-
1
-
-
2842567030
-
Oxazolidinone Antibacterial Agents
-
Brickner, S. J. Oxazolidinone Antibacterial Agents. Curr. Pharmaceut. Des. 1996, 2, 175-194.
-
(1996)
Curr. Pharmaceut. Des.
, vol.2
, pp. 175-194
-
-
Brickner, S.J.1
-
2
-
-
0023619963
-
Oxazolidinones, a New Class of Synthetic Antibacterial Agents: In Vitro and in Vivo Activities of DuP 105 and DuP 721
-
Slee, A. M.; Wuonola, M. A.; McRipley, R. J.; Zajac, I.; Zawada, M. J.; Bartholomew, P. T.; Gregory, W. A.; Forbes, M. Oxazolidinones, a New Class of Synthetic Antibacterial Agents: In Vitro and In Vivo Activities of DuP 105 and DuP 721. Antimicrob. Agents Chemother. 1987, 31, 1791-1797.
-
(1987)
Antimicrob. Agents Chemother.
, vol.31
, pp. 1791-1797
-
-
Slee, A.M.1
Wuonola, M.A.2
McRipley, R.J.3
Zajac, I.4
Zawada, M.J.5
Bartholomew, P.T.6
Gregory, W.A.7
Forbes, M.8
-
3
-
-
0023748768
-
Mechanism of Action of DuP 721: Inhibition of an Early Event during Initiation of Protein Synthesis
-
Eustice, D. C.; Feldman, P. A.; Zajac, I.; Slee, A. M. Mechanism of Action of DuP 721: Inhibition of an Early Event during Initiation of Protein Synthesis. Antimicrob. Agents Chemother. 1988, 32, 1218-1222.
-
(1988)
Antimicrob. Agents Chemother.
, vol.32
, pp. 1218-1222
-
-
Eustice, D.C.1
Feldman, P.A.2
Zajac, I.3
Slee, A.M.4
-
4
-
-
0025023153
-
Antibacterials. Synthesis and Structure-Activity Studies of 3-Aryl-2-oxooxazolidines. 2. The "A" Group
-
For early SAR work on compounds related to DuP 721, see: (a) Gregory, W. A.; Brittelli, D. R.; Wang, C.-L. J.; Kezar, H. S.; Carlson, R. K.; Park, C.-H.; Corless, P. F.; Miller, S. J.; Rajagopalan, P.; Wuonola, M. A.; McRipley, R. J.; Eberly, V. S.; Slee, A. M.; Forbes, M. Antibacterials. Synthesis and Structure-Activity Studies of 3-Aryl-2-oxooxazolidines. 2. The "A" Group. J. Med. Chem. 1990, 33, 2569-2578. (b) Gregory, W. A.; Brittelli, D. R.; Wang, C.-L. J.; Wuonola, M. A.; McRipley, R. J.; Eustice, D. C.; R. J.; Eberly, V. S.; Bartholomew, P. T.; Slee, A. M.; Forbes, M. Antibacterials. Synthesis and Structure-Activity Studies of 3-Aryl-2-oxooxazolidines. 1. The "B" Group. J. Med. Chem. 1989, 32, 1673-1681. (c) Park, C.-H.; Brittelli, D. R.; Wang, C. L.-J.; Marsh, F. D.; Gregory, W. A.; Wuonola, M. A.; McRipley, R. J.; Eberly, V. S.; Slee, A. M.; Forbes, M. Antibacterials. Synthesis and Structure-Activity Studies of 3-Aryl-2-oxooxazolidines. 4. Multiply-Substituted Aryl Derivatives. J. Med. Chem. 1992, 35, 1156-1165.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 2569-2578
-
-
Gregory, W.A.1
Brittelli, D.R.2
Wang, C.-L.J.3
Kezar, H.S.4
Carlson, R.K.5
Park, C.-H.6
Corless, P.F.7
Miller, S.J.8
Rajagopalan, P.9
Wuonola, M.A.10
McRipley, R.J.11
Eberly, V.S.12
Slee, A.M.13
Forbes, M.14
-
5
-
-
0024312371
-
