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Volumn 25, Issue 2, 2002, Pages 111-136

Prodrug and antedrug: Two diametrical approaches in designing safer drugs

Author keywords

Antedrug; Anti inflammation; Antibody directed enzyme prodrug; Asthma; Gene directed enzyme prodrug; Nucleoside prodrug; Nucleotide prodrug; Pro antedrug; Prodrug

Indexed keywords

ANTIBODY CONJUGATE; CYTOSINE DEAMINASE; DEAMINASE; FLUCYTOSINE; GANCICLOVIR; NUCLEOSIDE; NUCLEOTIDE; PRODRUG; THYMIDINE KINASE;

EID: 0036545413     PISSN: 02536269     EISSN: 02536269     Source Type: Journal    
DOI: 10.1007/BF02976552     Document Type: Review
Times cited : (31)

References (196)
  • 1
    • 0032481577 scopus 로고    scopus 로고
    • Synergistic anticancer effects of ganciclovir/thymidine kinase and 5-fluorocytosine deaminase gene therapies
    • Aghi, M., Kramm, C. M., Chou, T. C., Breakefield, X. O., and Chiocca, E. A., Synergistic anticancer effects of ganciclovir/thymidine kinase and 5-fluorocytosine deaminase gene therapies. J. Natl. Cancer Inst., 90, 370-380 (1998).
    • (1998) J. Natl. Cancer Inst. , vol.90 , pp. 370-380
    • Aghi, M.1    Kramm, C.M.2    Chou, T.C.3    Breakefield, X.O.4    Chiocca, E.A.5
  • 2
    • 0001199533 scopus 로고
    • Chemical aspects of selective toxicity
    • Albert, A., Chemical aspects of selective toxicity. Nature, 182, 421-423 (1958).
    • (1958) Nature , vol.182 , pp. 421-423
    • Albert, A.1
  • 4
    • 0027523517 scopus 로고
    • A first step in the development of gene therapy for colorectal carcinoma: Cloning, sequencing, and expression of E. coli cytosine deaminase
    • Austin, E. A. and Huber B. E., A first step in the development of gene therapy for colorectal carcinoma: cloning, sequencing, and expression of E. coli cytosine deaminase. Mol. Pharmacol. 43, 380-387 (1993).
    • (1993) Mol. Pharmacol. , vol.43 , pp. 380-387
    • Austin, E.A.1    Huber, B.E.2
  • 5
    • 0000136353 scopus 로고    scopus 로고
    • Antiinflammatory steroids
    • Wolff, M.E. (Ed.), John Wiley &Sons, Inc.
    • Avery, M. A. and Woolfrey, J. R., Antiinflammatory steroids. In Wolff, M.E. (Ed.), Medicinal Chemistry and Drug Discovery. John Wiley &Sons, Inc. 281-376 (1997).
    • (1997) Medicinal Chemistry and Drug Discovery , pp. 281-376
    • Avery, M.A.1    Woolfrey, J.R.2
  • 7
    • 0028592664 scopus 로고
    • Antibody-Directed Enzyme Prodrug Therapy (ADEPT): A review of some theoretical, experimental and clinical aspects
    • Bagshawe, K. D., Sharma, S. K., Springer, C. J., and Rogers, G. T., Antibody-Directed Enzyme Prodrug Therapy (ADEPT): a review of some theoretical, experimental and clinical aspects. Analytical Oncology, 5, 879 (1994).
    • (1994) Analytical Oncology , vol.5 , pp. 879
    • Bagshawe, K.D.1    Sharma, S.K.2    Springer, C.J.3    Rogers, G.T.4
  • 9
    • 0029989972 scopus 로고    scopus 로고
    • Activity of the (R)-Enantiomers of 9-(2-Phosphonylmethoxypropyl)adenine and 9-(2-Phosphonylmethoxypropyl)-2,6-Diaminopurine Against Human Immunodeficiency Virus in Different Human Cell Systems
    • Balzarini, J., Aquaro, S., Perno, C. -F., Witvrouw, M., Holy, A., and De Clerq, E., Activity of the (R)-Enantiomers of 9-(2-Phosphonylmethoxypropyl) adenine and 9-(2-Phosphonylmethoxypropyl)-2,6-Diaminopurine Against Human Immunodeficiency Virus in Different Human Cell Systems. Biochem. Biophys. Res. Comm., 219, 337-341 (1996).
    • (1996) Biochem. Biophys. Res. Comm. , vol.219 , pp. 337-341
    • Balzarini, J.1    Aquaro, S.2    Perno, C.F.3    Witvrouw, M.4    Holy, A.5    De Clerq, E.6
  • 10
    • 0029852052 scopus 로고    scopus 로고
    • Antiretrovirus Specificity and Intracellular Metabolism of 2′,3′-Didehydro-2′,3′-dideoxythymidine (Stavudine) and Its 5-Monophosphate Triester Prodrug So324
    • Balzarini, J., Egberink, H., Hartmann, K., Cahard, D., Vahlenkamp, T., Thormar, H., De Clercq, E., and McGuigan, C., Antiretrovirus Specificity and Intracellular Metabolism of 2′,3′-Didehydro-2′,3′- dideoxythymidine (Stavudine) and Its 5-Monophosphate Triester Prodrug So324. Mol. Pharmacol., 50, 1207-1213 (1996b).
    • (1996) Mol. Pharmacol. , vol.50 , pp. 1207-1213
    • Balzarini, J.1    Egberink, H.2    Hartmann, K.3    Cahard, D.4    Vahlenkamp, T.5    Thormar, H.6    De Clercq, E.7    McGuigan, C.8
  • 12
    • 0027534661 scopus 로고
    • Differential Antiherpesvirus and Antiretrovirus Effects of the (S) and ® Enantiomers of Acyclic Nucleoside Phosphonates: Potent and Selective in Vitro and in Vivo Antiretrovirus Activities of (R)-9-(2-Phosphonylmethoxypropyl) -2,6-Diaminopurine
    • Balzarini, J., Holy, A., Jindrich, J., Naesens, L., Snoeck, R., Schols, D., De Clercq E., Differential Antiherpesvirus and Antiretrovirus Effects of the (S) and ® Enantiomers of Acyclic Nucleoside Phosphonates: Potent and Selective In Vitro and In Vivo Antiretrovirus Activities of (R)-9-(2- Phosphonylmethoxypropyl)-2,6-Diaminopurine. Antimicrob. Agents and Chemother., 37, 332-338 (1993).
    • (1993) Antimicrob. Agents and Chemother. , vol.37 , pp. 332-338
    • Balzarini, J.1    Holy, A.2    Jindrich, J.3    Naesens, L.4    Snoeck, R.5    Schols, D.6    De Clercq, E.7
  • 14
    • 0030786410 scopus 로고    scopus 로고
    • Conversion of 2′,3′-Dideoxyadenosine (ddA) and 2′,3′-Didehydro-2′,3′-dideoxyadenosine (d4A) to Their Corresponding Aryloxyphosphoramidate Derivatives Markedly Potentiates Their Activity Against Human Immunodeficiency Virus and Hepatitis B Virus
    • Balzarini, J., Kruining, J., Wedgwood, O., Pannecouque, C., Aquaro, S., Perno, C. F., Naessens, L., Witvrouw, M., Heijtink, R., De Clercq, E., and McGuigan, C., Conversion of 2′,3′-Dideoxyadenosine (ddA) and 2′,3′-Didehydro-2′,3′-dideoxyadenosine (d4A) to Their Corresponding Aryloxyphosphoramidate Derivatives Markedly Potentiates Their Activity Against Human Immunodeficiency Virus and Hepatitis B Virus. FEBS Letters, 410, 324-328 (1997).
    • (1997) FEBS Letters , vol.410 , pp. 324-328
    • Balzarini, J.1    Kruining, J.2    Wedgwood, O.3    Pannecouque, C.4    Aquaro, S.5    Perno, C.F.6    Naessens, L.7    Witvrouw, M.8    Heijtink, R.9    De Clercq, E.10    McGuigan, C.11
  • 15
    • 0025979184 scopus 로고
    • 9-(2-Phosphonylmehtoxyethyl)adenine (PMEA) Effectively Inhibits Retrovirus Replication in Vitro and Simian Immunodeficiency Virus Infection in Rhesus Monkeys
    • Balzarini, J., Naesens, L., Slachmuylders, J., Niphuis, H., Rosenburg, I., Holy, A., and Schellekens, H., De Clerq, E., 9-(2-Phosphonylmehtoxyethyl) adenine (PMEA) Effectively Inhibits Retrovirus Replication In Vitro and Simian Immunodeficiency Virus Infection in Rhesus Monkeys. AIDS, 5, 21-28 (1991).
    • (1991) AIDS , vol.5 , pp. 21-28
    • Balzarini, J.1    Naesens, L.2    Slachmuylders, J.3    Niphuis, H.4    Rosenburg, I.5    Holy, A.6    Schellekens, H.7    De Clerq, E.8
  • 16
    • 0030583270 scopus 로고    scopus 로고
    • Anti-HIV and Anti-HBV Activity and Resistance Profile of 2′,3′-Dideoxy-3′-Thiacytidine (3TC) and Its Arylphosphoramidate Derivative CF 1109
    • Balzarini, J., Wedgwood, O., Kruining, J., Pelemans, H., Heijtink, R., De Clercq, E., and McGuigan, C., Anti-HIV and Anti-HBV Activity and Resistance Profile of 2′,3′-Dideoxy-3′-Thiacytidine (3TC) and Its Arylphosphoramidate Derivative CF 1109. Biochem. Biophys. Res. Comm., 225, 363-369 (1996c).
