-
1
-
-
2342481809
-
Lessons learned from marketed and investigational prodrugs
-
P. Ettmayer, G. Amidon, B. Clement, and B. Testa Lessons learned from marketed and investigational prodrugs J Med Chem. 47 2004 2393 2404
-
(2004)
J Med Chem.
, vol.47
, pp. 2393-2404
-
-
Ettmayer, P.1
Amidon, G.2
Clement, B.3
Testa, B.4
-
3
-
-
0346958512
-
Design of ester prodrugs to enhance oral absorption of poorly permeable compounds: Challenges to the discovery scientist
-
K. Beaumont, R. Webster, I. Gardner, and K. Dack Design of ester prodrugs to enhance oral absorption of poorly permeable compounds: challenges to the discovery scientist Curr Drug Metab. 4 2003 461 485
-
(2003)
Curr Drug Metab.
, vol.4
, pp. 461-485
-
-
Beaumont, K.1
Webster, R.2
Gardner, I.3
Dack, K.4
-
4
-
-
2442601735
-
Principles of drug metabolism
-
D.J. Abraham 6th ed. Wiley-Interscience Hoboken, NJ, USA
-
B. Testa, and W. Soine Principles of drug metabolism D.J. Abraham Burger's Medicinal Chemistry and Drug Discovery, vol. 2 6th ed. 2003 Wiley-Interscience Hoboken, NJ, USA 431 498
-
(2003)
Burger's Medicinal Chemistry and Drug Discovery, Vol. 2
, pp. 431-498
-
-
Testa, B.1
Soine, W.2
-
6
-
-
0033006069
-
Prodrug approaches in the improved delivery of peptide drugs
-
W. Wang, J. Jiang, C.E. Ballard, and B. Wang Prodrug approaches in the improved delivery of peptide drugs Curr Pharm Design 5 1999 265 287
-
(1999)
Curr Pharm Design
, vol.5
, pp. 265-287
-
-
Wang, W.1
Jiang, J.2
Ballard, C.E.3
Wang, B.4
-
8
-
-
0343724706
-
Prodrugs for improved CNS delivery
-
D.A. Bradley Prodrugs for improved CNS delivery Adv Drug Deliv Rev. 19 1996 171 202
-
(1996)
Adv Drug Deliv Rev.
, vol.19
, pp. 171-202
-
-
Bradley, D.A.1
-
9
-
-
0029865447
-
Prodrugs revisited - The "ad hoc" approach as a complement to ligand design
-
B. Testa, and J. Caldwell Prodrugs revisited - The "ad hoc" approach as a complement to ligand design Med Res Rev. 16 1996 233 241
-
(1996)
Med Res Rev.
, vol.16
, pp. 233-241
-
-
Testa, B.1
Caldwell, J.2
-
11
-
-
0021800252
-
Prodrugs. Do they have advantages in clinical practice?
-
V.J. Stella, Charman WNA, and V.H. Naringrekar Prodrugs. Do they have advantages in clinical practice? Drugs 29 1985 455 473
-
(1985)
Drugs
, vol.29
, pp. 455-473
-
-
Stella, V.J.1
Charman, W.N.A.2
Naringrekar, V.H.3
-
12
-
-
0004579318
-
Designing prodrugs and bioprecursors
-
G. Jolles K.R.H. Woolridge Academic Press London
-
C.G. Wermuth Designing prodrugs and bioprecursors G. Jolles K.R.H. Woolridge Drug Design: Fact or Fantasy? 1984 Academic Press London 47 72
-
(1984)
Drug Design: Fact or Fantasy?
, pp. 47-72
-
-
Wermuth, C.G.1
-
13
-
-
0345712954
-
Drug latentiation
-
E. Jucker Birkhauser Basel, Switzerland
-
N.J. Harper Drug latentiation E. Jucker Progress in Drug Research, vol. 4 1962 Birkhauser Basel, Switzerland 221 294
-
(1962)
Progress in Drug Research, Vol. 4
, pp. 221-294
-
-
Harper, N.J.1
-
14
-
-
0001199533
-
Chemical aspects of selective toxicity
-
A. Albert Chemical aspects of selective toxicity Nature 182 1958 421 422
-
(1958)
Nature
, vol.182
, pp. 421-422
-
-
Albert, A.1
-
15
-
-
0033966357
-
Soft drug design: General principles and recent applications
-
N. Bodor, and P. Buchwald Soft drug design: general principles and recent applications Med Res Rev. 20 2000 58 101
-
(2000)
Med Res Rev.
