-
1
-
-
80054860325
-
1, 4-Dihydropyridine Scaffold in Medicinal Chemistry, the Story so Far and Perspectives. (Part 1): Action in Ion Channels and GPCRs
-
Ioan, P.; Carosati, E.; Micucci, M.; Broccatelli, F.; Cruciani, G.; Zhorov, B.S.; Chiarini, A.; Budriesi, R. 1, 4-Dihydropyridine Scaffold in Medicinal Chemistry, The Story so Far And Perspectives. (Part 1): Action in Ion Channels and GPCRs. Curr. Med. Chem., 2011, 18, 4901-4922.
-
(2011)
Curr. Med. Chem.
, vol.18
, pp. 4901-4922
-
-
Ioan, P.1
Carosati, E.2
Micucci, M.3
Broccatelli, F.4
Cruciani, G.5
Zhorov, B.S.6
Chiarini, A.7
Budriesi, R.8
-
3
-
-
33645830172
-
A surface glycoprotein modulating drug permeability in Chinese hamster ovary cell mutants
-
Juliano, R.L.; Ling, V. A surface glycoprotein modulating drug permeability in Chinese hamster ovary cell mutants. Biochim. Biophys. Acta., 1976, 455, 152-162.
-
(1976)
Biochim. Biophys. Acta.
, vol.455
, pp. 152-162
-
-
Juliano, R.L.1
Ling, V.2
-
4
-
-
35148821944
-
Dihydropyridine derivatives to overcome atypical multidrug resistance: Design, synthesis, QSAR studies, and evaluation of their cytotoxic and pharmacological activities
-
Mehdipour, A.R.; Javidnia, K.; Hemmateenejad, B.; Amirghofran, Z.; Miri, R. Dihydropyridine derivatives to overcome atypical multidrug resistance: design, synthesis, QSAR studies, and evaluation of their cytotoxic and pharmacological activities. Chem. Biol. Drug Des., 2007, 70, 337-346.
-
(2007)
Chem. Biol. Drug Des.
, vol.70
, pp. 337-346
-
-
Mehdipour, A.R.1
Javidnia, K.2
Hemmateenejad, B.3
Amirghofran, Z.4
Miri, R.5
-
5
-
-
0020426820
-
Increased Accumulation of Vincristine and Adriamycin in Drug-resistant P388 Tumor Cells following Incubation with Calcium Antagonists and Calmodulin Inhibitors
-
Tsuruo, T.; Iida, H.; Tsukagoshi, S.; Sakurai, Y. Increased Accumulation of Vincristine and Adriamycin in Drug-resistant P388 Tumor Cells following Incubation with Calcium Antagonists and Calmodulin Inhibitors. Cancer Res., 1982, 42, 4730-4733.
-
(1982)
Cancer Res.
, vol.42
, pp. 4730-4733
-
-
Tsuruo, T.1
Iida, H.2
Tsukagoshi, S.3
Sakurai, Y.4
-
6
-
-
0020549246
-
Circumvention of vincristine and adriamycin resistance in vitro and in vivo by calcium influx blockers
-
Tsuruo, T.; Iida, H.; Nojiri, M.; Tsukagoshi, S.; Sakurai, Y. Circumvention of Vincristine and Adriamycin Resistance in Vitro and in Vivo by Calcium Influx Blockers. Cancer Res., 1983, 43, 2905-2910.
-
(1983)
Cancer Res.
, vol.43
, pp. 2905-2910
-
-
Tsuruo, T.1
Iida, H.2
Nojiri, M.3
Tsukagoshi, S.4
Sakurai, Y.5
-
7
-
-
0024595844
-
Analysis of structural features of dihydropyridine analogs needed to reverse multidrug resistance and to inhibit photoaffinity labeling of P-glycoprotein
-
Ichiro, N.; Kimitoshi, K.; Junko, K.; Michihiko, K.; Shin-Ichi, A.; Akira, K.; Ken-Ichi, S.; Yohji, Y.; Cornwell, M.M.; Pastan, I.; Gottesman, M.M. Analysis of structural features of dihydropyridine analogs needed to reverse multidrug resistance and to inhibit photoaffinity labeling of P-glycoprotein. Biochem. Pharmacol., 1989, 38, 519-527.
-
(1989)
Biochem. Pharmacol.
, vol.38
, pp. 519-527
-
-
Ichiro, N.1
Kimitoshi, K.2
Junko, K.3
Michihiko, K.4
Shin-Ichi, A.5
Akira, K.6
Ken-Ichi, S.7
Yohji, Y.8
Cornwell, M.M.9
Pastan, I.10
Gottesman, M.M.11
-
8
-
-
0026543580
-
A phase i study on the reversal of multidrug resistance (MDR) in vivo: Nifedipine plus etoposide
-
Philip, P.A.; Joel, S.; Monkman, S.C.; Dolega-Ossowski, E.; Tonkin, K.; Carmichael, J.; Idle, J.R.; Harris, A.L. A phase I study on the reversal of multidrug resistance (MDR) in vivo: nifedipine plus etoposide. Br. J. Cancer, 1992, 65, 267-270.
-
(1992)
Br. J. Cancer
, vol.65
, pp. 267-270
-
-
Philip, P.A.1
Joel, S.2
Monkman, S.C.3
Dolega-Ossowski, E.4
Tonkin, K.5
Carmichael, J.6
Idle, J.R.7
Harris, A.L.8
-
9
-
-
0025774639
-
B-859-35, a new drug with anti-tumor activity reverses multi-drug resistance
-
Hofmann, J.; Ueberall, F.; Egle, A.; Grunicke, H. B-859-35, a new drug with anti-tumor activity reverses multi-drug resistance. Int. J. Cancer, 1991, 47, 870-874.
-
(1991)
Int. J. Cancer
, vol.47
, pp. 870-874
-
-
Hofmann, J.1
Ueberall, F.2
Egle, A.3
Grunicke, H.4
-
10
-
-
0026583333
-
Reversal of multidrug resistance by B859-35, a metabolite of B859-35, niguldipine, verapamil and nitrendipine
-
Hofmann, J.; Wolf, A.; Spitaler, M.; Bock, G.; Drach, J.; Ludescher, C.; Grunicke, H. Reversal of multidrug resistance by B859-35, a metabolite of B859-35, niguldipine, verapamil and nitrendipine. J. Cancer Res. Clin. Oncol., 1992, 118, 361-366.
-
(1992)
J. Cancer Res. Clin. Oncol.
, vol.118
, pp. 361-366
-
-
Hofmann, J.1
Wolf, A.2
Spitaler, M.3
Bock, G.4
Drach, J.5
Ludescher, C.6
Grunicke, H.7
-
11
-
-
0028987531
-
Mechanism of action of dexniguldipine-HCl (B8509-035), a new potent modulator of multidrug resistance
-
Hofmann, J.; Gekeler, V.; Ise, W.; Noller, A.; Mitterdorfer, J.; Hofer, S.; Utz, I.; Gotwald, M.; Boer, R.; Glossmann, H.; Grunicke, H.H. Mechanism of action of dexniguldipine-HCl (B8509-035), a new potent modulator of multidrug resistance. Biochem. Pharmacol., 1995, 49, 603-609.
-
(1995)
Biochem. Pharmacol.
, vol.49
, pp. 603-609
-
-
Hofmann, J.1
Gekeler, V.2
Ise, W.3
Noller, A.4
Mitterdorfer, J.5
Hofer, S.6
Utz, I.7
Gotwald, M.8
Boer, R.9
Glossmann, H.10
Grunicke, H.H.11
-
12
-
-
0029036741
-
Tolerance safety, and kinetics of the new antineoplastic compound dexniguldipine-HCl after oral administration: A phase i doseescalation trial
-
Ukena, D.; Boewer, C.; Oldenkott, B.; Rathgeb, F.; Wurst, W.; Zech, K.; Sybrecht, G.W. Tolerance, safety, and kinetics of the new antineoplastic compound dexniguldipine-HCl after oral administration: a phase I doseescalation trial. Cancer Chemother. Pharmacol., 1995, 36, 160-164.
-
(1995)
Cancer Chemother. Pharmacol.
, vol.36
, pp. 160-164
-
-
Ukena, D.1
Boewer, C.2
Oldenkott, B.3
Rathgeb, F.4
Wurst, W.5
Zech, K.6
Sybrecht, G.W.7
-
13
-
-
0031738659
-
Newly synthesized dihydropyridine derivatives as modulators of P-glycoprotein-mediated multidrug resistance
-
Tanabe, H.; Tasaka, S.; Ohmori, H.; Gomi, N.; Sasaki, Y.; Machida, T.; Iino, M.; Kiue, A.; Naito, S.; Kuwano, M. Newly synthesized dihydropyridine derivatives as modulators of P-glycoprotein-mediated multidrug resistance. Bioorgan. Med. Chem., 1998, 6, 2219-2227.
-
(1998)
Bioorgan. Med. Chem.
, vol.6
, pp. 2219-2227
-
-
Tanabe, H.1
Tasaka, S.2
Ohmori, H.3
Gomi, N.4
Sasaki, Y.5
MacHida, T.6
Iino, M.7
Kiue, A.8
Naito, S.9
Kuwano, M.10
-
14
-
-
0035931556
-
Synthesis and structure-activity analysis of novel dihydropyridine derivatives to overcome multidrug resistance
-
Tasaka, S.; Ohmori, H.; Gomi, N.; Iino, M.; Machida, T.; Kiue, A.; Naito, S.; Kuwano, M. Synthesis and structure-activity analysis of novel dihydropyridine derivatives to overcome multidrug resistance. Bioorg. Med. Chem. Lett., 2001, 11, 275-277.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 275-277
-
-
Tasaka, S.1
Ohmori, H.2
Gomi, N.3
Iino, M.4
MacHida, T.5
Kiue, A.6
Naito, S.7
Kuwano, M.8
-
15
-
-
0028063555
-
Reversal of multidrug resistance by new dihydropyridines with low calcium antagonist activity
-
Capolongo, L.; Amboldi, N.; Ballinari, D.; Cozzi, P.; Melegaro, G.; Ripamonti, M.; Vaghi, F.; Grandi, M. Reversal of multidrug resistance by new dihydropyridines with low calcium antagonist activity. Acta Oncol., 1994, 33, 787-791.
-
(1994)
Acta Oncol.
, vol.33
, pp. 787-791
-
-
Capolongo, L.1
Amboldi, N.2
Ballinari, D.3
Cozzi, P.4
Melegaro, G.5
Ripamonti, M.6
Vaghi, F.7
Grandi, M.8
-
16
-
-
0036166651
-
3,5-dibenzoyl-1, 4-dihydropyridines: Synthesis and MDR reversal in tumor cells
-
Kawase, M.; Shah, A.; Gaveriya, H.; Motohashi, N.; Sakagami, H.; Varga, A.; Molnar, J. 3, 5-dibenzoyl-1, 4-dihydropyridines: synthesis and MDR reversal in tumor cells. Bioorgan. Med. Chem., 2002, 10, 1051-1055.
-
(2002)
Bioorgan. Med. Chem.
, vol.10
, pp. 1051-1055
-
-
Kawase, M.1
Shah, A.2
Gaveriya, H.3
Motohashi, N.4
Sakagami, H.5
Varga, A.6
Molnar, J.7
-
17
-
-
67349155960
-
DP7, a novel dihydropyridine multidrug resistance reverter, shows only weak inhibitory activity on human CYP3A enzyme(s)
-
D'Elia, P.; De Matteis, F.; Dragoni, S.; Shah, A.; Sgaragli, G.; Valoti, M. DP7, a novel dihydropyridine multidrug resistance reverter, shows only weak inhibitory activity on human CYP3A enzyme(s). Eur. J. Pharmacol., 2009, 614, 7-13.
-
(2009)
Eur. J. Pharmacol.
, vol.614
, pp. 7-13
-
-
D'Elia, P.1
De Matteis, F.2
Dragoni, S.3
Shah, A.4
Sgaragli, G.5
Valoti, M.6
-
18
-
-
1542299767
-
3, 5-Dibenzoyl-4-(3-phenoxyphenyl)-1, 4-dihydro-2, 6-dimethylpyridine (DP7) as a new multidrug resistance reverting agent devoid of effects on vascular smooth muscle contractility
-
Saponara, S.; Kawase, M.; Shah, A.; Motohashi, N.; Molnar, J.; Ugocsai, K.; Sgaragli, G.; Fusi, F., 3, 5-Dibenzoyl-4-(3-phenoxyphenyl)-1, 4-dihydro-2, 6-dimethylpyridine (DP7) as a new multidrug resistance reverting agent devoid of effects on vascular smooth muscle contractility. Brit. J. Pharmacol., 2004, 141, 415-422.
-
(2004)
Brit. J. Pharmacol.
, vol.141
, pp. 415-422
-
-
Saponara, S.1
Kawase, M.2
Shah, A.3
Motohashi, N.4
Molnar, J.5
Ugocsai, K.6
Sgaragli, G.7
Fusi, F.8
-
19
-
-
34247141496
-
3, 5-dibenzoyl-4-(3-phenoxyphenyl)-1, 4-dihydro-2, 6-dimethylpyridine (DP7): A new multidrug resistance inhibitor devoid of effects on Langendorff-perfused rat heart
-
Saponara, S.; Ferrara, A.; Gorelli, B.; Shah, A.; Kawase, M.; Motohashi, N.; Molnar, J.; Sgaragli, G.; Fusi, F., 3, 5-dibenzoyl-4-(3-phenoxyphenyl)-1, 4-dihydro-2, 6-dimethylpyridine (DP7): a new multidrug resistance inhibitor devoid of effects on Langendorff-perfused rat heart. Eur. J. Pharmacol., 2007, 563, 160-163.
-
(2007)
Eur. J. Pharmacol.