Antibacterials. Synthesis and Structure-Activity Studies of 3-Aryl-2-oxooxazolidines. 1. The "B" Group
-
For early SAR work on compounds related to DuP 721, see: (a) Gregory, W. A.; Brittelli, D. R.; Wang, C.-L. J.; Kezar, H. S.; Carlson, R. K.; Park, C.-H.; Corless, P. F.; Miller, S. J.; Rajagopalan, P.; Wuonola, M. A.; McRipley, R. J.; Eberly, V. S.; Slee, A. M.; Forbes, M. Antibacterials. Synthesis and Structure-Activity Studies of 3-Aryl-2-oxooxazolidines. 2. The "A" Group. J. Med. Chem. 1990, 33, 2569-2578. (b) Gregory, W. A.; Brittelli, D. R.; Wang, C.-L. J.; Wuonola, M. A.; McRipley, R. J.; Eustice, D. C.; R. J.; Eberly, V. S.; Bartholomew, P. T.; Slee, A. M.; Forbes, M. Antibacterials. Synthesis and Structure-Activity Studies of 3-Aryl-2-oxooxazolidines. 1. The "B" Group. J. Med. Chem. 1989, 32, 1673-1681. (c) Park, C.-H.; Brittelli, D. R.; Wang, C. L.-J.; Marsh, F. D.; Gregory, W. A.; Wuonola, M. A.; McRipley, R. J.; Eberly, V. S.; Slee, A. M.; Forbes, M. Antibacterials. Synthesis and Structure-Activity Studies of 3-Aryl-2-oxooxazolidines. 4. Multiply-Substituted Aryl Derivatives. J. Med. Chem. 1992, 35, 1156-1165.
-
(1989)
J. Med. Chem.
, vol.32
, pp. 1673-1681
-
-
Gregory, W.A.1
Brittelli, D.R.2
Wang, C.-L.J.3
Wuonola, M.A.4
McRipley, R.J.5
Eustice, D.C.6
R, J.7
Eberly, V.S.8
Bartholomew, P.T.9
Slee, A.M.10
Forbes, M.11
-
6
-
-
0026532148
-
Antibacterials. Synthesis and Structure-Activity Studies of 3-Aryl-2-oxooxazolidines. 4. Multiply-Substituted Aryl Derivatives
-
For early SAR work on compounds related to DuP 721, see: (a) Gregory, W. A.; Brittelli, D. R.; Wang, C.-L. J.; Kezar, H. S.; Carlson, R. K.; Park, C.-H.; Corless, P. F.; Miller, S. J.; Rajagopalan, P.; Wuonola, M. A.; McRipley, R. J.; Eberly, V. S.; Slee, A. M.; Forbes, M. Antibacterials. Synthesis and Structure-Activity Studies of 3-Aryl-2-oxooxazolidines. 2. The "A" Group. J. Med. Chem. 1990, 33, 2569-2578. (b) Gregory, W. A.; Brittelli, D. R.; Wang, C.-L. J.; Wuonola, M. A.; McRipley, R. J.; Eustice, D. C.; R. J.; Eberly, V. S.; Bartholomew, P. T.; Slee, A. M.; Forbes, M. Antibacterials. Synthesis and Structure-Activity Studies of 3-Aryl-2-oxooxazolidines. 1. The "B" Group. J. Med. Chem. 1989, 32, 1673-1681. (c) Park, C.-H.; Brittelli, D. R.; Wang, C. L.-J.; Marsh, F. D.; Gregory, W. A.; Wuonola, M. A.; McRipley, R. J.; Eberly, V. S.; Slee, A. M.; Forbes, M. Antibacterials. Synthesis and Structure-Activity Studies of 3-Aryl-2-oxooxazolidines. 4. Multiply-Substituted Aryl Derivatives. J. Med. Chem. 1992, 35, 1156-1165.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 1156-1165
-
-
Park, C.-H.1
Brittelli, D.R.2
Wang, C.L.-J.3
Marsh, F.D.4
Gregory, W.A.5
Wuonola, M.A.6
McRipley, R.J.7
Eberly, V.S.8
Slee, A.M.9
Forbes, M.10
-
8
-
-
0005952906
-
-
April 12, PJB Publications: Ltd., Richmond, Surrey, U.K.
