-
1
-
-
33645983649
-
Reactive intermediates and the pathogenesis of adverse drug reactions: The toxicology perspective
-
Amacher, D. E. Reactive intermediates and the pathogenesis of adverse drug reactions: The toxicology perspective. Curr. Drug Metab., 2006, 7, 219-229.
-
(2006)
Curr. Drug Metab.
, vol.7
, pp. 219-229
-
-
Amacher, D.E.1
-
2
-
-
79951599050
-
-
A. A. Elfarra, Ed.; American Association of Pharamceutical Scientists
-
Kalgutkar, A. S. In: Advances in Bioactivation Research; A. A. Elfarra, Ed.; American Association of Pharamceutical Scientists, 2008; pp. 27-55.
-
(2008)
Advances in Bioactivation Research
, pp. 27-55
-
-
Kalgutkar, A.S.1
-
3
-
-
38949099990
-
Mechanism-based inactivation of human cytochromes P450s: Experimental characterization, reactive intermediates, and clinical implications
-
DOI 10.1021/tx7002504
-
Hollenberg, P. F.; Kent, U. M.; Bumpus, N. N. Mechanism-Based Inactivation of Human Cytochromes P450s: experimental characterization, reactive intermediates, and clinical implications. Chem. Res. Toxicol., 2008, 21, 189-205. (Pubitemid 351219719)
-
(2008)
Chemical Research in Toxicology
, vol.21
, Issue.1
, pp. 189-205
-
-
Hollenberg, P.F.1
Kent, U.M.2
Bumpus, N.N.3
-
4
-
-
0036570099
-
Timing of new black box warnings and withdrawals for prescription medications
-
Lasser, K. E.; allen, P. D.; Woolhandler, S. J.; Himmelstein, D. U.; Wolfe, S. M.; Bor, D. H. Timing of new black box warning and withdrawals for prescription medications. J. Am. Med. Assoc., 2002, 287, 2215-2220. (Pubitemid 34441937)
-
(2002)
Journal of the American Medical Association
, vol.287
, Issue.17
, pp. 2215-2220
-
-
Lasser, K.E.1
Allen, P.D.2
Woolhandler, S.J.3
Himmelstein, D.U.4
Wolfe, S.M.5
Bor, D.H.6
-
5
-
-
49449102568
-
Toxicophores, reactive metabolites and drug safety: When is it a cause for concern?
-
Kalgutkar, A. S.; Fate, G.; Didiuk, M. T.; Bauman, J. Toxicophores, reactive metabolites and drug safety: when is it a cause for concern? Exp. Rev. Clin. Pharmacol., 2008, 1, 515-531.
-
(2008)
Exp. Rev. Clin. Pharmacol.
, vol.1
, pp. 515-531
-
-
Kalgutkar, A.S.1
Fate, G.2
Didiuk, M.T.3
Bauman, J.4
-
6
-
-
37849042912
-
Minimizing metabolic activation during pharmaceutical lead optimisation: Progress, knowledge gaps and future directions
-
Kumar, S.; Kassahun, K.; Tschirret-Guth, R. A.; Mitra, K.; Baillie, T. A. Minimizing metabolic activation during pharmaceutical lead optimisation: progress, knowledge gaps and future directions. Curr. Opin. Drug Discov., 2008, 11, 43-52.
-
(2008)
Curr. Opin. Drug Discov.
, vol.11
, pp. 43-52
-
-
Kumar, S.1
Kassahun, K.2
Tschirret-Guth, R.A.3
Mitra, K.4
Baillie, T.A.5
-
7
-
-
0030869610
-
Potential metabolic bioactivation pathways involving cyclic tertiary amines and azaarenes
-
DOI 10.1021/tx970096j
-
Castagnoli, Jr., N.; Rimoldi, J. M.; Bloomquist, J.; Castagnoli, K. P. Potential metabolic bioactivation pathways involving cyclic tertiary amines and azaarenes. Chem. Res. Toxicol., 1997, 10, 924-940. (Pubitemid 27418007)
-
(1997)
Chemical Research in Toxicology
, vol.10
, Issue.9
, pp. 924-940
-
-
Castagnoli N., Jr.1
Rimoldi, J.M.2
Bloomquist, J.3
Castagnoli, K.P.4
-
8
-
-
0028117125
-
The metabolism of alicyclic amines to reactive iminium ion intermediates
-
Gorrod, J. W.; Aislaitner, G. The metabolism of alicyclic amines to reactive iminium ion intermediates. Eur. J. Drug Metab. Phatmacokinet., 1994, 19, 209-217. (Pubitemid 24331190)
-
(1994)
European Journal of Drug Metabolism and Pharmacokinetics
, vol.19
, Issue.3
, pp. 209-217
-
-
Gorrod, J.W.1
Aislaitner, G.2
-
9
-
-
0035996573
-
On the diversity of oxidative bioactivation reactions on nitrogen-containing xenobiotics
-
DOI 10.2174/1389200023337360
-
Kalgutkar, A. S.; Dalvie, D. K.; O'Donnell, J. P.; Taylor, T. J.; Sahakian, D. C. On the diversity of oxidative bioactivation reactins on nitrogen-containing xenobiotics. Curr. Drug Metab., 2002, 3, 379-424. (Pubitemid 34778004)
-
(2002)
Current Drug Metabolism
, vol.3
, Issue.4
, pp. 379-424
-
-
Kalgutkar, A.S.1
Dalvie, D.K.2
O'Donnell, J.P.3
Taylor, T.J.4
Sahakian, D.C.5
-
10
-
-
0029118957
-
Haemoprotein-mediated metabolism of enamines and the possible involvement of one-electron oxidations
-
Sayre, L. M.; Engelhart, D. A.; Nadkarni, D. V.; Babu, M. K. M.; Klein, M. E.; McCoy, G. Haemoprotein-mediated metabolism of enamines and the possible involvement of one-electron oxidations. Xenobiotica, 1995, 7, 769-775.
-
(1995)
Xenobiotica
, vol.7
, pp. 769-775
-
-
Sayre, L.M.1
Engelhart, D.A.2
Nadkarni, D.V.3
Babu, M.K.M.4
Klein, M.E.5
McCoy, G.6
-
11
-
-
0025147290
-
The MPTP story: MAO activates tetrahydropyridine derivatives to toxins causing parkinsonism
-
Maret, G.; Testa, B.; Jenner, P.; El Taya, N.; and Carrupt, P-A. The MPTP story: MAO activates tetrahydropyridine derivatives to toxins causing Parkinsonism. Drug Metab. Rev., 1990, 22, 291-332. (Pubitemid 20340902)
-
(1990)
Drug Metabolism Reviews
, vol.22
, Issue.4
, pp. 291-332
-
-
Maret, G.1
Testa, B.2
Jenner, P.3
El Tayar, N.4
Carrupt, P.-A.5
-
12
-
-
0025988085
-
MPTP mechanism of neurotoxicity and their implications for Parkinson's disease
-
Gerlach, M.; Riederer, P.; Przuntek, H.; Youdim, M. B. H. MPTP mechanism of neurotoxicity and their implications for Parkinson's disease. Eur. J. Pharmacol., 1991, 208, 273-286.
-
(1991)
Eur. J. Pharmacol.
, vol.208
, pp. 273-286
-
-
Gerlach, M.1
Riederer, P.2
Przuntek, H.3
Youdim, M.B.H.4
-
13
-
-
0030437807
-
Astrocytes as the site for bioactivation of neurotoxins
-
Di Monte, D. A.; Royland, J. E.; Irwin, I.; Langston, J. W. Astrocytes as the site for bioactivation of neurotoxins. Neurotoxicology, 1996, 17, 697-704. (Pubitemid 27131818)
-
(1996)
NeuroToxicology
, vol.17
, Issue.3-4
, pp. 697-704
-
-
Di Monte, D.A.1
Royland, J.E.2
Irwin, I.3
Langston, J.W.4
-
14
-
-
0036038993
-
Studies on the oxidation of 1, 4-disubstituted-1, 2, 3, 6-tetrahydropyridines
-
Castagnoli, N. Jr.; Castagnoli, K.; Magnin, G.; Kuttab, S.; Shang, J. Studies on the oxidation of 1, 4-disubstituted-1, 2, 3, 6-tetrahydropyridines. Drug. Metab. Rev., 2002, 34, 533-547.