    • (1996) Biochem. Biophys. Res. Comm. , vol.225 , pp. 363-369
    • Balzarini, J.1    Wedgwood, O.2    Kruining, J.3    Pelemans, H.4    Heijtink, R.5    De Clercq, E.6    McGuigan, C.7
  • 17
    • 0031862891 scopus 로고    scopus 로고
    • Anti-inflammatory actions of glucocorticoids: Molecular mechanisms
    • Barnes, P. J., Anti-inflammatory actions of glucocorticoids: molecular mechanisms. Clinical Science, 94, 557-572 (1998).
    • (1998) Clinical Science , vol.94 , pp. 557-572
    • Barnes, P.J.1
  • 19
    • 0034101114 scopus 로고    scopus 로고
    • Mitochondrial amplification of death signals determines thymidine kinase/ganciclovir-triggered activation of apoptosis
    • Beltinger, C., Fulda, S., Kammertoens, T., Uckert, W., and Debatin, K. M., Mitochondrial amplification of death signals determines thymidine kinase/ganciclovir-triggered activation of apoptosis. Cancer Res., 60, 3213-3217 (2000).
    • (2000) Cancer Res. , vol.60 , pp. 3213-3217
    • Beltinger, C.1    Fulda, S.2    Kammertoens, T.3    Uckert, W.4    Debatin, K.M.5
  • 20
    • 0033950759 scopus 로고    scopus 로고
    • Cytosine deaminase suicide gene therapy for peritoneal carcinomatosis
    • Bentires-Alj, M., Hellin, A. C., and Lechanteur, C., Cytosine deaminase suicide gene therapy for peritoneal carcinomatosis. Cancer Gene Ther., 7, 20-26 (2000).
    • (2000) Cancer Gene Ther. , vol.7 , pp. 20-26
    • Bentires-Alj, M.1    Hellin, A.C.2    Lechanteur, C.3
  • 21
    • 0029731207 scopus 로고    scopus 로고
    • Synthesis, in Vitro Antiviral Evaluation, and Stability Studies of Bis(S-acyl-2-thioethyl) Ester Derivatives of 9-[2-(Phosphonomethoxy) ethyl]adenine (PMEA) as Potential PMEA Prodrugs with Improved Oral Bioavailability
    • Benzaria, S., Pélicano, H., Johnson, R., Maury, G., Imbach, J. L., Aubertin, A. M., Obert, G., and Gosselin, G., Synthesis, In Vitro Antiviral Evaluation, and Stability Studies of Bis(S-acyl-2-thioethyl) Ester Derivatives of 9-[2-(Phosphonomethoxy) ethyl]adenine (PMEA) as Potential PMEA Prodrugs with Improved Oral Bioavailability. J. Med. Chem., 39, 4958-4965 (1996).
    • (1996) J. Med. Chem. , vol.39 , pp. 4958-4965
    • Benzaria, S.1    Pélicano, H.2    Johnson, R.3    Maury, G.4    Imbach, J.L.5    Aubertin, A.M.6    Obert, G.7    Gosselin, G.8
  • 25
    • 0014127726 scopus 로고
    • The role of the 5-Hydroxyl Group of Adenosine in Determining Substrate Specificity for Adenosine Deaminase
    • Bloch, A., Robins, M. J., and McCarthy, J. R., Jr., The role of the 5-Hydroxyl Group of Adenosine in Determining Substrate Specificity for Adenosine Deaminase. J. Med. Chem., 10, 908-912 (1967).
    • (1967) J. Med. Chem. , vol.10 , pp. 908-912
    • Bloch, A.1    Robins, M.J.2    McCarthy Jr., J.R.3
  • 27
    • 0033966357 scopus 로고    scopus 로고
    • Soft drug design: General principles and recent applications
    • Bodor, N. and Buchwald, P., Soft drug design: general principles and recent applications. Med. Res. Rev., 20(1), 58-101 (2000).
    • (2000) Med. Res. Rev. , vol.20 , Issue.1 , pp. 58-101
    • Bodor, N.1    Buchwald, P.2
  • 28
    • 0034116724 scopus 로고    scopus 로고
    • Recent advances in retrometabolic drug design and targeting approaches
    • Bodor, N., Recent advances in retrometabolic drug design and targeting approaches. Pharmazie, 55(3), 163-166 (2000).
    • (2000) Pharmazie , vol.55 , Issue.3 , pp. 163-166
    • Bodor, N.1
  • 29
    • 0023976293 scopus 로고
    • Antiherpesvirus Activity of 9-(4-Hydroxy-3-hydroxymethylbut-1-yl)guanine (BRL 39123) in Animals
    • Boyd, M. R., Bacon, T. H., and Sutton, D., Antiherpesvirus Activity of 9-(4-Hydroxy-3-hydroxymethylbut-1-yl)guanine (BRL 39123) in Animals. Antimicrob. Agents Chemother., 32, 358-363 (1988).
    • (1988) Antimicrob. Agents Chemother. , vol.32 , pp. 358-363
    • Boyd, M.R.1    Bacon, T.H.2    Sutton, D.3
  • 30
    • 0027537214 scopus 로고
    • Comparative Activity of Penciclovir and Acyclovir in Mice Infected Intraperitoneally with Herpes Simplex Virus Type 1 SC 16
    • Boyd, M. R., Bacon, T. H., and Sutton, D., Comparative Activity of Penciclovir and Acyclovir in Mice Infected Intraperitoneally with Herpes Simplex Virus Type 1 SC 16. Antimicrob. Agents Chemother., 37, 642-645 (1993).
    • (1993) Antimicrob. Agents Chemother. , vol.37 , pp. 642-645
    • Boyd, M.R.1    Bacon, T.H.2    Sutton, D.3
  • 31
    • 10544247945 scopus 로고
    • In vivo Anti-retrovirus and Anti-cytomegalovirus Activity of 9-((2-Phosphonylmethoxy)-ethyl)adenine (PMEA)
    • Abstracts of Papers; Montreal, Canada, Abstract M.C.P. 74
    • Bronson, J. J., Ghazzouli, I., Hitchcock, M. J. M., Russel, J. W., Klunk, L. J., Kern E. R., and Martin, J. C., In vivo Anti-retrovirus and Anti-cytomegalovirus Activity of 9-((2-Phosphonylmethoxy)-ethyl)adenine (PMEA). Abstracts of Papers; 5th International Conference on AIDS, Montreal, Canada, Abstract M.C.P. 74 (1989).
    • (1989) 5th International Conference on AIDS
    • Bronson, J.J.1    Ghazzouli, I.2    Hitchcock, M.J.M.3    Russel, J.W.4    Klunk, L.J.5    Kern, E.R.6    Martin, J.C.7
  • 32
    • 0029938744 scopus 로고    scopus 로고
    • Soft drugs. 21. Design and evaluation of soft analogs of propantheline
    • Brouilette, G., Kawamura, M., Kumar, G. N., and Bodor, N., Soft drugs. 21. Design and evaluation of soft analogs of propantheline. J. Pharm. Sci. 85, 619 (1996).
    • (1996) J. Pharm. Sci. , vol.85 , pp. 619
    • Brouilette, G.1    Kawamura, M.2    Kumar, G.N.3    Bodor, N.4
  • 33
  • 34
    • 0025290649 scopus 로고
    • Brain Targeting of Anti-HIV Nucleosides: Synthesis and in Vitro and in Vivo Studies of Dihydopyridine Derivatives of 3-Azido-2,3-dideoxyuridine and 3-Azido-3-deoxythymidine
    • Chu, C. K., Bhadti, V. S., Doshi, K. J., Etse, J. T., Gallo, J. M., Boudinot, F. D., and Schinazi, R. F., Brain Targeting of Anti-HIV Nucleosides: Synthesis and In Vitro and In Vivo Studies of Dihydopyridine Derivatives of 3-Azido-2,3-dideoxyuridine and 3-Azido-3-deoxythymidine. J. Med. Chem., 33, 2188-2192 (1990).
    • (1990) J. Med. Chem. , vol.33 , pp. 2188-2192
    • Chu, C.K.1    Bhadti, V.S.2    Doshi, K.J.3    Etse, J.T.4    Gallo, J.M.5    Boudinot, F.D.6    Schinazi, R.F.7
  • 35
    • 0026772206 scopus 로고
    • In vivo gene transfer with retroviral vectorproducer cells for treatment of experimental brain tumors
    • Culver, K. W., Ram, Z., Wallbridge, S., Ishii, H., Oldfield, E. H., and Blaese, R. M., In vivo gene transfer with retroviral vectorproducer cells for treatment of experimental brain tumors. Science, 256, 1550-1552 (1992).