-
(b) Pharmaprojects, April 12, 1995, PJB Publications: Ltd., Richmond, Surrey, U.K.
-
(1995)
Pharmaprojects
-
-
-
9
-
-
0004243711
-
-
Feb, 7-I-484
-
(c) Pharmcast-International, Feb 1995, 7-I-484, 487.
-
(1995)
Pharmcast-International
, pp. 487
-
-
-
10
-
-
0030027833
-
Synthesis and Antibacterial Activity of U-100592 and U-100766, Two Oxazolidinone Antibacterial Agents for the Potential Treatment of Multidrug-Resistant Gram-Positive Bacterial Infections
-
(a) Brickner, S. J.; Hutchinson, D. K.; Barbachyn, M. R.; Manninen, P. R.; Ulanowicz, D. A.; Garmon, S. A.; Grega, K. C.; Hendges, S. K.; Toops, D. S.; Ford, C. W.; Zurenko, G. E. Synthesis and Antibacterial Activity of U-100592 and U-100766, Two Oxazolidinone Antibacterial Agents for the Potential Treatment of Multidrug-Resistant Gram-Positive Bacterial Infections. J. Med. Chem. 1996, 39, 673-679.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 673-679
-
-
Brickner, S.J.1
Hutchinson, D.K.2
Barbachyn, M.R.3
Manninen, P.R.4
Ulanowicz, D.A.5
Garmon, S.A.6
Grega, K.C.7
Hendges, S.K.8
Toops, D.S.9
Ford, C.W.10
Zurenko, G.E.11
-
11
-
-
0031040129
-
Oxazolidinone Antibacterial Agents: Development of the Clinical Candidates Eperezolid and Linezolid
-
(b) Zurenko, G. E.; Ford, C. W.; Hutchinson, D. K.; Brickner, S. J.; Barbachyn, M. R. Oxazolidinone Antibacterial Agents: Development of the Clinical Candidates Eperezolid and Linezolid. Exp. Opin. Invest. Drugs. 1997, 6, 151-158.
-
(1997)
Exp. Opin. Invest. Drugs.
, vol.6
, pp. 151-158
-
-
Zurenko, G.E.1
Ford, C.W.2
Hutchinson, D.K.3
Brickner, S.J.4
Barbachyn, M.R.5
-
12
-
-
15144360684
-
-
For related SAR work, see refs 9-13
-
(c) For related SAR work, see refs 9-13.
-
-
-
-
13
-
-
0029995925
-
Synthesis and Antibacterial Activity of New Tropone-Substituted Phenyloxazolidinone Antibacterial Agents. 1. Identification of Leads and Importance of the Tropone Substitution Pattern
-
Barbachyn, M. R.; Toops, D. S.; Ulanowicz, D. A.; Grega, K. C.; Brickner, S. J.; Ford, C. W.; Zurenko, G. E.; Harael, J. C.; Schaadt, R. D.; Stapert, D.; Yagi, B. H.; Buysse, J. M.; Demyan, W. F.; Kilburn, J. O.; Glickman, S. E. Synthesis and Antibacterial Activity of New Tropone-Substituted Phenyloxazolidinone Antibacterial Agents. 1. Identification of Leads and Importance of the Tropone Substitution Pattern. Bioorg. Med. Chem. Lett. 1996, 6, 1003-1008.
-
(1996)
Bioorg. Med. Chem. Lett.