-
(2002)
Drug. Metab. Rev.
, vol.34
, pp. 533-547
-
-
Castagnoli Jr., N.1
Castagnoli, K.2
Magnin, G.3
Kuttab, S.4
Shang, J.5
-
15
-
-
0022632791
-
Parkinson-like syndrome in nonhuman primates receiving a tetrahydropyridine derivative
-
Barsoum, N.j.; Gouh, A. W.; Sturgess, J. M.; De la Iglesia, F. W. Parkinson-like syndrome in nonhuman primates receiving a tetrahydropyridine derivatives. Neurotoxicology, 1986, 7, 119-126. (Pubitemid 16116626)
-
(1986)
NeuroToxicology
, vol.7
, Issue.1
, pp. 119-126
-
-
Barsoum, N.J.1
Gough, A.W.2
Sturgess, J.M.3
De La Iglesia, F.A.4
-
16
-
-
0005697982
-
-
Bernard, E. A. and Costa, E, Eds., Thieme Medical Publishers, New York
-
Taylor, C. P.; Sedman, A. J. In: Transmitter Amino Acid Receptors: Structures, Transduction And Models For Drug Development: Bernard, E. A. and Costa, E, Eds., Thieme Medical Publishers, New York, 1991, pp. 251-271.
-
(1991)
Transmitter Amino Acid Receptors: Structures, Transduction and Models for Drug Development
, pp. 251-271
-
-
Taylor, C.P.1
Sedman, A.J.2
-
17
-
-
0027174070
-
Identification of a pyridinium metabolite in human urine following a single oral dose of 1-[2-[bis[4-(trifluoromethyl)phenyl]methoxy]ethyl]- 1,2,5,6-tetrahydro-3-pyridinecarboxylic acid monohydrochloride, a γ- aminobutyric acid uptake inhibitor
-
Radulovic, L.; Woolf, T.; Bjorge, S.; Taylor, C.; Reiley, M.; Bockbrader, H.; Chang, T. Identification of a pyridinium metabolite in human urine following a single oral dose of 1-[2-[bis[4-(trifluoromethyl) phenyl]methoxy]ethyl]-1, 2, 5, 6-tetrahydro-3-pyridinecarboxylic acid monohydrochloride (CI-966), a.gamma.-aminobutyric acid uptake inhibitor. Chem. Res. Toxicol., 1993, 6, 341-344. (Pubitemid 23146597)
-
(1993)
Chemical Research in Toxicology
, vol.6
, Issue.3
, pp. 341-344
-
-
Radulovic, L.1
Woolf, T.2
Bjorge, S.3
Taylor, C.4
Reily, M.5
Bockbrader, H.6
Chang, T.7
-
18
-
-
0037404037
-
Influence of lipophilicity on the interactions of N-alkyl-4-phenyl-1,2,3, 6-tetrahydropyridines and their positively charged N-alkyl-4-phenylpyridinium metabolites with cytochrome P450 2D6
-
DOI 10.1124/dmd.31.5.596
-
Amit S. Kalgutkar, Sue Zhou, Odette A. Fahmi, Timothy J. Taylor. Influence of lipophilicity on the interactions of N-alkyl-4-phenyl-1, 2, 3, 6-tetrahydropyridines and their positively charged N-alkyl-4-phenylpyridinium metabolites with cytochrome P450 2D6. Drug Metab. Dispos., 2003, 31, 596-605. (Pubitemid 36444169)
-
(2003)
Drug Metabolism and Disposition
, vol.31
, Issue.5
, pp. 596-605
-
-
Kalgutkar, A.S.1
Zhou, S.2
Fahmi, O.A.3
Taylor, T.J.4
-
19
-
-
24644510168
-
Model electrochemical-mass spectrometric studies of the cytochrome P450-catalyzed oxidations of cyclic tertiary allylamines
-
DOI 10.1021/ja052048o
-
Jurva, U.; Bissel, P.; Isin, E. M.; Igarashi, K.; Kuttab, S.; Castagnoli, N. Jr. Model electrochemical-mass spectrometric studies of the cytochrome P450-catalyzed oxidations of cyclic tertiary allylamines. J. Am. Chem. Soc. 2005, 127, 12368-12377. (Pubitemid 41279264)
-
(2005)
Journal of the American Chemical Society
, vol.127
, Issue.35
, pp. 12368-12377
-
-
Jurva, U.1
Bissel, P.2
Isin, E.M.3
Igarashi, K.4
Kuttab, S.5
Castagnoli Jr., N.6
-
20
-
-
0035436665
-
Reactive metabolites and their role in drug reactions
-
Naisbitt, D. J.; Williams, D. P.; Pirmohamed, M.; Kitteringham, N. R.; and Park, B. K. Reactive metabolites and their role in drug reactions. Curr. Opin. Allergy Clin. Immunol, 2001, 1, 317-325.
-
(2001)
Curr. Opin. Allergy Clin. Immunol.
, vol.1
, pp. 317-325
-
-
Naisbitt, D.J.1
Williams, D.P.2
Pirmohamed, M.3
Kitteringham, N.R.4
Park, B.K.5
-
21
-
-
0035699746
-
Reactive metabolite screen for reducing candidate attrition in drug discovery
-
Chen, W. G.; Zhang, C.; Avery, M. J.; Fouda, H. G. Reactive metabolite screen for reducing candidate attrition in drug discovery. Adv. Exp. Med. Biol., 2001, 500, 521-524. (Pubitemid 34107049)
-
(2001)
Advances in Experimental Medicine and Biology
, vol.500
, pp. 521-524
-
-
Chen, W.G.1
Zhang, C.2
Avery, M.J.3
Fouda, H.G.4
-
22
-
-
0042308479
-
In vitro formation of quinoid metabolites of the dietary supplement Cimicifuga racemosa (black cohosh)
-
Johnson, B. M.; and van Breemen, R. B. In vitro formation of quinoid metabolites of the dietary supplement Cimicifuga racemosa (black cohosh). Chem. Res. Toxicol, 2003, 16, 838-846. (Pubitemid 36898998)
-
(2003)
Chemical Research in Toxicology
, vol.16
, Issue.7
, pp. 838-846
-
-
Johnson, B.M.1
Van Breemen, R.B.2
-
23
-
-
3242703146
-
Oxidation of raloxifene to quinoids: Potential toxic pathways via a diquinone methide and o-quinones
-
DOI 10.1021/tx0342722
-
Yu, L., Liu, H., Li, W., Zhang, F., Luckie, C., van Breemen, R. B., Thatcher, G. R., and Bolton, J. L. Oxidation of raloxifene to quinoids: potential toxic pathways via a diquinone methide and oquinones. Chem. Res. Toxicol, 2004, 17, 879-888. (Pubitemid 38955346)
-
(2004)
Chemical Research in Toxicology
, vol.17
, Issue.7
, pp. 879-888
-
-
Yu, L.1
Liu, H.2
Li, W.3
Zhang, F.4
Luckie, C.5
Van Breemen, R.B.6
Thatcher, G.R.J.7
Bolton, J.L.8
-
24
-
-
14844316005
-
A high-throughput liquid chromatography/tandem mass spectrometry method for screening glutathione conjugates using exact mass neutral loss acquisition
-
DOI 10.1002/rcm.1855
-
Castro-Perez, J.; Plumb, R.; Liang, L.; Yang, E. A high-throughput liquid chromatography/tandem mass spectrometry method for screening glutathione conjugates using exact mass neutral loss acquisition. Rapid Commun. Mass Spectrom., 2005, 19, 798-804. (Pubitemid 40349420)
-
(2005)
Rapid Communications in Mass Spectrometry
, vol.19
, Issue.6
, pp. 798-804
-
-
Castro-Perez, J.1
Plumb, R.2
Liang, L.3
Yang, E.4
-
25
-
-
0023756891
-
Protective role of glutathione and glutathione transferases in mutagenesis and carcinogenesis
-
Ketterer, B. Protective role of glutathione and glutathione transferases in mutagenesis and carcinogenesis. Mutat. Res., 1988, 202, 343-361.