    • (1992) Science , vol.256 , pp. 1550-1552
    • Culver, K.W.1    Ram, Z.2    Wallbridge, S.3    Ishii, H.4    Oldfield, E.H.5    Blaese, R.M.6
  • 36
    • 0020406681 scopus 로고
    • Defective hydroxylation of bufuralol associated with side-effects of the drug in poor metabolizers
    • Dayer, P., Kubli, A., Kupfer, A., Courvoisier, F., Balant, L., and Fabre, J. Defective hydroxylation of bufuralol associated with side-effects of the drug in poor metabolizers. Br. J. Clin. Pharmacol., 12, 750-751 (1982).
    • (1982) Br. J. Clin. Pharmacol. , vol.12 , pp. 750-751
    • Dayer, P.1    Kubli, A.2    Kupfer, A.3    Courvoisier, F.4    Balant, L.5    Fabre, J.6
  • 37
    • 0025837774 scopus 로고
    • Broad-spectrum anti-DNA virus and anti-retrovirus activity of phosphonylmethoxyalkylpurine and pyrimidines
    • De Clerq, E., Broad-spectrum anti-DNA virus and anti-retrovirus activity of phosphonylmethoxyalkylpurine and pyrimidines. Biochem. Pharmacol., 42, 963-972 (1991).
    • (1991) Biochem. Pharmacol. , vol.42 , pp. 963-972
    • De Clerq, E.1
  • 38
    • 0021089633 scopus 로고
    • Pharmacokinetics of Acyclovir after Intranvenous and Oral Administration
    • De Miranda, P., Blum, M. R., Pharmacokinetics of Acyclovir After Intranvenous and Oral Administration. J. Antimicrob. Chemother., 12 (Suppl. B) 29-37 (1983).
    • (1983) J. Antimicrob. Chemother. , vol.12 , Issue.SUPPL. B , pp. 29-37
    • De Miranda, P.1    Blum, M.R.2
  • 40
    • 0027268254 scopus 로고
    • Transport of 5-fluorouracil and uracil into human erythrocytes
    • Domin, B. A., Mahony, W. B., and Zimmerman, T. P., Transport of 5-fluorouracil and uracil into human erythrocytes. Biochem. Pharmacol., 46, 503-510 (1993).
    • (1993) Biochem. Pharmacol. , vol.46 , pp. 503-510
    • Domin, B.A.1    Mahony, W.B.2    Zimmerman, T.P.3
  • 41
    • 0021025352 scopus 로고
    • The biochemistry and mechanism of action of acyclovir
    • Elion, G. B., The biochemistry and mechanism of action of acyclovir. Antimicrob. Chemother., 12, Suppl. B:9-17 (1983).
    • (1983) Antimicrob. Chemother. , vol.12 , Issue.SUPPL. B , pp. 9-17
    • Elion, G.B.1
  • 44
    • 0020448543 scopus 로고
    • Ultrashort-acting b-adrenergic blocking agent. 1. (Aryloxy)- propanolamines containing esters in the nitrogen substituent
    • Erhardt, P. W., Woo, C. M., Gorzynski, R. J., and Anderson, W. G., Ultrashort-acting b-adrenergic blocking agent. 1. (Aryloxy)-propanolamines containing esters in the nitrogen substituent. J. Med. Chem., 25, 1402-1407 (1982).
    • (1982) J. Med. Chem. , vol.25 , pp. 1402-1407
    • Erhardt, P.W.1    Woo, C.M.2    Gorzynski, R.J.3    Anderson, W.G.4
  • 45
    • 0027943194 scopus 로고
    • Synthesis and Antitumor Evaluation of Bis[(Pivaloyloxy)methyl]-2-Deoxy-5- Fluorouridine 5-Monophosphate (FdUMP): A Strategy to Introduce Nucleotides into Cells
    • Farquhar, D., Khan, S., Srivastva, D. N., and Saunders, P. P., Synthesis and Antitumor Evaluation of Bis[(Pivaloyloxy)methyl]-2-Deoxy-5-Fluorouridine 5-Monophosphate (FdUMP): A Strategy to Introduce Nucleotides into Cells. J. Med. Chem., 37, 3902-3909 (1994).
    • (1994) J. Med. Chem. , vol.37 , pp. 3902-3909
    • Farquhar, D.1    Khan, S.2    Srivastva, D.N.3    Saunders, P.P.4
  • 46
    • 0028283593 scopus 로고
    • Metabolic and Pharmacokinetic Studies Following Oral Administration of 14C-Famciclovir to Healthy Subjects
    • Filer, C. W., Allen, G. D., and Brown, T. A., Metabolic and Pharmacokinetic Studies Following Oral Administration of 14C-Famciclovir to Healthy Subjects. Xenbiotica, 24, 357-368 (1994).
    • (1994) Xenbiotica , vol.24 , pp. 357-368
    • Filer, C.W.1    Allen, G.D.2    Brown, T.A.3
  • 47
    • 11244262182 scopus 로고    scopus 로고
    • Current and future treatment of inflammatory bowel disease
    • Fiorino, T., Current and future treatment of inflammatory bowel disease. Drug & Market Development. 42-48 (2000).
    • (2000) Drug & Market Development , pp. 42-48
    • Fiorino, T.1
  • 50
    • 0031023474 scopus 로고    scopus 로고
    • Immune system in suicide gene therapy
    • Freeman, S. M., Ramesh, R., and Marrogi, A. J., Immune system in suicide gene therapy. Lancet, 349, 2-3 (1997).
    • (1997) Lancet , vol.349 , pp. 2-3
    • Freeman, S.M.1    Ramesh, R.2    Marrogi, A.J.3
  • 52
    • 0026079070 scopus 로고
    • Colon-specific drug delivery from a glucoside prodrug in the guinea pig. Efficacy study
    • Friend, D. R., Phillips, S., and Tozer, T. N., Colon-specific drug delivery from a glucoside prodrug in the guinea pig. Efficacy study. J. Control Release, 15, 47-54 (1991).
    • (1991) J. Control Release , vol.15 , pp. 47-54
    • Friend, D.R.1    Phillips, S.2    Tozer, T.N.3
  • 53
    • 0008798541 scopus 로고    scopus 로고
    • Beta-adrenergic blocking drugs in cardiac disorders
    • Messerli, F. H., Ed.; W. B. Saunders Co., New York
    • nd ed., Messerli, F. H., Ed.; W. B. Saunders Co., New York, 465-474 (1996).
    • (1996) nd Ed. , pp. 465-474
    • Frishman, W.H.1    Hershman, D.2
  • 54
    • 0031011611 scopus 로고    scopus 로고
    • Transduction of cytosine deaminase gene makes rat glioma cells highly sensitive to 5-fluorocytosine
    • Ge, K., Xu, L., Zheng, Z., Xu, D., Sun, L. and Liu, X., Transduction of cytosine deaminase gene makes rat glioma cells highly sensitive to 5-fluorocytosine. Int. J. Cancer, 71, 675-679 (1997).
    • (1997) Int. J. Cancer , vol.71 , pp. 675-679
    • Ge, K.1    Xu, L.2    Zheng, Z.3    Xu, D.4    Sun, L.5    Liu, X.6
  • 55
    • 0026636419 scopus 로고
    • Inhaled corticosteroids: Benefits and risks
    • Geddes, D. M., Inhaled corticosteroids: Benefits and risks. Thorax, 47, 404-407 (1992).
    • (1992) Thorax , vol.47 , pp. 404-407
    • Geddes, D.M.1
  • 58
    • 0023267580 scopus 로고
    • Inhibitory Effects of 2′,3′-Didehydro-2′,3′- Dideoxynucleosides on Infectivity, Cytopathic Effects and Replication of Human Immunodeficiency Virus
    • Hamamoto, U., Nakashima, H., Matsui, A., Matsuda, A., Ueda, T., and Yamamoto, N., Inhibitory Effects of 2′,3′-Didehydro-2′, 3′-Dideoxynucleosides on Infectivity, Cytopathic Effects and Replication of Human Immunodeficiency Virus. Antimicrob. Agents Chemother., 31, 908 (1987).
    • (1987) Antimicrob. Agents Chemother. , vol.31 , pp. 908
    • Hamamoto, U.1    Nakashima, H.2    Matsui, A.3    Matsuda, A.4    Ueda, T.5    Yamamoto, N.6
  • 59
    • 0023267580 scopus 로고
    • Inhibitory Effects of 2′,3′-Didehydro-2′,3′- Dideoxynucleosides on Infectivity, Cytopathic Effects and Replication of Human Immunodeficiency Virus
    • Hamamoto, U., Nakashima, H., Matsui, A., Matsuda, A., Ueda, T., and Yamamoto, N., Inhibitory Effects of 2′,3′-Didehydro-2′, 3′-Dideoxynucleosides on Infectivity, Cytopathic Effects and Replication of Human Immunodeficiency Virus. Antimicrob. Agents Chemother., 31, 908 (1987).
    • (1987) Antimicrob. Agents Chemother. , vol.31 , pp. 908
    • Hamamoto, U.1    Nakashima, H.2    Matsui, A.3    Matsuda, A.4    Ueda, T.5    Yamamoto, N.6
  • 60
    • 0017645875 scopus 로고
    • Bufuralol, a new betaadrenoceptor blocking agent in a series of benzofuran-2-ethanolamines. Part 2: Pharmacology
    • Hamilton, T. C. and Parkes, M. W., Bufuralol, a new betaadrenoceptor blocking agent in a series of benzofuran-2-ethanolamines. Part 2: Pharmacology. Arzneim.-Forsch. 27, 1410-1417 (1977).
