-
1
-
-
33746255370
-
Future of toxicology-metabolic activation and drug design: Challenges and opportunities in chemical toxicology
-
DOI 10.1021/tx060062o
-
Baillie TA. (2006). Future of toxicology-metabolic activation and drug design: challenges and opportunities in chemical toxicology. Chem Res Toxicol 19: 889-93. (Pubitemid 44092354)
-
(2006)
Chemical Research in Toxicology
, vol.19
, Issue.7
, pp. 889-893
-
-
Baillie, T.A.1
-
2
-
-
62249155473
-
Can in vitro metabolism-dependent covalent binding data distinguish hepatotoxic from nonhepatotoxic drugs? An analysis using human hepatocytes and liver S-9 fraction
-
Bauman JN, Kelly JM, Tripathy S, et al. (2009). Can in vitro metabolism-dependent covalent binding data distinguish hepatotoxic from nonhepatotoxic drugs? An analysis using human hepatocytes and liver S-9 fraction. Chem Res Toxicol 22: 332-40.
-
(2009)
Chem Res Toxicol
, vol.22
, pp. 332-340
-
-
Bauman, J.N.1
Kelly, J.M.2
Tripathy, S.3
-
3
-
-
0027199712
-
Predictability of the covalent binding of acidic drugs in man
-
Benet LZ, Spahn-Langguth H, Iwakawa S, et al. (1993). Predictability of the covalent binding of acidic drugs in man. Life Sci 53:PL141-6.
-
(1993)
Life Sci
, vol.53
-
-
Benet, L.Z.1
Spahn-Langguth, H.2
Iwakawa, S.3
-
4
-
-
7744224004
-
Standardization of a LC/ MS/MS method for the determination of acyl glucuronides and their isomers
-
Bolze S, Lacombe O, Durand G, et al. (2002). Standardization of a LC/ MS/MS method for the determination of acyl glucuronides and their isomers. Curr Sep 20: 55-9.
-
(2002)
Curr Sep
, vol.20
, pp. 55-59
-
-
Bolze, S.1
Lacombe, O.2
Durand, G.3
-
5
-
-
0027275566
-
Physiological parameters in laboratory animals and humans
-
DOI 10.1023/A:1018943613122
-
Davies B, Morris T. (1993). Physiological parameters in laboratory animals and humans. Pharm Res (NY) 10: 1093-5. (Pubitemid 23211439)
-
(1993)
Pharmaceutical Research
, vol.10
, Issue.7
, pp. 1093-1095
-
-
Davies, B.1
Morris, T.2
-
6
-
-
79959417881
-
Species independence in brain tissue binding using brain homogenates
-
Di L, Umland JP, Chang G, et al. (2011). Species independence in brain tissue binding using brain homogenates. Drug Metab Dispos 39: 1270-7.
-
(2011)
Drug Metab Dispos
, vol.39
, pp. 1270-1277
-
-
Di Umland L, J.P.1
Chang, G.2
-
7
-
-
84870055979
-
Mechanistic insights from comparing intrinsic clearance values between human liver microsomes and hepatocytes to guide drug design
-
Di L, Keefer C, Scott DO, et al. (2012). Mechanistic insights from comparing intrinsic clearance values between human liver microsomes and hepatocytes to guide drug design. Eur J Med Chem 57: 441-8.
-
(2012)
Eur J Med Chem
, vol.57
, pp. 441-448
-
-
Di Keefer L, C.1
Scott, D.O.2
-
8
-
-
0032826052
-
Disposition and chemical stability of telmisartan 1-O-acylglucuronide
-
Ebner T, Heinzel G, Prox A, et al. (1999). Disposition and chemical stability of telmisartan 1-O-acylglucuronide. Drug Metab Dispos 27: 1143-9. (Pubitemid 29463600)
-
(1999)
Drug Metabolism and Disposition
, vol.27
, Issue.10
, pp. 1143-1149
-
-
Ebner, T.1
Heinzel, G.2
Prox, A.3
Beschke, K.4
Wachsmuth, H.5
-
9
-
-
28144461609
-
In vitro inhibitory effect of 1-aminobenzotriazole on drug oxidations catalyzed by human cytochrome P450 enzymes: A comparison with SKF-525A and ketoconazole
-
Emoto C, Murase S, Sawada Y, et al. (2003). In vitro inhibitory effect of 1-aminobenzotriazole on drug oxidations catalyzed by human cytochrome P450 enzymes: a comparison with SKF-525A and ketoconazole. Drug Metab Pharmacokinet 18: 287-95.