-
(1988)
Mutat. Res.
, vol.202
, pp. 343-361
-
-
Ketterer, B.1
-
26
-
-
0027205012
-
Mass spectrometry in the analysis of glutathione conjugates
-
DOI 10.1002/bms.1200220602
-
Baillie, T. A.; Davis, M. R. Mass spectrometry in the analysis of glutathione conjugates. Biol. Mass Spectrom., 1993, 22, 319-325. (Pubitemid 23165443)
-
(1993)
Biological Mass Spectrometry
, vol.22
, Issue.6
, pp. 319-325
-
-
Baillie, T.A.1
Davis, M.R.2
-
27
-
-
0344851843
-
Mechanistic Studies on the Bioactivation of Diclofenac: Identification of Diclofenac-S-acyl-glutathione in Vitro in Incubations with Rat and Human Hepatocytest
-
DOI 10.1021/tx034038b
-
Grillo, M. P.; Hua, F.; Knutson, C. G.; Ware, J. A.; and Li, C. Mechanistic studies on the bioactivation of diclofenac: identification of diclofenac-S-acyl-glutathione in vitro in incubations with rat and human hepatocytes. Chem. Res. Toxicol., 2003, 16, 1410-1417. (Pubitemid 37464462)
-
(2003)
Chemical Research in Toxicology
, vol.16
, Issue.11
, pp. 1410-1417
-
-
Grillo, M.P.1
Hua, F.2
Knutson, C.G.3
Ware, J.A.4
Li, C.5
-
28
-
-
27144477300
-
Cyanide trapping of iminium ion reactive intermediates followed by detection and structure identification using liquid chromatography-tandem mass spectrometry (LC-MS/MS)
-
DOI 10.1021/tx0501637
-
Argoti, D.; Liang, L.; Conteh, A.; Liangfu Chen, L.; Bershas, D.; Yu, C. P.; Vouros, P.; Yang, E. Cyanide trapping of iminium ion reactive intermediates followed by detection and structure identification using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Chem. Res. Toxicol., 2005, 18, 1537-1544. (Pubitemid 41504473)
-
(2005)
Chemical Research in Toxicology
, vol.18
, Issue.10
, pp. 1537-1544
-
-
Argoti, D.1
Liang, L.2
Conteh, A.3
Chen, L.4
Bershas, D.5
Yu, C.-P.6
Vouros, P.7
Yang, E.8
-
29
-
-
0025986938
-
Trapping of reactive intermediates by incorporation of 14C-sodium cyanide during microsomal oxidation
-
Gorrod, J. W.; Whittlesea, C. M.; Lam, S. P. Trapping of reactive intermediates by incorporation of 14C-sodium cyanide during microsomal oxidation. Adv. Exp. Med. Biol., 1991, 283, 657-664.
-
(1991)
Adv. Exp. Med. Biol.
, vol.283
, pp. 657-664
-
-
Gorrod, J.W.1
Whittlesea, C.M.2
Lam, S.P.3
-
30
-
-
33645278643
-
A quantitative high-throughput trapping assay as a measurement of potential for bioactivation
-
Meneses-Lorente, G.; Zea Sakatis, M.; Schulz-Utermoehl, T.; De Nardi, C.; Watt, A. P. A quantitative high-throughput trapping assay as a measurement of potential for bioactivation. Anal. Biochem., 2006, 351, 266-272.
-
(2006)
Anal. Biochem.
, vol.351
, pp. 266-272
-
-
Meneses-Lorente, G.1
Zea Sakatis, M.2
Schulz-Utermoehl, T.3
De Nardi, C.4
Watt, A.P.5
-
31
-
-
1642281756
-
Drug-Protein Adducts: An Industry Perspective on Minimizing the Potential for Drug Bioactivation in Drug Discovery and Development
-
DOI 10.1021/tx034170b
-
Evans, D. C.; Watt, A. P.; Nicoll-Griffith, D. A.; and Baillie, T. A. Drug-protein adducts: an industry perspective on minimizing the potential for drug bioactivation in drug discovery and development. Chem. Res. Toxicol, 2004, 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
-
32
-
-
20244376331
-
In vitro bioactivation of dihydrobenzoxathiin selective estrogen receptor modulators by cytochrome P450 3A4 in human liver microsomes: Formation of reactive iminium and quinone type metabolites
-
DOI 10.1021/tx0496789
-
Zhang, Z.; Chen, Q.; Li, Y.; Doss, G. A.; Dean, B. J.; Ngui, J. S.; Elipe, M. S.; Kim, S.; Wu, J. Y.; DiNinno, F.; Hammond, M. L.; Stearns, R. A.; Evans, D. C.; Baillie, T. A.; Tang, W. In vitro bioactivation of dihydrobenzoxathiin selective estrogen receptor modulators by cytochrome P450 3A4 in human liver microsomes: formation of reactive iminium and quinone type metabolites. Chem. Res. Toxicol, 2005, 18, 675-685. (Pubitemid 40563281)
-
(2005)
Chemical Research in Toxicology
, vol.18
, Issue.4
, pp. 675-685
-
-
Zhang, Z.1
Chen, Q.2
Li, Y.3
Doss, G.A.4
Dean, B.J.5
Ngui, J.S.6
Elipe, M.S.7
Kim, S.8
Wu, J.Y.9
DiNinno, F.10
Hammond, M.L.11
Stearns, R.A.12
Evans, D.C.13
Baillie, T.A.14
Tang, W.15
-
34
-
-
9644307848
-
Discovery of (2S)-N-[(1R)-2-[4-cyclohexyl-4-[[(1,1-dimethylethyl)amino] carbonyl]-1-piperidinyl]-1-[(4-fluorophenyl)methyl]-2-oxoethyl] -4-methyl-2-piperazinecarboxamide (MB243), a potent and selective melanocortin subtype-4 receptor agonist
-
DOI 10.1016/j.bmcl.2004.10.020, PII S0960894X0401248X
-
Palucki, B. L.; Park, M. K.; Nargund, R. P.; Ye, Z.; Sebhat, I. K.; Pollard, P. G.; Kalyani, R. N.; Tang, R.; MacNeil, T.; Weinberg, D. H.; Vongs, A.; Rosenblum, C. I.; Doss, G. A.; Miller, R. R.; Stearns, R. A.; Peng, Q.; Tamvakopoulos, C.; McGowan, E.; Martin, W. J.; Metzger, J. M.; Shepherd, C. A.; Strack, A. M.; MacIntyre, D. E.; Van der Ploeg, L. H. T.; Patchett, A. A. Discovery of (2S)-N-[(1 R)-2-[4-cyclohexyl-4-[[(1, 1-dimethylethyl) amino] carbonyl]-1-piperidinyl]-1-[(4-fluorophenyl) methyl]-2-oxoethyl]-4-methyl-2- piperazinecarboxamide (MB243), a potent and selective melanocortin subtype-4 receptor agonist. Bioorg. Med. Chem. Lett., 2005, 15, 171-175. (Pubitemid 39575806)
-
(2005)
Bioorganic and Medicinal Chemistry Letters
, vol.15
, Issue.1
, pp. 171-175
-
-
Palucki, B.L.1
Park, M.K.2
Nargund, R.P.3
Ye, Z.4
Sebhat, I.K.5
Pollard, P.G.6
Kalyani, R.N.7
Tang, R.8
MacNeil, T.9
Weinberg, D.H.10
Vongs, A.11
Rosenblum, C.I.12
Doss, G.A.13
Miller, R.R.14
Stearns, R.A.15
Peng, Q.16
Tamvakopoulos, C.17
McGowan, E.18
Martin, W.J.19
Metzger, J.M.20
Shepherd, C.A.21
Strack, A.M.22
MacIntyre, D.E.23
Van Der Ploeg, L.H.T.24
Patchett, A.A.25
more..