, vol.6
, pp. 1003-1008
-
-
Barbachyn, M.R.1
Toops, D.S.2
Ulanowicz, D.A.3
Grega, K.C.4
Brickner, S.J.5
Ford, C.W.6
Zurenko, G.E.7
Harael, J.C.8
Schaadt, R.D.9
Stapert, D.10
Yagi, B.H.11
Buysse, J.M.12
Demyan, W.F.13
Kilburn, J.O.14
Glickman, S.E.15
-
14
-
-
0029978552
-
Synthesis and Antibacterial Activity of New Tropone-Substituted Phenyloxazolidinone Antibacterial Agents. 2. Modification of the Phenyl Ring - The Potentiating Effect of Fluorine Substitution on in Vivo Activity
-
Barbachyn, M. R.; Toops, D. S.; Grega, K. C.; Hendges, S. K.; Ford, C. W.; Zurenko, G. E.; Hamel, J. C.; Schaadt, R. D.; Stapert, D.; Yagi, B. H.; Buysse, J. M.; Demyan, W. F.; Kilburn, J. O.; Glickman, S. E. Synthesis and Antibacterial Activity of New Tropone-Substituted Phenyloxazolidinone Antibacterial Agents. 2. Modification of the Phenyl Ring - The Potentiating Effect of Fluorine Substitution on In Vivo Activity. Bioorg. Med. Chem. Lett. 1996, 6, 1009-1014.
-
(1996)
Bioorg. Med. Chem. Lett.
, vol.6
, pp. 1009-1014
-
-
Barbachyn, M.R.1
Toops, D.S.2
Grega, K.C.3
Hendges, S.K.4
Ford, C.W.5
Zurenko, G.E.6
Hamel, J.C.7
Schaadt, R.D.8
Stapert, D.9
Yagi, B.H.10
Buysse, J.M.11
Demyan, W.F.12
Kilburn, J.O.13
Glickman, S.E.14
-
15
-
-
0029790883
-
Oxazolidinone Antibacterial Agents. An Enantioselective Synthesis of the [6,5,5] Tricyclic Fused Oxazolidinone Ring System and Application to the Synthesis of a Rigid DuP 721 Analogue
-
Gleave, M. D.; Brickner, S. J. Oxazolidinone Antibacterial Agents. An Enantioselective Synthesis of the [6,5,5] Tricyclic Fused Oxazolidinone Ring System and Application to the Synthesis of a Rigid DuP 721 Analogue. J. Og. Chem. 1996, 61, 6470-6474.
-
(1996)
J. Og. Chem.
, vol.61
, pp. 6470-6474
-
-
Gleave, M.D.1
Brickner, S.J.2
-
16
-
-
0032546516
-
Synthesis and Antibacterial Activity of [6,5,5] and [6,6,5] Tricyclic Fused Oxazolidinones
-
Gleave, D. M.; Brickner, S. J.; Manninen, P. R.; Allwine, D. A.; Lovasz, K. D.; Rohrer, D. C.; Tucker, J. A.; Zurenko, G. E.; Ford, C. W. Synthesis and Antibacterial Activity of [6,5,5] and [6,6,5] Tricyclic Fused Oxazolidinones. Bioorg. Med. Chem. Lett. 1998, 8, 1231-1236.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 1231-1236
-
-
Gleave, D.M.1
Brickner, S.J.2
Manninen, P.R.3
Allwine, D.A.4
Lovasz, K.D.5
Rohrer, D.C.6
Tucker, J.A.7
Zurenko, G.E.8
Ford, C.W.9
-
17
-
-
5644244213
-
Piperazinyl Oxazolidinones: Structure Activity Relationships of a New Class of Oxazolidinone Antibacterial Agents
-
Abstracts of Papers; San Francisco, CA, Sept 1995; American Society for Microbiology: Washington, DC, Abstract No. F207
-
Hutchinson, D. K.; Barbachyn, M. K.; Brickner, S. J.; Buysse, J. M.; Demyan, W.; Ford, C. W.; Garmon, S. A.; Glickman, S. E.; Grega, K. C.; Hendges, S. K.; Kilburn, J. O.; Manninen, P. R.; Reid, R. J.; Toops, D. A.; Ulanowicz, D. A. Zurenko, G. E. Piperazinyl Oxazolidinones: Structure Activity Relationships of a New Class of Oxazolidinone Antibacterial Agents. Abstracts of Papers; 35th Interscience Conference on Antimicrobial Agents and Chemotherapy, San Francisco, CA, Sept 1995; American Society for Microbiology: Washington, DC, 1995; Abstract No. F207.