    • (1977) Arzneim.-Forsch. , vol.27 , pp. 1410-1417
    • Hamilton, T.C.1    Parkes, M.W.2
  • 61
    • 0030768615 scopus 로고    scopus 로고
    • Viral directed cytosine deaminase/5-fluorocytosine gene therapy enhances radiation response in human cancer xenografts
    • Hanna, N. N., Mauceri, H. J., Wayne, J. D., Hallahan, D. E., Kufe, D. W., and Weichselbaum, R. R., Viral directed cytosine deaminase/5-fluorocytosine gene therapy enhances radiation response in human cancer xenografts. Cancer Res., 57, 4205-4209 (1997).
    • (1997) Cancer Res. , vol.57 , pp. 4205-4209
    • Hanna, N.N.1    Mauceri, H.J.2    Wayne, J.D.3    Hallahan, D.E.4    Kufe, D.W.5    Weichselbaum, R.R.6
  • 62
    • 0024354624 scopus 로고
    • Prodrugs of Selective Antiherpesvirus Agent 9-[4-Hydroxy-3- (hydroxymethyl)but-1-yl]guanine (BRL 39123) with Improved Gastrointestinal Absorption Properties
    • Harden, M. R., Jarvest, R. L., Boyd, M. R., Sutton, D., and Vere Hodge, R. A., Prodrugs of Selective Antiherpesvirus Agent 9-[4-Hydroxy-3- (hydroxymethyl)but-1-yl]guanine (BRL 39123) with Improved Gastrointestinal Absorption Properties. J. Med. Chem., 32, 1738-1743 (1989).
    • (1989) J. Med. Chem. , vol.32 , pp. 1738-1743
    • Harden, M.R.1    Jarvest, R.L.2    Boyd, M.R.3    Sutton, D.4    Vere Hodge, R.A.5
  • 63
    • 0023259332 scopus 로고
    • Synthesis and Antiviral Activity of 9 [4-Hydroxy-3-(hydroxymethyl) but-1-yl]purines
    • Harnden, M. R., Jarvest, R. L., Bacon, T. H., and Boyd, M. R., Synthesis and Antiviral Activity of 9 [4-Hydroxy-3-(hydroxymethyl) but-1-yl]purines J. Med. Chem., 30, 1636-1642 (1987).
    • (1987) J. Med. Chem. , vol.30 , pp. 1636-1642
    • Harnden, M.R.1    Jarvest, R.L.2    Bacon, T.H.3    Boyd, M.R.4
  • 64
    • 0006750632 scopus 로고
    • Prodrugs of the Selective Antiherpesvirus Agent 9-[4-Hydroxy-3- (hydroxymethyl)but-1-yl]guanine (BRL 39123) with Improved Gastrointestinal Absorption Properties
    • Harnden, M. R., Jarvest, R. L., Boyd, M. R., Sutton, D., and Vere Hodge, R. A., Prodrugs of the Selective Antiherpesvirus Agent 9-[4-Hydroxy-3- (hydroxymethyl)but-1-yl]guanine (BRL 39123) with Improved Gastrointestinal Absorption Properties. J. Med. Chem., 33, 1765-1773 (1989a).
    • (1989) J. Med. Chem. , vol.33 , pp. 1765-1773
    • Harnden, M.R.1    Jarvest, R.L.2    Boyd, M.R.3    Sutton, D.4    Vere Hodge, R.A.5
  • 65
    • 0024354624 scopus 로고
    • Prodrugs of the Selective Antiherpesvirus Agent 9-[4-Hydroxy-3- (hydroxymethyl)but-1-yl]guanine (BRL 39123) with Improved Gastrointestinal Absorption Properties
    • Harnden, M. R., Jarvest, R. L., Boyd, M. R., Sutton, D., Vere and Hodge, R. A., Prodrugs of the Selective Antiherpesvirus Agent 9-[4-Hydroxy-3- (hydroxymethyl)but-1-yl]guanine (BRL 39123) with Improved Gastrointestinal Absorption Properties. J. Med. Chem., 32, 1738-1743 (1989b).
    • (1989) J. Med. Chem. , vol.32 , pp. 1738-1743
    • Harnden, M.R.1    Jarvest, R.L.2    Boyd, M.R.3    Sutton, D.4    Vere Hodge, R.A.5
  • 66
    • 0032443703 scopus 로고    scopus 로고
    • New steroidal anti-inflammatory antedrugs bind to macrophage glucocorticoid receptors and inhibit nitric oxide generation
    • Heiman, A. S., Hickman, F., Ko, D. -H., and Lee, H. J., New steroidal anti-inflammatory antedrugs bind to macrophage glucocorticoid receptors and inhibit nitric oxide generation. Steroids, 63, 644-649 (1998).
    • (1998) Steroids , vol.63 , pp. 644-649
    • Heiman, A.S.1    Hickman, F.2    Ko, D.H.3    Lee, H.J.4
  • 67
    • 0031009643 scopus 로고    scopus 로고
    • New steroidal anti-inflammatory antedrugs: Methyl 3,20-dioxo-9α- fluoro-11β, 17α,21-trihydroxy-1,4-pregnadiene-16α-carboxylate and methyl 21-acetyloxy-3,20-dioxo-11β,17α-dihydroxy-9α-fluoro- 1,4-pregnadiene-16a-carboxylate
    • Heiman, A. S., Ko, D.-H., Chen, M., and Lee, H. J., New steroidal anti-inflammatory antedrugs: Methyl 3,20-dioxo-9α-fluoro-11β, 17α,21-trihydroxy-1,4-pregnadiene-16α-carboxylate and methyl 21-acetyloxy-3,20-dioxo-11β,17α-dihydroxy-9α-fluoro-1, 4-pregnadiene-16a-carboxylate. Steroids, 62, 491-499 (1997).
    • (1997) Steroids , vol.62 , pp. 491-499
    • Heiman, A.S.1    Ko, D.-H.2    Chen, M.3    Lee, H.J.4
  • 69
    • 0006647307 scopus 로고
    • Complementary Chemotherapy in Acute Leukemia. Recent Results
    • Holland, J. F. and Glidewell, O., Complementary Chemotherapy in Acute Leukemia. Recent Results Cancer Res., 30, 95 (1970).
    • (1970) Cancer Res. , vol.30 , pp. 95
    • Holland, J.F.1    Glidewell, O.2
  • 70
    • 0022496698 scopus 로고
    • 1β-D-Arabinofuranosylcytosine Conjugates of Thioether Phospholipids as a New Class of Potential Antitumor Drugs
    • Hong, C. I., Kirisitis, A. J., Buchheit, D. J., Nechaev, A., and West, C. R., 1β-D-Arabinofuranosylcytosine Conjugates of Thioether Phospholipids as a New Class of Potential Antitumor Drugs. Cancer Drug Delivery, 3, 101-113 (1986).
    • (1986) Cancer Drug Delivery , vol.3 , pp. 101-113
    • Hong, C.I.1    Kirisitis, A.J.2    Buchheit, D.J.3    Nechaev, A.4    West, C.R.5
  • 71
    • 0030002326 scopus 로고    scopus 로고
    • Nucleoside Conjugates. 15. Synthesis and Biological Activity of Anti-HIV Nucleoside Conjugates of Ether and Thioether Phospholipids
    • Hong, C. I., Nechaev, A., Kirisits, A. J., Vig, R., West, C. R., Manouilov, K. K., and Chu, C. K., Nucleoside Conjugates. 15. Synthesis and Biological Activity of Anti-HIV Nucleoside Conjugates of Ether and Thioether Phospholipids. J. Med. Chem., 39, 1771-1777 (1996).
    • (1996) J. Med. Chem. , vol.39 , pp. 1771-1777
    • Hong, C.I.1    Nechaev, A.2    Kirisits, A.J.3    Vig, R.4    West, C.R.5    Manouilov, K.K.6    Chu, C.K.7
  • 72
    • 0018575385 scopus 로고
    • Nucleoside Conjugates as Potential Antitumor Agents. 2. Synthesis and Biological Activity of 1-(β-D-Arabinofuranosyl)cytosine Conjugates of Prednisolone and Prednisone
    • Hong, C. I., Nechaev, A., and West, C. R., Nucleoside Conjugates as Potential Antitumor Agents. 2. Synthesis and Biological Activity of 1-(β-D-Arabinofuranosyl)cytosine Conjugates of Prednisolone and Prednisone. J. Med. Chem., 22, 1428-1432 (1979a).
    • (1979) J. Med. Chem. , vol.22 , pp. 1428-1432
    • Hong, C.I.1    Nechaev, A.2    West, C.R.3
  • 73
    • 0018575385 scopus 로고
    • Nucleoside Conjugates as Potential Antitumor Agents. 2. Synthesis and Biological Activity of 1-(β-D-Arabinofuranosyl)cytosine Conjugates of Prednisolone and Prednisone
    • Hong, C. I., Nechaev, A., and West, C. R., Nucleoside Conjugates as Potential Antitumor Agents. 2. Synthesis and Biological Activity of 1-(β-D-Arabinofuranosyl)cytosine Conjugates of Prednisolone and Prednisone. J. Med. Chem., 22, 1428-1432 (1979b).