-
35
-
-
13844250566
-
Metabolic activation of a 1,3-disubstituted piperazine derivative: Evidence for a novel ring contraction to an imidazoline
-
DOI 10.1021/tx049711r
-
Doss, G. A.; Miller, R. R.; Zhang, Z.; Teffera, Y.; Nargund, R. P.; Palucki, B.; Park, M. K.; Tang, Y. S.; Evans, D. C.; Baillie, T. A.; Stearns, R. A. Metabolic Activation of a 1, 3-Disubstituted Piperazine Derivative: Evidence for a Novel Ring Contraction to an Imidazoline. Chem. Res. Toxicol., 2005, 18, 271-276. (Pubitemid 40256246)
-
(2005)
Chemical Research in Toxicology
, vol.18
, Issue.2
, pp. 271-276
-
-
Doss, G.A.1
Miller, R.R.2
Zhang, Z.3
Teffera, Y.4
Nargund, R.P.5
Palucki, B.6
Park, M.K.7
Tang, Y.S.8
Evans, D.C.9
Baillie, T.A.10
Stearns, R.A.11
-
36
-
-
0032465960
-
Identification of rodent carcinogens and noncarcinogens using genetic toxicity tests: Premises, promises, and performance
-
DOI 10.1006/rtph.1998.1234
-
Zeiger, E. Identification of rodent carcinogens and noncarcinogens using genetic toxicity tests: premises, promises, and performance. Regul. Toxicol. Pharmacol., 1998, 28, 85-95. (Pubitemid 29076774)
-
(1998)
Regulatory Toxicology and Pharmacology
, vol.28
, Issue.2
, pp. 85-95
-
-
Zeiger, E.1
-
37
-
-
0343621452
-
Prediction of rodent carcinogenicity utilizing a battery of in vitro and in vivo genotoxicity tests
-
Kim, B. S.; Margolin, B. H. Prediction of rodent carcinogenicity utilizing a battery of in vitro and in vivo genotoxicity tests. Environ. Mol. Mutagen., 1999, 34, 297-304. (Pubitemid 30039047)
-
(1999)
Environmental and Molecular Mutagenesis
, vol.34
, Issue.4
, pp. 297-304
-
-
Kim, B.S.1
Margolin, B.H.2
-
38
-
-
34249103662
-
2c receptor agonist for the treatment of obesity: Role of metabolic activation
-
DOI 10.1124/dmd.106.013649
-
Kalgutkar, A. S.; Dalvie, D. K.; Aubrecht, J.; Smith, E. B.; Coffing, S. L.; Cheung, J. R.; Vage, C.; Lame, M. E.; Chiang, P.; McClure, K. F.; Maurer, T. S.; Coelho, Jr., R. V.; Soliman, V. F.; Schildknegt, K. Genotoxicity of 2-(3-chlorobenzyloxy)-6-(piperazinyl) pyrazine, a novel 5-hHydroxytryptamine2c receptor agonist for the treatment of obesity: role of metabolic activation. Drug. Metab. Dispos., 2007, 35, 848-858. (Pubitemid 46798595)
-
(2007)
Drug Metabolism and Disposition
, vol.35
, Issue.6
, pp. 848-858
-
-
Kalgutkar, A.S.1
Dalvie, D.K.2
Aubrecht, J.3
Smith, E.B.4
Coffing, S.L.5
Cheung, J.R.6
Vage, C.7
Lame, M.E.8
Chiang, P.9
McClure, K.F.10
Maurer, T.S.11
Coelho Jr., R.V.12
Soliman, V.F.13
Schildknegt, K.14
-
39
-
-
0034894282
-
Efficacy and safety of mirtazapine in major depressive disorder patients after SSRI treatment failure: An open-label trial
-
Fava, M.; Dunner, D. L.; Greist, J. H.; Preskorn, S. H.; Trivedi, M. H.; Zajecka, J.; Cohen, M. Efficacy and safety of mirtazapine in major depressive disorder patients after SSRI treatment failure: An open-label trial. J. Clin. Psychiatry, 2001, 62, 413-420. (Pubitemid 32717873)
-
(2001)
Journal of Clinical Psychiatry
, vol.62
, Issue.6
, pp. 413-420
-
-
Fava, M.1
Dunner, D.L.2
Greist, J.H.3
Preskorn, S.H.4
Trivedi, M.H.5
Zajecka, J.6
Cohen, M.7
-
40
-
-
0023742928
-
Safety of midazolam
-
Inman, W. H. W. Safety of midazolam. Lancet, 1988, 2, 683-684.
-
(1988)
Lancet
, vol.2
, pp. 683-684
-
-
Inman, W.H.W.1
-
41
-
-
0032853328
-
Isoform-selective metabolism of mianserin by cytochrome P-450 2D
-
Chow, T.; Hiroi, T.; Imaoka, S.; Chiba, K.; Funae, Y. Isoformselective metabolism of mianserin by cytochrome P-450 2D. Drug. Metab. Dispos., 1999, 27, 1200-1204. (Pubitemid 29463608)
-
(1999)
Drug Metabolism and Disposition
, vol.27
, Issue.10
, pp. 1200-1204
-
-
Chow, T.1
Hiroi, T.2
Imaoka, S.3
Chiba, K.4
Funae, Y.5
-
42
-
-
0024451145
-
Structural requirements for bioactivation of anticonvulsants to cytotoxic metabolites in vitro
-
Riley, R. J.; Kitteringham, N. R.; Park, B. K. Structural requirements for bioactivation of anticonvulsants to cytotoxic metabolites in vitro. Br. J. Clin. Pharmacol., 1989, 28, 482-487. (Pubitemid 19269788)
-
(1989)
British Journal of Clinical Pharmacology
, vol.28
, Issue.4
, pp. 482-487
-
-
Roley, R.J.1
Kitteringham, N.R.2
Park, B.K.3
-
43
-
-
0025352538
-
Formation of cytotoxic metabolites from phenytoin, imipramine, desipramine, amitriptyline and mianserin by mouse and human hepatic microsomes
-
DOI 10.1016/0006-2952(90)90614-Q
-
Riley, R. J.; Roberts, P.; Kitteringham, M. R. Park, B. K. Formation of cytotoxic metabolites from phenytoin, imipramine, desipramine, amitriptyline and mianserin by mouse and human hepatic microsomes. Biochem. Pharmacol., 1990, 39, 1951-1958. (Pubitemid 20187331)
-
(1990)
Biochemical Pharmacology
, vol.39
, Issue.12
, pp. 1951-1958
-
-
Riley, R.J.1
Roberts, P.2
Kitteringham, N.R.3
Park, B.K.4
-
44
-
-
58249118866
-
Screening and characterization of reactive metabolites using glutathione ethyl ester in combination with Q-trapmass spectrometry J
-
Wen, B. and Fitch, L. Screening and characterization of reactive metabolites using glutathione ethyl ester in combination with Q-trapmass spectrometry J. Mass Spectrometry, 2009, 44, 90-99.
-
(2009)
Mass Spectrometry
, vol.44
, pp. 90-99
-
-
Wen, B.1
Fitch, L.2
-
45
-
-
0242658899
-
Drug-induced hepatotoxicity
-
Andrade, R. J.; Lucena, M. I. Drug-induced hepatotoxicity. N. Eng.l J. Med., 2003, 349, 1974-1976.