, vol.563
, pp. 160-163
-
-
Saponara, S.1
Ferrara, A.2
Gorelli, B.3
Shah, A.4
Kawase, M.5
Motohashi, N.6
Molnar, J.7
Sgaragli, G.8
Fusi, F.9
-
20
-
-
33747197446
-
Cancer cell permeability-glycoprotein as a target of MDR reverters: Possible role of novel dihydropyridine derivatives
-
Fusi, F.; Saponara, S.; Valoti, M.; Dragoni, S.; D'Elia, P.; Sgaragli, T.; Alderighi, D.; Kawase, M.; Shah, A.; Motohashi, N.; Sgaragli, G. Cancer cell permeability-glycoprotein as a target of MDR reverters: possible role of novel dihydropyridine derivatives. Curr. Drug Targets, 2006, 7, 949-959.
-
(2006)
Curr. Drug Targets
, vol.7
, pp. 949-959
-
-
Fusi, F.1
Saponara, S.2
Valoti, M.3
Dragoni, S.4
D'Elia, P.5
Sgaragli, T.6
Alderighi, D.7
Kawase, M.8
Shah, A.9
Motohashi, N.10
Sgaragli, G.11
-
21
-
-
41149150846
-
Imidazo[2 1-b] thiazole System: A Scaffold Endowing Dihydropyridines with Selective Cardiodepressant Activity
-
Budriesi, R.; Ioan, P.; Locatelli, A.; Cosconati, S.; Leoni, A.; Ugenti, M.P.; Andreani, A.; Di Toro, R.; Bedini, A.; Spampinato, S.; Marinelli, L.; Novellino, E.; Chiarini, A. Imidazo[2, 1-b]thiazole System: A Scaffold Endowing Dihydropyridines with Selective Cardiodepressant Activity. J. Med. Chem., 2008, 51, 1592-1600.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 1592-1600
-
-
Budriesi, R.1
Ioan, P.2
Locatelli, A.3
Cosconati, S.4
Leoni, A.5
Ugenti, M.P.6
Andreani, A.7
Di Toro, R.8
Bedini, A.9
Spampinato, S.10
Marinelli, L.11
Novellino, E.12
Chiarini, A.13
-
22
-
-
78651106621
-
Inhibition of MDR1 activity and induction of apoptosis by analogues of nifedipine and diltiazem: An in vitro analysis
-
Viale, M.; Cordazzo, C.; de Totero, D.; Budriesi, R.; Rosano, C.; Leoni, A.; Ioan, P.; Aiello, C.; Croce, M.; Andreani, A.; Rambaldi, M.; Russo, P.; Chiarini, A.; Spinelli, D. Inhibition of MDR1 activity and induction of apoptosis by analogues of nifedipine and diltiazem: an in vitro analysis. Invest. New Drugs, 2011, 29, 98-109.
-
(2011)
Invest. New Drugs
, vol.29
, pp. 98-109
-
-
Viale, M.1
Cordazzo, C.2
De Totero, D.3
Budriesi, R.4
Rosano, C.5
Leoni, A.6
Ioan, P.7
Aiello, C.8
Croce, M.9
Andreani, A.10
Rambaldi, M.11
Russo, P.12
Chiarini, A.13
Spinelli, D.14
-
23
-
-
27944510952
-
Effects of new 4-aryl-1, 4-dihydropyridines and 4-arylpyridines on drug efflux mediated by multidrug resistance-associated protein 1
-
Zhou, X.F.; Coburn, R.A.; Morris, M.E. Effects of new 4-aryl-1, 4-dihydropyridines and 4-arylpyridines on drug efflux mediated by multidrug resistance-associated protein 1. J. Pharm. Sci.-Us., 2005, 94, 2256-2265.
-
(2005)
J. Pharm. Sci.-Us.
, vol.94
, pp. 2256-2265
-
-
Zhou, X.F.1
Coburn, R.A.2
Morris, M.E.3
-
24
-
-
14044250851
-
New 4-aryl-1, 4-dihydropyridines and 4-arylpyridines as P-glycoprotein inhibitors
-
Zhou, X.F.; Zhang, L.; Tseng, E.; Scott-Ramsay, E.; Schentag, J.J.; Coburn, R.A.; Morris, M.E. New 4-aryl-1, 4-dihydropyridines and 4-arylpyridines as P-glycoprotein inhibitors. Drug Metab. Dispos., 2005, 33, 321-328.
-
(2005)
Drug Metab. Dispos.
, vol.33
, pp. 321-328
-
-
Zhou, X.F.1
Zhang, L.2
Tseng, E.3
Scott-Ramsay, E.4
Schentag, J.J.5
Coburn, R.A.6
Morris, M.E.7
-
25
-
-
22944449708
-
Effects of dihydropyridines and pyridines on multidrug resistance mediated by breast cancer resistance protein: In vitro and in vivo studies
-
Zhou, X.F.; Yang, X.; Wang, Q.; Coburn, R.A.; Morris, M.E. Effects of dihydropyridines and pyridines on multidrug resistance mediated by breast cancer resistance protein: in vitro and in vivo studies. Drug Metab. Dispos., 2005, 33, 1220-1228.
-
(2005)
Drug Metab. Dispos.
, vol.33
, pp. 1220-1228
-
-
Zhou, X.F.1
Yang, X.2
Wang, Q.3
Coburn, R.A.4
Morris, M.E.5
-
26
-
-
34249939511
-
Structure-activity relationships of novel N-acyloxy-1, 4-dihydropyridines as P-glycoprotein inhibitors
-
Voigt, B.; Coburger, C.; Monar, J.; Hilgeroth, A. Structure-activity relationships of novel N-acyloxy-1, 4-dihydropyridines as P-glycoprotein inhibitors. Bioorgan. Med. Chem., 2007, 15, 5110-5113.
-
(2007)
Bioorgan. Med. Chem.
, vol.15
, pp. 5110-5113
-
-
Voigt, B.1
Coburger, C.2
Monar, J.3
Hilgeroth, A.4
-
27
-
-
51449096211
-
Dihydropyridines and atypical MDR: A novel perspective of designing general reversal agents for both typical and atypical MDR
-
Miri, R.; Mehdipour, A. Dihydropyridines and atypical MDR: a novel perspective of designing general reversal agents for both typical and atypical MDR. Bioorgan. Med. Chem., 2008, 16, 8329-8334.
-
(2008)
Bioorgan. Med. Chem.
, vol.16
, pp. 8329-8334
-
-
Miri, R.1
Mehdipour, A.2
-
28
-
-
57749185247
-
Impact of novel MDR modulators on human cancer cells: Reversal activities and induction studies
-
Coburger, C.; Lage, H.; Molnar, J.; Hilgeroth, A. Impact of novel MDR modulators on human cancer cells: reversal activities and induction studies. Pharm. Res., 2009, 26, 182-188.
-
(2009)
Pharm. Res.
, vol.26
, pp. 182-188
-
-
Coburger, C.1
Lage, H.2
Molnar, J.3
Hilgeroth, A.4
-
29
-
-
77955324516
-
Novel structure-activity relationships and selectivity profiling of cage dimeric 1, 4-dihydropyridines as multidrug resistance (MDR) modulators
-
Coburger, C.; Wollmann, J.; Krug, M.; Baumert, C.; Seifert, M.; Molnar, J.; Lage, H.; Hilgeroth, A. Novel structure-activity relationships and selectivity profiling of cage dimeric 1, 4-dihydropyridines as multidrug resistance (MDR) modulators. Bioorgan. Med. Chem., 2010, 18, 4983-4990.
-
(2010)
Bioorgan. Med. Chem.
, vol.18
, pp. 4983-4990
-
-
Coburger, C.1
Wollmann, J.2
Krug, M.3
Baumert, C.4
Seifert, M.5
Molnar, J.6
Lage, H.7
Hilgeroth, A.8
-
30
-
-
33646465986
-
Biological evaluation of bishydroxymethyl-substituted cage dimeric 1, 4-dihydropyridines as a novel class of P-glycoprotein modulating agents in cancer cells
-
Richter, M.; Molnar, J.; Hilgeroth, A. Biological evaluation of bishydroxymethyl-substituted cage dimeric 1, 4-dihydropyridines as a novel class of P-glycoprotein modulating agents in cancer cells. J. Med. Chem., 2006, 49, 2838-2840.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 2838-2840
-
-
Richter, M.1
Molnar, J.2
Hilgeroth, A.3
-
31
-
-
23644441767
-
First insight into the symmetry and flexibility of membrane efflux pump P-glycoprotein by novel bifunctional modulators
-
Wollmann, J.; Richter, M.; Molnar, J.; Hilgeroth, A. First insight into the symmetry and flexibility of membrane efflux pump P-glycoprotein by novel bifunctional modulators. Chem. Bio. Chem., 2005, 6, 1353-1356.
-
(2005)
Chem. Bio. Chem.
, vol.6
, pp. 1353-1356
-
-
Wollmann, J.1
Richter, M.2
Molnar, J.3
Hilgeroth, A.4
-
32
-
-
33750989090
-
Physicochemical characteristics of novel P-glycoprotein inhibitors of the cage dimeric 1, 4-dihydropyridine type
-
Wollmann, J.; Molnar, J.; Hilgeroth, A. Physicochemical characteristics of novel P-glycoprotein inhibitors of the cage dimeric 1, 4-dihydropyridine type. Med. Chem., 2006, 2, 565-568.
-
(2006)
Med. Chem.
, vol.2
, pp. 565-568
-
-
Wollmann, J.1
Molnar, J.2
Hilgeroth, A.3
-
33
-
-
0345411341
-
P-Glycoprotein and cytochrome P-450 3A inhibition: Dissociation of inhibitory potencies
-
Wandel, C.; Kim, R.B.; Kajiji, S.; Guengerich, F.P.; Wilkinson, G.R.; Wood, A.J.J. P-Glycoprotein and Cytochrome P-450 3A Inhibition: Dissociation of Inhibitory Potencies. Cancer Res., 1999, 59, 3944-3948.
-
(1999)
Cancer Res.
, vol.59
, pp. 3944-3948
-
-
Wandel, C.1
Kim, R.B.2
Kajiji, S.3
Guengerich, F.P.4
Wilkinson, G.R.5
Wood, A.J.J.6
-
34
-
-
38549122929
-
Glucocorticoid receptor physiology
-
Heitzer, M.D.; Wolf, I.M.; Sanchez, E.R.; Witchel, S.F.; DeFranco, D.B. Glucocorticoid receptor physiology. Rev. Endocr. Metab. Disord., 2007, 8, 321-330.
-
(2007)
Rev. Endocr. Metab. Disord.
, vol.8
, pp. 321-330
-
-
Heitzer, M.D.1
Wolf, I.M.2
Sanchez, E.R.3
Witchel, S.F.4
Defranco, D.B.5
-
35
-
-
0034130707
-
Cell mediators of inflammation in the Alzheimer disease brain
-
Akiyama, H.; Arai, T.; Kondo, H.; Tanno, E.; Haga, C.; Ikeda, K. Cell mediators of inflammation in the Alzheimer disease brain. Alzheimer Dis. Assoc. Disord., 2000, 14 Suppl 1, S47-S53.
-
(2000)
Alzheimer Dis. Assoc. Disord.
, vol.14
, Issue.SUPPL. 1
-
-
Akiyama, H.1
Arai, T.2
Kondo, H.3
Tanno, E.4
Haga, C.5
Ikeda, K.6
-
36
-
-
76349084466
-
Complement in neuroprotection and neurodegeneration
-
Yanamadala, V.; Friedlander, R.M. Complement in neuroprotection and neurodegeneration. Trends Mol. Med., 2010, 16, 69-76.
-
(2010)
Trends Mol. Med.
, vol.16
, pp. 69-76
-
-
Yanamadala, V.1
Friedlander, R.M.2
-
37
-
-
0034101592
-
New anti-inflammatory treatment strategy in Alzheimer's disease
-
Sugaya, K.; Uz, T.; Kumar, V.; Manev, H. New anti-inflammatory treatment strategy in Alzheimer's disease. Jpn. J. Pharmacol., 2000, 82, 85-94.
-
(2000)
Jpn. J. Pharmacol.
, vol.82
, pp. 85-94
-
-
Sugaya, K.1
Uz, T.2
Kumar, V.3
Manev, H.4
-
38
-
-
33748681122
-
Study of the interaction of 1, 4-dihydropyridine derivatives with glucocorticoid hormone receptors from the rat liver
-
Vaitkuviene, A.; Ulinskaite, A.; Meskys, R.; Duburs, G.; Klusa, V.; Liutkevicius, E. Study of the interaction of 1, 4-dihydropyridine derivatives with glucocorticoid hormone receptors from the rat liver. Pharmacol. Rep. PR, 2006, 58, 551-558.
-
(2006)
Pharmacol. Rep. PR
, vol.58
, pp. 551-558
-
-
Vaitkuviene, A.1
Ulinskaite, A.2
Meskys, R.3
Duburs, G.4
Klusa, V.5
Liutkevicius, E.6
-
39
-
-
0021863519
-
The isolation and characterization of kadsurenone from haifenteng (Piper futokadsura) as an orally active specific receptor antagonist of platelet-activating factor
-
Shen, T.Y.; Hwang, S.B.; Chang, M.N.; Doebber, T.W.; Lam, M.H.; Wu, M.S.; Wang, X. The isolation and characterization of kadsurenone from haifenteng (Piper futokadsura) as an orally active specific receptor antagonist of platelet-activating factor. Int. J. Tissue React., 1985, 7, 339-343.
-
(1985)
Int. J. Tissue React.