    • (1979) J. Med. Chem. , vol.22 , pp. 1428-1432
    • Hong, C.I.1    Nechaev, A.2    West, C.R.3
  • 74
    • 0030713362 scopus 로고    scopus 로고
    • Anthracyclines in the treatment of cancer: An overview
    • Hortobagyi, G. N., Anthracyclines in the treatment of cancer: an overview. Drugs, 54, 1-7 (1997).
    • (1997) Drugs , vol.54 , pp. 1-7
    • Hortobagyi, G.N.1
  • 75
    • 0028221349 scopus 로고
    • Antiviral Activity of Phosphatidyl-dideoxycytidine in Hepatitis B Infected Cells and Enhanced Hepatitic Uptake in Mice
    • Hostetler, K. Y., Richman, D. D., Sridhar, C. N., and Gardner, M. F., Antiviral Activity of Phosphatidyl-dideoxycytidine in Hepatitis B Infected Cells and Enhanced Hepatitic Uptake in Mice. Antiviral Res., 24, 59-67 (1994).
    • (1994) Antiviral Res. , vol.24 , pp. 59-67
    • Hostetler, K.Y.1    Richman, D.D.2    Sridhar, C.N.3    Gardner, M.F.4
  • 76
    • 0028108469 scopus 로고
    • Metabolism of 5 fluorocytosine in human colorectal tumor cells transduced with the cytosine deaminase gene: Significant antitumor effects when only a small percentage of tumor cells express cytosine deaminase
    • Huber, B. E., Austin, E. A., Richards, C. A., Davis, S. T., and Good, S. S., Metabolism of 5 fluorocytosine in human colorectal tumor cells transduced with the cytosine deaminase gene: significant antitumor effects when only a small percentage of tumor cells express cytosine deaminase. Proc. Natl. Acad. Sci. USA, 91, 8302-8306 (1994).
    • (1994) Proc. Natl. Acad. Sci. USA , vol.91 , pp. 8302-8306
    • Huber, B.E.1    Austin, E.A.2    Richards, C.A.3    Davis, S.T.4    Good, S.S.5
  • 77
    • 0027496518 scopus 로고
    • In vivo antitumor activity of 5-fluorocytosine on human colorectal carcinoma cells genetically modified to express cytosine deaminase
    • Huber, B. E., Austin, E. S., Good, S. S., Knick, V. C., Tibbels, S., and Richards, C. A., In vivo antitumor activity of 5-fluorocytosine on human colorectal carcinoma cells genetically modified to express cytosine deaminase. Cancer Res., 53, 4619-4626 (1993).
    • (1993) Cancer Res. , vol.53 , pp. 4619-4626
    • Huber, B.E.1    Austin, E.S.2    Good, S.S.3    Knick, V.C.4    Tibbels, S.5    Richards, C.A.6
  • 78
    • 0034692180 scopus 로고    scopus 로고
    • Design, synthesis and evaluation of soft bufuralol analogues
    • Hwang, S. K., Juhasz, A., Yoon, S. H., and Bodor, N., Design, synthesis and evaluation of soft bufuralol analogues. J. Med. Chem., 43(8), 1525-1532 (2000).
    • (2000) J. Med. Chem. , vol.43 , Issue.8 , pp. 1525-1532
    • Hwang, S.K.1    Juhasz, A.2    Yoon, S.H.3    Bodor, N.4
  • 79
    • 0033961839 scopus 로고    scopus 로고
    • In vivo efficacy and toxicity of 5-fluorocytosine/cytosine deaminase gene therapy for malignant gliomas mediated by adenovirus
    • Ichikawa, T., Tamiya, T., Adachi, Y., Ono, Y., Matsumoto, K., Furuta, T., Yoshida, Y., Hamada, H., and Ohmato, T., In vivo efficacy and toxicity of 5-fluorocytosine/cytosine deaminase gene therapy for malignant gliomas mediated by adenovirus. Cancer Gene Ther., 7, 74-82 (2000).
    • (2000) Cancer Gene Ther. , vol.7 , pp. 74-82
    • Ichikawa, T.1    Tamiya, T.2    Adachi, Y.3    Ono, Y.4    Matsumoto, K.5    Furuta, T.6    Yoshida, Y.7    Hamada, H.8    Ohmato, T.9
  • 80
    • 0025285677 scopus 로고
    • Monophosphoric Acid Diesters of 7b Hydroxycholestrol and of Pyrimidine Nucleosides as Potential Antitumor Agents: Synthesis and Preliminary Evaluation of Antitumor Activity
    • Ji Y., Moog, C., Schmitt, G., Bischoff, P., and Luu, B., Monophosphoric Acid Diesters of 7b Hydroxycholestrol and of Pyrimidine Nucleosides as Potential Antitumor Agents: Synthesis and Preliminary Evaluation of Antitumor Activity. J. Med. Chem., 33, 2264-2270 (1990).
    • (1990) J. Med. Chem. , vol.33 , pp. 2264-2270
    • Ji, Y.1    Moog, C.2    Schmitt, G.3    Bischoff, P.4    Luu, B.5
  • 81
    • 0034075060 scopus 로고    scopus 로고
    • Design, synthesis and evaluation of soft glycopyrrolate and its analog
    • Ji, F., Huang, F., Juhasz, A., Wu, W., and Bodor, N., Design, synthesis and evaluation of soft glycopyrrolate and its analog. Pharmazie., 55(3), 187-191 (2000).
    • (2000) Pharmazie. , vol.55 , Issue.3 , pp. 187-191
    • Ji, F.1    Huang, F.2    Juhasz, A.3    Wu, W.4    Bodor, N.5
  • 83
    • 0342369451 scopus 로고    scopus 로고
    • Cardiovascular studies on different classes of soft drugs
    • Juhasz, A. and Bodor, N., Cardiovascular studies on different classes of soft drugs. Pharmazie., 55(3), 228-238 (2000).
    • (2000) Pharmazie. , vol.55 , Issue.3 , pp. 228-238
    • Juhasz, A.1    Bodor, N.2
  • 85
    • 0029112774 scopus 로고
    • Gene therapy of hepatoma: Bystander effects and non-apoptotic cell death induced by thymidine kinase and ganciclovir
    • Kaneko, Y. and Tsukamoto, A., Gene therapy of hepatoma: bystander effects and non-apoptotic cell death induced by thymidine kinase and ganciclovir. Cancer Lett., 96, 105-110 (1995).
    • (1995) Cancer Lett. , vol.96 , pp. 105-110
    • Kaneko, Y.1    Tsukamoto, A.2
  • 86
    • 0029095503 scopus 로고
    • Regressions and cures of melanoma xenografts following treatment with monoclonal antibody beta-lactamase conjugates in combination with anticancer prodrugs
    • Kerr, D. E., Schreiber, G. J., Vrudhula, V. M., Svensson, H. P., Hellstrom, I., Hellstrom, K. E., and Senter, P. D., Regressions and cures of melanoma xenografts following treatment with monoclonal antibody beta-lactamase conjugates in combination with anticancer prodrugs . Cancer Res., 55, 3558-3563 (1995).
    • (1995) Cancer Res. , vol.55 , pp. 3558-3563
    • Kerr, D.E.1    Schreiber, G.J.2    Vrudhula, V.M.3    Svensson, H.P.4    Hellstrom, I.5    Hellstrom, K.E.6    Senter, P.D.7
  • 87
    • 0000396872 scopus 로고
    • A novel approach to the development of safer anti inflammatory steroids: Antedrugs
    • Khalil, M. A., Kwon, T., and Lee, H. J., A novel approach to the development of safer anti inflammatory steroids: Antedrugs. Current Topics in Med. Chem., 1, 173-202 (1993).
    • (1993) Current Topics in Med. Chem. , vol.1 , pp. 173-202
    • Khalil, M.A.1    Kwon, T.2    Lee, H.J.3
  • 88
    • 0002104784 scopus 로고    scopus 로고
    • New antiinflammatory steroids: [16α,17α-d]-3- hydroxyiminoformylisoxazoline derivatives of prednisolone and 9α-fluoroprednisolone
    • Khalil, M. A., Maponya, M. F., Ko, D. -H., You, Z., Oriaku, E. T., and Lee, H. J., New antiinflammatory steroids: [16αa,17α-d]-3- hydroxyiminoformylisoxazoline derivatives of prednisolone and 9α-fluoroprednisolone. Med. Chem. Res., 6, 52-60 (1996).
    • (1996) Med. Chem. Res. , vol.6 , pp. 52-60
    • Khalil, M.A.1    Maponya, M.F.2    Ko, D.H.3    You, Z.4    Oriaku, E.T.5    Lee, H.J.6
  • 89
    • 0028225668 scopus 로고
    • Colonic mucosa-specific pro-antedrugs for oral treatment of ulcerative colitis: Design, synthesis and fate of methyl 20- glucopyranosyloxyprednisolonates
    • Kimura, T., Yamaguchi, T., Usuki, K., Kurosaki, Y., Nakayama, T., Fujiwara, Y., Matsuda, Y., Unno, K., and Suzuki, T., Colonic mucosa-specific pro-antedrugs for oral treatment of ulcerative colitis: design, synthesis and fate of methyl 20-glucopyranosyloxyprednisolonates. J. Control Release, 30, 125-135 (1994).
