-
2
-
-
0028278916
-
Acute antiemetic efficacy and safety of dolasetron mesylate, a 5-HT3 antagonist, in cancer patients treated with cisplatin
-
T. Conroy, P. Cappelare, M. Fabbro, A. A. Fauser, T. A. Splinter, M. Spielmann, M. Scheider, B. Chevalier, A. Goupil, and J. Chauvergne: Acute antiemetic efficacy and safety of dolasetron mesylate, a 5-HT3 antagonist, in cancer patients treated with cisplatin. Am. J. Clin. Oncol. 17, 97-102 (1994).
-
(1994)
Am. J. Clin. Oncol.
, vol.17
, pp. 97-102
-
-
Conroy, T.1
Cappelare, P.2
Fabbro, M.3
Fauser, A.A.4
Splinter, T.A.5
Spielmann, M.6
Scheider, M.7
Chevalier, B.8
Goupil, A.9
Chauvergne, J.10
-
3
-
-
0026480620
-
Human dolasetron pharmacokinetics. I. Disposition following single dose intravenous administration to normal male subjects
-
H. Boxenbaum, T. Gillespie, K. Heck, and W. Hahne: Human dolasetron pharmacokinetics. I. Disposition following single dose intravenous administration to normal male subjects. Biopharm. Drug Dispos. 13, 693-701 (1992).
-
(1992)
Biopharm. Drug Dispos.
, vol.13
, pp. 693-701
-
-
Boxenbaum, H.1
Gillespie, T.2
Heck, K.3
Hahne, W.4
-
4
-
-
0027533117
-
Human dolasetron pharmacokinetics. II. Absorption and disposition following single dose oral administration to normal male subjects
-
H. Boxenbaum, T. Gillespie, K. Heck, and W. Hahne: Human dolasetron pharmacokinetics. II. Absorption and disposition following single dose oral administration to normal male subjects. Biopharm. Drug Dispos. 14, 131-141 (1993).
-
(1993)
Biopharm. Drug Dispos.
, vol.14
, pp. 131-141
-
-
Boxenbaum, H.1
Gillespie, T.2
Heck, K.3
Hahne, W.4
-
5
-
-
0029086806
-
Stereoselectivity of the carbonyl reduction of dolasetron in rats, dogs and humans
-
J. Dow and C. Berg: Stereoselectivity of the carbonyl reduction of dolasetron in rats, dogs and humans. Chirality 7, 342-348 (1995).
-
(1995)
Chirality
, vol.7
, pp. 342-348
-
-
Dow, J.1
Berg, C.2
-
6
-
-
9244259375
-
Identification of enzymes responsible for dolasetron metabolism using human hepatic cytosol and characterized human liver
-
M. K. Reith, G. A. Leeson, and L. K. Cheng: Identification of enzymes responsible for dolasetron metabolism using human hepatic cytosol and characterized human liver. ISSX Proc. 6, 254 (1994).
-
(1994)
ISSX Proc.
, vol.6
, pp. 254
-
-
Reith, M.K.1
Leeson, G.A.2
Cheng, L.K.3
-
7
-
-
0026200222
-
3 receptor antagonists, a new approach in emesis: A review of ondansetron, granisetron and tropisetron
-
3 receptor antagonists, a new approach in emesis: a review of ondansetron, granisetron and tropisetron. Anticancer Drugs 2, 343-355 (1991).
-
(1991)
Anticancer Drugs
, vol.2
, pp. 343-355
-
-
Seynaeve, C.1
Verweij, J.2
De Mulder, P.H.3
-
8
-
-
0026764731
-
Tropisetron - A review of clinical experience
-
K. M. Bruijn: Tropisetron - a review of clinical experience. Drugs 43 (Suppl. 3), 11-22 (1992).
-
(1992)
Drugs
, vol.43
, Issue.3 SUPPL.
, pp. 11-22
-
-
Bruijn, K.M.1
-
9
-
-
0025831485
-
Ondansetron - The first of a new class of antiemetic agents
-
B. J. Chaffee and R. M. Tankanow: Ondansetron - the first of a new class of antiemetic agents. Clin. Pharmacol. 10, 430-446 (1991).
-
(1991)
Clin. Pharmacol.
, vol.10
, pp. 430-446
-
-
Chaffee, B.J.1
Tankanow, R.M.2
-
10
-
-
0025639014
-
Genetic polymorphisms of drug metabolism
-
U. A. Meyer: Genetic polymorphisms of drug metabolism. Fundam. Clin. Pharmacol. 4, 595-615 (1990).
-
(1990)
Fundam. Clin. Pharmacol.
