-
1
-
-
0025204647
-
2 production in synovial fibroblasts
-
Ito A, Mori Y. Effect of a novel anti-inflammatory drug, 2-(10, 11-dihydro-10-oxo-dibenzo [b, f ] -thiepin-2-yl) propionic acid (CN-100), on the proteoglycan biosynthesis in articular chondrocytes and prostaglandin E2 production in synovial fibroblasts. Res Commun Chem Pathol Pharmacol 1990; 70: 131-142.
-
(1990)
Res Commun Chem Pathol Pharmacol
, vol.70
, pp. 131-142
-
-
Ito, A.1
Mori, Y.2
-
2
-
-
0010468706
-
Pharmacokinetics of CN-100 for 80 mg tablet of final preparation in healthy volunteers
-
Sasaki K, Iizuka K, Sano H, Miwa M, Haruki S. Pharmacokinetics of CN-100 for 80 mg tablet of final preparation in healthy volunteers. Jpn Pharmacol Ther 1992; 20: 2167-2174.
-
(1992)
Jpn Pharmacol Ther
, vol.20
, pp. 2167-2174
-
-
Sasaki, K.1
Iizuka, K.2
Sano, H.3
Miwa, M.4
Haruki, S.5
-
3
-
-
0028858960
-
Cytochrome P450 inhibitors: Evaluation of specificities in the in vitro metabolism of therapeutic agents by human liver microsomes
-
Newton DJ, Wang RW, Lu AYH. Cytochrome P450 inhibitors: evaluation of specificities in the in vitro metabolism of therapeutic agents by human liver microsomes. Drug Metab Dispos 1995; 23: 154-158.
-
(1995)
Drug Metab Dispos
, vol.23
, pp. 154-158
-
-
Newton, D.J.1
Wang, R.W.2
Lu, A.Y.H.3
-
4
-
-
0028970047
-
Ketoconazole and sulphaphenazole as the respective selective inhibitors of P4503A and 2C9
-
Baldwin SJ, Bloomer JC, Smith GJ, et al. Ketoconazole and sulphaphenazole as the respective selective inhibitors of P4503A and 2C9. Xenobiotica 1995; 25: 261-270.
-
(1995)
Xenobiotica
, vol.25
, pp. 261-270
-
-
Baldwin, S.J.1
Bloomer, J.C.2
Smith, G.J.3
-
5
-
-
0032970480
-
Fully automated analysis of activities catalysed by the major human liver cytochrome P450 (CYP) enzymes: Assessment of human CYP inhibition potential
-
Moody GC, Griffin SJ, Mather AN, McGinnity DF, Riley RJ. Fully automated analysis of activities catalysed by the major human liver cytochrome P450 (CYP) enzymes: Assessment of human CYP inhibition potential. Xenobiotica 1999; 29: 53-75.
-
(1999)
Xenobiotica
, vol.29
, pp. 53-75
-
-
Moody, G.C.1
Griffin, S.J.2
Mather, A.N.3
McGinnity, D.F.4
Riley, R.J.5
-
6
-
-
0035062308
-
Inhibition of drug metabolism in human liver microsomes by nizatidine, cimetidine and omeprazole
-
Furuta S, Kamada E, Suzuki T, et al. Inhibition of drug metabolism in human liver microsomes by nizatidine, cimetidine and omeprazole. Xenobiotica 2001; 31: 1-10
-
(2001)
Xenobiotica
, vol.31
, pp. 1-10
-
-
Furuta, S.1
Kamada, E.2
Suzuki, T.3
-
7
-
-
0035119491
-
In vitro inhibition of cytochrome P450 enzymes in human liver microsomes by a potent CYP2A6 inhibitor, trans-2-phenylcyclopropylamine (tranylcypromine), and its nonamine analog, cyclopropylbenzene
-
Taavitsainen P, Juvonen R, Pelkonen O. In vitro inhibition of cytochrome P450 enzymes in human liver microsomes by a potent CYP2A6 inhibitor, trans-2-phenylcyclopropylamine (tranylcypromine), and its nonamine analog, cyclopropylbenzene. Drug Metab Dispos 2001; 29: 217-222
-
(2001)
Drug Metab Dispos
, vol.29
, pp. 217-222
-
-
Taavitsainen, P.1
Juvonen, R.2
Pelkonen, O.3
-
8
-
-
0030056594
-
Specificity of substrate and inhibitor probes for cytochrome P450s: Evaluation of in vitro metabolism using cDNA-expressed human P450s and human liver microsomes
-
Ono S, Hatanaka T, Hotta H, et al. Specificity of substrate and inhibitor probes for cytochrome P450s: Evaluation of in vitro metabolism using cDNA-expressed human P450s and human liver microsomes. Xenobiotica 1996; 26: 681-693
-
(1996)
Xenobiotica
, vol.26
, pp. 681-693
-
-
Ono, S.1
Hatanaka, T.2
Hotta, H.3
-
9
-
-
0034015751
-
Inhibitory effects of amiodarone and its N-deethylated metabolite on human cytochrome P450 activities: Prediction of in vivo drug interactions
-
Ohyama K, Nakajima M, Suzuki M, et al. Inhibitory effects of amiodarone and its N-deethylated metabolite on human cytochrome P450 activities: Prediction of in vivo drug interactions. Br J Clin Pharmacol 2000; 49: 244-253.