, vol.7
, pp. 339-343
-
-
Shen, T.Y.1
Hwang, S.B.2
Chang, M.N.3
Doebber, T.W.4
Lam, M.H.5
Wu, M.S.6
Wang, X.7
-
40
-
-
0009645885
-
Characterization of a platelet-activating factor receptor antagonist isolated from haifenteng (Piper futokadsura): Specific inhibition of in vitro and in vivo platelet-activating factor-induced effects
-
Shen, T.Y.; Hwang, S.B.; Chang, M.N.; Doebber, T.W.; Lam, M.H.; Wu, M.S.; Wang, X.; Han, G.Q.; Li, R.Z. Characterization of a platelet-activating factor receptor antagonist isolated from haifenteng (Piper futokadsura): specific inhibition of in vitro and in vivo platelet-activating factor-induced effects. P. Natl. Acad. Sci. USA, 1985, 82, 672-676.
-
(1985)
P. Natl. Acad. Sci. USA
, vol.82
, pp. 672-676
-
-
Shen, T.Y.1
Hwang, S.B.2
Chang, M.N.3
Doebber, T.W.4
Lam, M.H.5
Wu, M.S.6
Wang, X.7
Han, G.Q.8
Li, R.Z.9
-
41
-
-
0022355670
-
Bn 52021 and related-compounds -A new series of highly specific paf-acether receptor antagonists
-
Braquet, P., Bn 52021 and Related-Compounds -a New Series of Highly Specific Paf-Acether Receptor Antagonists. Prostaglandins, 1985, 30, 687-687.
-
(1985)
Prostaglandins
, vol.30
, pp. 687-687
-
-
Braquet, P.1
-
42
-
-
0037140827
-
Syntheses and bioactivities of novel carbamates combining platelet activating factor (PAF) receptor antagonist with thromboxane synthase inhibitor (TxSI)
-
Fujita, M.; Seki, T. Syntheses and bioactivities of novel carbamates combining platelet activating factor (PAF) receptor antagonist with thromboxane synthase inhibitor (TxSI). Bioorg. Med. Chem. Lett., 2002, 12, 1383-1386.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 1383-1386
-
-
Fujita, M.1
Seki, T.2
-
43
-
-
0023815481
-
Biological effects of the orally active platelet activating factor receptor antagonist SDZ 64-412
-
Handley, D.A.; Van Valen, R.G.; Melden, M.K.; Houlihan, W.J.; Saunders, R.N. Biological effects of the orally active platelet activating factor receptor antagonist SDZ 64-412. J. Pharmacol. Exp. Ther., 1988, 247, 617-623.
-
(1988)
J. Pharmacol. Exp. Ther.
, vol.247
, pp. 617-623
-
-
Handley, D.A.1
Van Valen, R.G.2
Melden, M.K.3
Houlihan, W.J.4
Saunders, R.N.5
-
44
-
-
0025295120
-
Long-acting dihydropyridine calcium antagonists. 5. Synthesis and structure-activity relationships for a series of 2-[[(N-substitutedheterocyclyl) ethoxy]methyl]-1, 4-dihydropyridine calcium antagonists
-
Alker, D.; Campbell, S.F.; Cross, P.E.; Burges, R.A.; Carter, A.J.; Gardiner, D.G. Long-acting dihydropyridine calcium antagonists. 5. Synthesis and structure-activity relationships for a series of 2-[[(N- substitutedheterocyclyl) ethoxy]methyl]-1, 4-dihydropyridine calcium antagonists. J. Med. Chem., 1990, 33, 1805-1811.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 1805-1811
-
-
Alker, D.1
Campbell, S.F.2
Cross, P.E.3
Burges, R.A.4
Carter, A.J.5
Gardiner, D.G.6
-
45
-
-
0026712338
-
1, 4-Dihydropyridines as antagonists of platelet activating factor. 1. Synthesis and structure-activity relationships of 2-(4-heterocyclyl)phenyl derivatives
-
Cooper, K.; Fray, M.J.; Parry, M.J.; Richardson, K.; Steele, J. 1, 4-Dihydropyridines as antagonists of platelet activating factor. 1. Synthesis and structure-activity relationships of 2-(4-heterocyclyl)phenyl derivatives. J. Med. Chem., 1992, 35, 3115-3129.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 3115-3129
-
-
Cooper, K.1
Fray, M.J.2
Parry, M.J.3
Richardson, K.4
Steele, J.5
-
46
-
-
0029002906
-
Effect of a novel potent platelet-activating factor antagonist, modipafant, in clinical asthma
-
Kuitert, L.M.; Angus, R.M.; Barnes, N.C.; Barnes, P.J.; Bone, M.F.; Chung, K.F.; Fairfax, A.J.; Higenbotham, T.W.; O'Connor, B.J.; Piotrowska, B. Effect of a novel potent platelet-activating factor antagonist, modipafant, in clinical asthma. Am. J. Respir. Crit. Care Med., 1995, 151, 1331-1335.
-
(1995)
Am. J. Respir. Crit. Care Med.
, vol.151
, pp. 1331-1335
-
-
Kuitert, L.M.1
Angus, R.M.2
Barnes, N.C.3
Barnes, P.J.4
Bone, M.F.5
Chung, K.F.6
Fairfax, A.J.7
Higenbotham, T.W.8
O'Connor, B.J.9
Piotrowska, B.10
-
47
-
-
0023678961
-
Synthesis, platelet aggregation inhibitory activity, and in vivo antithrombotic activity of new 1, 4-dihydropyridines
-
Sunkel, C.E.; Fau de Casa-Juana, M.; Cillero, F.J.; Priego, J.G.; Ortega, M.P. Synthesis, platelet aggregation inhibitory activity, and in vivo antithrombotic activity of new 1, 4-dihydropyridines. J. Med. Chem., 1988, 31, 1886-1890.
-
(1988)
J. Med. Chem.
, vol.31
, pp. 1886-1890
-
-
Sunkel, C.E.1
Fau De Casa-Juana, M.2
Cillero, F.J.3
Priego, J.G.4
Ortega, M.P.5
-
48
-
-
0025147287
-
1, 4-Dihydropyridines, a new class of platelet-activating factor receptor antagonists: In vitro pharmacologic studies
-
Ortega, M.P.; Garcia, M.C.; Gijon, M.A.; de Casa-Juana, M.F.; Priego, J.G.; Sanchez Crespo, M.; Sunkel, C. 1, 4-Dihydropyridines, a new class of platelet-activating factor receptor antagonists: in vitro pharmacologic studies. J. Pharmacol. Exp. Ther., 1990, 255, 28-33.
-
(1990)
J. Pharmacol. Exp. Ther.
, vol.255
, pp. 28-33
-
-
Ortega, M.P.1
Garcia, M.C.2
Gijon, M.A.3
De Casa-Juana, M.F.4
Priego, J.G.5
Sanchez Crespo, M.6
Sunkel, C.7
-
49
-
-
0025052174
-
Pharmacological actions of PCA 4248, a new platelet-activating factor receptor antagonist: In vivo studies
-
Fernandez-Gallardo, S.; Ortega, M.P.; Priego, J.G.; de Casa-Juana, M.F.; Sunkel, C.; Sanchez Crespo, M. Pharmacological actions of PCA 4248, a new platelet-activating factor receptor antagonist: in vivo studies. J. Pharmacol. Exp. Ther., 1990, 255, 34-39.
-
(1990)
J. Pharmacol. Exp. Ther.
, vol.255
, pp. 34-39
-
-
Fernandez-Gallardo, S.1
Ortega, M.P.2
Priego, J.G.3
De Casa-Juana, M.F.4
Sunkel, C.5
Sanchez Crespo, M.6
-
50
-
-
77951034721
-
-
US 6, 566, 359 B1, May 20
-
Bazan, N.G.; Sunkel, C.; Marcheselli, V.L.; Buillia, G.J. 2, 4, 6-trimethyl-1, 4-dihydro-pyridine-3, 5-dicarboxylic acid esters as neuroprotective drugs. US 6, 566, 359 B1, May, 20, 2003.
-
(2003)
2,4,6-trimethyl-1,4-dihydro-pyridine-3,5-dicarboxylic Acid Esters As Neuroprotective Drugs
-
-
Bazan, N.G.1
Sunkel, C.2
Marcheselli, V.L.3
Buillia, G.J.4
-
51
-
-
0042020173
-
Treatment of Alzheimer's disease: Current status and new perspectives
-
Scarpini, E.; Scheltens, P.; Feldman, H. Treatment of Alzheimer's disease: current status and new perspectives. Lancet Neurol. 2003, 2, 539-547.
-
(2003)
Lancet Neurol.
, vol.2
, pp. 539-547
-
-
Scarpini, E.1
Scheltens, P.2
Feldman, H.3
-
52
-
-
0024433932
-
Alzheimer's disease and THA: A review of the cholinergic theory and of preliminary results
-
Boller, F.; Forette, F. Alzheimer's disease and THA: a review of the cholinergic theory and of preliminary results. Biomed. Pharmacother. 1989, 43, 487-491.
-
(1989)
Biomed. Pharmacother.
, vol.43
, pp. 487-491
-
-
Boller, F.1
Forette, F.2
-
53
-
-
4544295150
-
Rationale for the development of cholinesterase inhibitors as anti-Alzheimer agents
-
Lahiri, D.K.; Rogers, J.T.; Greig, N.H.; Sambamurti, K. Rationale for the development of cholinesterase inhibitors as anti-Alzheimer agents. Curr. Pharm. Des., 2004, 10, 3111-3119.
-
(2004)
Curr. Pharm. Des.
, vol.10
, pp. 3111-3119
-
-
Lahiri, D.K.1
Rogers, J.T.2
Greig, N.H.3
Sambamurti, K.4
-
54
-
-
77956220629
-
Neuronal calcium signaling, mitochondrial dysfunction, and Alzheimer's disease
-
Supnet, C.; Bezprozvanny, I. Neuronal calcium signaling, mitochondrial dysfunction, and Alzheimer's disease. J. Alzheimers Dis., 2010, 20 Suppl 2, S487-S498.
-
(2010)
J. Alzheimers Dis.
, vol.20
, Issue.SUPPL. 2
-
-
Supnet, C.1
Bezprozvanny, I.2
-
55
-
-
47749113650
-
Abeta plaques lead to aberrant regulation of calcium homeostasis in vivo resulting in structural and functional disruption of neuronal networks
-
Kuchibhotla, K.V.; Goldman, S.T.; Lattarulo, C.R.; Wu, H.Y.; Hyman, B.T.; Bacskai, B.J. Abeta plaques lead to aberrant regulation of calcium homeostasis in vivo resulting in structural and functional disruption of neuronal networks. Neuron, 2008, 59, 214-225.
-
(2008)
Neuron
, vol.59
, pp. 214-225
-
-
Kuchibhotla, K.V.1
Goldman, S.T.2
Lattarulo, C.R.3
Wu, H.Y.4
Hyman, B.T.5
Bacskai, B.J.6
-
56
-
-
77952033875
-
Bivalent -carbolines as potential multitarget anti-Alzheimer agents
-
Rook, Y.; Schmidtke, K.U.; Gaube, F.; Schepmann, D.; Wunsch, B.; Heilmann, J.; Lehmann, J.; Winckler, T. Bivalent -carbolines as potential multitarget anti-Alzheimer agents. J. Med. Chem., 2010, 53, 3611-3617.
-
(2010)
J. Med. Chem.
, vol.53
, pp. 3611-3617
-
-
Rook, Y.1
Schmidtke, K.U.2
Gaube, F.3
Schepmann, D.4
Wunsch, B.5
Heilmann, J.6
Lehmann, J.7
Winckler, T.8
-
57
-
-
33845961279
-
Novel multipotent tacrinedihydropyridine hybrids with improved acetylcholinesterase inhibitory and neuroprotective activities as potential drugs for the treatment of Alzheimer's disease
-
Marco-Contelles, J.; Leon, R.; de Los Rios, C.; Guglietta, A.; Terencio, J.; Lopez, M.G.; Garcia, A.G.; Villarroya, M. Novel multipotent tacrinedihydropyridine hybrids with improved acetylcholinesterase inhibitory and neuroprotective activities as potential drugs for the treatment of Alzheimer's disease. J. Med. Chem., 2006, 49, 7607-7610.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 7607-7610
-
-
Marco-Contelles, J.1
Leon, R.2
De Los Rios, C.3
Guglietta, A.4
Terencio, J.5
Lopez, M.G.6
Garcia, A.G.7
Villarroya, M.8
-
58
-
-
65649142161
-
Tacripyrines the first tacrine-dihydropyridine hybrids as multitargetdirected ligands for the treatment of Alzheimer's disease
-
Marco-Contelles, J.; Leon, R.; de los Rios, C.; Samadi, A.; Bartolini, M.; Andrisano, V.; Huertas, O.; Barril, X.; Luque, F.J.; Rodriguez-Franco, M.I.; Lopez, B.; Lopez, M.G.; Garcia, A.G.; Carreiras Mdo, C.; Villarroya, M. Tacripyrines, the first tacrine-dihydropyridine hybrids, as multitargetdirected ligands for the treatment of Alzheimer's disease. J. Med. Chem., 2009, 52, 2724-2732.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 2724-2732
-
-
Marco-Contelles, J.1
Leon, R.2
De Los Rios, C.3
Samadi, A.4
Bartolini, M.5
Andrisano, V.6
Huertas, O.7
Barril, X.8
Luque, F.J.9
Rodriguez-Franco, M.I.10
Lopez, B.11
Lopez, M.G.12
Garcia, A.G.13
Carreiras Mdo, C.14
Villarroya, M.15
-
59
-
-
0348108039
-
Synthesis, biological activity, and docking studies of new acetylcholinesterase inhibitors of the bispyridinium type
-
Kapkova, P.; Stiefl, N.; Surig, U.; Engels, B.; Baumann, K.; Holzgrabe, U. Synthesis, biological activity, and docking studies of new acetylcholinesterase inhibitors of the bispyridinium type. Arch. Pharm. (Weinheim), 2003, 336, 523-540.