, vol.20
, pp. 58-101
-
-
Bodor, N.1
Buchwald, P.2
-
16
-
-
0000120844
-
Novel approaches to the design of safer drugs: Soft drugs and site-specific chemical delivery systems
-
B. Testa Academic Press London
-
N. Bodor Novel approaches to the design of safer drugs: soft drugs and site-specific chemical delivery systems B. Testa Advances in Drug Research, vol. 13 1984 Academic Press London 255 331
-
(1984)
Advances in Drug Research, Vol. 13
, pp. 255-331
-
-
Bodor, N.1
-
17
-
-
0023277876
-
Esmolol: A preliminary review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy
-
P. Benfield, and E.M. Sorkin Esmolol: a preliminary review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy Drugs 33 1987 392 412
-
(1987)
Drugs
, vol.33
, pp. 392-412
-
-
Benfield, P.1
Sorkin, E.M.2
-
19
-
-
0026757191
-
Drug-polymer conjugates: Potential for improved chemotherapy
-
R. Duncan Drug-polymer conjugates: potential for improved chemotherapy Anti-Canc. Drugs 3 1992 175 210
-
(1992)
Anti-Canc. Drugs
, vol.3
, pp. 175-210
-
-
Duncan, R.1
-
20
-
-
0033180164
-
Receptor-mediated and enzyme-dependent targeting of cytotoxic anticancer drugs
-
G.M. Dubowchik, and M.A. Walker Receptor-mediated and enzyme-dependent targeting of cytotoxic anticancer drugs Pharmacol. Therap. 83 1999 67 123
-
(1999)
Pharmacol. Therap.
, vol.83
, pp. 67-123
-
-
Dubowchik, G.M.1
Walker, M.A.2
-
22
-
-
0031726953
-
Design of intramolecularly activated prodrugs
-
B. Testa, and J.M. Mayer Design of intramolecularly activated prodrugs Drug Metab Rev. 30 1998 787 807
-
(1998)
Drug Metab Rev.
, vol.30
, pp. 787-807
-
-
Testa, B.1
Mayer, J.M.2
-
23
-
-
0342437513
-
Improvement of oral peptide bioavailability: Peptidomimetics and prodrug strategies
-
G.M. Pauletti, S. Gangwar, T.J. Siahaan, J. Aube, and R.T. Borchardt Improvement of oral peptide bioavailability: Peptidomimetics and prodrug strategies Adv Drug Deliv Rev. 27 1997 235 256
-
(1997)
Adv Drug Deliv Rev.
, vol.27
, pp. 235-256
-
-
Pauletti, G.M.1
Gangwar, S.2
Siahaan, T.J.3
Aube, J.4
Borchardt, R.T.5
-
24
-
-
0031126947
-
Prodrug strategies to enhance the intestinal absorption of peptides
-
S. Gangwar, G.M. Pauletti, B. Wang, T.J. Siahaan, V.J. Stella, and R.T. Borchardt Prodrug strategies to enhance the intestinal absorption of peptides Drug Discov Today 2 1997 148 155
-
(1997)
Drug Discov Today
, vol.2
, pp. 148-155
-
-
Gangwar, S.1
Pauletti, G.M.2
Wang, B.3
Siahaan, T.J.4
Stella, V.J.5
Borchardt, R.T.6
-
26
-
-
0029054737
-
Amino acid derivatives of dapsone as water-soluble prodrugs
-
N.L. Pochopin, W.N. Charman, and V.J. Stella Amino acid derivatives of dapsone as water-soluble prodrugs Int. J. Pharmaceut. 121 1995 157 167
-
(1995)
Int. J. Pharmaceut.
, vol.121
, pp. 157-167
-
-
Pochopin, N.L.1
Charman, W.N.2
Stella, V.J.3
-
27
-
-
0028948839
-
A theoretical basis for a biopharmaceutic drug classification: The correlation of in vitro drug product dissolution and in vivo bioavailability
-
G.L. Amidon, H. Lennernäs, V.P. Shah, and J.R. Crison A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability Pharm Res. 12 1995 413 420
-
(1995)
Pharm Res.