-
(1995)
35th Interscience Conference on Antimicrobial Agents and Chemotherapy
-
-
Hutchinson, D.K.1
Barbachyn, M.K.2
Brickner, S.J.3
Buysse, J.M.4
Demyan, W.5
Ford, C.W.6
Garmon, S.A.7
Glickman, S.E.8
Grega, K.C.9
Hendges, S.K.10
Kilburn, J.O.11
Manninen, P.R.12
Reid, R.J.13
Toops, D.A.14
Zurenko G E, U.D.A.15
-
18
-
-
0029940428
-
In Vivo Activities of U-100592 and U-100766, Novel Oxazolidinone Antimicrobial Agents, against Experimental Bacterial Infections
-
Ford, C. W.; Hamel, J. C.; Wilson, D. M.; Moerman, J. K.; Stapert, D.; Yancey, R. J.; Hutchinson, D. K.; Barbachyn, M. R.; Brickner, S. J. In Vivo Activities of U-100592 and U-100766, Novel Oxazolidinone Antimicrobial Agents, against Experimental Bacterial Infections. Antimicrob. Agents Chemother. 1996, 1508-1513.
-
(1996)
Antimicrob. Agents Chemother.
, pp. 1508-1513
-
-
Ford, C.W.1
Hamel, J.C.2
Wilson, D.M.3
Moerman, J.K.4
Stapert, D.5
Yancey, R.J.6
Hutchinson, D.K.7
Barbachyn, M.R.8
Brickner, S.J.9
-
19
-
-
0029942573
-
In Vitro Activities of U-100592 and U-100766, Novel Oxazolidinone Antibacterial Agents
-
Zurenko, G. E.; Yagi, B. H.; Schaadt, R. D.; Allison, J. W.; Kilburn, J. O.; Glickman, S. E.; Hutchinson, D. K.; Barbachyn, M. R.; Brickner, S. J. In Vitro Activities of U-100592 and U-100766, Novel Oxazolidinone Antibacterial Agents. Antimicrob. Agents Chemother. 1996, 839-845.
-
(1996)
Antimicrob. Agents Chemother.
, pp. 839-845
-
-
Zurenko, G.E.1
Yagi, B.H.2
Schaadt, R.D.3
Allison, J.W.4
Kilburn, J.O.5
Glickman, S.E.6
Hutchinson, D.K.7
Barbachyn, M.R.8
Brickner, S.J.9
-
20
-
-
0029912276
-
In Vitro Antimicrobial Activities and Spectra of U-100592 and U-100766, Two Novel Fluorinated Oxazolidinones
-
Jones, R. N.; Johnson, D. M.; Erwin, M. E. In Vitro Antimicrobial Activities and Spectra of U-100592 and U-100766, Two Novel Fluorinated Oxazolidinones. Antimicrob. Agents Chemother. 1996, 720-726.
-
(1996)
Antimicrob. Agents Chemother.
, pp. 720-726
-
-
Jones, R.N.1
Johnson, D.M.2
Erwin, M.E.3
-
21
-
-
0029976183
-
In Vitro Activities of Oxazolidinone Compounds U100592 and U100766 against Staphylococcus aureus and Staphylococcus epidermis
-
Kaatz, G. W.; Seo, S. M. In Vitro Activities of Oxazolidinone Compounds U100592 and U100766 against Staphylococcus aureus and Staphylococcus epidermis, Antimicrob. Agents Chemother. 1996, 799-801.
-
(1996)
Antimicrob. Agents Chemother.
, pp. 799-801
-
-
Kaatz, G.W.1
Seo, S.M.2
-
22
-
-
0029922958
-
In Vitro Activities of Oxazolidinones U-100592 and U-100766 against Penicillin-Resistant and Cephalosporin-Resistant Strains of Streptococcus pneumoniae
-
Mason, E. O.; Lamberth, L. B.; Kaplan, S. L. In Vitro Activities of Oxazolidinones U-100592 and U-100766 against Penicillin-Resistant and Cephalosporin-Resistant Strains of Streptococcus pneumoniae. Antimicrob. Agents Chemother. 1996, 1039-1040.