-
(2003)
Arch. Pharm. (Weinheim)
, vol.336
, pp. 523-540
-
-
Kapkova, P.1
Stiefl, N.2
Surig, U.3
Engels, B.4
Baumann, K.5
Holzgrabe, U.6
-
60
-
-
28844431542
-
Search for dual function inhibitors for Alzheimer's disease: Synthesis and biological activity of acetylcholinesterase inhibitors of pyridinium-type and their Abeta fibril formation inhibition capacity
-
Kapkova, P.; Alptuzun, V.; Frey, P.; Erciyas, E.; Holzgrabe, U. Search for dual function inhibitors for Alzheimer's disease: synthesis and biological activity of acetylcholinesterase inhibitors of pyridinium-type and their Abeta fibril formation inhibition capacity. Bioorg. Med. Chem., 2006, 14, 472-478.
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 472-478
-
-
Kapkova, P.1
Alptuzun, V.2
Frey, P.3
Erciyas, E.4
Holzgrabe, U.5
-
61
-
-
77549083797
-
Interaction of (benzylidene-hydrazono)-1, 4-dihydropyridines with betaamyloid, acetylcholine, and butyrylcholine esterases
-
Alptuzun, V.; Prinz, M.; Horr, V.; Scheiber, J.; Radacki, K.; Fallarero, A.; Vuorela, P.; Engels, B.; Braunschweig, H.; Erciyas, E.; Holzgrabe, U. Interaction of (benzylidene-hydrazono)-1, 4-dihydropyridines with betaamyloid, acetylcholine, and butyrylcholine esterases. Bioorg. Med. Chem., 2010, 18, 2049-2059.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 2049-2059
-
-
Alptuzun, V.1
Prinz, M.2
Horr, V.3
Scheiber, J.4
Radacki, K.5
Fallarero, A.6
Vuorela, P.7
Engels, B.8
Braunschweig, H.9
Erciyas, E.10
Holzgrabe, U.11
-
62
-
-
0019843193
-
Site-specific sustained release of drugs to the brain
-
Bodor, N.; Farag, H.H.; Brewster, M.E. Site-specific, sustained release of drugs to the brain. Science, 1981, 214, 1370-1372.
-
(1981)
Science
, vol.214
, pp. 1370-1372
-
-
Bodor, N.1
Farag, H.H.2
Brewster, M.E.3
-
63
-
-
77549083797
-
Interaction of (benzylidene-hydrazono)-1, 4-dihydropyridines with betaamyloid, acetylcholine, and butyrylcholine esterases
-
Alptuzun, V.; Prinz, M.; Horr, V.; Scheiber, J.; Radacki, K.; Fallarero, A.; Vuorela, P.; Engels, B.; Braunschweig, H.; Erciyas, E.; Holzgrabe, U. Interaction of (benzylidene-hydrazono)-1, 4-dihydropyridines with betaamyloid, acetylcholine, and butyrylcholine esterases. Bioorg. Med. Chem., 2010, 18, 2049-2059.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 2049-2059
-
-
Alptuzun, V.1
Prinz, M.2
Horr, V.3
Scheiber, J.4
Radacki, K.5
Fallarero, A.6
Vuorela, P.7
Engels, B.8
Braunschweig, H.9
Erciyas, E.10
Holzgrabe, U.11
-
64
-
-
33947708348
-
The molecular mechanisms of the antiamyloid effects of phenols
-
Shoval, H.; Lichtenberg, D.; Gazit, E. The molecular mechanisms of the antiamyloid effects of phenols. Amyloid, 2007, 14, 73-87.
-
(2007)
Amyloid
, vol.14
, pp. 73-87
-
-
Shoval, H.1
Lichtenberg, D.2
Gazit, E.3
-
65
-
-
33750705653
-
A century of Alzheimer's disease
-
Goedert, M.; Spillantini M.G. A century of Alzheimer's disease. Science, 2006, 314, 777-781.
-
(2006)
Science
, vol.314
, pp. 777-781
-
-
Goedert, M.1
Spillantini, M.G.2
-
66
-
-
78649849389
-
Identification of dihydropyridines that reduce cellular tau levels
-
Evans, C.G.; Jinwal, U.K.; Makley, L.N.; Dickey, C.A.; Gestwicki, J.E. Identification of dihydropyridines that reduce cellular tau levels. Chem. Commun. (Camb), 2011, 47, 529-531.
-
(2011)
Chem. Commun. (Camb)
, vol.47
, pp. 529-531
-
-
Evans, C.G.1
Jinwal, U.K.2
Makley, L.N.3
Dickey, C.A.4
Gestwicki, J.E.5
-
67
-
-
70349617699
-
Chemical manipulation of hsp70 ATPase activity regulates tau stability
-
Jinwal, U.K.; Miyata, Y.; Koren, J. 3rd; Jones, J.R.; Trotter, J.H.; Chang, L.; O'Leary, J.; Morgan, D.; Lee, D.C.; Shults, C.L.; Rousaki, A.; Weeber, E.J.; Zuiderweg, E.R.; Gestwicki, J.E.; Dickey, C.A. Chemical manipulation of hsp70 ATPase activity regulates tau stability. J. Neurosci., 2009, 29, 12079-12088.
-
(2009)
J. Neurosci.
, vol.29
, pp. 12079-12088
-
-
Jinwal, U.K.1
Miyata III, Y.2
Koren, J.3
Jones, J.R.4
Trotter, J.H.5
Chang, L.6
O'Leary, J.7
Morgan, D.8
Lee, D.C.9
Shults, C.L.10
Rousaki, A.11
Weeber, E.J.12
Zuiderweg, E.R.13
Gestwicki, J.E.14
Dickey, C.A.15
-
68
-
-
77749310853
-
Drug-resistant tuberculosis: A worldwide epidemic poses a new challenge
-
Loddenkemper, R.; Hauer, B. Drug-resistant tuberculosis: a worldwide epidemic poses a new challenge. Dtsch. Arztebl. Int., 2010, 107, 10-19.
-
(2010)
Dtsch. Arztebl. Int.
, vol.107
, pp. 10-19
-
-
Loddenkemper, R.1
Hauer, B.2
-
69
-
-
0037441632
-
American thoracic society/centers for disease control and prevention/infectious diseases society of America: Treatment of tuberculosis
-
Blumberg, H. M.; Burman, W.J.; Chaisson, R.E.; Daley, C.L.; Etkind, S.C.; Friedman, L.N.; Fujiwara, P.; Grzemska, M.; Hopewell, P.C.; Iseman, M.D.; Jasmer, R.M.; Koppaka, V.; Menzies, R.I.; O'Brien, R.J.; Reves, R.R.; Reichman, L.B.; Simone, P.M.; Starke, J.R.; Vernon, A.A. American Thoracic Society/Centers for Disease Control and Prevention/Infectious Diseases Society of America: treatment of tuberculosis. Am. J. Respir. Crit. Care Med., 2003, 167, 603-662.
-
(2003)
Am. J. Respir. Crit. Care Med.
, vol.167
, pp. 603-662
-
-
Blumberg, H.M.1
Burman, W.J.2
Chaisson, R.E.3
Daley, C.L.4
Etkind, S.C.5
Friedman, L.N.6
Fujiwara, P.7
Grzemska, M.8
Hopewell, P.C.9
Iseman, M.D.10
Jasmer, R.M.11
Koppaka, V.12
Menzies, R.I.13
O'Brien, R.J.14
Reves, R.R.15
Reichman, L.B.16
Simone, P.M.17
Starke, J.R.18
Vernon, A.A.19
-
70
-
-
0021849846
-
Biological activity of 1, 4-dihydropyridine derivatives
-
Fiszer-Maliszewska, L.; Wieczorek, J.; Mordarski, M.; Balicki, R.; Kaczmarek, L.; Nantka-Namirski, P. Biological activity of 1, 4-dihydropyridine derivatives. Arch. Immunol. Ther. Exp. (Warsz), 1985, 33, 345-352.
-
(1985)
Arch. Immunol. Ther. Exp. (Warsz)
, vol.33
, pp. 345-352
-
-
Fiszer-Maliszewska, L.1
Wieczorek, J.2
Mordarski, M.3
Balicki, R.4
Kaczmarek, L.5
Nantka-Namirski, P.6
-
71
-
-
0032543736
-
Antimycobacterial activity of substituted isosteres of pyridine-and pyrazinecarboxylic acids
-
Wachter, G.A.; Davis, M.C.; Martin, A.R.; Franzblau, S.G. Antimycobacterial activity of substituted isosteres of pyridine-and pyrazinecarboxylic acids. J. Med. Chem., 1998, 41, 2436-2438.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2436-2438
-
-
Wachter, G.A.1
Davis, M.C.2
Martin, A.R.3
Franzblau, S.G.4
-
72
-
-
0034897586
-
Synthesis and QSAR studies of 4-substituted phenyl-2, 6-dimethyl-3, 5-bis-N-(substituted phenyl)carbamoyl-1, 4-dihydropyridines as potential antitubercular agents
-
Desai, B.; Sureja, D.; Naliapara, Y.; Shah, A.; Saxena, A.K. Synthesis and QSAR studies of 4-substituted phenyl-2, 6-dimethyl-3, 5-bis-N-(substituted phenyl)carbamoyl-1, 4-dihydropyridines as potential antitubercular agents. Bioorg. Med. Chem., 2001, 9, 1993-1998.
-
(2001)
Bioorg. Med. Chem.
, vol.9
, pp. 1993-1998
-
-
Desai, B.1
Sureja, D.2
Naliapara, Y.3
Shah, A.4
Saxena, A.K.5
-
73
-
-
14244261320
-
Synthesis and antitbercular avtivity studies of some unsymmetrical 1, 4-dihydropyridines
-
Gaveriya, H.; Desai, B.; Vora, V.; Shah, A. Synthesis and antitbercular avtivity studies of some unsymmetrical 1, 4-dihydropyridines. Indian J. Pharm. Sci., 2002, 64, 59-62.
-
(2002)
Indian J. Pharm. Sci.
, vol.64
, pp. 59-62
-
-
Gaveriya, H.1
Desai, B.2
Vora, V.3
Shah, A.4
-
74
-
-
0037168055
-
Three-dimensional quantitative structure-activity relationship of 1, 4-dihydropyridines as antitubercular agents
-
Kharkar, P.S.; Desai, B.; Gaveria, H.; Varu, B.; Loriya, R.; Naliapara, Y.; Shah, A.; Kulkarni, V.M., Three-dimensional quantitative structure-activity relationship of 1, 4-dihydropyridines as antitubercular agents. J. Med. Chem., 2002, 45, 4858-4867.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 4858-4867
-
-
Kharkar, P.S.1
Desai, B.2
Gaveria, H.3
Varu, B.4
Loriya, R.5
Naliapara, Y.6
Shah, A.7
Kulkarni, V.M.8
-
75
-
-
77954664594
-
Synthesis, in vitro antitubercular activity and 3DQSAR study of 1, 4-dihydropyridines
-
Manvar, A.T.; Pissurlenkar, R.R.; Virsodia, V.R.; Upadhyay, K.D.; Manvar, D.R.; Mishra, A.K.; Acharya, H.D.; Parecha, A.R.; Dholakia, C.D.; Shah, A.K.; Coutinho, E.C. Synthesis, in vitro antitubercular activity and 3DQSAR study of 1, 4-dihydropyridines. Mol. Divers., 2010, 14, 285-305.
-
(2010)
Mol. Divers.
, vol.14
, pp. 285-305
-
-
Manvar, A.T.1
Pissurlenkar, R.R.2
Virsodia, V.R.3
Upadhyay, K.D.4
Manvar, D.R.5
Mishra, A.K.6
Acharya, H.D.7
Parecha, A.R.8
Dholakia, C.D.9
Shah, A.K.10
Coutinho, E.C.11
-
76
-
-
67349236409
-
Synthesis and antitubercular activity of novel 4-substituted imidazolyl-2, 6-dimethyl-N3, N5-bisaryl-1, 4-dihydropyridine-3, 5-dicarboxamides
-
Fassihi, A.; Azadpour, Z.; Delbari, N.; Saghaie, L.; Memarian, H.R.; Sabet, R.; Alborzi, A.; Miri, R.; Pourabbas, B.; Mardaneh, J.; Mousavi, P.; Moeinifard, B.; Sadeghi-Aliabadi, H. Synthesis and antitubercular activity of novel 4-substituted imidazolyl-2, 6-dimethyl-N3, N5-bisaryl-1, 4-dihydropyridine-3, 5-dicarboxamides. Eur. J. Med. Chem., 2009, 44, 3253-3258.
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 3253-3258
-
-
Fassihi, A.1
Azadpour, Z.2
Delbari, N.3
Saghaie, L.4
Memarian, H.R.5
Sabet, R.6
Alborzi, A.7
Miri, R.8
Pourabbas, B.9
Mardaneh, J.10
Mousavi, P.11
Moeinifard, B.12
Sadeghi-Aliabadi, H.13
-
77
-
-
60049093578
-
Synthesis and biological evaluation of some new 1, 4-dihydropyridines containing different ester substitute and diethyl carbamoyl group as anti-tubercular agents
-
Khoshneviszadeh, M.; Edraki, N.; Javidnia, K.; Alborzi, A.; Pourabbas, B.; Mardaneh, J.; Miri, R. Synthesis and biological evaluation of some new 1, 4-dihydropyridines containing different ester substitute and diethyl carbamoyl group as anti-tubercular agents. Bioorg. Med. Chem., 2009, 17, 1579-1586.