, vol.4
, pp. 595-615
-
-
Meyer, U.A.1
-
11
-
-
0028223289
-
The polymorphic cytochrome P-4502D6 is involved in the metabolism of both 5-hydroxytryptamine antagonists, tropisetron, and ondansetron
-
V. Fischer, A. E. M. Vickers, F. Heitz, S. Mahadevan, J. Baldeck, P. Minery, and R. Tynes: The polymorphic cytochrome P-4502D6 is involved in the metabolism of both 5-hydroxytryptamine antagonists, tropisetron, and ondansetron. Drug Metab. Dispos. 22, 269-274 (1994).
-
(1994)
Drug Metab. Dispos.
, vol.22
, pp. 269-274
-
-
Fischer, V.1
Vickers, A.E.M.2
Heitz, F.3
Mahadevan, S.4
Baldeck, J.5
Minery, P.6
Tynes, R.7
-
12
-
-
0029024335
-
In vitro characterization of cytochrome P450 catalysed metabolism of the antiemetic tropisetron
-
L. Firkusny, H. K. Kroemer, and M. Eichelbaum: In vitro characterization of cytochrome P450 catalysed metabolism of the antiemetic tropisetron. Biochem. Pharmacol. 49, 1777-1784 (1995).
-
(1995)
Biochem. Pharmacol.
, vol.49
, pp. 1777-1784
-
-
Firkusny, L.1
Kroemer, H.K.2
Eichelbaum, M.3
-
13
-
-
0011368056
-
Cytochrome P-450 metabolism of ondansetron by CYP1A2, CYP1A1 and CYP2D6
-
B. M. Kerr, S. Y. Boulding-Brown, C. A. Lee, C. C. Boehlert, J. F. Pritchard, C. M. Dixon, P. V. Colthup, M. K. Bayliss, M. H. Tarbit, and C. J. Serabjit-Singh: Cytochrome P-450 metabolism of ondansetron by CYP1A2, CYP1A1 and CYP2D6. ISSX Proc. 4, 137 (1994).
-
(1994)
ISSX Proc.
, vol.4
, pp. 137
-
-
Kerr, B.M.1
Boulding-Brown, S.Y.2
Lee, C.A.3
Boehlert, C.C.4
Pritchard, J.F.5
Dixon, C.M.6
Colthup, P.V.7
Bayliss, M.K.8
Tarbit, M.H.9
Serabjit-Singh, C.J.10
-
14
-
-
0025114258
-
Identification of the primary gene defect at the cytochrome P-450 CYP2D6 locus
-
A. C. Gough, J. S. Miles, N. K. Spurr, J. E. Moss, A. Gaedigk, M. Eichelbaum, and C. W. Wolf: Identification of the primary gene defect at the cytochrome P-450 CYP2D6 locus. Nature 347, 773-776 (1990).
-
(1990)
Nature
, vol.347
, pp. 773-776
-
-
Gough, A.C.1
Miles, J.S.2
Spurr, N.K.3
Moss, J.E.4
Gaedigk, A.5
Eichelbaum, M.6
Wolf, C.W.7
-
15
-
-
0017184389
-
A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding
-
M. M. Bradford: A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72, 248-254 (1976).
-
(1976)
Anal. Biochem.
, vol.72
, pp. 248-254
-
-
Bradford, M.M.1
-
16
-
-
78651165715
-
The carbon monoxide-binding pigment of liver microsomes
-
T. Omura and R. Sato: The carbon monoxide-binding pigment of liver microsomes. J. Biol. Chem. 239, 2370-2385 (1964).
-
(1964)
J. Biol. Chem.
, vol.239
, pp. 2370-2385
-
-
Omura, T.1
Sato, R.2
-
17
-
-
0024418697
-
The specificity of inhibition of debrisoquine 4-hydroxylase activity by quinidine and quinine in the rat is inverse of that in man
-
S. Kobayashi, S. Murray, D. Watson, D. Sesardic, D. S. Davies, and A. R. Boobis: The specificity of inhibition of debrisoquine 4-hydroxylase activity by quinidine and quinine in the rat is inverse of that in man. Biochem. Pharmacol. 38, 2797-2799 (1989).
-
(1989)
Biochem. Pharmacol.