    • (1994) J. Control Release , vol.30 , pp. 125-135
    • Kimura, T.1    Yamaguchi, T.2    Usuki, K.3    Kurosaki, Y.4    Nakayama, T.5    Fujiwara, Y.6    Matsuda, Y.7    Unno, K.8    Suzuki, T.9
  • 91
    • 0034098564 scopus 로고    scopus 로고
    • New steroidal anti-inflammatory antedrugs: Methyl 21-desoxy-21-chloro- 11β,17α-dihydroxy-3,20-dioxo-1,4-pregnadiene-16α-carboxylate, methyl 21-desoxy-21-chloro-11β-hydroxy-3,20-dioxo-1,4-pregnadiene- 16α-carboxylate, and their 9α-fluoro derivatives
    • Ko, D.-H., Heima, A. S., Chen, M., and Lee, H. J., New steroidal anti-inflammatory antedrugs: Methyl 21-desoxy-21-chloro-11β,17α- dihydroxy-3,20-dioxo-1,4-pregnadiene-16α-carboxylate, methyl 21-desoxy-21-chloro-11β-hydroxy-3,20-dioxo-1,4-pregnadiene-16α- carboxylate, and their 9α-fluoro derivatives. Steroids, 65, 210-218 (2000).
    • (2000) Steroids , vol.65 , pp. 210-218
    • Ko, D.-H.1    Heima, A.S.2    Chen, M.3    Lee, H.J.4
  • 92
    • 11244285855 scopus 로고    scopus 로고
    • New steroidal antiinflammatory antedrugs: Methyl 3,20-dioxo-9α- fluoro-11β,17α,21-trihydroxy-1,4-pregnadiene-16α-carboxylate and its 21-O-acyl derivatives
    • in the press
    • Ko, D. -H., Heiman, A. S., Hudson, C. E., and Lee, H. J., New steroidal antiinflammatory antedrugs: Methyl 3,20-dioxo-9α-fluoro-11β, 17α,21-trihydroxy-1,4-pregnadiene-16α-carboxylate and its 21-O-acyl derivatives. Steroids, in the press (2001).
    • (2001) Steroids
    • Ko, D.H.1    Heiman, A.S.2    Hudson, C.E.3    Lee, H.J.4
  • 93
    • 0000506441 scopus 로고    scopus 로고
    • New anti inflammatory steroids: [16α,17α-d]-isoxazoline derivatives of prednisolone and 9α-fluoroprednisolone
    • Ko, D. -H., Maponya, M. F., Khalil, M. A., Oriaku, E. T., You, Z. and Lee, H. J., New anti inflammatory steroids: [16α,17α-d]-isoxazoline derivatives of prednisolone and 9α-fluoroprednisolone. Med. Chem. Res., 7, 313-323 (1997).
    • (1997) Med. Chem. Res. , vol.7 , pp. 313-323
    • Ko, D.H.1    Maponya, M.F.2    Khalil, M.A.3    Oriaku, E.T.4    You, Z.5    Lee, H.J.6
  • 94
    • 0024797070 scopus 로고
    • Antitumor Activity and Pharmacology of 1-β-D- Arabinofuranosylcytosine-5-stearylphosphate: An Orally Active Derivative of 1-b-D-Arabinofuranosylcytosine
    • Kodama, K., Morozumi, M., Saitoh, K., Kuninaka, A., Yoshino, H., and Saneyoshi, M., Antitumor Activity and Pharmacology of 1-β-D- Arabinofuranosylcytosine-5-stearylphosphate: An Orally Active Derivative of 1-b-D-Arabinofuranosylcytosine. Jpn. J. Cancer Res., 80, 679 (1989).
    • (1989) Jpn. J. Cancer Res. , vol.80 , pp. 679
    • Kodama, K.1    Morozumi, M.2    Saitoh, K.3    Kuninaka, A.4    Yoshino, H.5    Saneyoshi, M.6
  • 95
    • 0032717286 scopus 로고    scopus 로고
    • Comparison of gene therapy with the herpes simplex virus thymidine kinase gene and the bacterial cytosine deaminase gene for the treatment of hepatocellular carcinoma
    • Kuriyama, S., Mitoro, A., Yamazaki, M., Tsujinoue, H., Nakatani, T., Akahane, T., Toyokawa, Y., Kojima, H., Okamoto, S., and Fukui, H., Comparison of gene therapy with the herpes simplex virus thymidine kinase gene and the bacterial cytosine deaminase gene for the treatment of hepatocellular carcinoma. Scand. J. Gastroenterol., 34, 1033-1041 (1999).
    • (1999) Scand. J. Gastroenterol. , vol.34 , pp. 1033-1041
    • Kuriyama, S.1    Mitoro, A.2    Yamazaki, M.3    Tsujinoue, H.4    Nakatani, T.5    Akahane, T.6    Toyokawa, Y.7    Kojima, H.8    Okamoto, S.9    Fukui, H.10
  • 96
    • 0028970008 scopus 로고
    • New steroidal antiinflammatory antedrugs: Steroidal [16α, 17α-d]-3-carbethoxyisoxazolines
    • Kwon T, Heiman A. S., Oriaku E. T., Yoon, K., and Lee, H. J., New steroidal antiinflammatory antedrugs: steroidal [16α, 17α-d]-3- carbethoxyisoxazolines. J. Med. Chem., 38, 1048-1051 (1995).
    • (1995) J. Med. Chem. , vol.38 , pp. 1048-1051
    • Kwon, T.1    Heiman, A.S.2    Oriaku, E.T.3    Yoon, K.4    Lee, H.J.5
  • 97
    • 0035942484 scopus 로고    scopus 로고
    • Estradiol-16a-carboxylic acid esters as locally active estrogens
    • Labaree, D. C., Reynolds, T. Y., and Hochberg, R. B., Estradiol-16a-carboxylic acid esters as locally active estrogens. J. Med. Chem., 44, 1802-1814 (2001).
    • (2001) J. Med. Chem. , vol.44 , pp. 1802-1814
    • Labaree, D.C.1    Reynolds, T.Y.2    Hochberg, R.B.3
  • 98
    • 0033144772 scopus 로고    scopus 로고
    • A novel approach to the discovery of non-systemic anti-inflammatory steroids: Antedrug
    • Lee, H. J. and Ko, D. -H., A novel approach to the discovery of non-systemic anti-inflammatory steroids: Antedrug. Arch. Pharm. Res., 22(3), 279-287 (1999).
    • (1999) Arch. Pharm. Res. , vol.22 , Issue.3 , pp. 279-287
    • Lee, H.J.1    Ko, D.H.2
  • 99
    • 0020037486 scopus 로고
    • Anti-inflammatory steroids without pituitary adrenal suppression
    • Lee, H. J. and Soliman, M. R. I., Anti-inflammatory steroids without pituitary adrenal suppression. Science, 215, 989-991 (1982).
    • (1982) Science , vol.215 , pp. 989-991
    • Lee, H.J.1    Soliman, M.R.I.2
  • 101
    • 0031725758 scopus 로고    scopus 로고
    • New steroidal anti-inflammatory agents: Prednisolone derivatives with an isoxazoline fusion at the 16- and 17-carbons and an alkyl carboxylate at the 16a-position
    • Lee, H. J., You, Z., Ko, D. -H., and Yoon, K. J., New steroidal anti-inflammatory agents: Prednisolone derivatives with an isoxazoline fusion at the 16- and 17-carbons and an alkyl carboxylate at the 16a-position. Drugs Exptl. Clin. Res., 24(2), 57-66 (1998).
    • (1998) Drugs Exptl. Clin. Res. , vol.24 , Issue.2 , pp. 57-66
    • Lee, H.J.1    You, Z.2    Ko, D.-H.3    Yoon, K.J.4
  • 102
    • 0028819889 scopus 로고
    • Mononucleoside Phosphotriester Deravitives with S-Acyl-2-thioethyl Bioreversible Phosphate-Protecting Groups: Intracellular Delivery of 3-Azido-2,3-dideoxythymidine 5-Monophosphate
    • Lefebvre, I., Périgaud, C., Pompon, A., Aubertin, A. M., Girardet, J.L., Kirn, A., Gosselin, G., and Imbach, J. L., Mononucleoside Phosphotriester Deravitives with S-Acyl-2-thioethyl Bioreversible Phosphate-Protecting Groups: Intracellular Delivery of 3-Azido-2,3-dideoxythymidine 5-Monophosphate. J. Med. Chem., 38, 3941-3950 (1995).
    • (1995) J. Med. Chem. , vol.38 , pp. 3941-3950
    • Lefebvre, I.1    Périgaud, C.2    Pompon, A.3    Aubertin, A.M.4    Girardet, J.L.5    Kirn, A.6    Gosselin, G.7    Imbach, J.L.8
  • 103
    • 0022994060 scopus 로고
    • Human Gastrointestinal Absorption of Acyclovir from Tablet Duodenal Infusion and Sipped Solution
    • Lewis, L. D., Fowle, A. S. E., and Bittiner, S. B., Human Gastrointestinal Absorption of Acyclovir from Tablet Duodenal Infusion and Sipped Solution. Br. J. Clin. Pharmacol., 21, 459-462 (1986).