-
(2000)
Br J Clin Pharmacol
, vol.49
, pp. 244-253
-
-
Ohyama, K.1
Nakajima, M.2
Suzuki, M.3
-
10
-
-
0031723235
-
Prediction of pharmacokinetic alterations caused by drug-drug interactions: Metabolic interaction in the liver
-
Ito K, Iwatsubo T, Kanamitsu S, et al. Prediction of pharmacokinetic alterations caused by drug-drug interactions: Metabolic interaction in the liver. Pharmacol Rev 1998; 50: 387-411.
-
(1998)
Pharmacol Rev
, vol.50
, pp. 387-411
-
-
Ito, K.1
Iwatsubo, T.2
Kanamitsu, S.3
-
11
-
-
0033956664
-
Prediction of pharmacokinetic drug/drug interactions from in vitro data: Interactions of the nonsteroidal anti-inflammatory drug lornoxicam with oral anticoagulants
-
Kohl C, Steinkellner M. Prediction of pharmacokinetic drug/drug interactions fromin vitro data: Interactions of the nonsteroidal anti-inflammatory drug lornoxicam with oral anticoagulants. Drug Metab Dispos 2000; 28: 161-168
-
(2000)
Drug Metab Dispos
, vol.28
, pp. 161-168
-
-
Kohl, C.1
Steinkellner, M.2
-
12
-
-
0034014925
-
Identification of the major human liver cytochrome P450 isoform (s) responsible for the formation of the primary metabolites of ziprasidone and prediction of possible drug interactions
-
Prakash C, Kamel A, Cui D, et al. Identification of the major human liver cytochrome P450 isoform (s) responsible for the formation of the primary metabolites of ziprasidone and prediction of possible drug interactions. Br J Clin Pharmacol 2000; 49(Suppl 1): 35S-42S.
-
(2000)
Br J Clin Pharmacol
, vol.49
, Issue.SUPPL. 1
-
-
Prakash, C.1
Kamel, A.2
Cui, D.3
-
13
-
-
0027433317
-
Complementary deoxyribonucleic acid cloning and expression of a human liver uridine diphosphate-glucuronosyltransferase glucuronidating carboxylic acid-containing drugs
-
Jin C, Miners JO, Lillywhite KJ, Mackenzie PI. Complementary deoxyribonucleic acid cloning and expression of a human liver uridine diphosphate-glucuronosyltransferase glucuronidating carboxylic acid-containing drugs. J Pharmacol Exp Ther 1993; 264: 475-479.
-
(1993)
J Pharmacol Exp Ther
, vol.264
, pp. 475-479
-
-
Jin, C.1
Miners, J.O.2
Lillywhite, K.J.3
Mackenzie, P.I.4
-
14
-
-
0031894377
-
The glucuronidation of opioids, other xenobiotics, and androgens by human UGT2B7Y (268) and UGT2B7H (268)
-
Coffman BL, King CD, Rios GR, Tephly TR. The glucuronidation of opioids, other xenobiotics, and androgens by human UGT2B7Y (268) and UGT2B7H (268). Drug Metab Dispos 1998; 26: 73-77.