-
(2003)
N. Eng.l J. Med.
, vol.349
, pp. 1974-1976
-
-
Andrade, R.J.1
Lucena, M.I.2
-
46
-
-
0345376184
-
Nefazodone (Serzone) withdrawn because of hepatotoxicity
-
Choi, S. Nefazodone (serzone) withdrawn because of hepatotoxicity. CMAJ., 2003, 169, 1187. (Pubitemid 37491525)
-
(2003)
Canadian Medical Association Journal
, vol.169
, Issue.11
, pp. 1187
-
-
Choi, S.1
-
47
-
-
20844454730
-
Bioactivation of the nontricyclic antidepressant nefazodone to a reactive quinone-imine species in human liver microsomes and recombinant cytochrome P450 3A4
-
DOI 10.1124/dmd.104.001735
-
Kalgutkar, A. S.; Vaz, A. D.; Lame, M. E.; Henne, K. R.; Soglia, J.; Zhao, S. X.; Abramov, Y. A.; Lombardo, F.; Collin, C.; Hendsch, Z. S.; Hop, C. E. C. A. Bioactivation of the nontricyclic antidepressant nefazodone to a reactive quinone-imine species in human liver microsomes and recombinant cytochrome P450 3A4. Drug. Metab. Dispos., 2005, 33, 243-253. (Pubitemid 40216592)
-
(2005)
Drug Metabolism and Disposition
, vol.33
, Issue.2
, pp. 243-253
-
-
Kalgutkar, A.S.1
Vaz, A.D.N.2
Lame, M.E.3
Henne, K.R.4
Soglia, J.5
Zhao, S.X.6
Abramov, Y.A.7
Lombarde, F.8
Collin, C.9
Hendsch, Z.S.10
Hop, C.E.C.A.11
-
48
-
-
34547672814
-
N-dealkylation of arylpiperazine derivatives: Disposition and metabolism of the 1-aryl-piperazines formed
-
DOI 10.2174/138920007781368908
-
Caccia, S. N-Dealkylation of arylpiprazine derivatives: Disposition and metabolism of the 1-arylpiperazines formed. Curr. Drug. Metab., 2007, 8, 612-622. (Pubitemid 47209098)
-
(2007)
Current Drug Metabolism
, vol.8
, Issue.6
, pp. 612-622
-
-
Caccia, S.1
-
49
-
-
44149108220
-
Comparison of the bioactivation potential of the antidepressant and hepatotoxin nefazodone with aripiprazole, a structural analog and marketed drug
-
DOI 10.1124/dmd.108.020545
-
Bauman, J. N.; Frederick, K. S.; Sawant, A.; Walsky, R. L.; Cox, L. M.; Obach, R. S.; Kalgutkar, A. S. Comparison of the bioactivation potential of the antidepressant and hepatotoxin nefazodone with aripiprazole, a structural analog and marketed drug. Drug. Metab. Dispos., 2008, 36, 1016-1029. (Pubitemid 351717458)
-
(2008)
Drug Metabolism and Disposition
, vol.36
, Issue.6
, pp. 1016-1029
-
-
Bauman, J.N.1
Frederick, K.S.2
Sawant, A.3
Walsky, R.L.4
Cox, L.M.5
Obach, R.S.6
Kalgutkar, A.S.7
-
50
-
-
0020535550
-
Prazosin update. A review of its pharmacological properties and therapeutic use in hypertension and congestive heart failure
-
Stanaszek, W. F.; Kellerman, D.; Brogden, R. N.; Romankiewicz, J. A. Prazosin update. A review of its pharmacological properties and therapeutic use in hypertension and congestive heart failure. Drugs, 1983, 25, 339-384. (Pubitemid 13112223)
-
(1983)
Drugs
, vol.25
, Issue.4
, pp. 339-384
-
-
Stanaszek, W.F.1
Kellerman, D.2
Brogden, R.N.3
Romankiewicz, J.A.4
-
51
-
-
34249088106
-
Metabolism of prazosin in rat, dog, and human liver microsomes and cryopreserved rat and human hepatocytes and characterization of metabolites by liquid chromatography/tandem mass spectrometry
-
DOI 10.1124/dmd.106.013219
-
Erve, J. C. L.; Vashishtha, S. C.; DeMaio, W.; Talaat, R. E. Metabolism of prazosin in rat, dog, and human liver microsomes and cryopreserved rat and human hepatocytes and characterization of metabolites by liquid chromatography/tandem mass spectrometry. Drug. Metab. Dispos., 2007, 35, 908-916. (Pubitemid 46798601)
-
(2007)
Drug Metabolism and Disposition
, vol.35
, Issue.6
, pp. 908-916
-
-
Erve, J.C.L.1
Vashishtha, S.C.2
DeMaio, W.3
Talaat, R.E.4
-
52
-
-
35848937130
-
Bioactivation of phencyclidine in rat and human liver microsomes and recombinant P450 2B enzymes: Evidence for the formation of a novel quinone methide intermediate
-
DOI 10.1021/tx700145k
-
Driscoll, J. P.; Kornecki, K.; Wolkowski, J. P.; Chupak, L.; Kalgutkar, A. S.; O'Donnell, J. P. Bioactivation of phencyclidine in rat and human liver microsomes and recombinant P450 2B enzymes: Evidence for the formation of a novel quinone methide intermediate. Chem. Res. Toxicol., 2007, 20, 1488-1497. (Pubitemid 350057218)
-
(2007)
Chemical Research in Toxicology
, vol.20
, Issue.10
, pp. 1488-1497
-
-
Driscoll, J.P.1
Kornecki, K.2
Wolkowski, J.P.3
Chupak, L.4
Kalgutkar, A.S.5
O'Donnell, J.P.6
-
53
-
-
0026041960
-
Generation and fate of enamines in the microsomal metabolism of cyclic tertiary amines
-
Sayre, L. M.; Engelhart, D. A.; Venkataraman, B.; Babu, M. K. M.; McCoy, G. D. Generation and fate of enamines in the microsomal metabolism of cyclic tertiary amines. Biocem. Biophy. Res. Comm., 1991, 179, 1368-1376.
-
(1991)
Biocem. Biophy. Res. Comm.
, vol.179
, pp. 1368-1376
-
-
Sayre, L.M.1
Engelhart, D.A.2
Venkataraman, B.3
Babu, M.K.M.4
McCoy, G.D.5
-
54
-
-
0025899971
-
Application of chemical cytochrome P-450 model system to studies on drug metabolism
-
Masumoto, H.; Ohta, S.; Hirobe, M. Application of chemical cytochrome P-450 model system to studies on drug metabolism. Drug. Metab. Dispos., 1991, 19, 768-778.
-
(1991)
Drug. Metab. Dispos.