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 1579-1586
-
-
Khoshneviszadeh, M.1
Edraki, N.2
Javidnia, K.3
Alborzi, A.4
Pourabbas, B.5
Mardaneh, J.6
Miri, R.7
-
78
-
-
0034702247
-
A small-molecule nitroimidazopyran drug candidate for the treatment of tuberculosis
-
Stover, C.K.; Warrener, P.; VanDevanter, D.R.; Sherman, D.R.; Arain, T.M.; Langhorne, M.H.; Anderson, S.W.; Towell, J.A.; Yuan, Y.; McMurray, D.N.; Kreiswirth, B.N.; Barry, C.E.; Baker, W.R. A small-molecule nitroimidazopyran drug candidate for the treatment of tuberculosis. Nature, 2000, 405, 962-966.
-
(2000)
Nature
, vol.405
, pp. 962-966
-
-
Stover, C.K.1
Warrener, P.2
Vandevanter, D.R.3
Sherman, D.R.4
Arain, T.M.5
Langhorne, M.H.6
Anderson, S.W.7
Towell, J.A.8
Yuan, Y.9
McMurray, D.N.10
Kreiswirth, B.N.11
Barry, C.E.12
Baker, W.R.13
-
79
-
-
0028151053
-
Effect of NS-3, a thyrotropin-releasing hormone analog, on in vivo acetylcholine release in rat brain: Regional differences and its sites of action
-
Itoh, Y.; Ogasawara, T.; Mushiroi, T.; yamazaki, A.; Ukai, Y.; Kimura, K. Effect of NS-3, a thyrotropin-releasing hormone analog, on in vivo acetylcholine release in rat brain: regional differences and its sites of action. J. Pharmacol. Exp. Ther., 1994, 271, 884-890.
-
(1994)
J. Pharmacol. Exp. Ther.
, vol.271
, pp. 884-890
-
-
Itoh, Y.1
Ogasawara, T.2
Mushiroi, T.3
Yamazaki, A.4
Ukai, Y.5
Kimura, K.6
-
80
-
-
0021239054
-
Synthesis of thyrotropinreleasing hormone analogues. 1. Complete dissociation of central nervous system effects from thyrotropin-releasing activity
-
Szirtes, T.; Kisfaludy, L.; Palosi, E.; Szporny, L. Synthesis of thyrotropinreleasing hormone analogues. 1. Complete dissociation of central nervous system effects from thyrotropin-releasing activity. J. Med. Chem., 1984, 27, 741-745.
-
(1984)
J. Med. Chem.
, vol.27
, pp. 741-745
-
-
Szirtes, T.1
Kisfaludy, L.2
Palosi, E.3
Szporny, L.4
-
81
-
-
8644224096
-
Centrally acting and metabolically stable thyrotropinreleasing hormone analogues by replacement of histidine with substituted pyridinium
-
Prokai, L.; Prokai-Tatrai, K.; Zharikova, A.D.; Nguyen, V.; Perjesi, P.; Stevens, S.M.Jr. Centrally acting and metabolically stable thyrotropinreleasing hormone analogues by replacement of histidine with substituted pyridinium. J. Med. Chem., 2004, 47, 6025-6033.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 6025-6033
-
-
Prokai, L.1
Prokai-Tatrai, K.2
Zharikova, A.D.3
Nguyen, V.4
Perjesi, P.5
Stevens Jr., S.M.6
-
82
-
-
0034827301
-
Calcium channel modulators of the dihydropyridine family are human pregnane X receptor activators and inducers of CYP3A, CYP2B, and CYP2C in human hepatocytes
-
Drocourt, L.; Pascussi, J. M.; Assenat, E.; Fabre, J.M.; Maurel, P.; Vilarem, M.J. Calcium channel modulators of the dihydropyridine family are human pregnane X receptor activators and inducers of CYP3A, CYP2B, and CYP2C in human hepatocytes. Drug Metab. Dispos., 2001, 29, 1325-1331.
-
(2001)
Drug Metab. Dispos.
, vol.29
, pp. 1325-1331
-
-
Drocourt, L.1
Pascussi, J.M.2
Assenat, E.3
Fabre, J.M.4
Maurel, P.5
Vilarem, M.J.6
-
83
-
-
9644260442
-
Liver microsomal biotransformation of nitro-aryl drugs: Mechanism for potential oxidative stress induction
-
Letelier, M.E.; Izquierdo, P.; Godoy, L.; Lepe, A.M.; Faundez, M. Liver microsomal biotransformation of nitro-aryl drugs: mechanism for potential oxidative stress induction. J. Appl. Toxicol., 2004, 24, 519-525.
-
(2004)
J. Appl. Toxicol.
, vol.24
, pp. 519-525
-
-
Letelier, M.E.1
Izquierdo, P.2
Godoy, L.3
Lepe, A.M.4
Faundez, M.5
-
84
-
-
20644460143
-
Microsomal UDP-glucuronyltransferase in rat liver: Oxidative activation
-
Letelier, M.E.; Pimentel, A.; Pino, P.; Lepe, A.M.; Faundez, M.; Aracena, P.; Speisky, H. Microsomal UDP-glucuronyltransferase in rat liver: oxidative activation. Basic Clin. Pharmacol. Toxicol., 2005, 96, 480-486.
-
(2005)
Basic Clin. Pharmacol. Toxicol.
, vol.96
, pp. 480-486
-
-
Letelier, M.E.1
Pimentel, A.2
Pino, P.3
Lepe, A.M.4
Faundez, M.5
Aracena, P.6
Speisky, H.7
-
85
-
-
0032567798
-
Different potencies of dihydropyridine derivatives in blocking T-type but not L-type Ca2+ channels in neuroblastoma-glioma hybrid cells
-
Stengel, W.; Jainz, M.; Andreas, K. Different potencies of dihydropyridine derivatives in blocking T-type but not L-type Ca2+ channels in neuroblastoma-glioma hybrid cells. Eur. J. Pharmacol., 1998, 342, 339-345.
-
(1998)
Eur. J. Pharmacol.
, vol.342
, pp. 339-345
-
-
Stengel, W.1
Jainz, M.2
Andreas, K.3
-
86
-
-
0029965979
-
Differential membrane interactions of calcium channel blockers. Implications for antioxidant activity
-
Mason, R.P.; Trumbore, M.W. Differential membrane interactions of calcium channel blockers. Implications for antioxidant activity. Biochem. Pharmacol., 1996, 51, 653-660.
-
(1996)
Biochem. Pharmacol.
, vol.51
, pp. 653-660
-
-
Mason, R.P.1
Trumbore, M.W.2
-
87
-
-
0033552883
-
Atherosclerosis-an inflammatory disease
-
Ross, R. Atherosclerosis-an inflammatory disease. N. Engl. J. Med., 1999, 340, 115-126.
-
(1999)
N. Engl. J. Med.
, vol.340
, pp. 115-126
-
-
Ross, R.1
-
88
-
-
0033304494
-
Molecular control of immune/inflammatory responses: Interactions between nuclear factor-kappa B and steroid receptorsignaling pathways
-
McKay, L.I.; Cidlowski, J.A. Molecular control of immune/inflammatory responses: interactions between nuclear factor-kappa B and steroid receptorsignaling pathways. Endocr. Rev., 1999, 20, 435-459.
-
(1999)
Endocr. Rev.
, vol.20
, pp. 435-459
-
-
McKay, L.I.1
Cidlowski, J.A.2
-
89
-
-
0037155057
-
Matrix metalloproteinases in vascular remodeling and atherogenesis: The good, the bad, and the ugly
-
Galis, Z.S.; Khatri, J.J. Matrix metalloproteinases in vascular remodeling and atherogenesis: the good, the bad, and the ugly. Circ. Res., 2002, 90, 251-262.
-
(2002)
Circ. Res.
, vol.90
, pp. 251-262
-
-
Galis, Z.S.1
Khatri, J.J.2
-
90
-
-
0025679025
-
Atherogenesis calcium and calcium-antagonists
-
Henry, P.D. Atherogenesis, Calcium and Calcium-Antagonists. Am. J. Cardiol., 1990, 66, I3-I6.
-
(1990)
Am. J. Cardiol.
, vol.66
-
-
Henry, P.D.1
-
91
-
-
0033793333
-
The calcium-channel blocker lacidipine reduces the development of atherosclerotic lesions in the apoEdeficient mouse
-
Cristofori, P.; Lanzoni, A.; Quartaroli, M.; Pastorino, A.M.; Zancanaro, C.; Cominacini, L.; Gaviraghi, G.; Turton, J. The calcium-channel blocker lacidipine reduces the development of atherosclerotic lesions in the apoEdeficient mouse. J. Hypertens., 2000, 18, 1429-1436.
-
(2000)
J. Hypertens.
, vol.18
, pp. 1429-1436
-
-
Cristofori, P.1
Lanzoni, A.2
Quartaroli, M.3
Pastorino, A.M.4
Zancanaro, C.5
Cominacini, L.6
Gaviraghi, G.7
Turton, J.8
-
92
-
-
0029860461
-
Calcium-channel blockers inhibit human low-density lipoprotein oxidation by oxygen radicals
-
Napoli, C.; Chiariello, M.; Palumbo, G.; Ambrosio, G. Calcium-channel blockers inhibit human low-density lipoprotein oxidation by oxygen radicals. Cardiovasc. Drugs Ther., 1996, 10, 417-424.
-
(1996)
Cardiovasc. Drugs Ther.
, vol.10
, pp. 417-424
-
-
Napoli, C.1
Chiariello, M.2
Palumbo, G.3
Ambrosio, G.4
-
93
-
-
0029926066
-
Inhibition of lipid hydroperoxidation of low density lipoprotein by the Ca2+-channel and alpha(1)-adrenoceptor antagonist monatepil maleate
-
Hayashi, K.; Kuga, Y.; Nomura, S.; Okura, Y.; Tanaka, K.; Yasunobu, Y.; Nomura, K.; Shingu, T.; Kuwashima, J.; Kajiyama, G. Inhibition of lipid hydroperoxidation of low density lipoprotein by the Ca2+-channel and alpha(1)-adrenoceptor antagonist monatepil maleate. Arzneimittel-Forsch., 1996, 46, 378-381.
-
(1996)
Arzneimittel-Forsch.
, vol.46
, pp. 378-381
-
-
Hayashi, K.1
Kuga, Y.2
Nomura, S.3
Okura, Y.4
Tanaka, K.5
Yasunobu, Y.6
Nomura, K.7
Shingu, T.8
Kuwashima, J.9
Kajiyama, G.10
-
94
-
-
0030948956
-
Impact of a combination of a calcium antagonist and a betablocker on cell-and copper-mediated oxidation of LDL and on the accumulation and efflux of cholesterol in human macrophages and murine J774 cells
-
Lesnik, P.; Dachet, C.; Petit, L.; Moreau, M.; Griglio, S.; Brudi, P.; Chapman, M.J. Impact of a combination of a calcium antagonist and a betablocker on cell-and copper-mediated oxidation of LDL and on the accumulation and efflux of cholesterol in human macrophages and murine J774 cells. Arterioscler. Thromb. Vasc. Biol., 1997, 17, 979-988.
-
(1997)
Arterioscler. Thromb. Vasc. Biol.
, vol.17
, pp. 979-988
-
-
Lesnik, P.1
Dachet, C.2
Petit, L.3
Moreau, M.4
Griglio, S.5
Brudi, P.6
Chapman, M.J.7
-
95
-
-
0030030436
-
Structure-function relationships of calcium antagonists. Effect on oxidative modification of low density lipoprotein
-
Rojstaczer, N.; Triggle, D.J. Structure-function relationships of calcium antagonists. Effect on oxidative modification of low density lipoprotein. Biochem. Pharmacol., 1996, 51, 141-150.
-
(1996)
Biochem. Pharmacol.
, vol.51
, pp. 141-150
-
-
Rojstaczer, N.1
Triggle, D.J.2
-
96
-
-
0026476406
-
Improved measurement of low-density-lipoprotein susceptibility to copperinduced oxidation: Application of a short procedure for isolating low-density lipoprotein
-
Kleinveld, H.A.; Hak-Lemmers, H.L.; Stalenhoef, A.F.; Demacker, P.N. Improved measurement of low-density-lipoprotein susceptibility to copperinduced oxidation: application of a short procedure for isolating low-density lipoprotein. Clin. Chem., 1992, 38, 2066-2072.
-
(1992)
Clin. Chem.
, vol.38
, pp. 2066-2072
-
-
Kleinveld, H.A.1
Hak-Lemmers, H.L.2
Stalenhoef, A.F.3
Demacker, P.N.4
-
97
-
-
0037459202
-
Antioxidant activity of different dihydropyridines
-
Cominacini, L.; Fratta Pasini, A.; Garbin, U.; Pastorino, A.M.; Davoli, A.; Nava, C.; Campagnola, M.; Rossato, P.; Lo Cascio, V. Antioxidant activity of different dihydropyridines. Biochem. Bioph. Res. Co., 2003, 302, 679-684.
-
(2003)
Biochem. Bioph. Res. Co.
, vol.302
, pp. 679-684
-
-
Cominacini, L.1
Fratta Pasini, A.2
Garbin, U.3
Pastorino, A.M.4
Davoli, A.5
Nava, C.6
Campagnola, M.7
Rossato, P.8
Lo Cascio, V.9
-
98
-
-
0002179154
-
Calcium channel blockers with antioxidant activity
-
Bellomo, G.; Finardi, G.; Maggi, E.; Rice-Evans, E., Eds. Richelieu Press: London
-
Gaviraghi, G.; Pastorino, A.M.; Ratti, E.; Trist, D.G. Calcium channel blockers with antioxidant activity. In Free Radicals, Lipoprotein Oxidation and Atherosclerosis, Bellomo, G.; Finardi, G.; Maggi, E.; Rice-Evans, E., Eds. Richelieu Press: London, 1995; pp 431-456.