    • (1986) Br. J. Clin. Pharmacol. , vol.21 , pp. 459-462
    • Lewis, L.D.1    Fowle, A.S.E.2    Bittiner, S.B.3
  • 104
    • 0033542041 scopus 로고    scopus 로고
    • Systemic adverse effects of inhaled corticosteroid therapy: A systematic review and meta-analysis
    • Lipworth, B. J., Systemic adverse effects of inhaled corticosteroid therapy: A systematic review and meta-analysis. Arch. Intern. Med., 159(9), 941-955 (1999).
    • (1999) Arch. Intern. Med. , vol.159 , Issue.9 , pp. 941-955
    • Lipworth, B.J.1
  • 105
    • 0030764432 scopus 로고    scopus 로고
    • New Synthesis and Antitumor Activity of CycloSal-Derivatives of 5-Fluoro-2′-deoxyuridinemonophosphate
    • Lorey, M., Meier, C., De Clerq, E., and Balzarini, J., New Synthesis and Antitumor Activity of CycloSal-Derivatives of 5-Fluoro-2′- deoxyuridinemonophosphate. Nucleosides & Nucleotides, 16, 789-792 (1997).
    • (1997) Nucleosides & Nucleotides , vol.16 , pp. 789-792
    • Lorey, M.1    Meier, C.2    De Clerq, E.3    Balzarini, J.4
  • 107
    • 0029005041 scopus 로고
    • Lymphatic Targeting of Anti-HIV Nucleosides: Distribution of 3-Azido-3-Deoxythymidine (AZT) and 3-Azido-2,3-Deoxyuridine (AzdU) after Administration of Dipalmitoylphosphatidyl Prodrugs to Mice
    • Manouilov, K. K., Fedorov, I. I., Boudinot, F. D., White, C. A., Kotra, K. P., Schinazi, R. F., Hong, C. I., and Chu, C. K., Lymphatic Targeting of Anti-HIV Nucleosides: Distribution of 3-Azido-3-Deoxythymidine (AZT) and 3-Azido-2,3-Deoxyuridine (AzdU) after Administration of Dipalmitoylphosphatidyl Prodrugs to Mice. Antiviral Chem. Chemother., 6, 230-238 (1995).
    • (1995) Antiviral Chem. Chemother. , vol.6 , pp. 230-238
    • Manouilov, K.K.1    Fedorov, I.I.2    Boudinot, F.D.3    White, C.A.4    Kotra, K.P.5    Schinazi, R.F.6    Hong, C.I.7    Chu, C.K.8
  • 108
    • 0030994635 scopus 로고    scopus 로고
    • Lymphatic Targeting of Anti-HIV Nucleosides: Distribution of 2′,3′-Dideoxyinosine after Intravenous and Oral Administration of Dipalmitoylphosphatidyl Prodrug in Mice
    • Manouilov, K. K., Xu, Z. S., Boudinot, F. D., Schinazi, R. F., and Chu, C. K. Lymphatic Targeting of Anti-HIV Nucleosides: Distribution of 2′,3′-Dideoxyinosine after Intravenous and Oral Administration of Dipalmitoylphosphatidyl Prodrug in Mice. Antiviral Res., 34, 91-99 (1997).
    • (1997) Antiviral Res. , vol.34 , pp. 91-99
    • Manouilov, K.K.1    Xu, Z.S.2    Boudinot, F.D.3    Schinazi, R.F.4    Chu, C.K.5
  • 109
    • 0022345218 scopus 로고
    • Human cytomegalovirus-indeced DNA polymerase and its interaction with the triphosphates of 1-(2′-deoxy-2′-fluoro-beta-D-arabinofuranosyl)-5- methyuracil, -5-iodocytosine, and 5-methylcytosine
    • Mar, E, C., Chiou, J. F., Cheng, Y. C., and Huang, E. S., Human cytomegalovirus-indeced DNA polymerase and its interaction with the triphosphates of 1-(2′-deoxy-2′-fluoro-beta-D-arabinofuranosyl)-5- methyuracil, -5-iodocytosine, and 5-methylcytosine. J. Virol., 56, 846-851 (1995).
    • (1995) J. Virol. , vol.56 , pp. 846-851
    • Mar, E.C.1    Chiou, J.F.2    Cheng, Y.C.3    Huang, E.S.4
  • 110
    • 0032972940 scopus 로고    scopus 로고
    • Growth and collagen synthesis disorders in asthmatic children treated with inhaled steroids
    • Suisse Romande
    • Martin-du Pan, R. C., Vonlanthen, M. C., and Dubuis, J. M., Growth and collagen synthesis disorders in asthmatic children treated with inhaled steroids. Rev. Med., Suisse Romande, 119(6), 475-479 (1999).
    • (1999) Rev. Med. , vol.119 , Issue.6 , pp. 475-479
    • Martin-du Pan, R.C.1    Vonlanthen, M.C.2    Dubuis, J.M.3
  • 111
    • 0029975897 scopus 로고    scopus 로고
    • Aryl Phosphoramidate Derivatives of d4T Have Improved Anti-HIV Efficacy in Tissue Culture and May Act by the Generation of a Novel Intracellular Metabolite
    • McGuigan, C., Cahard, D., Sheeka, H. M., De Clercq, E., and Balzarini, J., Aryl Phosphoramidate Derivatives of d4T Have Improved Anti-HIV Efficacy in Tissue Culture and May Act by the Generation of a Novel Intracellular Metabolite. J. Med. Chem., 39, 1748-1753 (1996).
    • (1996) J. Med. Chem. , vol.39 , pp. 1748-1753
    • McGuigan, C.1    Cahard, D.2    Sheeka, H.M.3    De Clercq, E.4    Balzarini, J.5
  • 113
    • 0027284753 scopus 로고
    • Intracellular Delivery of Bioactive AZT Nucleotides by Aryl Phosphate Derivatives of AZT
    • McGuigan, C., Pathirana, R. N., Balzarini, J., and De Clercq, E., Intracellular Delivery of Bioactive AZT Nucleotides by Aryl Phosphate Derivatives of AZT. J. Med. Chem., 36, 1048-1052 (1993).
    • (1993) J. Med. Chem. , vol.36 , pp. 1048-1052
    • McGuigan, C.1    Pathirana, R.N.2    Balzarini, J.3    De Clercq, E.4
  • 115
    • 11244318100 scopus 로고    scopus 로고
    • Synthesis and pharmacological evaluations of novel conjugates of steroidal antedrugs and non-steroidal anti-inflammatory drugs
    • submitted
    • McLean, H. M., Heiman, A. S., and Lee, H. J., Synthesis and pharmacological evaluations of novel conjugates of steroidal antedrugs and non-steroidal anti-inflammatory drugs . Med. Chem. Res., submitted (2001).
    • (2001) Med. Chem. Res.
    • McLean, H.M.1    Heiman, A.S.2    Lee, H.J.3
  • 116
    • 0002451023 scopus 로고    scopus 로고
    • 4H-1.3.2.-Benzodioxaphosphorin-2-nucleosyl-2-oxide a New Concept for Lipophilic, Potential Prodrugs of Biologically Active Nucleoside Monophosphates
    • Meier, C. 4H-1.3.2.-Benzodioxaphosphorin-2-nucleosyl-2-oxide A New Concept for Lipophilic, Potential Prodrugs of Biologically Active Nucleoside Monophosphates. Angew. Chem., 108, 77-79 (1996).
    • (1996) Angew. Chem. , vol.108 , pp. 77-79
    • Meier, C.1
  • 117
    • 0030811807 scopus 로고    scopus 로고
    • Cyclo-Saligenyl-3′-azido-2′,3′-dideoxythymidine monophosphate (CycloSal-AZTMP) a New Pro-nucleotide Approach
    • Meier, C., De Clerq, E., and Balzarini, J., Cyclo-Saligenyl-3′- azido-2′,3′-dideoxythymidine monophosphate (CycloSal-AZTMP) A New Pro-nucleotide Approach. Nucleosides and Nucleotides, 16, 793-796 (1997c).
    • (1997) Nucleosides and Nucleotides , vol.16 , pp. 793-796
    • Meier, C.1    De Clerq, E.2    Balzarini, J.3
  • 118
    • 0030927126 scopus 로고    scopus 로고
    • ADA-Bypass by Lipophilic CycloSal-ddAMP Pro-nucleotides a Second Example of the Efficiency of the CycloSal-concept
    • Meier, C., Knispel, T., De Clerq, E., and Balzarini, J., ADA-Bypass by Lipophilic CycloSal-ddAMP Pro-nucleotides a Second Example of the Efficiency of the CycloSal-concept. Bioorg. Med. Chem. Lett., 7, 1577-1582 (1997d).
    • (1997) Bioorg. Med. Chem. Lett. , vol.7 , pp. 1577-1582
    • Meier, C.1    Knispel, T.2    De Clerq, E.3    Balzarini, J.4
  • 119
    • 0033529048 scopus 로고    scopus 로고
    • CycloSal-pronucleotides of 2′,3′-Dideoxyadenosine and 2′,3′-Dideoxy-2′,3′-didehydroadenosine: Synthesis and Antiviral Evaluation of a Highly Efficient Nucleotide Delivery System
    • Meier, C., Knispel, T., De Clerq, E., and Balzarini, J., CycloSal-pronucleotides of 2′,3′-Dideoxyadenosine and 2′,3′-Dideoxy-2′,3′-didehydroadenosine: Synthesis and Antiviral Evaluation of a Highly Efficient Nucleotide Delivery System. J. Med. Chem., 42, 1604-1614 (1999a).