, vol.38
, pp. 2797-2799
-
-
Kobayashi, S.1
Murray, S.2
Watson, D.3
Sesardic, D.4
Davies, D.S.5
Boobis, A.R.6
-
18
-
-
0026595179
-
Effects of imidazole derivatives on cytochromes P450 from human hepatocytes in primary culture
-
M. Maurice, L. Pichard, M. Daujat, I. Fabre, H. Joyeux, J. Domergue, and P. Maurel: Effects of imidazole derivatives on cytochromes P450 from human hepatocytes in primary culture. FASEB 6, 752-758 (1992).
-
(1992)
FASEB
, vol.6
, pp. 752-758
-
-
Maurice, M.1
Pichard, L.2
Daujat, M.3
Fabre, I.4
Joyeux, H.5
Domergue, J.6
Maurel, P.7
-
19
-
-
0023924549
-
In vitro inhibition studies of tolbutamide hydroxylase activity of human liver microsomes by azoles, sulphonamides and quinolines
-
D. J. Back, J. F. Tjia, J. Karbwang, and J. Colbert: In vitro inhibition studies of tolbutamide hydroxylase activity of human liver microsomes by azoles, sulphonamides and quinolines. Br. J. Clin. Pharmacol. 26, 23-29 (1988).
-
(1988)
Br. J. Clin. Pharmacol.
, vol.26
, pp. 23-29
-
-
Back, D.J.1
Tjia, J.F.2
Karbwang, J.3
Colbert, J.4
-
20
-
-
0028362263
-
Characterization of the inhibition of P4501A2 by furafylline
-
S. E. Clarke, A. D. Ayrton, and R. J. Chenery: Characterization of the inhibition of P4501A2 by furafylline. Xenobiotica 24, 517-526 (1994).
-
(1994)
Xenobiotica
, vol.24
, pp. 517-526
-
-
Clarke, S.E.1
Ayrton, A.D.2
Chenery, R.J.3
-
21
-
-
0026035519
-
Role of human cytochrome P-450 IIE1 in the oxidation of many low molecular weight cancer suspects
-
F. P. Guengerich, D. Kim, and M. Iwasaki: Role of human cytochrome P-450 IIE1 in the oxidation of many low molecular weight cancer suspects. Chem. Res. Toxicol. 4, 168-179 (1991).
-
(1991)
Chem. Res. Toxicol.
, vol.4
, pp. 168-179
-
-
Guengerich, F.P.1
Kim, D.2
Iwasaki, M.3
-
22
-
-
0027967659
-
Simultaneous measurement of the major metabolites of dolasetron mesilate in human urine using solid-phase extraction and high-performance liquid chromatography
-
P. Sanwald, N. D. Huebert, and K. D. Haegele: Simultaneous measurement of the major metabolites of dolasetron mesilate in human urine using solid-phase extraction and high-performance liquid chromatography. J. Chromatogr. B. 661, 101-107 (1994).
-
(1994)
J. Chromatogr. B.
, vol.661
, pp. 101-107
-
-
Sanwald, P.1
Huebert, N.D.2
Haegele, K.D.3
-
23
-
-
9244248370
-
The use of electrospray ionization-liquid chromatography-mass spectometry to study the role of CYP2D6 in the in vitro metabolism of 5-hydroxytryptamine receptor antagonists
-
in press
-
P. Sanwald, M. David and J. Dow: The use of electrospray ionization-liquid chromatography-mass spectometry to study the role of CYP2D6 in the in vitro metabolism of 5-hydroxytryptamine receptor antagonists. J. Chromatogr. B. in press.
-
J. Chromatogr. B.
-
-
Sanwald, P.1
David, M.2
Dow, J.3
-
25
-
-
0015893413
-
The absorption of nicotine-1-N-oxide and its reduction in the gastro-intestinal tract in man
-
P. Jenner, J. W. Gorrod, and A. H. Beckett: The absorption of nicotine-1-N-oxide and its reduction in the gastro-intestinal tract in man. Xenobiotica 3, 341-349 (1977).
-
(1977)
Xenobiotica
, vol.3
, pp. 341-349
-
-
Jenner, P.1
Gorrod, J.W.2
Beckett, A.H.3
-
26
-
-
0018712382
-
Metabolic conversion of indicine N-oxide to indicine in rabbits and humans
-
G. Powis, M. M. Ames, and J. S. Kovach: Metabolic conversion of indicine N-oxide to indicine in rabbits and humans. Cancer Res. 39, 3564-3570 (1979).