, vol.12
, pp. 413-420
-
-
Amidon, G.L.1
Lennernäs, H.2
Shah, V.P.3
Crison, J.R.4
-
28
-
-
0346958512
-
Design of ester prodrugs to enhance oral absorption of poorly permeable compounds: Challenges to the discovery scientist
-
K. Beaumont, R. Webster, I. Gardner, and K. Dack Design of ester prodrugs to enhance oral absorption of poorly permeable compounds: challenges to the discovery scientist Curr Drug Metab. 4 2003 461 485
-
(2003)
Curr Drug Metab.
, vol.4
, pp. 461-485
-
-
Beaumont, K.1
Webster, R.2
Gardner, I.3
Dack, K.4
-
29
-
-
0031786423
-
Targeting influenza virus neuraminidase - A new strategy for antiviral therapy
-
J.S. Oxford, and R. Lambkin Targeting influenza virus neuraminidase - a new strategy for antiviral therapy Drug Discov. Today 3 1998 448 456
-
(1998)
Drug Discov. Today
, vol.3
, pp. 448-456
-
-
Oxford, J.S.1
Lambkin, R.2
-
30
-
-
0034084227
-
Discovery and development of GS 4104 (oseltamivir): An orally active influenza neuraminidase inhibitor
-
W. Lew, X. Chen, and C.U. Kim Discovery and development of GS 4104 (oseltamivir): an orally active influenza neuraminidase inhibitor Curr Med Chem. 7 2000 663 672
-
(2000)
Curr Med Chem.
, vol.7
, pp. 663-672
-
-
Lew, W.1
Chen, X.2
Kim, C.U.3
-
31
-
-
0023820851
-
3H-bambuterol, a carbamate prodrug of terbutaline, in blood from humans and laboratory animals in vitro
-
3H- bambuterol, a carbamate prodrug of terbutaline, in blood from humans and laboratory animals in vitro Biochem Pharmacol. 37 1988 3867 3876
-
(1988)
Biochem Pharmacol.
, vol.37
, pp. 3867-3876
-
-
Tunek, A.1
Levin, E.2
Svensson, L.A.3
-
32
-
-
0026330790
-
A prodrug approach to a long-acting beta2 agonist
-
L.Å. Svensson A prodrug approach to a long-acting beta2 agonist Drug News Perspect. 4 1991 544 549
-
(1991)
Drug News Perspect.
, vol.4
, pp. 544-549
-
-
Svensson, L.Å.1
-
33
-
-
0029029678
-
Oral bambuterol versus terbutaline in patients with asthma
-
G. Persson, O. Pahlm, and Y. Gnosspelius Oral bambuterol versus terbutaline in patients with asthma Curr Therap Res. 56 1995 457 465
-
(1995)
Curr Therap Res.
, vol.56
, pp. 457-465
-
-
Persson, G.1
Pahlm, O.2
Gnosspelius, Y.3
-
34
-
-
0024166436
-
The design and bioactivation of presystematically stable prodrugs
-
L.A. Svensson, and A. Tunek The design and bioactivation of presystematically stable prodrugs Drug Metab Rev. 19 1988 165 194
-
(1988)
Drug Metab Rev.
, vol.19
, pp. 165-194
-
-
Svensson, L.A.1
Tunek, A.2
-
35
-
-
0034807893
-
A physiologically based pharmacokinetic analysis of capecitabine, a triple prodrug of 5-FU, in humans: The mechanism for tumor-selective accumulation of 5-FU
-
Y. Tsukamoto, Y. Kato, M. Ura, I. Horii, H. Ishitsuka, and K. Kusuhara A physiologically based pharmacokinetic analysis of capecitabine, a triple prodrug of 5-FU, in humans: the mechanism for tumor-selective accumulation of 5-FU Pharm. Res. 18 2001 1190 1202
-
(2001)
Pharm. Res.
, vol.18
, pp. 1190-1202
-
-
Tsukamoto, Y.1
Kato, Y.2
Ura, M.3
Horii, I.4
Ishitsuka, H.5
Kusuhara, K.6
-
36
-
-
0036079395
-
Capecitabine: Fulfilling the promise of oral chemotherapy
-
J.J. Hwang, and J.L. Marshall Capecitabine: fulfilling the promise of oral chemotherapy Exp. Opin. Pharmacother. 3 2002 733 743
-
(2002)
Exp. Opin. Pharmacother.