, vol.19
, pp. 768-778
-
-
Masumoto, H.1
Ohta, S.2
Hirobe, M.3
-
55
-
-
0020322386
-
Metabolic formation of iminium species: Metabolism of phencyclidine
-
DOI 10.1021/jm00347a002
-
Ward, D.; Kalir, A.; Trevor, A.; Adams, J. Metabolic formation of iminium species: metabolism of phencyclidine. J. Med. Chem., 1982, 25, 491-492. (Pubitemid 12051969)
-
(1982)
Journal of Medicinal Chemistry
, vol.25
, Issue.5
, pp. 491-492
-
-
Ward, D.1
Kalir, A.2
Trevor, A.3
-
56
-
-
0021990110
-
Metabolism of phencyclidine. The role of the carbinolamine intermediate in the formation of lactam and amino acid metabolites of nitrogen heterocycles
-
DOI 10.1021/jm00379a011
-
Baker, J. K.; Little, T. L. Metabolism of phencyclidine. The role of the carbinolamine intermediate in the formation of lactam and amino acid metabolites of nitrogen heterocycles. J. Med. Chem., 1985, 28, 46-50. (Pubitemid 15156295)
-
(1985)
Journal of Medicinal Chemistry
, vol.28
, Issue.1
, pp. 46-50
-
-
Baker, J.K.1
Little, T.L.2
-
57
-
-
0037671381
-
The mechanism-based inactivation of human cytochrome P450 2B6 by phencyclidine
-
DOI 10.1124/dmd.31.1.46
-
Jushchyshyn, M. I.; Kent, U. M.; Hollenberg, P. F. The mechanismbased inactivation of human cytochrome P450 2B6 by phencyclidine. Drug. Metab. Dispos., 2003, 31, 46-52. (Pubitemid 36735257)
-
(2003)
Drug Metabolism and Disposition
, vol.31
, Issue.1
, pp. 46-52
-
-
Jushchyshyn, M.I.1
Kent, U.M.2
Hollenberg, P.F.3
-
58
-
-
0033775525
-
Molecular mechanisms of selective estrogen receptor modulator (SERM) action
-
Dutertre, M.; and Smith, C. L. Molecular mechanisms of selective estrogen receptor modulator (SERM) action. J. Pharmacol. Exp. Ther., 2000, 295, 431-437.
-
(2000)
J. Pharmacol. Exp. Ther.
, vol.295
, pp. 431-437
-
-
Dutertre, M.1
Smith, C.L.2
-
59
-
-
0034068228
-
Role of quinones in toxicology
-
DOI 10.1021/tx9902082
-
Bolton, J. L.; Trush, M. A.; Penning, T. M.; Dryhurst, G.; Monks, T. J. Role of quinones in toxicology. Chem. Res. Toxicol, 2000, 13, 135-160. (Pubitemid 30169958)
-
(2000)
Chemical Research in Toxicology
, vol.13
, Issue.3
, pp. 135-160
-
-
Bolton, J.L.1
Trush, M.A.2
Penning, T.M.3
Dryhurst, G.4
Monks, T.J.5
-
60
-
-
11144356286
-
Estrogen Receptor Ligands. II. Discovery of Benzoxathiins as Potent, Selective Estrogen Receptor α Modulators
-
DOI 10.1021/jm034243o
-
Kim, S., Wu, J. Y., Birzin, E. T., Frisch, K., Chan, W., Pai, L., Yang, Y. T., Mosley, R. T., Fitzgerald, P. M. D., Sharma, N., Dahllund, J., Thorsell, A., Dininno, F., Rohrer, S. P., Schaeffer, J. M., Hammond, M. L. Estrogen receptor ligands. II. Discovery of benzoxathiins as potent, selective estrogen receptor a modulators. J. Med. Chem., 2004, 47, 2171-2175. (Pubitemid 38478840)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.9
, pp. 2171-2175
-
-
Kim, S.1
Wu, J.Y.2
Birzin, E.T.3
Frisch, K.4
Chan, W.5
Pai, L.-Y.6
Yang, Y.T.7
Mosley, R.T.8
Fitzgerald, P.M.D.9
Sharma, N.10
Dahllund, J.11
Thorsell, A.-G.12
DiNinno, F.13
Rohrer, S.P.14
Schaeffer, J.M.15
Hammond, M.L.16
-
61
-
-
2342467515
-
Estrogen receptor ligands. Part 4: The SAR of the syn-dihydrobenzoxathiin SERAMs
-
DOI 10.1016/j.bmcl.2004.03.074, PII S0960894X04004470
-
Kim, S.; Wu, J.; Chen, H. Y.; Birzin, E. T.; Chan, W.; Yang, Y. T.; Colwell, L.; Li, S.; Dahllund, J.; Dininno, F.; Rohrer, S. P.; Schaeffer, J. M.; Hammond, M. L. Estrogen receptor ligands. Part 4. The SAR of the syn-dihydrobenzoxathiin SERMs. Bioorg. Med. Chem. Lett., 2004, 14, 2741-2745. (Pubitemid 38569730)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.11
, pp. 2741-2745
-
-
Kim, S.1
Wu, J.2
Chen, H.Y.3
Birzin, E.T.4
Chan, W.5
Yang, Y.T.6
Colwell, L.7
Li, S.8
Dahllund, J.9
DiNinno, F.10
Rohrer, S.P.11
Schaeffer, J.M.12
Hammond, M.L.13
-
62
-
-
20244376331
-
In vitro bioactivation of dihydrobenzoxathiin selective estrogen receptor modulators by cytochrome P450 3A4 in human liver microsomes: Formation of reactive iminium and quinone type metabolites
-
DOI 10.1021/tx0496789
-
Zhang, Z.; Chen, Q.; Li, Y.; Doss, G. A.; Dean, B. J.; Ngui, J. S.; Elipe, M. S.; Wu, S. K. J. Y.; DiNinno, F.; Hammond, M. L.; Stearns, R. A.; Evans, D. C.; Baillie, T. A.; Tang, W. In vitro bioactivation of dihydrobenzoxathiin selective estrogen receptor modulators by cytochrome P450 3A4 in human liver microsomes: formation of reactive iminium and quinone type metabolites. Chem. Res. Toxicol, 2005, 18, 675-685. (Pubitemid 40563281)
-
(2005)
Chemical Research in Toxicology
, vol.18
, Issue.4
, pp. 675-685
-
-
Zhang, Z.1
Chen, Q.2
Li, Y.3
Doss, G.A.4
Dean, B.J.5
Ngui, J.S.6
Elipe, M.S.7
Kim, S.8
Wu, J.Y.9
DiNinno, F.10
Hammond, M.L.11
Stearns, R.A.12
Evans, D.C.13
Baillie, T.A.14
Tang, W.15
-
63
-
-
0026066622
-
Dehydration is the first step in the bioactivation of haloperidol to its pyridinium metabolite
-
Rang, J.; Gorrod, J. W. E. Dehydration is the first step in the bioactivation of haloperidol to its pyridinium metabolite. Toxicol. Lett., 1991, 59, 117-123.
-
(1991)
Toxicol. Lett.