-
(1996)
Antimicrob. Agents Chemother.
, pp. 1039-1040
-
-
Mason, E.O.1
Lamberth, L.B.2
Kaplan, S.L.3
-
23
-
-
0030773903
-
The Oxazolidinone Eperezolid Binds to the 50S Ribosomal Subunit and Competes with Binding of Chloramphenicol and Lincomycin
-
Lin, A. H.; Murray, K. W.; Vidmar, T. J.; Marotti, K. R. The Oxazolidinone Eperezolid Binds to the 50S Ribosomal Subunit and Competes with Binding of Chloramphenicol and Lincomycin. Antimicrob. Agents Chemother. 1997, 41, 2127-2131.
-
(1997)
Antimicrob. Agents Chemother.
, vol.41
, pp. 2127-2131
-
-
Lin, A.H.1
Murray, K.W.2
Vidmar, T.J.3
Marotti, K.R.4
-
24
-
-
0030793842
-
Mechanism of Action of Oxazolidinones: Effects of Linezolid and Eperezolid on Translation Reactions
-
Shinabarger, D. L.; Marotti, K. R.; Murray, R. W.; Lin, A. H.; Melchior, E. P.; Swaney, S. M.; Dunyak, D. S.; Demyan, W. F.; Buysse, J. M. Mechanism of Action of Oxazolidinones: Effects of Linezolid and Eperezolid on Translation Reactions. Antimicrob. Agents Chemother. 1997, 41, 2132-2136.
-
(1997)
Antimicrob. Agents Chemother.
, vol.41
, pp. 2132-2136
-
-
Shinabarger, D.L.1
Marotti, K.R.2
Murray, R.W.3
Lin, A.H.4
Melchior, E.P.5
Swaney, S.M.6
Dunyak, D.S.7
Demyan, W.F.8
Buysse, J.M.9
-
25
-
-
0024593744
-
Characterization of the Human Colon Carcinoma Cell Line (Caco-2) as a Model System for Intestinal Permeability
-
Hildalgo, I. L.; Raub, T. J.; Borchardt, R. T. Characterization of the Human Colon Carcinoma Cell Line (Caco-2) as a Model System for Intestinal Permeability. Gastroenterology. 1989, 96, 736-749.
-
(1989)
Gastroenterology
, vol.96
, pp. 736-749
-
-
Hildalgo, I.L.1
Raub, T.J.2
Borchardt, R.T.3
-
26
-
-
0030588714
-
Caco-2 Monolayers in Experimental and Theoretical Predictions of Drug Transport
-
Artursson, P.; Palm, K.; Luthman, K. Caco-2 Monolayers in Experimental and Theoretical Predictions of Drug Transport. Adv. Drug Delivery Rev. 1996, 23, 77-98.
-
(1996)
Adv. Drug Delivery Rev.
, vol.23
, pp. 77-98
-
-
Artursson, P.1
Palm, K.2
Luthman, K.3
-
27
-
-
0029998275
-
Comparative Studies of Drug-Metabolizing Enzymes in Dog, Monkey, and Human Small Intestines, and in Caco-2 Cells
-
Prueksaritanont, T.; Gorham, L. M.; Hochman, J. H.; Tran, L. O.; Vyas, K. P. Comparative Studies of Drug-Metabolizing Enzymes in Dog, Monkey, and Human Small Intestines, and in Caco-2 Cells. Drug Metab. Disp. 1996, 24, 634-642.
-
(1996)
Drug Metab. Disp.
, vol.24
, pp. 634-642
-
-
Prueksaritanont, T.1
Gorham, L.M.2
Hochman, J.H.3
Tran, L.O.4
Vyas, K.P.5
-
28
-
-
0024789567
-
Time-Dependent Activity and Expression of Glutathione-S-Transferases in the Human Colon Adenocarcinoma Cell Line Caco-2
-
Peters, W. H. N.; Roelofs, H. M. J. Time-Dependent Activity and Expression of Glutathione-S-Transferases in the Human Colon Adenocarcinoma Cell Line Caco-2. Biochem. J. 1989, 264, 613-616.