-
(2003)
Drug Metab Pharmacokinet
, vol.18
, pp. 287-295
-
-
Emoto, C.1
Murase, S.2
Sawada, Y.3
-
10
-
-
1642281756
-
Drug-Protein Adducts: An Industry Perspective on Minimizing the Potential for Drug Bioactivation in Drug Discovery and Development
-
DOI 10.1021/tx034170b
-
Evans DC, Watt AP, Nicoll-Griffith DA, Baillie TA. (2004). Drugprotein adducts: an industry perspective on minimizing the potential for drug bioactivation in drug discovery and development. Chem Res Toxicol 17: 3-16. (Pubitemid 38134055)
-
(2004)
Chemical Research in Toxicology
, vol.17
, Issue.1
, pp. 3-16
-
-
Evans, D.C.1
Watt, A.P.2
Nicoll-Griffith, D.A.3
Baillie, T.A.4
-
11
-
-
84867243137
-
Inhibition of morphine glucuronidation in the liver microsomes of rats and humans by monoterpenoid alcohols
-
Ishii Y, Iida N, Miyauchi Y, et al. (2012). Inhibition of morphine glucuronidation in the liver microsomes of rats and humans by monoterpenoid alcohols. Biol Pharm Bull 35: 1811-17.
-
(2012)
Biol Pharm Bull
, vol.35
, pp. 1811-1817
-
-
Ishii, Y.1
Iida, N.2
Miyauchi, Y.3
-
12
-
-
0030937636
-
Prediction of in vivo drug metabolism in the human liver from in vitro metabolism data
-
DOI 10.1016/S0163-7258(96)00184-2, PII S0163725896001842
-
Iwatsubo T, Hirota N, Ooie T, et al. (1997). Prediction of in vivo drug metabolism in the human liver from in vitro metabolism data. Pharmacol Ther 73: 147-71. (Pubitemid 27191615)
-
(1997)
Pharmacology and Therapeutics
, vol.73
, Issue.2
, pp. 147-171
-
-
Iwatsubo, T.1
Hirota, N.2
Ooie, T.3
Suzuki, H.4
Shimada, N.5
Chiba, K.6
Ishizaki, T.7
Green, C.E.8
Tyson, C.A.9
Sugiyama, Y.10
-
13
-
-
0029910243
-
Oxidation of tienilic acid by human yeast-expressed cytochromes P-450 2C8, 2C9, 2C18 and 2C19. Evidence that this drug is a mechanism-based inhibitor specific for cytochrome P-450 2C9
-
Jean P, Lopez-Garcia P, Dansette P, et al. (1996). Oxidation of tienilic acid by human yeast-expressed cytochromes P-450 2C8, 2C9, 2C18 and 2C19. Evidence that this drug is a mechanism-based inhibitor specific for cytochrome P-450 2C9. Eur J Biochem 241: 797-804. (Pubitemid 26379382)
-
(1996)
European Journal of Biochemistry
, vol.241
, Issue.3
, pp. 797-804
-
-
Jean, P.1
Lopez-Garcia, P.2
Dansette, P.3
Mansuy, D.4
Goldstein, J.L.5
-
14
-
-
84884609633
-
A simple method to evaluate reactivity of acylglucuronides optimized for early stage drug discovery
-
Jinno N, Ohashi S, Tagashira M, et al. (2013). A simple method to evaluate reactivity of acylglucuronides optimized for early stage drug discovery. Biol Pharm Bull 36: 1509-13.