, vol.59
, pp. 117-123
-
-
Rang, J.1
Gorrod, J.W.E.2
-
64
-
-
4143090802
-
Identification of an N-methyl-4-phenylpyridinium-like metabolite of the antidiarrheal agent loperamide in human liver microsomes: Underlying reason(s) for the lack of neurotoxicity despite the bioactivation event
-
Kalgutkar, A. S.; Nguyen, H. T. Identification of N-methyl-4- phenylpyridinium-like metabolite of the antidarrheal agent loperamide in human liver microsomes: undelying reason (s) for the lack of neurotoxicity despite the bioactivation event. Drug. Metab. Dispos., 2004, 32, 943-952. (Pubitemid 39096054)
-
(2004)
Drug Metabolism and Disposition
, vol.32
, Issue.9
, pp. 943-952
-
-
Kalgutkar, A.S.1
Nguyen, H.T.2
-
65
-
-
0030965178
-
Pyrrolidides: Synthesis and structure-activity relationship as inhibitors of dipeptidyl peptidase IV
-
DOI 10.1016/S0223-5234(97)89082-4
-
Augustyns, K. J. L.; Lambeir, A. M.; Borloo, M.; De Meester, I.; Vedernikova, I.; Vanhoof, G.; Hendriks, D.; Scharpé, S.; Haemers, A. Pyrrolidides: synthesis and structure-activity relationship as inhibitors of dipeptidyl peptidase IV. Eur. J. Med. Chem., 1997, 32, 301-309. (Pubitemid 27220261)
-
(1997)
European Journal of Medicinal Chemistry
, vol.32
, Issue.4
, pp. 301-309
-
-
Augustyns, K.J.L.1
Lambeir, A.M.2
Borloo, M.3
De Meester, I.4
Vedernikova, I.5
Vanhoof, G.6
Hendriks, D.7
Scharpe, S.8
Haemers, A.9
-
66
-
-
10744233045
-
Fluoropyrrolidine amides as dipeptidyl peptidase IV inhibitors
-
DOI 10.1016/j.bmcl.2003.12.040
-
Caldwell, C. G.; Chen, P.; He, J.; Parmee, E. R.; Leiting, B.; Marsilio, F.; Patel, R. A.; Wu, J. K.; Eiermann, G. J.; Petrov, A. Fluoropyrrolidine amides as dipeptidyl peptidase IV inhibitors. Bioorg. Med. Chem. Lett., 2004, 14, 1265-1268 (Pubitemid 38229869)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.5
, pp. 1265-1268
-
-
Caldwell, C.G.1
Chen, P.2
He, J.3
Parmee, E.R.4
Leiting, B.5
Marsilio, F.6
Patel, R.A.7
Wu, J.K.8
Eiermann, G.J.9
Petrov, A.10
He, H.11
Lyons, K.A.12
Thornberry, N.A.13
Weber, A.E.14
-
67
-
-
11144285534
-
Metabolic activation of fluoropyrrolidine dipeptidyl peptidase-IV inhibitors by rat liver microsomes
-
DOI 10.1124/dmd.104.001842
-
Shiyao Xu, Bing Zhu, Yohannes Teffera, Deborah E. Pan, Charles G. Caldwell, George Doss, Ralph A. Stearns, David C. Evans, Maria G. Beconi. Metabolic activation of fluoropyrrolidine dipeptidyl peptidase-IV inhibitors by rat liver microsomes. Drug. Metab. Dispos., 2005, 33, 121-130. (Pubitemid 40023523)
-
(2005)
Drug Metabolism and Disposition
, vol.33
, Issue.1
, pp. 121-130
-
-
Xu, S.1
Zhu, B.2
Teffera, Y.3
Pan, D.E.4
Caldwell, C.G.5
Doss, G.6
Stearns, R.A.7
Evans, D.C.8
Beconi, M.G.9
-
68
-
-
13344293709
-
Inhibition of monoamine oxidase B in the brains of smokers
-
DOI 10.1038/379733a0
-
Fowler, J. S.; Volkow, N. D.; Wang, G-J.; Pappas, N.; Logan, J.; MacGregor, R.; Alexoff, D.; Shea, C.; Schlyer, D.; Wolf, A. P.; Warner, D.; Zezulkova, I.; Cilento, R. Inhibition of monoamine oxidase B in the brains of smokers. Nature, 1996, 379, 733-736. (Pubitemid 26061736)
-
(1996)
Nature
, vol.379
, Issue.6567
, pp. 733-736
-
-
Fowler, J.S.1
Volkow, N.D.2
Wang, G.-J.3
Pappas, N.4
Logan, J.5
MacGregor, R.6
Alexoff, D.7
Shea, C.8
Schlyer, D.9
Wolf, A.P.10
Warner, D.11
Zezulkova, I.12
Cilento, R.13
-
69
-
-
0033018662
-
Studies on the pyrrolinone metabolites derived from the tobacco alkaloid 1-methyl-2-(3-pyridinyl)pyrrole (β-nicotyrine)
-
DOI 10.1021/tx990019j
-
Liu, X.; Zang, L.;. Van der Schyf, C. J.; Igarashi, K.; Castagnoli, K.; Castagnoli, Jr. N. Studies on the pyrrolinone metabolites derived from the tobacco alkaloid 1-methyl-2-(3-pyridinyl) pyrrole (pnicotyrine). Chem. Res. Toxicol, 1999, 12, 508-512. (Pubitemid 29282921)
-
(1999)
Chemical Research in Toxicology
, vol.12
, Issue.6
, pp. 508-512
-
-
Liu, X.1
Zang, L.2
Van Der Schyf, C.J.3
Igarashi, K.4
Castagnoli, K.5
Castagnoli Jr., N.6
-
70
-
-
0034075321
-
Studies on the in vivo biotransformation of the tobacco alkaloid β- nicotyrine
-
DOI 10.1021/tx990124t
-
Liu, X.; Castagnoli, K.; Van der Schyf, C. J.; Castagnoli, Jr. N. Studies on the in vivo biotransformation of the tobacco alkaloid (3-nicotyrine. Chem. Res. Toxicol, 2000, 13, 336-341. (Pubitemid 30327152)
-
(2000)
Chemical Research in Toxicology
, vol.13
, Issue.5
, pp. 336-341
-
-
Liu, X.1
Castagnoli, K.2
Van Der Schyf, C.J.3
Castagnoli Jr., N.4
-
71
-
-
0024506245
-
+
-
DOI 10.1016/0304-3940(89)90704-0
-
Booth, R. G.; Castagnoli,. N Jr.; Rollema, H. Intracerebral microdialysis neurotoxicity studies of quinoline and isoquinoline derivatives related to MPTP/MPP+. Neurosci. Lett., 1989, 100, 306-312. (Pubitemid 19128194)
-
(1989)
Neuroscience Letters
, vol.100
, Issue.1-3
, pp. 306-312
-
-
Booth, R.G.1
Castagnoli Jr., N.2
Rollema, H.3
-
72
-
-
20044391231
-
Discovery of novel non-peptidic ketopiperazine-based renin inhibitors
-
DOI 10.1016/j.bmc.2005.01.048
-
Holsworth, D. D.; Powell, N. A.; Downing, D. M.; Cai, C.; Cody, W. L.; Ryan, J. M.; Ostroski, R.; Jalaie, M.; Bryant, J. W.; Edmunds, J. J. Discovery of novel non-peptidic ketopiperazine-based renin inhibitors. Bioorg. Med. Chem., 2005, 13, 2657-2664. (Pubitemid 40341668)
-
(2005)
Bioorganic and Medicinal Chemistry
, vol.13
, Issue.7
, pp. 2657-2664
-
-
Holsworth, D.D.1
Powell, N.A.2
Downing, D.M.3
Cai, C.4
Cody, W.L.5
Ryan, J.M.6
Ostroski, R.7
Jalaie, M.8
Bryant, J.W.9
Edmunds, J.J.10
-
73
-
-
33644967829
-
Ketopiperazine-based renin inhibitors: Optimization of the "C" ring
-
Holsworth, D. D.; Cai, C.; Cheng, X.; Cody, W. L.; Downing, D. M.; Erasga, N.; Lee, C.; Powell, N. A.; Edmunds, J. J.; Stier, M. Ketopiperazine-based renin inhibitors: optimization of the "C" ring. Bioorg. Med. Chem. Lett., 2006, 16, 2500-2504.
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 2500-2504
-
-
Holsworth, D.D.1
Cai, C.2
Cheng, X.3
Cody, W.L.4
Downing, D.M.5
Erasga, N.6
Lee, C.7
Powell, N.A.8
Edmunds, J.J.9
Stier, M.10
-
74
-
-
33751530433
-
Metabolic aromatization of N-alkyl-1,2,3,4-tetrahydroquinoline substructures to quinolinium by human liver microsomes and horseradish peroxidase
-
DOI 10.1124/dmd.106.012286
-
Gu, G.; Collins, R.; Holsworth, D. D.; Walker, G. S.; Voorman, R. L. Metabolic aromatization of N-alkyl-1, 2, 3, 4-tetrahydroquinoline substructures to quinolinium by human liver microsomes and horseradish peroxidase. Drug Metab. Dispos., 2006, 34, 2044-2055. (Pubitemid 44837765)
-
(2006)
Drug Metabolism and Disposition
, vol.34
, Issue.12
, pp. 2044-2055
-
-
Gu, C.1
Collins, R.2
Holsworth, D.D.3
Walker, G.S.4
Voorman, R.L.5
-
75
-
-
0021838250
-
The role of metabolite-specific antibodies in nomifensine-dependent immune hemolytic anemia
-
Salama, A.; Mueller-Eckhardt, C. The role of metabolite-specific antibodies in nomifensine-dependent immune hemolytic anemia. N. Engl. J. Med., 1985, 313, 469-474. (Pubitemid 15015074)
-
(1985)
New England Journal of Medicine
, vol.313
, Issue.8
, pp. 469-474
-
-
Salama, A.1
Mueller-Eckhardt, C.2
-
76
-
-
33746035132
-
Nomifensine and haemolytic Anemia
-
Mann, R. D.; Andrews, E. B. eds, Wiley, New York
-
Stonier, P. D.; Edwards, J. G. Nomifensine And Haemolytic Anemia, In Pharmacovigilance; Mann, R. D.; Andrews, E. B. eds), 2002; pp. 155-166, Wiley, New York.