-
(1995)
Free Radicals, Lipoprotein Oxidation and Atherosclerosis
, pp. 431-456
-
-
Gaviraghi, G.1
Pastorino, A.M.2
Ratti, E.3
Trist, D.G.4
-
99
-
-
55049123446
-
Lercanidipine decreases vascular matrix metalloproteinase-2 activity and protects against vascular dysfunction in diabetic rats
-
Martinez, M.L.; Rizzi, E.; Castro, M.M.; Fernandes, K.; Bendhack, L.M.; Gerlach, R.F.; Tanus-Santos, J.E. Lercanidipine decreases vascular matrix metalloproteinase-2 activity and protects against vascular dysfunction in diabetic rats. Eur. J. Pharmacol., 2008, 599, 110-116.
-
(2008)
Eur. J. Pharmacol.
, vol.599
, pp. 110-116
-
-
Martinez, M.L.1
Rizzi, E.2
Castro, M.M.3
Fernandes, K.4
Bendhack, L.M.5
Gerlach, R.F.6
Tanus-Santos, J.E.7
-
100
-
-
0035253838
-
Calcium antagonists as inhibitors of in vitro low density lipoprotein oxidation and glycation
-
Sobal, G.; Menzel, E.J.; Sinzinger, H. Calcium antagonists as inhibitors of in vitro low density lipoprotein oxidation and glycation. Biochem. Pharmacol., 2001, 61, 373-379.
-
(2001)
Biochem. Pharmacol.
, vol.61
, pp. 373-379
-
-
Sobal, G.1
Menzel, E.J.2
Sinzinger, H.3
-
101
-
-
78649808628
-
-
Prasanna Kumar, K.; Rama Narsimha Reddy, A.; Narsimha Reddy, Y.; Anbu, J. Lipid lowering activity of lercadipine in hyperlipidemic rats. I.J.P.T., 2010, 9, 73-75.
-
(2010)
Lipid lowering activity of lercadipine in hyperlipidemic rats I.J.P.T.
, vol.9
, pp. 73-75
-
-
Prasanna Kumar, K.1
Rama Narsimha Reddy, A.2
Narsimha Reddy, Y.3
Anbu, J.4
-
102
-
-
79952805318
-
-
Vaz, R.J.; Klabunde, T., Eds. WILEYVCH
-
Schuster, D.; Laggner, C.; Langer, T., In Antitargets: Prediction and Prevention of Drug Side Effects, Vaz, R.J.; Klabunde, T., Eds. WILEYVCH: 2008; pp 3-22.
-
(2008)
Antitargets: Prediction and Prevention of Drug Side Effects
, pp. 3-22
-
-
Schuster, D.1
Laggner, C.2
Langer, T.3
-
103
-
-
77952641150
-
Transporter-mediated efflux influences CNS side effects: ABCB1, from antitarget to target
-
Broccatelli, F.; Carosati, E.; Cruciani, G.; Oprea, T.I. Transporter-Mediated Efflux Influences CNS Side Effects: ABCB1, from Antitarget to Target. Mol. Inf., 2010, 29, 16-26.
-
(2010)
Mol. Inf.
, vol.29
, pp. 16-26
-
-
Broccatelli, F.1
Carosati, E.2
Cruciani, G.3
Oprea, T.I.4
-
104
-
-
0034604796
-
Low-affinity block of cardiac K(+) currents by nifedipine
-
Zhabyeyev, P.; Missan, S.; Jones, S.E.; McDonald, T.F. Low-affinity block of cardiac K(+) currents by nifedipine. Eur. J. Pharmacol., 2000, 401, 137-143.
-
(2000)
Eur. J. Pharmacol.
, vol.401
, pp. 137-143
-
-
Zhabyeyev, P.1
Missan, S.2
Jones, S.E.3
McDonald, T.F.4
-
105
-
-
0031752779
-
HERG and KvLQT1/IsK, the cardiac K+ channels involved in long QT syndromes, are targets for calcium channel blockers
-
Chouabe, C.; Drici, M.D.; Romey, G.; Barhanin, J.; Lazdunski, M. HERG and KvLQT1/IsK, the Cardiac K+ Channels Involved in Long QT Syndromes, Are Targets for Calcium Channel Blockers. Mol. Pharmacol., 1998, 54, 695-703.
-
(1998)
Mol. Pharmacol.
, vol.54
, pp. 695-703
-
-
Chouabe, C.1
Drici, M.D.2
Romey, G.3
Barhanin, J.4
Lazdunski, M.5
-
106
-
-
1842686775
-
A model for identifying HERG K+ channel blockers
-
Aronov, A.M.; Goldman, B.B. A model for identifying HERG K+ channel blockers. Bioorg. Med. Chem., 2004, 12, 2307-2315.
-
(2004)
Bioorg. Med. Chem.
, vol.12
, pp. 2307-2315
-
-
Aronov, A.M.1
Goldman, B.B.2
-
107
-
-
83555174958
-
BDDCS applied to over 900 drugs. 2011
-
Benet, L.Z.; Broccatelli, F.; Oprea, T.I. BDDCS applied to over 900 drugs. 2011, AAPS J., 2011, 13, 519-547.
-
(2011)
AAPS J.
, vol.13
, pp. 519-547
-
-
Benet, L.Z.1
Broccatelli, F.2
Oprea, T.I.3
-
108
-
-
0031975185
-
Update: Clinically significant cytochrome P-450 drug interactions
-
Michalets, E.L. Update: clinically significant cytochrome P-450 drug interactions. Pharmacotherapy, 1998, 18, 84-112.
-
(1998)
Pharmacotherapy
, vol.18
, pp. 84-112
-
-
Michalets, E.L.1
-
110
-
-
0029868372
-
Peripheral edema due to Nifedipine-Itraconazole interaction: A case report
-
Tailor, S.A.N.; Gupta, A.K.; Walker, S.E.; Shear, N.H. Peripheral edema due to Nifedipine-Itraconazole interaction: a case report. Arch. Dermatol., 1996, 132, 350-352.
-
(1996)
Arch. Dermatol.
, vol.132
, pp. 350-352
-
-
Tailor, S.A.N.1
Gupta, A.K.2
Walker, S.E.3
Shear, N.H.4
-
111
-
-
0022354273
-
Felodipine kinetics in healthy men
-
Edgar, B.; Regårdh, C.G.; Johnsson, G.; Johansson, L.; Lundborg, P.; Löfberg, I.; Rönn, O. Felodipine kinetics in healthy men. Clin. Pharmacol. Ther., 1985, 38, 205-211.
-
(1985)
Clin. Pharmacol. Ther.
, vol.38
, pp. 205-211
-
-
Edgar, B.1
Regårdh, C.G.2
Johnsson, G.3
Johansson, L.4
Lundborg, P.5
Löfberg, I.6
Rönn, O.7
-
112
-
-
0031001463
-
Effects of grapefruit juice ingestion: Pharmacokinetics and haemodynamics of intravenously and orally administered felodipine in healthy men
-
Lundahl, J.; Regårdh, C.G.; Edgar, B.; Johnsson, G. Effects of grapefruit juice ingestion: pharmacokinetics and haemodynamics of intravenously and orally administered felodipine in healthy men. Eur. J. Clin. Pharmacol., 1997, 52, 139-145.
-
(1997)
Eur. J. Clin. Pharmacol.
, vol.52
, pp. 139-145
-
-
Lundahl, J.1
Regårdh, C.G.2
Edgar, B.3
Johnsson, G.4
-
113
-
-
0035145127
-
Seville orange juicefelodipine interaction: Comparison with dilute grapefruit juice and involvement of furocoumarins
-
Malhotra, S.; Bailey D.G.; Paine, M.F.; Watkins, P.B. Seville orange juicefelodipine interaction: comparison with dilute grapefruit juice and involvement of furocoumarins. Clin. Pharmacol. Ther., 2001, 69, 14-23.
-
(2001)
Clin. Pharmacol. Ther.
, vol.69
, pp. 14-23
-
-
Malhotra, S.1
Bailey, D.G.2
Paine, M.F.3
Watkins, P.B.4
-
114
-
-
0028153858
-
Grapefruit juice and drugs: How significant is the interaction?
-
Bailey, D.G.; Arnold, J.M.O.; Spence, J.D. Grapefruit juice and drugs: how significant is the interaction? Clin. Pharmacokinet., 1994, 26, 91-98.
-
(1994)
Clin. Pharmacokinet.
, vol.26
, pp. 91-98
-
-
Bailey, D.G.1
Arnold, J.M.O.2
Spence, J.D.3
-
115
-
-
0031966729
-
Drug interactions with grapefruit juice: Extent, probable mechanism and clinical relevance
-
Fuhr, U. Drug Interactions with Grapefruit Juice: Extent, Probable Mechanism and Clinical Relevance. Drug Saf., 1998, 18, 251-272.
-
(1998)
Drug Saf.
, vol.18
, pp. 251-272
-
-
Fuhr, U.1
-
116
-
-
77249122159
-
Physicochemical space for optimum oral bioavailability: Contribution of human intestinal absorption and first-pass elimination
-
Manthena V.S.; Varma, R.; Obach, S.; Rotter, C.; Miller, H.R.; Chang, G.; Steyn, S.J.; El-Kattan, A.; Troutman, M.D. Physicochemical space for optimum oral bioavailability: contribution of human intestinal absorption and first-pass elimination. J. Med. Chem., 2010, 53, 1098-1108.
-
(2010)
J. Med. Chem.
, vol.53
, pp. 1098-1108
-
-
Manthena, V.S.1
Varma, R.2
Obach, S.3
Rotter, C.4
Miller, H.R.5
Chang, G.6
Steyn, S.J.7
El-Kattan, A.8
Troutman, M.D.9
-
117
-
-
38149041686
-
Relationship between lipophilicities of 1, 4-dihydropyridine derivatives and pharmacokinetic interaction strengths with grapefruit juice
-
Uesawa, Y.; Mohri, K. Relationship between lipophilicities of 1, 4-dihydropyridine derivatives and pharmacokinetic interaction strengths with grapefruit juice, Yakugaku Zasshi, 2008, 128, 117-122.
-
(2008)
Yakugaku Zasshi
, vol.128
, pp. 117-122
-
-
Uesawa, Y.1
Mohri, K.2
-
118
-
-
14144254049
-
PIII-89 an open trial of nifedipine-herb interactions: Nifedipine with St John's wort, ginseng or ginkgo biloba
-
Smith, M.; Lin, K.M.; Zheng, Y.P. PIII-89 an open trial of nifedipine-herb interactions: nifedipine with St John's wort, ginseng or ginkgo biloba. Clin. Pharmacol. Ther., 2001, 69, P86.
-
(2001)
Clin. Pharmacol. Ther.
, vol.69
-
-
Smith, M.1
Lin, K.M.2
Zheng, Y.P.3
-
119
-
-
0034033399
-
Inhibition of human cytochrome P450 enzymes by 1, 4-dihydropyridine calcium antagonists: Prediction of in vivo drug-drug interactions
-
Katoh, M.; Nakajima, M.; Shimada, N.; Yamazaki, H.; Yokoi, T. Inhibition of human cytochrome P450 enzymes by 1, 4-dihydropyridine calcium antagonists: prediction of in vivo drug-drug interactions. Eur. J. Clin. Pharmacol., 2000, 55, 843-852.
-
(2000)
Eur. J. Clin. Pharmacol.
, vol.55
, pp. 843-852
-
-
Katoh, M.1
Nakajima, M.2
Shimada, N.3
Yamazaki, H.4
Yokoi, T.5
-
120
-
-
0025091419
-
Pharmacokinetic drug interactions with cyclosporin (Part I) 1
-
Yee, G.C.; McGuire, T.R. Pharmacokinetic drug interactions with cyclosporin (Part I) 1. Clin. Pharmacokinet., 1990, 19, 319-322.
-
(1990)
Clin. Pharmacokinet.
, vol.19
, pp. 319-322
-
-
Yee, G.C.1
McGuire, T.R.2
-
121
-
-
0020518173
-
Interaction between digoxin and the calcium antagonists nicardipine and tiapamil
-
Lessem, J.; Bellinetto, A. Interaction between digoxin and the calcium antagonists nicardipine and tiapamil. Clin. Ther., 1983, 5, 595-602.
-
(1983)
Clin. Ther.
, vol.5
, pp. 595-602
-
-
Lessem, J.1
Bellinetto, A.2
-
122
-
-
0033636618
-
Inhibitory potencies of 1, 4-dihydropyridine calcium antagonists to P-glycoprotein-mediated transport: Comparison with the effects on CYP3A4
-
Katoh M.; Nakajima, M.; Yamazaki, H.; Yokoi, T. Inhibitory Potencies of 1, 4-dihydropyridine Calcium Antagonists to P-glycoprotein-Mediated Transport: Comparison with the Effects on CYP3A4. Pharm. Res., 2000, 17, 1189-1197.
-
(2000)
Pharm. Res.
, vol.17
, pp. 1189-1197
-
-
Katoh, M.1
Nakajima, M.2
Yamazaki, H.3
Yokoi, T.4
-
123
-
-
0022651899
-
Noninteraction between nifedipine and digoxin
-
Pedersen, K.E.; Madsen, J.L.; Klitgaard, N.A.; Ljoer, K.; Hvidt, S. Noninteraction between nifedipine and digoxin. Dan. Med. Bull., 1986, 33, 109-110.
-
(1986)
Dan. Med. Bull.
, vol.33
, pp. 109-110
-
-
Pedersen, K.E.1
Madsen, J.L.2
Klitgaard, N.A.3
Ljoer, K.4
Hvidt, S.5
-
124
-
-
0034763005
-
Rational use of in vitro P-glycoprotein assays in drug discovery
-
Polli, J.W.; Wring, S.A.; Humphreys, J.E.; Huang, L.; Morgan, J.B. Webster, L.O.; Serabjit-Singh, C.S. Rational use of in vitro P-glycoprotein assays in drug discovery. J. Pharmacol. Exp. Ther., 2001, 299, 620-628.