-
(2013)
Biol Pharm Bull
, vol.36
, pp. 1509-1513
-
-
Jinno, N.1
Ohashi, S.2
Tagashira, M.3
-
15
-
-
80052267476
-
PhRMA CPCDC initiative on predictive models of human pharmacokinetics, part 2: Comparative assessment of prediction methods of human volume of distribution
-
Jones RD, Jones HM, Rowland M, et al. (2011). PhRMA CPCDC initiative on predictive models of human pharmacokinetics, part 2: comparative assessment of prediction methods of human volume of distribution. J Pharm Sci 100: 4074-89.
-
(2011)
J Pharm Sci
, vol.100
, pp. 4074-4089
-
-
Jones, R.D.1
Jones, H.M.2
Rowland, M.3
-
16
-
-
20844444779
-
Idiosyncratic drug hepatotoxicity
-
DOI 10.1038/nrd1750
-
Kaplowitz N. (2005). Idiosyncratic drug hepatotoxicity. Nat Rev Drug Discov 4: 489-99. (Pubitemid 40861991)
-
(2005)
Nature Reviews Drug Discovery
, vol.4
, Issue.6
, pp. 489-499
-
-
Kaplowitz, N.1
-
17
-
-
84862934885
-
Differential modulation of cytochrome P450 activity and the effect of 1-aminobenzotriazole on hepatic transport in sandwich-cultured human hepatocytes
-
Kimoto E, Walsky R, Zhang H, et al. (2012). Differential modulation of cytochrome P450 activity and the effect of 1-aminobenzotriazole on hepatic transport in sandwich-cultured human hepatocytes. Drug Metab Dispos 40: 407-11.
-
(2012)
Drug Metab Dispos
, vol.40
, pp. 407-411
-
-
Kimoto, E.1
Walsky, R.2
Zhang, H.3
-
18
-
-
78650743790
-
Toxicological evaluation of acyl glucuronides of nonsteroidal anti-inflammatory drugs using human embryonic kidney 293 cells stably expressing human UDP-glucuronosyltransferase and human hepatocytes
-
Koga T, Fujiwara R, Nakajima M, Yokoi T. (2011). Toxicological evaluation of acyl glucuronides of nonsteroidal anti-inflammatory drugs using human embryonic kidney 293 cells stably expressing human UDP-glucuronosyltransferase and human hepatocytes. Drug Metab Dispos 39: 54-60.
-
(2011)
Drug Metab Dispos
, vol.39
, pp. 54-60
-
-
Koga, T.1
Fujiwara, R.2
Nakajima, M.3
Yokoi, T.4
-
19
-
-
0037058253
-
A review of the common properties of drugs with idiosyncratic hepatotoxicity and the "multiple determinant hypothesis" for the manifestation of idiosyncratic drug toxicity
-
DOI 10.1016/S0009-2797(02)00051-0, PII S0009279702000510
-
Li AP. (2002). A review of the common properties of drugs with idiosyncratic hepatotoxicity and the ''multiple determinant hypothesis'' for the manifestation of idiosyncratic drug toxicity. Chem Biol Interact 142: 7-23. (Pubitemid 35232550)
-
(2002)
Chemico-Biological Interactions
, vol.142
, Issue.1-2
, pp. 7-23
-
-
Li, A.P.1
-
20
-
-
84875783673
-
Comprehensive assessment of human pharmacokinetic prediction based on in vivo animal pharmacokinetic data, part 1: Volume of distribution at steady state
-
Lombardo F, Waters NJ, Argikar UA, et al. (2013a). Comprehensive assessment of human pharmacokinetic prediction based on in vivo animal pharmacokinetic data, part 1: volume of distribution at steady state. J Clin Pharmacol 53: 167-77.
-
(2013)
J Clin Pharmacol
, vol.53
, pp. 167-177
-
-
Lombardo, F.1
Waters, N.J.2
Argikar, U.A.3
-
21
-
-
84865484675
-
Comprehensive assessment of human pharmacokinetic prediction based on in vivo animal pharmacokinetic data, part 2: Clearance
-
Lombardo F, Waters NJ, Argikar UA, et al. (2013b). Comprehensive assessment of human pharmacokinetic prediction based on in vivo animal pharmacokinetic data, part 2: clearance. J Clin Pharmacol 53: 178-91.