-
(1998)
Drug Metab Dispos
, vol.26
, pp. 73-77
-
-
Coffman, B.L.1
King, C.D.2
Rios, G.R.3
Tephly, T.R.4
-
15
-
-
0017363296
-
Characteristics of a microsomal cytochrome P-448-mediated reaction. Ethoxyresorufin O-de-ethylation
-
Burke MD, Prough RA, Mayer RT. Characteristics of a microsomal cytochrome P-448-mediated reaction. Ethoxyresorufin O-de-ethylation. Drug Metab Dispos 1977; 5: 1-8.
-
(1977)
Drug Metab Dispos
, vol.5
, pp. 1-8
-
-
Burke, M.D.1
Prough, R.A.2
Mayer, R.T.3
-
16
-
-
0023873591
-
Tolbutamide hydroxylation by human liver microsomes. Kinetic characterisation and relationship to other cytochrome P-450 dependent xenobiotic oxidations
-
Miners JO, Smith KJ, Robson RA, et al. Tolbutamide hydroxylation by human liver microsomes. Kinetic characterisation and relationship to other cytochrome P-450 dependent xenobiotic oxidations. Biochem Pharmacol 1988; 37: 1137-1144.
-
(1988)
Biochem Pharmacol
, vol.37
, pp. 1137-1144
-
-
Miners, J.O.1
Smith, K.J.2
Robson, R.A.3
-
17
-
-
0030812882
-
In vitro comparison of cytochrome P450-mediated metabolic activities in human, dog, cat, and horse
-
Chauret N, Gauthier A, Martin J, Nicoll-Griffith DA.In vitro comparison of cytochrome P450-mediated metabolic activities in human, dog, cat, and horse. Drug Metab Dispos 1997; 25: 1130-1136.
-
(1997)
Drug Metab Dispos
, vol.25
, pp. 1130-1136
-
-
Chauret, N.1
Gauthier, A.2
Martin, J.3
Nicoll-Griffith, D.A.4
-
18
-
-
0023258883
-
High-performance liquid chromatographic assays for bufuralol 1′-hydroxylase, debrisoquine 4-hydroxylase, and dextromethorphan O-demethylase in microsomes and purified cytochrome P-450 isozymes of human liver
-
Kronbach T, Mathys D, Gut J, Catin T, Meyer UA. High-performance liquid chromatographic assays for bufuralol 1′-hydroxylase, debrisoquine 4-hydroxylase, and dextromethorphan O-demethylase in microsomes and purified cytochrome P-450 isozymes of human liver. Anal Biochem 1987; 162: 24-32.
-
(1987)
Anal Biochem
, vol.162
, pp. 24-32
-
-
Kronbach, T.1
Mathys, D.2
Gut, J.3
Catin, T.4
Meyer, U.A.5
-
19
-
-
0002110504
-
Induction by oxyisobutyrates of hepatic and kidney microsomal cytochrome P-450 with specificity towards hydroxylation of fatty acids
-
eds Gustafsson JÅ, Carlstedt-Duke J, Mode A, Rafter J. Elsevier/North Holland Biomedical Press, Amsterdam
-
Parker GL, Orton TC. Induction by oxyisobutyrates of hepatic and kidney microsomal cytochrome P-450 with specificity towards hydroxylation of fatty acids. In Biochemistry, Biophysics and Regulation of Cytochrome P-450, eds Gustafsson JÅ, Carlstedt-Duke J, Mode A, Rafter J. Elsevier/North Holland Biomedical Press, Amsterdam, 373-377.
-
Biochemistry, Biophysics and Regulation of Cytochrome P-450
, pp. 373-377
-
-
Parker, G.L.1
Orton, T.C.2
-
20
-
-
0023654735
-
Regulation of testosterone hydroxylation by rat liver microsomal cytochrome P-450
-
Sonderfan AJ, Arlotto MP, Dutton DR, McMillen SK, Parkinson A. Regulation of testosterone hydroxylation by rat liver microsomal cytochrome P-450. Arch Biochem Biophys 1987; 255: 27-41.
-
(1987)
Arch Biochem Biophys
, vol.255
, pp. 27-41
-
-
Sonderfan, A.J.1
Arlotto, M.P.2
Dutton, D.R.3
McMillen, S.K.4
Parkinson, A.5
-
21
-
-
0029122943
-
Drug interaction of zaltoprofen, a novel anti-inflammatory drug, and its effect on hepatic drug metabolizing enzyme
-
Sano H, Segawa Y, Furuta S, et al. Drug interaction of zaltoprofen, a novel anti-inflammatory drug, and its effect on hepatic drug metabolizing enzyme. Jpn Pharmacol Ther 1995; 23: 1477-1487.