-
(2001)
J. Pharmacol. Exp. Ther.
, vol.299
, pp. 620-628
-
-
Polli, J.W.1
Wring, S.A.2
Humphreys, J.E.3
Huang, L.4
Morgan, J.B.5
Webster, L.O.6
Serabjit-Singh, C.S.7
-
125
-
-
0036175307
-
Unmasking the dynamic interplay between intestinal P-glycoprotein and CYP3A4
-
Cummins, C.L.; Jacobsen, W. Benet, L.Z. Unmasking the Dynamic Interplay between Intestinal P-Glycoprotein and CYP3A4. J. Pharmacol. Exp. Ther., 2002, 300, 1036-1045.
-
(2002)
J. Pharmacol. Exp. Ther.
, vol.300
, pp. 1036-1045
-
-
Cummins, C.L.1
Jacobsen, W.2
Benet, L.Z.3
-
126
-
-
0025860978
-
Oxidation of dihydropyridine calcium channel blockers and analogues by human liver cytochrome P-450 IIIA4
-
Guengerich, F.P.; Brian, W.R.; Iwasaki, M.; Sari, M.A.; Baarnhielm, C.; Berntsson, P. Oxidation of dihydropyridine calcium channel blockers and analogues by human liver cytochrome P-450 IIIA4. J. Med. Chem., 1991, 34, 1838-1844.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 1838-1844
-
-
Guengerich, F.P.1
Brian, W.R.2
Iwasaki, M.3
Sari, M.A.4
Baarnhielm, C.5
Berntsson, P.6
-
127
-
-
0021716675
-
Cytochrome P-450-dependent oxidation of felodipine-A 1, 4-dihydropyridine-to the corresponding pyridine
-
Bäärnhielm, C.; Skånberg, I.; Borg, K.O. Cytochrome P-450-dependent oxidation of felodipine-a 1, 4-dihydropyridine-to the corresponding pyridine. Xenobiotica, 1984, 14, 719-726.
-
(1984)
Xenobiotica
, vol.14
, pp. 719-726
-
-
Bäärnhielm, C.1
Skånberg, I.2
Borg, K.O.3
-
128
-
-
0022998708
-
Characterization of rat and human liver microsomal cytochrome P-450 forms involved in nifedipine oxidation, a prototype for genetic polymorphism in oxidative drug metabolism
-
Guengerich, F.P.; Martin, M.V.; Beaune, P.H.; Kremers, P.; Wolff, T.; Waxman, D.J. Characterization of rat and human liver microsomal cytochrome P-450 forms involved in nifedipine oxidation, a prototype for genetic polymorphism in oxidative drug metabolism. J. Biol. Chem., 1986, 261, 5051-5060.
-
(1986)
J. Biol. Chem.
, vol.261
, pp. 5051-5060
-
-
Guengerich, F.P.1
Martin, M.V.2
Beaune, P.H.3
Kremers, P.4
Wolff, T.5
Waxman, D.J.6
-
129
-
-
0022550688
-
Oxidation of 4-aryl-and 4-alkyl-substituted 2, 6-dimethyl-3, 5-bis(alkoxycarbonyl)-1, 4-dihydropyridines by human liver microsomes and immunochemical evidence for the involvement of a form of cytochrome P-450
-
Böcker, R.H.; Guengerich, F.P. Oxidation of 4-aryl-and 4-alkyl-substituted 2, 6-dimethyl-3, 5-bis(alkoxycarbonyl)-1, 4-dihydropyridines by human liver microsomes and immunochemical evidence for the involvement of a form of cytochrome P-450. J. Med. Chem., 1986, 29, 1596-1603.
-
(1986)
J. Med. Chem.
, vol.29
, pp. 1596-1603
-
-
Böcker, R.H.1
Guengerich, F.P.2
-
130
-
-
0023928052
-
Cytochrome P-450-catalyzed dehydrogenation of 1, 4-dihydropyridines
-
Guengerich, F.P.; Böcker, R.H. Cytochrome P-450-catalyzed dehydrogenation of 1, 4-dihydropyridines. J. Biol. Chem., 1988, 263, 8168-8175.
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 8168-8175
-
-
Guengerich, F.P.1
Böcker, R.H.2
-
131
-
-
0023899032
-
Cytochrome P-450-catalyzed hydroxylation and carboxylic acid ester cleavage of Hantzsch pyridine esters
-
Guengerich, F.P.; Peterson, L.A.; Böcker, R.H. Cytochrome P-450-catalyzed hydroxylation and carboxylic acid ester cleavage of Hantzsch pyridine esters. J. Biol. Chem., 1988, 263, 8176-8183.
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 8176-8183
-
-
Guengerich, F.P.1
Peterson, L.A.2
Böcker, R.H.3
-
132
-
-
0024368623
-
In vivo oxidative cleavage of a pyridinecarboxylic acid ester metabolite of nifedipine
-
Funaki, T.; Soons, P.A.; Guengerich, F.P.; Breimer, D.D. In vivo oxidative cleavage of a pyridinecarboxylic acid ester metabolite of nifedipine. Biochem. Pharmacol., 1989, 38, 4213-4216.
-
(1989)
Biochem. Pharmacol.
, vol.38
, pp. 4213-4216
-
-
Funaki, T.1
Soons, P.A.2
Guengerich, F.P.3
Breimer, D.D.4
-
133
-
-
0031975185
-
Update: Clinically significant cytochrome P-450 drug interactions
-
Michalets, E.L. Update: clinically significant cytochrome P-450 drug interactions. Pharmacotherapy, 1998, 18, 84-112.
-
(1998)
Pharmacotherapy
, vol.18
, pp. 84-112
-
-
Michalets, E.L.1
-
134
-
-
34547663626
-
The effect of cytochrome P450 metabolism on drug response, interactions, and adverse effects
-
Lynch, T.; Price A. The effect of cytochrome P450 metabolism on drug response, interactions, and adverse effects. Am. Fam. Physician., 2007, 76, 391-396.
-
(2007)
Am. Fam. Physician.
, vol.76
, pp. 391-396
-
-
Lynch, T.1
Price, A.2
-
135
-
-
34248140809
-
Enzymes and pharmacogenetics of cardiovascular drugs
-
Siest, G.; Jeannesson, E.; Visvikis-Siest, S. Enzymes and pharmacogenetics of cardiovascular drugs. Clin. Chim. Acta., 2007, 381, 26-31.
-
(2007)
Clin. Chim. Acta.
, vol.381
, pp. 26-31
-
-
Siest, G.1
Jeannesson, E.2
Visvikis-Siest, S.3
-
136
-
-
0032924934
-
Cytochrome P-450 3A4: Regulation and role in drug metabolism
-
Guengerich, F.P. Cytochrome P-450 3A4: Regulation and role in drug metabolism. Ann. Rev. Pharmacol. Toxicol., 1999, 39, 1-17.
-
(1999)
Ann. Rev. Pharmacol. Toxicol.
, vol.39
, pp. 1-17
-
-
Guengerich, F.P.1
-
137
-
-
21144458074
-
Inhibitory effects of nicardipine to cytochrome P450 (CYP) in human liver microsomes
-
Nakamura, K.; Ariyoshi, N.; Iwatsubo, T.; Fukunaga, Y.; Higuchi, S.; Itoh, K.; Shimada, N.; Nagashima, K.; Yokoi, T.; Yamamoto, K.; Horiuchi, R.; Kamataki, T. Inhibitory effects of nicardipine to cytochrome P450 (CYP) in human liver microsomes. Biol. Pharm. Bull., 2005, 28, 882-885.
-
(2005)
Biol. Pharm. Bull.
, vol.28
, pp. 882-885
-
-
Nakamura, K.1
Ariyoshi, N.2
Iwatsubo, T.3
Fukunaga, Y.4
Higuchi, S.5
Itoh, K.6
Shimada, N.7
Nagashima, K.8
Yokoi, T.9
Yamamoto, K.10
Horiuchi, R.11
Kamataki, T.12
-
138
-
-
34548536326
-
Effect of benidipine on simvastatin metabolism in human liver microsomes
-
Sugiyama, Y.; Mimura, N.; Kuwabara, T.; Kobayashi, H.; Ushiki, J.; Fuse, E. Effect of benidipine on simvastatin metabolism in human liver microsomes. Drug Metab. Pharmacokinet., 2007, 22, 199-205.
-
(2007)
Drug Metab. Pharmacokinet.
, vol.22
, pp. 199-205
-
-
Sugiyama, Y.1
Mimura, N.2
Kuwabara, T.3
Kobayashi, H.4
Ushiki, J.5
Fuse, E.6
-
139
-
-
33646568084
-
Enzymatic characteristics of CYP3A5 and CYP3A4: A comparison of in vitro kinetic and drug-drug interaction patterns
-
Emoto, C.; Iwasaki, K. Enzymatic characteristics of CYP3A5 and CYP3A4: a comparison of in vitro kinetic and drug-drug interaction patterns. Xenobiotica, 2006, 36, 219-233.
-
(2006)
Xenobiotica
, vol.36
, pp. 219-233
-
-
Emoto, C.1
Iwasaki, K.2
-
140
-
-
0030770247
-
Examination of metabolic pathways and identification of human liver cytochrome P450 isozymes responsible for the metabolism of barnidipine, a calcium channel blocker
-
Teramura, T.; Fukunaga, Y.; Van Hoogdalem, E.J.; Watanabe, T.; Higuchi, S. Examination of metabolic pathways and identification of human liver cytochrome P450 isozymes responsible for the metabolism of barnidipine, a calcium channel blocker, Xenobiotica, 1997, 27, 885-900.
-
(1997)
Xenobiotica
, vol.27
, pp. 885-900
-
-
Teramura, T.1
Fukunaga, Y.2
Van Hoogdalem, E.J.3
Watanabe, T.4
Higuchi, S.5
-
141
-
-
34548089507
-
Characterization of benidipine and its enantiomers' metabolism by human liver cytochrome P450 enzymes
-
Yoon, Y.J.; Kim, K.B.; Kim, H.; Seo, K.A.; Kim, H.S.; Cha, I.J.; Kim, E.Y.; Liu, K.H.; Shin, J.G. Characterization of benidipine and its enantiomers' metabolism by human liver cytochrome P450 enzymes. Drug Metab. Dispos., 2007, 35, 1518-1524.
-
(2007)
Drug Metab. Dispos.
, vol.35
, pp. 1518-1524
-
-
Yoon, Y.J.1
Kim, K.B.2
Kim, H.3
Seo, K.A.4
Kim, H.S.5
Cha, I.J.6
Kim, E.Y.7
Liu, K.H.8
Shin, J.G.9
-
142
-
-
0030969001
-
Pharmacokinetics and pharmacodynamics in toxicology
-
Smith, D.A. Pharmacokinetics and pharmacodynamics in toxicology, Xenobiotica, 1997, 27, 513-525.
-
(1997)
Xenobiotica
, vol.27
, pp. 513-525
-
-
Smith, D.A.1
-
143
-
-
0037336297
-
Metabolism and metabolic inhibition of cilnidipine in human liver microsomes
-
Liu, X.Q.; Zhao, Y.; Li, D.; Qian, Z.Y.; Wang, G.J. Metabolism and metabolic inhibition of cilnidipine in human liver microsomes. Acta Pharmacol. Sin., 2003, 24, 263-268.
-
(2003)
Acta Pharmacol. Sin.
, vol.24
, pp. 263-268
-
-
Liu, X.Q.1
Zhao, Y.2
Li, D.3
Qian, Z.Y.4
Wang, G.J.5
-
144
-
-
0036199483
-
Interaction potential of lercanidipine, a new vasoselective dihydropyridine calcium antagonist
-
Klotz, U. Interaction potential of lercanidipine, a new vasoselective dihydropyridine calcium antagonist. Arzneimittelforschung, 2002, 52, 155-161.
-
(2002)
Arzneimittelforschung
, vol.52
, pp. 155-161
-
-
Klotz, U.1
-
145
-
-
0032913679
-
Cytochrome P-450 isoforms involved in carboxylic acid ester cleavage of Hantzsch pyridine ester of pranidipine
-
Kudo, S.; Okumura, H.; Miyamoto, G.; Ishizaki, T. Cytochrome P-450 isoforms involved in carboxylic acid ester cleavage of Hantzsch pyridine ester of pranidipine, Drug Metab. Dispos., 1999, 27, 303-308.
-
(1999)
Drug Metab. Dispos.
, vol.27
, pp. 303-308
-
-
Kudo, S.1
Okumura, H.2
Miyamoto, G.3
Ishizaki, T.4
-
146
-
-
0037974573
-
In vitro metabolism of midazolam, triazolam, nifedipine, and testosterone by human liver microsomes and recombinant cytochromes P450: Role of CYP3A4 and CYP3A5
-
Patki, K.C.; Von Moltke, L.L.; Greenblatt, D.J. In vitro metabolism of midazolam, triazolam, nifedipine, and testosterone by human liver microsomes and recombinant cytochromes P450: role of CYP3A4 and CYP3A5. Drug Metab. Dispos., 2003, 31, 938-944.
-
(2003)
Drug Metab. Dispos.
, vol.31
, pp. 938-944
-
-
Patki, K.C.1
Von Moltke, L.L.2
Greenblatt, D.J.3
-
147
-
-
14044278775
-
Development and validation of a high-throughput radiometric CYP2C9 inhibition assay using tritiated diclofenac
-
Di Marco, A.; Marcucci, I.; Chaudhary, A.; Taliani, M.; Laufer, R. Development and validation of a high-throughput radiometric CYP2C9 inhibition assay using tritiated diclofenac. Drug Metab. Dispos., 2005, 33, 359-364.
-
(2005)
Drug Metab. Dispos.