-
(1989)
Biochem. J.
, vol.264
, pp. 613-616
-
-
Peters, W.H.N.1
Roelofs, H.M.J.2
-
29
-
-
0027480292
-
Glutathione Conjugate Transport by Human Colon Adenocarcinoma Cells (Caco-2 Cells)
-
Oude-Elferink, R. P.; Baker, C. T.; Jansen, P. L. Glutathione Conjugate Transport by Human Colon Adenocarcinoma Cells (Caco-2 Cells). Biochem. J. 1993, 290 (3), 759-764.
-
(1993)
Biochem. J.
, vol.290
, Issue.3
, pp. 759-764
-
-
Oude-Elferink, R.P.1
Baker, C.T.2
Jansen, P.L.3
-
30
-
-
0025132942
-
Caco-2 cell Monolayers as a Model for Drug Transport Across the Intestinal Mucosa
-
Hilgers, A. R.; Conradi, R. A.; Burton, P. S. Caco-2 cell Monolayers as a Model for Drug Transport Across the Intestinal Mucosa. Pharm. Res. 1990, 7, 902-910.
-
(1990)
Pharm. Res.
, vol.7
, pp. 902-910
-
-
Hilgers, A.R.1
Conradi, R.A.2
Burton, P.S.3
-
31
-
-
0025999171
-
The Influence of Peptide Structure on Transport Across Caco-2 Cells
-
Conradi, R. A.; Hilgers, A. R.; Ho, N. F. H.; Burton, P. S. The Influence of Peptide Structure on Transport Across Caco-2 Cells. Pharm. Res. 1991, 8, 1453-1460.
-
(1991)
Pharm. Res.
, vol.8
, pp. 1453-1460
-
-
Conradi, R.A.1
Hilgers, A.R.2
Ho, N.F.H.3
Burton, P.S.4
-
32
-
-
0028335309
-
Transcellular Permeability of Chloropromazine demonstrating the Roles of Protein Binding and Membrane Partitioning
-
Sawada, G. A.; Ho, N. F. H.; Williams, L. K.; Barshun, C. L.; Raub, T. J. Transcellular Permeability of Chloropromazine demonstrating the Roles of Protein Binding and Membrane Partitioning. Pharm. Res. 1994, 11, 665-673.
-
(1994)
Pharm. Res.
, vol.11
, pp. 665-673
-
-
Sawada, G.A.1
Ho, N.F.H.2
Williams, L.K.3
Barshun, C.L.4
Raub, T.J.5
-
33
-
-
0028948839
-
A Theoretical Basis for a Biopharmaceutic Drug Classification: The Correlation of in Vitro Drug Product Dissolution and in Vivo Bioavailability
-
Amidon, G. L.; Lennernas, H.; Shah, V. P.; Crison, J. R. A Theoretical Basis for a Biopharmaceutic Drug Classification: The Correlation of In Vitro Drug Product Dissolution and In Vivo Bioavailability. Pharm. Res. 1995, 12, 413-420.
-
(1995)
Pharm. Res.
, vol.12
, pp. 413-420
-
-
Amidon, G.L.1
Lennernas, H.2
Shah, V.P.3
Crison, J.R.4
-
34
-
-
84993915717
-
A New Approach fur the Synthesis of Fused Imidazoles: The Synthesis of 3-Acyl-Substituted Imidazo[1,2-x]azines
-
Podergajs, S.; Stanovnik, B.; Tisler, M. A New Approach fur the Synthesis of Fused Imidazoles: The Synthesis of 3-Acyl-Substituted Imidazo[1,2-x]azines. Synthesis 1984, 263-265.
-
(1984)
Synthesis
, pp. 263-265
-
-
Podergajs, S.1
Stanovnik, B.2
Tisler, M.3
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