, vol.3
, pp. 733-743
-
-
Hwang, J.J.1
Marshall, J.L.2
-
37
-
-
0033678468
-
Identification and biological activity of the active metabolite of clopidogrel
-
P. Savi, J.M. Pereillo, M.F. Uzabiaga, J. Combalbert, C. Picard, and J.P. Maffrand Identification and biological activity of the active metabolite of clopidogrel Thromb Haemost. 84 2000 891 896
-
(2000)
Thromb Haemost.
, vol.84
, pp. 891-896
-
-
Savi, P.1
Pereillo, J.M.2
Uzabiaga, M.F.3
Combalbert, J.4
Picard, C.5
Maffrand, J.P.6
-
38
-
-
0038508970
-
The metabolism of clopidogrel is catalyzed by human cytochrome P450 3A and is inhibited by atorvastin
-
T.A. Clarke, and L.A. Waskell The metabolism of clopidogrel is catalyzed by human cytochrome P450 3A and is inhibited by atorvastin Drug Metab. Disposit. 31 2003 53 59
-
(2003)
Drug Metab. Disposit.
, vol.31
, pp. 53-59
-
-
Clarke, T.A.1
Waskell, L.A.2
-
39
-
-
0346497703
-
Potent mechanism-based inhibition of human CYP2B6 by clopidogrel and ticlopidine
-
T. Richter, T.E. Miirdter, G. Heinkele, J. Pleiss, S. Tatzel, and M. Schwab Potent mechanism-based inhibition of human CYP2B6 by clopidogrel and ticlopidine J Pharmacol Exp Ther. 308 2004 189 197
-
(2004)
J Pharmacol Exp Ther.
, vol.308
, pp. 189-197
-
-
Richter, T.1
Miirdter, T.E.2
Heinkele, G.3
Pleiss, J.4
Tatzel, S.5
Schwab, M.6
-
40
-
-
79953769061
-
Synthetic DNA-targeted chemotherapeutic agents and related tumor-activated prodrugs
-
D.J. Abraham 6th ed. Wiley Hoboken, NJ, USA
-
W.A. Denny Synthetic DNA-targeted chemotherapeutic agents and related tumor-activated prodrugs DJ. Abraham Burger's Medicinal Chemistry and Drug Discovery, vol. 5 6th ed. 2003 Wiley Hoboken, NJ, USA 51 105
-
(2003)
Burger's Medicinal Chemistry and Drug Discovery, Vol. 5
, pp. 51-105
-
-
Denny, W.A.1
-
41
-
-
0344687262
-
Comparative efficacy of novel platinum(IV) compounds with established chemotherapeutic drugs in solid tumour models
-
M.D. Hall, C. Martin, Ferguson DJP, R.M. Phillips, T.W. Hambley, and R. Callaghan Comparative efficacy of novel platinum(IV) compounds with established chemotherapeutic drugs in solid tumour models Biochem Pharmacol. 67 2004 17 30
-
(2004)
Biochem Pharmacol.
, vol.67
, pp. 17-30
-
-
Hall, M.D.1
Martin, C.2
Ferguson, D.J.P.3
Phillips, R.M.4
Hambley, T.W.5
Callaghan, R.6
-
42
-
-
0026502752
-
Enzymology of the reduction of the potent benzotriazine-di-N-oxide hypoxic cell cytotoxin SR 4233 (WIN 59075) by NAD(P)H: (Quinone acceptor) oxidoreductase (EC 1.6.99.2) purified from Walker 256 rat tumour cells
-
R.J. Riley, and P. Workman Enzymology of the reduction of the potent benzotriazine-di-N-oxide hypoxic cell cytotoxin SR 4233 (WIN 59075) by NAD(P)H: (quinone acceptor) oxidoreductase (EC 1.6.99.2) purified from Walker 256 rat tumour cells Biochem. Pharmacol. 43 1992 167 174
-
(1992)
Biochem. Pharmacol.
, vol.43
, pp. 167-174
-
-
Riley, R.J.1
Workman, P.2
|