, vol.33
, pp. 359-364
-
-
Di Marco, A.1
Marcucci, I.2
Chaudhary, A.3
Taliani, M.4
Laufer, R.5
-
148
-
-
33750547308
-
CYP2C9 inhibition: Impact of probe selection and pharmacogenetics on in vitro inhibition profiles
-
Kumar, V.; Wahlstrom, J.L.; Rock, D.A.; Warren, C.J.; Gorman, L.A.; Tracy, T.S. CYP2C9 inhibition: impact of probe selection and pharmacogenetics on
-
(2006)
Drug Metab. Dispos.
, vol.34
, pp. 1966-1975
-
-
Kumar, V.1
Wahlstrom, J.L.2
Rock, D.A.3
Warren, C.J.4
Gorman, L.A.5
Tracy, T.S.6
-
149
-
-
33947603205
-
Comparison of cytochrome P450 inhibition assays for drug discovery using human liver microsomes with LCMS, rhCYP450 isozymes with fluorescence, and double cocktail with LCMS
-
Di, L.; Kerns, E.H.; Li, S.Q.; Carter, G.T. Comparison of cytochrome P450 inhibition assays for drug discovery using human liver microsomes with LCMS, rhCYP450 isozymes with fluorescence, and double cocktail with LCMS. Int. J. Pharm. 2007, 335, 1-11.
-
(2007)
Int. J. Pharm.
, vol.335
, pp. 1-11
-
-
Di, L.1
Kerns, E.H.2
Li, S.Q.3
Carter, G.T.4
-
150
-
-
0035015324
-
High-throughput cytochrome P450 (CYP) inhibition screening via a cassette probe-dosing strategy. VI. Simultaneous evaluation of inhibition potential of drugs on human hepatic isozymes CYP2A6, 3A4, 2C9, 2D6 and 2E1
-
Bu, H.Z.; Magis, L.; Knuth, K.; Teitelbaum, P. High-throughput cytochrome P450 (CYP) inhibition screening via a cassette probe-dosing strategy. VI. Simultaneous evaluation of inhibition potential of drugs on human hepatic isozymes CYP2A6, 3A4, 2C9, 2D6 and 2E1. Rapid. Commun. Mass Spectrom. 2001, 15, 741-748.
-
(2001)
Rapid. Commun. Mass Spectrom.
, vol.15
, pp. 741-748
-
-
Bu, H.Z.1
Magis, L.2
Knuth, K.3
Teitelbaum, P.4
-
151
-
-
14044256740
-
Examination of 209 drugs for inhibition of cytochrome P450 2C8
-
Walsky, R.L.; Gaman, E.A.; Obach, R.S. Examination of 209 drugs for inhibition of cytochrome P450 2C8. J. Clin. Pharmacol., 2005, 45, 68-78.
-
(2005)
J. Clin. Pharmacol.
, vol.45
, pp. 68-78
-
-
Walsky, R.L.1
Gaman, E.A.2
Obach, R.S.3
-
152
-
-
33750711672
-
Evaluation of 227 drugs for in vitro inhibition of cytochrome P450 2B6
-
Walsky, R.L.; Astuccio, A.V.; Obach, R.S. Evaluation of 227 drugs for in vitro inhibition of cytochrome P450 2B6. J. Clin. Pharmacol., 2006, 46, 1426-1438.
-
(2006)
J. Clin. Pharmacol.
, vol.46
, pp. 1426-1438
-
-
Walsky, R.L.1
Astuccio, A.V.2
Obach, R.S.3
-
153
-
-
0032735988
-
CYP3A4 drug interactions: Correlation of 10 in vitro probe substrates
-
Kenworthy, K.E.; Bloomer, J.C.; Clarke, S.E.; Houston, J.B. CYP3A4 drug interactions: correlation of 10 in vitro probe substrates. Br. J. Clin. Pharmacol., 1999, 48, 716-727.
-
(1999)
Br. J. Clin. Pharmacol.
, vol.48
, pp. 716-727
-
-
Kenworthy, K.E.1
Bloomer, J.C.2
Clarke, S.E.3
Houston, J.B.4
-
154
-
-
33645836309
-
Human cytochrome p450 induction and inhibition potential of clevidipine and its primary metabolite h152/81
-
Zhang, J.G.; Dehal, S.S.; Ho, T.; Johnson, J.; Chandler, C.; Blanchard, A.P.; Clark, R.J.Jr; Crespi, C.L.; Stresser, D.M.; Wong, J. Human cytochrome p450 induction and inhibition potential of clevidipine and its primary metabolite h152/81. Drug Metab. Dispos., 2006, 34, 734-737.
-
(2006)
Drug Metab. Dispos.
, vol.34
, pp. 734-737
-
-
Zhang, J.G.1
Dehal, S.S.2
Ho, T.3
Johnson, J.4
Chandler, C.5
Blanchard, A.P.6
Clark Jr., R.J.7
Crespi, C.L.8
Stresser, D.M.9
Wong, J.10
-
155
-
-
4644331461
-
Differences in the inhibition of cytochromes P450 3A4 and 3A5 by metabolite-inhibitor complex-forming drugs
-
McConn, D.J. 2nd; Lin, Y.S.; Allen, K.; Kunze, K.L.; Thummel, K.E. Differences in the inhibition of cytochromes P450 3A4 and 3A5 by metabolite-inhibitor complex-forming drugs. Drug Metab. Dispos., 2004, 32, 1083-1091.
-
(2004)
Drug Metab. Dispos.
, vol.32
, pp. 1083-1091
-
-
McConn, I.I.D.J.1
Lin, Y.S.2
Allen, K.3
Kunze, K.L.4
Thummel, K.E.5
-
156
-
-
34548070044
-
Computational approaches that predict metabolic intermediate complex formation with CYP3A4 (+b5)
-
Jones, D.R.; Ekins, S.; Li, L.; Hall, S.D. Computational approaches that predict metabolic intermediate complex formation with CYP3A4 (+b5). Drug Metab. Dispos., 2007, 35, 1466-1475.
-
(2007)
Drug Metab. Dispos.
, vol.35
, pp. 1466-1475
-
-
Jones, D.R.1
Ekins, S.2
Li, L.3
Hall, S.D.4
-
157
-
-
0033959578
-
Drug interactions with calcium channel blockers: Possible involvement of metabolite-intermediate complexation with CYP3A
-
Ma, B.; Prueksaritanont, T.; Lin, J.H. Drug Interactions with Calcium Channel Blockers: Possible Involvement of Metabolite-Intermediate Complexation with CYP3A. Drug Metab. Dispos., 2000, 28, 125-130.
-
(2000)
Drug Metab. Dispos.
, vol.28
, pp. 125-130
-
-
Ma, B.1
Prueksaritanont, T.2
Lin, J.H.3
-
158
-
-
0032420517
-
Clinical pharmacokinetics of mibefradil. 1998
-
Welker, H.A.; Wiltshire, H.; Bullingham, R. Clinical pharmacokinetics of mibefradil. 1998 Clin. Pharmacokinet., 1998, 35, 405-423.
-
(1998)
Clin. Pharmacokinet.
, vol.35
, pp. 405-423
-
-
Welker, H.A.1
Wiltshire, H.2
Bullingham, R.3
-
159
-
-
0033026601
-
Metabolic interactions between mibefradil and HMG-CoA reductase inhibitors: An in vitro investigation with human liver preparations
-
Prueksaritanont, T.; Ma, B.; Tang, C.; Meng, Y.; Assang, C.; Lu, P.; Reider, P.J.; Lin, J.H.; Baillie, T.A. Metabolic interactions between mibefradil and HMG-CoA reductase inhibitors: An in vitro investigation with human liver preparations. Br. J. Clin. Pharmacol., 1999, 47, 291-298.
-
(1999)
Br. J. Clin. Pharmacol.
, vol.47
, pp. 291-298
-
-
Prueksaritanont, T.1
Ma, B.2
Tang, C.3
Meng, Y.4
Assang, C.5
Lu, P.6
Reider, P.J.7
Lin, J.H.8
Baillie, T.A.9
-
160
-
-
34250716928
-
Risk assessment for drug-drug interaction caused by metabolism-based inhibition of CYP3A using automated in vitro assay systems and its application in the early drug discovery process
-
Watanabe, A.; Nakamura, K.; Okudaira, N.; Okazaki, O.; Sudo, K. Risk assessment for drug-drug interaction caused by metabolism-based inhibition of CYP3A using automated in vitro assay systems and its application in the early drug discovery process. Drug Metab. Dispos., 2007, 35, 1232-1238.
-
(2007)
Drug Metab. Dispos.
, vol.35
, pp. 1232-1238
-
-
Watanabe, A.1
Nakamura, K.2
Okudaira, N.3
Okazaki, O.4
Sudo, K.5
-
161
-
-
1542649526
-
Studies on the interactions between drug and estrogen. II. on the inhibitory effect of 29 drugs reported to induce gynecomastia on the oxidation of estradiol at C-2 or C-17
-
Satoh, T.; Munakata, H.; Fujita, K.; Itoh, S.; Itoh, S.; Kamataki, T.; Yoshizawa, I. Studies on the interactions between drug and estrogen. II. On the inhibitory effect of 29 drugs reported to induce gynecomastia on the oxidation of estradiol at C-2 or C-17. Biol. Pharm. Bull., 2003, 26, 695-700.
-
(2003)
Biol. Pharm. Bull.
, vol.26
, pp. 695-700
-
-
Satoh, T.1
Munakata, H.2
Fujita, K.3
Itoh, S.4
Itoh, S.5
Kamataki, T.6
Yoshizawa, I.7
-
162
-
-
16544377013
-
Effect of nilvadipine, a dihydropyridine calcium antagonist, on cytochrome p450 activities in human hepatic microsomes
-
Niwa, T.; Shiraga, T.; Hashimoto, T.; Kagayama, A. Effect of nilvadipine, a dihydropyridine calcium antagonist, on cytochrome p450 activities in human hepatic microsomes. Biol. Pharm. Bull., 2004, 27, 415-417.
-
(2004)
Biol. Pharm. Bull.
, vol.27
, pp. 415-417
-
-
Niwa, T.1
Shiraga, T.2
Hashimoto, T.3
Kagayama, A.4
-
163
-
-
0037389628
-
In vitro and pharmacophore insights into CYP3A enzymes
-
Ekins, S.; Stresser, D.M.; Williams, J.A. In vitro and pharmacophore insights into CYP3A enzymes. Trends Pharmacol. Sci., 2003, 24, 161-166.
-
(2003)
Trends Pharmacol. Sci.
, vol.24
, pp. 161-166
-
-
Ekins, S.1
Stresser, D.M.2
Williams, J.A.3
-
164
-
-
0141789965
-
QSAR analysis of the inhibition of recombinant CYP 3A4 activity by structurally diverse compounds using a genetic algorithm-combined partial least squares method
-
Wanchana, S.; Yamashita, F.; Hashida, M. QSAR analysis of the inhibition of recombinant CYP 3A4 activity by structurally diverse compounds using a genetic algorithm-combined partial least squares method. Pharm. Res., 2003, 20, 1401-1408.
-
(2003)
Pharm. Res.
, vol.20
, pp. 1401-1408
-
-
Wanchana, S.1
Yamashita, F.2
Hashida, M.3
-
165
-
-
0027364928
-
Specificity of substrate and inhibitor probes for human cytochromes P4501A1 and 1A2
-
Tassaneeyakul, W.; Birkett, D.J.; Veronese, M.E.; McManus, M.E.; Tukey, R.H.; Quattrochi, L.C.; Gelboin, H.V.; Miners, J.O. Specificity of substrate and inhibitor probes for human cytochromes P4501A1 and 1A2. J. Pharmacol. Exp. Ther., 1993, 265, 401-407.
-
(1993)
J. Pharmacol. Exp. Ther.
, vol.265
, pp. 401-407
-
-
Tassaneeyakul, W.1
Birkett, D.J.2
Veronese, M.E.3
McManus, M.E.4
Tukey, R.H.5
Quattrochi, L.C.6
Gelboin, H.V.7
Miners, J.O.8
-
166
-
-
0032498303
-
An orphan nuclear receptor activated by pregnanes defines a novel steroid signaling pathway
-
Kliewer, S.A.; Moore, J.T.; Wade, L.; Staudinger, J.L.; Watson, M.A.; Jones, S.A.; McKee, D.D.; Oliver, B.B.; Willson, T.M.; Zetterstrom, R.H.; Perlmann, T.; Lehmann, J.M. An orphan nuclear receptor activated by pregnanes defines a novel steroid signaling pathway. Cell, 1998, 92, 73-82.
-
(1998)
Cell
, vol.92
, pp. 73-82
-
-
Kliewer, S.A.1
Moore, J.T.2
Wade, L.3
Staudinger, J.L.4
Watson, M.A.5
Jones, S.A.6
McKee, D.D.7
Oliver, B.B.8
Willson, T.M.9
Zetterstrom, R.H.10
Perlmann, T.11
Lehmann, J.M.12
-
167
-
-
13144260727
-
Identification of the human nuclear receptor defines a new signaling pathway for CYP3A induction
-
Bertilsson G.; Heidrich, J.; Svensson, K.; Asman, M.; Jendeberg, L.; Sydow-Backman, M.; Ohlsson, R.; Postlind, H.; Blomquist, P.; Berkenstam, A. Identification of the human nuclear receptor defines a new signaling pathway for CYP3A induction. Proc. Natl. Acad. Sci. USA, 1998, 95, 12208-12213.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 12208-12213
-
-
Bertilsson, G.1
Heidrich, J.2
Svensson, K.3
Asman, M.4
Jendeberg, L.5
Sydow-Backman, M.6
Ohlsson, R.7
Postlind, H.8
Blomquist, P.9
Berkenstam, A.10
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