Gibson, J.R.2
Marks, B.D.3
-
37
-
-
18844387928
-
Determination of drug glucuronidation and UDP-glucuronosyltransferase selectivity using a 96-well radiometric assay
-
Di Marco A, D'Antoni M, Attaccalite S, Carotenuto P, Laufer R: Determination of drug glucuronidation and UDP-glucuronosyltransferase selectivity using a 96-well radiometric assay. Drug Metab Dispos 2005;33:812-819.
-
(2005)
Drug Metab Dispos
, vol.33
, pp. 812-819
-
-
Di Marco, A.1
D'Antoni, M.2
Attaccalite, S.3
Carotenuto, P.4
Laufer, R.5
-
38
-
-
0036890353
-
Complexities of glucuronidation affecting in vitro in vivo extrapolation
-
Lin JH, Wong BK: Complexities of glucuronidation affecting in vitro in vivo extrapolation. Curr Drug Metab 2002;3:623-646.
-
(2002)
Curr Drug Metab
, vol.3
, pp. 623-646
-
-
Lin, J.H.1
Wong, B.K.2
-
39
-
-
0344610168
-
Predicting human drug glucuronidation parameters: Application of in vitro and in silico modeling approaches
-
Miners JO, Smith PA, Sorich MJ, McKinnon RA, Mackenzie PI: Predicting human drug glucuronidation parameters: application of in vitro and in silico modeling approaches. Annu Rev Pharmacol Toxicol 2004;44:1-25.
-
(2004)
Annu Rev Pharmacol Toxicol
, vol.44
, pp. 1-25
-
-
Miners, J.O.1
Smith, P.A.2
Sorich, M.J.3
McKinnon, R.A.4
Mackenzie, P.I.5
-
40
-
-
33744804311
-
Comprehensive analysis of UGT1A polymorphisms predictive for pharmacokinetics and treatment outcome in patients with non-small-cell lung cancer treated with irinotecan and cisplatin
-
Han JY, Lim HS, Shin ES, Yoo YK, Park YH, Lee JE, et al.: Comprehensive analysis of UGT1A polymorphisms predictive for pharmacokinetics and treatment outcome in patients with non-small-cell lung cancer treated with irinotecan and cisplatin. J Clin Oncol 2006;24:2237-2244.
-
(2006)
J Clin Oncol
, vol.24
, pp. 2237-2244
-
-
Han, J.Y.1
Lim, H.S.2
Shin, E.S.3
Yoo, Y.K.4
Park, Y.H.5
Lee, J.E.6
-
41
-
-
33746780621
-
Pharmacogenetics of uridine diphosphoglucuronosyltransferase (UGT) 1A family members and its role in patient response to irinotecan
-
Nagar S, Blanchard RL: Pharmacogenetics of uridine diphosphoglucuronosyltransferase (UGT) 1A family members and its role in patient response to irinotecan. Drug Metab Rev 2006;38:393-409.
-
(2006)
Drug Metab Rev
, vol.38
, pp. 393-409
-
-
Nagar, S.1
Blanchard, R.L.2
-
43
-
-
0031974584
-
A universal radiochemical high-performance liquid chromatographic assay for the determination of UDP-glucuronosyltransferase activity
-
Ethell BT, Anderson GD, Beaumont K, Rance DJ, Burchell B: A universal radiochemical high-performance liquid chromatographic assay for the determination of UDP-glucuronosyltransferase activity. Anal Biochem 1998;255: 142-147.
-
(1998)
Anal Biochem
, vol.255
, pp. 142-147
-
-
Ethell, B.T.1
Anderson, G.D.2
Beaumont, K.3
Rance, D.J.4
Burchell, B.5
-
44
-
-
4644299238
-
Development of an assay using 4-trifluoromethylumbelliferyl as a marker substrate for assessment of drug-drug interactions to multiple isoforms of UDP-glucuronosyltransferases
-
Baranczewski P, Kallin A, Andersson A, Hagigi S, Aberg M, Postlind H, et al.: Development of an assay using 4-trifluoromethylumbelliferyl as a marker substrate for assessment of drug-drug interactions to multiple isoforms of UDP-glucuronosyltransferases. Assay Drug Dev Technol 2004;2:345-352.
-
(2004)
Assay Drug Dev Technol
, vol.2
, pp. 345-352
-
-
Baranczewski, P.1
Kallin, A.2
Andersson, A.3
Hagigi, S.4
Aberg, M.5
Postlind, H.6
-
45
-
-
0034009448
-
In vitro glucuronidation using human liver microsomes and the pore-forming peptide alamethicin
-
Fisher MB, Campanale K, Ackermann BL, VandenBranden M, Wrighton SA: In vitro glucuronidation using human liver microsomes and the pore-forming peptide alamethicin. Drug Metab Dispos 2000;28:560-566.
-
(2000)
Drug Metab Dispos
, vol.28
, pp. 560-566
-
-
Fisher, M.B.1
Campanale, K.2
Ackermann, B.L.3
VandenBranden, M.4
Wrighton, S.A.5
-
46
-
-
0026602510
-
Optimal detergent activation of rat liver microsomal UDP-glucuronosyl transferases toward morphine and 1-naphthol: Contribution to induction and latency studies
-
Lett E, Kriszt W, de Sandro V, Ducrotoy G, Richert L: Optimal detergent activation of rat liver microsomal UDP-glucuronosyl transferases toward morphine and 1-naphthol: contribution to induction and latency studies. Biochem Pharmacol 1992;43:1649-1653.
-
(1992)
Biochem Pharmacol
, vol.43
, pp. 1649-1653
-
-
Lett, E.1
Kriszt, W.2
de Sandro, V.3
Ducrotoy, G.4
Richert, L.5
-
47
-
-
12244277451
-
Pharmacophore and quantitative structure activity relationship modeling of UDP- glucuronosyltransferase 1A1 (UGT1A1) substrates
-
Sorich MJ, Smith PA, McKinnon RA, Miners JO: Pharmacophore and quantitative structure activity relationship modeling of UDP- glucuronosyltransferase 1A1 (UGT1A1) substrates. Pharmacogenetics 2002;12:635-645.
-
(2002)
Pharmacogenetics
, vol.12
, pp. 635-645
-
-
Sorich, M.J.1
Smith, P.A.2
McKinnon, R.A.3
Miners, J.O.4
|