-
(1979)
Cancer Res.
, vol.39
, pp. 3564-3570
-
-
Powis, G.1
Ames, M.M.2
Kovach, J.S.3
-
27
-
-
0023607597
-
Disclosure of the metabolic retroversion of trimethylamine N-oxide in humans: A pharmacogenetic approach
-
M. Al-Waiz, R. Ayesh, S. C. Mitchell, J. R. Idle, and R. L. Smith: Disclosure of the metabolic retroversion of trimethylamine N-oxide in humans: a pharmacogenetic approach. Clin. Pharmacol. Ther. 42, 608-612 (1987).
-
(1987)
Clin. Pharmacol. Ther.
, vol.42
, pp. 608-612
-
-
Al-Waiz, M.1
Ayesh, R.2
Mitchell, S.C.3
Idle, J.R.4
Smith, R.L.5
-
28
-
-
0028858960
-
Cytochrome P450 inhibitors. Evaluation of specificities in the in vitro metabolism of therapeutic agents by human liver microsomes
-
D. J. Newton, R. W. Wang, and A. Y. H. Lu: Cytochrome P450 inhibitors. Evaluation of specificities in the in vitro metabolism of therapeutic agents by human liver microsomes. Drug Metab. Dispos. 23, 154-158 (1995).
-
(1995)
Drug Metab. Dispos.
, vol.23
, pp. 154-158
-
-
Newton, D.J.1
Wang, R.W.2
Lu, A.Y.H.3
-
29
-
-
0028171950
-
Characterisation of the cytochrome P450 enzymes involved in the in vitro metabolism of granisetron
-
J. C Bloomer, S. J. Baldwin, G. J. Smith, A. D. Ayrton, S. E. Clarke, and R. J. Chenery: Characterisation of the cytochrome P450 enzymes involved in the in vitro metabolism of granisetron. Br. J. Clin. Pharmacol. 38, 557-566 (1994).
-
(1994)
Br. J. Clin. Pharmacol.
, vol.38
, pp. 557-566
-
-
Bloomer, J.C.1
Baldwin, S.J.2
Smith, G.J.3
Ayrton, A.D.4
Clarke, S.E.5
Chenery, R.J.6
-
30
-
-
0028229191
-
The pharmacokinetics of ondansetron after intravenous injection in healthy volunteers phenotyped as poor or extensive metabolisers of debrisoquine
-
E. I. L. Ashford, J. L. Palmer, A. Bye, and A. Bedding: The pharmacokinetics of ondansetron after intravenous injection in healthy volunteers phenotyped as poor or extensive metabolisers of debrisoquine. Br. J. Clin. Pharmacol. 37, 389-391 (1994).
-
(1994)
Br. J. Clin. Pharmacol.
, vol.37
, pp. 389-391
-
-
Ashford, E.I.L.1
Palmer, J.L.2
Bye, A.3
Bedding, A.4
-
31
-
-
0011897540
-
Bioavailability and the effect of food on the pharmacokinetics of dolasetron mesilate and its active metabolite, MDL74156, in man
-
N. D. Huebert, J.-J. Schwartz, C. Hinze, and K. D. Haegele: Bioavailability and the effect of food on the pharmacokinetics of dolasetron mesilate and its active metabolite, MDL74156, in man. Br. J. Clin. Pharmacol. 37, 120P (1994).
-
(1994)
Br. J. Clin. Pharmacol.
, vol.37
-
-
Huebert, N.D.1
Schwartz, J.-J.2
Hinze, C.3
Haegele, K.D.4
-
32
-
-
0028289040
-
Clinical implication of genetic polymorphism in drug metabolism
-
G. T. Tucker: Clinical implication of genetic polymorphism in drug metabolism. J. Pharm. Pharmacol. 46 (Suppl. 1), 417-424 (1994).
-
(1994)
J. Pharm. Pharmacol.
, vol.46
, Issue.1 SUPPL.
, pp. 417-424
-
-
Tucker, G.T.1
-
33
-
-
0026801232
-
Ondansetron - Metabolism and pharmacokinetics
-
J. F. Pritchard: Ondansetron - metabolism and pharmacokinetics. Semin. Oncol. 19 (Suppl. 4), 9-15 (1992).
-
(1992)
Semin. Oncol.
, vol.19
, Issue.4 SUPPL.
, pp. 9-15
-
-
Pritchard, J.F.1
|