-
(2002)
Pharmacovigilance
, pp. 155-166
-
-
Stonier, P.D.1
Edwards, J.G.2
-
77
-
-
33746073769
-
Metabolism of nomifensine to a dihydroisoquinolinium ion metabolite by human myeloperoxidase, hemoglobin, monoamine oxidase A, and cytochrome P450 enzymes
-
DOI 10.1124/dmd.106.010173
-
Obach, R. S.; Dalvie, D. K. Metabolism of nomifensine to a dihydroisoquinolinium ion metabolite by human myeloperoxidase, hemoglobin, monoamine oxidase A, and cytochrome P450 enzymes. Drug Metab. Dispos., 2006, 34, 1310-1316. (Pubitemid 44079871)
-
(2006)
Drug Metabolism and Disposition
, vol.34
, Issue.8
, pp. 1310-1316
-
-
Obach, R.S.1
Dalvie, D.K.2
-
78
-
-
0037243921
-
The thienopyridine derivatives (platelet adenosine diphosphate receptor antagonists), pharmacology and clinical developments
-
DOI 10.1046/j.1365-2044.2003.02960.x
-
Kam, P. C. A.; Nethery, C. M. The thienopyridine derivatives (platelet adenosine diphosphate receptor antagonists), pharmacology and clinical developments. Anaesthesia, 2003, 58, 28-35. (Pubitemid 36113325)
-
(2003)
Anaesthesia
, vol.58
, Issue.1
, pp. 28-35
-
-
Kam, P.C.A.1
Nethery, C.M.2
-
79
-
-
0029873941
-
Ticlopidine: A review of its pharmacology, clinical efficacy and tolerability in the prevention of cerebral ischemia and stroke
-
Noble, S.; Goa, K. L. Ticlopidine: a review of its pharmacology, clinical efficacy and tolerability in the prevention of cerebral ischemia and stroke. Drugs Aging., 1996, 8, 214-232.
-
(1996)
Drugs Aging.
, vol.8
, pp. 214-232
-
-
Noble, S.1
Goa, K.L.2
-
80
-
-
1642498326
-
Characterization of novel dihydrothienopyridinium and thienopyridinium metabolites of ticlopidine in vitro: Role of peroxidases, cytochromes P450, and monoamine oxidases
-
DOI 10.1124/dmd.32.1.49
-
Dalvie, D. K.; O'Connell, T. N. Characterisation of novel dihydrothienopyridinium and thienopyridinium metabolites of ticlopidine in vitro: role of peroxidases, cytochromes P450, and monoamine oxidases. Drug Metab. Dispos., 2004, 32, 49-57. (Pubitemid 38112535)
-
(2004)
Drug Metabolism and Disposition
, vol.32
, Issue.1
, pp. 49-57
-
-
Dalvie, D.K.1
O'Connell, T.N.2
-
81
-
-
38949088196
-
Metabolism and toxicity of drugs. Two decades of progress in industrial drug metabolism
-
DOI 10.1021/tx7002273
-
Baillie, T. A. Metabolism and toxicity of drugs. Two decades of progress in industrial drug metabolism. Chem. Res. Toxicol., 2008, 21, 129-137. (Pubitemid 351219714)
-
(2008)
Chemical Research in Toxicology
, vol.21
, Issue.1
, pp. 129-137
-
-
Baillie, T.A.1
-
82
-
-
19944399431
-
A comprehensive listing of bioactivation pathways of organic functional groups
-
DOI 10.2174/1389200054021799
-
Kalgutkar, A. S.; Gardne, I.; Obach, R. S.; Shaffer, C. L.; Callegari, E.; Henne, K. R.; Mutlib, A. E.; Dalvie, D. K.; Lee, J. S.; Nakai, Y.; O'Donnell, J. P.; Boer, J.; Harriman, S. P. A comprehensive listing of bioactivation pathways of organic functional groups. Curr. Drug Metab., 2005, 6, 161-225. (Pubitemid 40753853)
-
(2005)
Current Drug Metabolism
, vol.6
, Issue.3
, pp. 161-225
-
-
Kalgutkar, A.S.1
Gardner, I.2
Obach, R.S.3
Shaffer, C.L.4
Callegari, E.5
Henne, K.R.6
Mutlib, A.E.7
Dalvie, D.K.8
Lee, J.S.9
Nakai, Y.10
O'Donnell, J.P.11
Boer, J.12
Harriman, S.P.13
-
83
-
-
0035996330
-
Cytochrome P450 3A4-mediated bioactivation of raloxifene: Irreversible enzyme inhibition and thiol adduct formation
-
DOI 10.1021/tx0200109
-
Chen, Q.; Ngui, J. S.; Doss, G. A.; Wang, R. W.; Cai, X.; DiNinno, F. P.; Blizzard, T. A.; Hammond, M. L.; Stearns, R. S.; Evans, D. C.; Baillie, T. A.; Tang, W. Cytochrome P450 3A4-mediated bioactivation of raloxifene: irreversible enzyme inhibition and thiol adduct formation. Chem. Res. Toxicol., 2002, 15, 907-914. (Pubitemid 34774444)
-
(2002)
Chemical Research in Toxicology
, vol.15
, Issue.7
, pp. 907-914
-
-
Chen, Q.1
Ngui, J.S.2
Doss, G.A.3
Wang, R.W.4
Cai, X.5
DiNinno, F.P.6
Blizzard, T.A.7
Hammond, M.L.8
Stearns, R.A.9
Evans, D.C.10
Baillie, T.A.11
Tang, W.12
-
84
-
-
3242703146
-
Oxidation of raloxifene to quinoids: Potential toxic pathways via a diquinone methide and o-quinones
-
DOI 10.1021/tx0342722
-
Yu, L.; Liu, H.; Li, W.; Zhang, F.; Luckie, C.; van Breemen, R. B.; Thacher, G. R. J.; Bolton, J. L. Oxidation of raloxifene to quinoids: potential toxic pathways via a diquinone methide and o-quinones. Chem. Res. Toxicol., 2004, 17, 879-888. (Pubitemid 38955346)
-
(2004)
Chemical Research in Toxicology
, vol.17
, Issue.7
, pp. 879-888
-
-
Yu, L.1
Liu, H.2
Li, W.3
Zhang, F.4
Luckie, C.5
Van Breemen, R.B.6
Thatcher, G.R.J.7
Bolton, J.L.8
-
85
-
-
33748994836
-
Bioactivation of selective estrogen receptor modulators (SERMs)
-
DOI 10.1021/tx060126v
-
Dowers, T. S.; Qin, Z. H.; Thatcher, G. R. J.; Bolton, J. L. Bioactivation of selective estrogen receptor modulators (SERMs). Chem. Res. Toxicol., 2006, 19, 1125-1137. (Pubitemid 44454028)
-
(2006)
Chemical Research in Toxicology
, vol.19
, Issue.9
, pp. 1125-1137
-
-
Dowers, T.S.1
Qin, Z.-H.2
Thatcher, G.R.J.3
Bolton, J.L.4
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