-
(2013)
J Clin Pharmacol
, vol.53
, pp. 178-191
-
-
Lombardo, F.1
Waters, N.J.2
Argikar, U.A.3
-
22
-
-
35548965586
-
The UDP-glucuronosyltransferase 2B7 isozyme is responsible for gemfibrozil glucuronidation in the human liver
-
DOI 10.1124/dmd.107.017269
-
Mano Y, Usui T, Kamimura H. (2007). The UDP-glucuronosyltransferase 2B7 isozyme is responsible for gemfibrozil glucuronidation in the human liver. Drug Metab Dispos 35: 2040-4. (Pubitemid 350005193)
-
(2007)
Drug Metabolism and Disposition
, vol.35
, Issue.11
, pp. 2040-2044
-
-
Mano, Y.1
Usui, T.2
Kamimura, H.3
-
23
-
-
34047275727
-
Prediction of in vivo potential for metabolic activation of drugs into chemically reactive intermediate: Correlation of in vitro and in vivo generation of reactive intermediates and in vitro glutathione conjugate formation in rats and humans
-
DOI 10.1021/tx060234h
-
Masubuchi N, Makino C, Murayama N. (2007). Prediction of in vivo potential for metabolic activation of drugs into chemically reactive intermediate: correlation of in vitro and in vivo generation of reactive intermediates and in vitro glutathione conjugate formation in rats and humans. Chem Res Toxicol 20: 455-64. (Pubitemid 46548692)
-
(2007)
Chemical Research in Toxicology
, vol.20
, Issue.3
, pp. 455-464
-
-
Masubuchi, N.1
Makino, C.2
Murayama, N.3
-
24
-
-
33845464619
-
Investigation of the immunogenicity of diclofenac and diclofenac metabolites
-
DOI 10.1016/j.toxlet.2006.10.014, PII S0378427406013142
-
Naisbitt DJ, Sanderson LS, Meng X, et al. (2007). Investigation of the immunogenicity of diclofenac and diclofenac metabolites. Toxicol Lett 168: 45-50. (Pubitemid 44909720)
-
(2007)
Toxicology Letters
, vol.168
, Issue.1
, pp. 45-50
-
-
Naisbitt, D.J.1
Sanderson, L.S.2
Meng, X.3
Stachulski, A.V.4
Clarke, S.E.5
Park, B.K.6
-
25
-
-
70349103856
-
A zone classification system for risk assessment of idiosyncratic drug toxicity using daily dose and covalent binding
-
Nakayama S, Atsumi R, Takakusa H, et al. (2009). A zone classification system for risk assessment of idiosyncratic drug toxicity using daily dose and covalent binding. Drug Metab Dispos 37: 1970-7.
-
(2009)
Drug Metab Dispos
, vol.37
, pp. 1970-1977
-
-
Nakayama, S.1
Atsumi, R.2
Takakusa, H.3
-
26
-
-
79959400794
-
Combination of GSH trapping and time-dependent inhibition assays as a predictive method of drugs generating highly reactive metabolites
-
Nakayama S, Takakusa H, Watanabe A, et al. (2011). Combination of GSH trapping and time-dependent inhibition assays as a predictive method of drugs generating highly reactive metabolites. Drug Metab Dispos 39: 1247-54.
-
(2011)
Drug Metab Dispos
, vol.39
, pp. 1247-1254
-
-
Nakayama, S.1
Takakusa, H.2
Watanabe, A.3
-
27
-
-
53549100467
-
Can in vitro metabolism-dependent covalent binding data in liver microsomes distinguish hepatotoxic from nonhepatotoxic drugs? An analysis of 18 drugs with consideration of intrinsic clearance and daily dose
-
Obach RS, Kalgutkar AS, Soglia JR, Zhao SX. (2008). Can in vitro metabolism-dependent covalent binding data in liver microsomes distinguish hepatotoxic from nonhepatotoxic drugs? An analysis of 18 drugs with consideration of intrinsic clearance and daily dose. Chem Res Toxicol 21: 1814-22.