-
(1995)
Jpn Pharmacol Ther
, vol.23
, pp. 1477-1487
-
-
Sano, H.1
Segawa, Y.2
Furuta, S.3
-
22
-
-
0025001434
-
Absorption, distribution, metabolism and excretion of CN-100, (±) -2-(10, 11-dihydro-10-oxodibenzo[b, f]thiepin-2-yl) propionic acid in rats
-
Haruki S, Yamada A. Absorption, distribution, metabolism and excretion of CN-100, (±) -2-(10, 11-dihydro-10-oxodibenzo[b, f ]thiepin-2-yl) propionic acid in rats. Jpn Pharmacol Ther 1990; 18: 3843-3863.
-
(1990)
Jpn Pharmacol Ther
, vol.18
, pp. 3843-3863
-
-
Haruki, S.1
Yamada, A.2
-
24
-
-
0031841377
-
Cytochrome P4502C9 is an enzyme of major importance in human drug metabolism
-
Miners JO, Birkett DJ. Cytochrome P4502C9 is an enzyme of major importance in human drug metabolism. Br J Clin Pharmacol 1998; 45: 525-538.
-
(1998)
Br J Clin Pharmacol
, vol.45
, pp. 525-538
-
-
Miners, J.O.1
Birkett, D.J.2
-
25
-
-
0034818966
-
Is cytochrome P450 2C9 genotype associated with NSAID gastric ulceration?
-
Martin JH, Begg EJ, Kennedy MA, Roberts R, Barclay ML. Is cytochrome P450 2C9 genotype associated with NSAID gastric ulceration? Br J Clin Pharmacol 2001; 51: 627-630
-
(2001)
Br J Clin Pharmacol
, vol.51
, pp. 627-630
-
-
Martin, J.H.1
Begg, E.J.2
Kennedy, M.A.3
Roberts, R.4
Barclay, M.L.5
-
27
-
-
0024187313
-
Species, organ and cellular variation in the flavin-containing monooxygenase
-
Hodgson E, Levi PE. Species, organ and cellular variation in the flavin-containing monooxygenase. Drug Metabol Drug Interact 1988; 6: 219-233.
-
(1988)
Drug Metabol Drug Interact
, vol.6
, pp. 219-233
-
-
Hodgson, E.1
Levi, P.E.2
-
28
-
-
0035039708
-
Metabolism of sulfinpyrazone sulfide and sulfinpyrazone by human liver microsomes and cDNA-expressed cytochrome P450s
-
He M, Rettie AE, Neal J, Trager WF. Metabolism of sulfinpyrazone sulfide and sulfinpyrazone by human liver microsomes and cDNA-expressed cytochrome P450s. Drug Metab Dispos 2001; 29: 701-711.
-
(2001)
Drug Metab Dispos
, vol.29
, pp. 701-711
-
-
He, M.1
Rettie, A.E.2
Neal, J.3
Trager, W.F.4
-
29
-
-
0035052562
-
In-vitro metabolism of celecoxib, a cyclooxygenase-2 inhibitor, by allelic variant forms of human liver microsomal cytochrome P450 2C9: Correlation with CYP2C9 genotype and in-vivo pharmacokinetics
-
Tang C, Shou M, Rushmore TH, et al. In-vitro metabolism of celecoxib, a cyclooxygenase-2 inhibitor, by allelic variant forms of human liver microsomal cytochrome P450 2C9: Correlation with CYP2C9 genotype and in-vivo pharmacokinetics. Pharmacogenetics 2001; 11: 223-235
-
(2001)
Pharmacogenetics
, vol.11
, pp. 223-235
-
-
Tang, C.1
Shou, M.2
Rushmore, T.H.3
-
30
-
-
0032733974
-
Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: An examination of in vitro half-life approach and nonspecific binding to microsomes
-
Obach RS. Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: An examination of in vitro half-life approach and nonspecific binding to microsomes. Drug Metab Dispos 1999; 27: 1350-1359.
-
(1999)
Drug Metab Dispos
, vol.27
, pp. 1350-1359
-
-
Obach, R.S.1
|