-
(2008)
Chem Res Toxicol
, vol.21
, pp. 1814-1822
-
-
Obach, R.S.1
Kalgutkar, A.S.2
Soglia, J.R.3
Zhao, S.X.4
-
28
-
-
79958063692
-
An integrated reactive metabolite evaluation approach to assess and reduce safety risk during drug discovery and development
-
Reese M, Sakatis M, Ambroso J, et al. (2010). An integrated reactive metabolite evaluation approach to assess and reduce safety risk during drug discovery and development. Chem Biol Interact 192: 60-4.
-
(2010)
Chem Biol Interact
, vol.192
, pp. 60-64
-
-
Reese, M.1
Sakatis, M.2
Ambroso, J.3
-
29
-
-
80052268294
-
PhRMA CPCDC initiative on predictive models of human pharmacokinetics, part 3: Comparative assessment of prediction methods of human clearance
-
Ring BJ, Chien JY, Adkison KK, et al. (2011). PhRMA CPCDC initiative on predictive models of human pharmacokinetics, part 3: comparative assessment of prediction methods of human clearance. J Pharm Sci 100: 4090-110.
-
(2011)
J Pharm Sci
, vol.100
, pp. 4090-4110
-
-
Ring, B.J.1
Chien, J.Y.2
Adkison, K.K.3
-
30
-
-
0022609024
-
Correlation between in-vitro microsomal enzyme activity and whole organ hepatic elimination kinetics: Analysis with a dispersion model
-
Roberts MS, Rowland M. (1986). Correlation between in-vitro microsomal enzyme activity and whole organ hepatic elimination kinetics: analysis with a dispersion model. J Pharm Pharmacol 38: 177-81. (Pubitemid 16162503)
-
(1986)
Journal of Pharmacy and Pharmacology
, vol.38
, Issue.3
, pp. 177-181
-
-
Roberts, M.S.1
Rowland, M.2
-
31
-
-
1642504441
-
Glucuronidation of carboxylic acid containing compounds by UDP-glucuronosyltransferase isoforms
-
DOI 10.1016/j.abb.2004.02.004, PII S0003986104000645
-
Sakaguchi K, Green M, Stock N, et al. (2004). Glucuronidation of carboxylic acid containing compounds by UDP-glucuronosyltransferase isoforms. Arch Biochem Biophys 424: 219-25. (Pubitemid 38401955)
-
(2004)
Archives of Biochemistry and Biophysics
, vol.424
, Issue.2
, pp. 219-225
-
-
Sakaguchi, K.1
Green, M.2
Stock, N.3
Reger, T.S.4
Zunic, J.5
King, C.6
-
32
-
-
77957114353
-
Predictability of idiosyncratic drug toxicity risk for carboxylic acid-containing drugs based on the chemical stability of acyl glucuronide
-
Sawamura R, Okudaira N, Watanabe K, et al. (2010). Predictability of idiosyncratic drug toxicity risk for carboxylic acid-containing drugs based on the chemical stability of acyl glucuronide. Drug Metab Dispos 38: 1857-64.
-
(2010)
Drug Metab Dispos
, vol.38
, pp. 1857-1864
-
-
Sawamura, R.1
Okudaira, N.2
Watanabe, K.3
-
33
-
-
0036320379
-
Prediction of hepatic clearance and availability by cryopreserved human hepatocytes: An application of serum incubation method
-
DOI 10.1124/dmd.30.8.892
-
Shibata Y, Takahashi H, Chiba M, Ishii Y. (2002). Prediction of hepatic clearance and availability by cryopreserved human hepatocytes: an application of serum incubation method. Drug Metab Dispos 30: 892-6. (Pubitemid 34815418)
-
(2002)
Drug Metabolism and Disposition
, vol.30
, Issue.8
, pp. 892-896
-
-
Shibata, Y.1
Takahashi, H.2
Chiba, M.3
Ishii, Y.4
-
34
-
-
0026532030
-
Acyl glucuronides revisited: Is the glucuronidation process a toxification as well as a detoxification mechanism?
-
Spahn-Langguth H, Benet LZ. (1992). Acyl glucuronides revisited: is the glucuronidation process a toxification as well as a detoxification mechanism? Drug Metab Rev 24: 5-47.
-
(1992)
Drug Metab Rev
, vol.24
, pp. 5-47
-
-
Spahn-Langguth, H.1
Benet, L.Z.2
-
35
-
-
77955591482
-
Evaluation of the human prediction of clearance from hepatocyte and microsome intrinsic clearance for 52 drug compounds
-
Sohlenius-Sternbeck AK, Afzelius L, Prusis P, et al. (2010). Evaluation of the human prediction of clearance from hepatocyte and microsome intrinsic clearance for 52 drug compounds. Xenobiotica 40: 637-49.
-
(2010)
Xenobiotica
, vol.40
, pp. 637-649
-
-
Sohlenius-Sternbeck, A.K.1
Afzelius, L.2
Prusis, P.3
-
36
-
-
84863794190
-
Practical use of the regression offset approach for the prediction of in vivo intrinsic clearance from hepatocytes
-
Sohlenius-Sternbeck AK, Jones C, Ferguson D, et al. (2012). Practical use of the regression offset approach for the prediction of in vivo intrinsic clearance from hepatocytes. Xenobiotica 42: 841-53.
-
(2012)
Xenobiotica
, vol.42
, pp. 841-853
-
-
Sohlenius-Sternbeck, A.K.1
Jones, C.2
Ferguson, D.3
-
37
-
-
79958047253
-
Risk assessment and mitigation strategies for reactive metabolites in drug discovery and development
-
Thompson RA, Isin EM, Li Y, et al. (2010). Risk assessment and mitigation strategies for reactive metabolites in drug discovery and development. Chem Biol Interact 192: 65-71.
-
(2010)
Chem Biol Interact
, vol.192
, pp. 65-71
-
-
Thompson, R.A.1
Isin, E.M.2
Li, Y.3
-
38
-
-
84865208356
-
In vitro approach to assess the potential for risk of idiosyncratic adverse reactions caused by candidate drugs
-
Thompson RA, Isin EM, Li Y et al. (2012). In vitro approach to assess the potential for risk of idiosyncratic adverse reactions caused by candidate drugs. Chem Res Toxicol 25:161632.
-
(2012)
Chem Res Toxicol
, vol.25
, pp. 161632
-
-
Thompson, R.A.1
Isin, E.M.2
Li, Y.3
-
39
-
-
0035147506
-
Prediction of a new drug's potential to cause idiosyncratic reactions
-
Uetrecht J. (2001). Prediction of a new drug's potential to cause idiosyncratic reactions. Curr Opin Drug Discov Dev 4: 55-9. (Pubitemid 32118459)
-
(2001)
Current Opinion in Drug Discovery and Development
, vol.4
, Issue.1
, pp. 55-59
-
-
Uetrecht, J.1
-
40
-
-
33847081148
-
Idiosyncratic drug reactions: Current understanding
-
Uetrecht J. (2007). Idiosyncratic drug reactions: current understanding. Annu Rev Pharmacol Toxicol 47: 513-39.
-
(2007)
Annu Rev Pharmacol Toxicol
, vol.47
, pp. 513-539
-
-
Uetrecht, J.1
-
41
-
-
71049174955
-
Evaluation of the potential for drug-induced liver injury based on in vitro covalent binding to human liver proteins
-
Usui T, Mise M, Hashizume T, et al. (2009). Evaluation of the potential for drug-induced liver injury based on in vitro covalent binding to human liver proteins. Drug Metab Dispos 37: 2383-92.
-
(2009)
Drug Metab Dispos
, vol.37
, pp. 2383-2392
-
-
Usui, T.1
Mise, M.2
Hashizume, T.3
-
42
-
-
80052258840
-
PhRMA CPCDC initiative on predictive models of human pharmacokinetics, part 4: Prediction of plasma concentration-time profiles in human from in vivo preclinical data by using the Wajima approach
-
Vuppugalla R, Marathe P, He H, et al. (2011). PhRMA CPCDC initiative on predictive models of human pharmacokinetics, part 4: prediction of plasma concentration-time profiles in human from in vivo preclinical data by using the Wajima approach. J Pharm Sci 100: 4111-26.
-
(2011)
J Pharm Sci
, vol.100
, pp. 4111-4126
-
-
Vuppugalla, R.1
Marathe, P.2
He, H.3
|