    • (1999) J. Med. Chem. , vol.42 , pp. 1604-1614
    • Meier, C.1    Knispel, T.2    De Clerq, E.3    Balzarini, J.4
  • 120
    • 0030707857 scopus 로고    scopus 로고
    • CycloSal-Pronucleotides: The Design and Biological Evaluation of a New Class of Lipophilic Nucleotide Prodrugs
    • Meier, C., Knispel, T., Lorey, M., and Balzarini, J., CycloSal-Pronucleotides: The Design and Biological Evaluation of a New Class of Lipophilic Nucleotide Prodrugs. Int. Antiviral News, 5, 183-186 (1997a).
    • (1997) Int. Antiviral News , vol.5 , pp. 183-186
    • Meier, C.1    Knispel, T.2    Lorey, M.3    Balzarini, J.4
  • 121
    • 0033529065 scopus 로고    scopus 로고
    • CycloSal-Pronucleotides of 2-Fluoroara-and 2-Fluoro-ribo-2,3- dideoxyadenosine as a Strategy to Bypass a Metabolic Blockade
    • Meier, C., Knispel, T., Marquez, V. E., Siddiqui, M. A., De Clerq, E., and Balzarini, J., CycloSal-Pronucleotides of 2-Fluoroara-and 2-Fluoro-ribo-2,3-dideoxyadenosine as a Strategy to Bypass a Metabolic Blockade. J. Med. Chem., 42, 1615-1624 (1999b).
    • (1999) J. Med. Chem. , vol.42 , pp. 1615-1624
    • Meier, C.1    Knispel, T.2    Marquez, V.E.3    Siddiqui, M.A.4    De Clerq, E.5    Balzarini, J.6
  • 122
    • 0031013734 scopus 로고    scopus 로고
    • Cyclic Saligenyl Phosphotriesters of 2′,3′-Dideoxy-2′, 3′-didehydrothymidine (d4T) - A New Pro-nucleotide Approach
    • Meier, C., Lorey, M., De Clerq, E., and Balzarini, J., Cyclic Saligenyl Phosphotriesters of 2′,3′-Dideoxy-2′,3′- didehydrothymidine (d4T)-A New Pro-nucleotide Approach. Bioorg. Med. Chem. Lett., 7, 99-104 (1997b).
    • (1997) Bioorg. Med. Chem. Lett. , vol.7 , pp. 99-104
    • Meier, C.1    Lorey, M.2    De Clerq, E.3    Balzarini, J.4
  • 123
    • 0032560234 scopus 로고    scopus 로고
    • CycloSal-2′,3′-dideoxy-2′,3′-didehydrothymidine Monophosphate (CycloSald4TMP): Synthesis and Antiviral Evaluation of a New d4TMP Delivery System
    • Meier, C., Lorey, M., De Clerq, E., Balzarini, J., CycloSal-2′, 3′-dideoxy-2′,3′-didehydrothymidine Monophosphate (CycloSald4TMP): Synthesis and Antiviral Evaluation of a New d4TMP Delivery System. J. Med. Chem., 41, 1417-1427 (1998).
    • (1998) J. Med. Chem. , vol.41 , pp. 1417-1427
    • Meier, C.1    Lorey, M.2    De Clerq, E.3    Balzarini, J.4
  • 124
    • 0031836938 scopus 로고    scopus 로고
    • Tumor immunogenicity is determined by the mechanism of cell death via induction of heat shock protein expression
    • Melcher, A., Todryk, S., Hardwick, N., Ford, M, Jacobson, M., and Vile, R. G., Tumor immunogenicity is determined by the mechanism of cell death via induction of heat shock protein expression. Nat. Med., 4, 581-587 (1998).
    • (1998) Nat. Med. , vol.4 , pp. 581-587
    • Melcher, A.1    Todryk, S.2    Hardwick, N.3    Ford, M.4    Jacobson, M.5    Vile, R.G.6
  • 126
    • 0025194134 scopus 로고
    • The potential of carboxypeptidase G2 antibody conjugates as anti-tumour agents. II. In vivo localizing and clearance properties in a choriocarcinoma model
    • Melton, R. G., Searle, F., Sherwood, R. F., Bagshawe, K. D., and Boden, J. A., The potential of carboxypeptidase G2 antibody conjugates as anti-tumour agents. II. In vivo localizing and clearance properties in a choriocarcinoma model. Br. J. Cancer, 61, 420-424 (1990).
    • (1990) Br. J. Cancer , vol.61 , pp. 420-424
    • Melton, R.G.1    Searle, F.2    Sherwood, R.F.3    Bagshawe, K.D.4    Boden, J.A.5
  • 127
    • 0029996360 scopus 로고    scopus 로고
    • Bystander killing of cancer cells by herpes simplex virus thymidine kinase gene is mediated by connexins
    • Mesnil, M., Piccoli, C., Tiraby, G., Willecke, K., and Yamasaki, H., Bystander killing of cancer cells by herpes simplex virus thymidine kinase gene is mediated by connexins. Proc. Natl. Acad. Sci. USA, 93, 1831-1835 (1996).
    • (1996) Proc. Natl. Acad. Sci. USA , vol.93 , pp. 1831-1835
    • Mesnil, M.1    Piccoli, C.2    Tiraby, G.3    Willecke, K.4    Yamasaki, H.5
  • 128
    • 0022485359 scopus 로고
    • Tumor chemotherapy conferred by inserted herpes thymidine kinase genes: Paradigm for a prospective cancer control strategy
    • Moolten, F. L., Tumor chemotherapy conferred by inserted herpes thymidine kinase genes: paradigm for a prospective cancer control strategy. Cancer Res., 46, 5276-5281 (1986).
    • (1986) Cancer Res. , vol.46 , pp. 5276-5281
    • Moolten, F.L.1
  • 129
    • 0028297316 scopus 로고
    • Tumor expressing the cytosine deaminase suicide gene can be eliminated in vivo with 5-fluorocytosine and induce protective immunity to wild type tumor
    • Mullen, C. A., Coale, M. M., Lowe, R., and Blaese, R. M., Tumor expressing the cytosine deaminase suicide gene can be eliminated in vivo with 5-fluorocytosine and induce protective immunity to wild type tumor . Cancer Res., 54, 1503-1506 (1994).
    • (1994) Cancer Res. , vol.54 , pp. 1503-1506
    • Mullen, C.A.1    Coale, M.M.2    Lowe, R.3    Blaese, R.M.4
  • 131
    • 0028560018 scopus 로고
    • Therapeutic potential of PMEA as an antiviral drug
    • Nassens, L., Balazarini, J., and De Clerq, E., Therapeutic potential of PMEA as an antiviral drug. Med. Virol., 4, 147-159 (1993).
    • (1993) Med. Virol. , vol.4 , pp. 147-159
    • Nassens, L.1    Balazarini, J.2    De Clerq, E.3
  • 133
    • 0028907668 scopus 로고
    • Adenovirus-mediated gene therapy for human head and neck squamous cell cancer in a nude mouse model
    • O'Malley, B. W. Jr., Chen, S. H., Schwartz, M. R., and Woo, S. L., Adenovirus-mediated gene therapy for human head and neck squamous cell cancer in a nude mouse model. Cancer Res., 55, 1080-1085 (1995).
    • (1995) Cancer Res. , vol.55 , pp. 1080-1085
    • O'Malley Jr., B.W.1    Chen, S.H.2    Schwartz, M.R.3    Woo, S.L.4
  • 134
    • 0024500236 scopus 로고
    • A Dihydropyridine Carriers System for Sustained Delivery of 2′,3′-Dideoxynucleosides to the Brain
    • Palomino, E., Kessel, D., and Horwitz, J. P., A Dihydropyridine Carriers System for Sustained Delivery of 2′,3′-Dideoxynucleosides to the Brain. J. Med. Chem., 32, 622 (1989).
    • (1989) J. Med. Chem. , vol.32 , pp. 622
    • Palomino, E.1    Kessel, D.2    Horwitz, J.P.3
  • 136
    • 0028096091 scopus 로고
    • Synthesis of the Phosphodiester of 3β(7β-Hydroxy-cholestrol) and of 5′(3′Deoxy, 3Azido-thymidine)
    • Pannecoucke, X., Parmentier, G., Schmitt, G., Dolle, F., and Luu, B., Synthesis of the Phosphodiester of 3β(7β-Hydroxy-cholestrol) and of 5′(3′Deoxy, 3Azido-thymidine). Tetrahedron, 50, 1173-1178 (1994).
    • (1994) Tetrahedron , vol.50 , pp. 1173-1178
    • Pannecoucke, X.1    Parmentier, G.2    Schmitt, G.3    Dolle, F.4    Luu, B.5
  • 138
    • 0027980948 scopus 로고
    • Equal Inhibition of the Replication of Human Immunodeficiency Virus in Human T-Cell Culture by ddA Bis (SATE) Phosphotriester and 3-Azido-2′, 3′-dideoxythymidine
    • Périgaud, C., Aubertin, A.M., Benzaria, S., Pélicano, H., Girardet, J. L., Maury, G., Gosselin, G., Kirn, A., and Imbach, J. L., Equal Inhibition of the Replication of Human Immunodeficiency Virus in Human T-Cell Culture by ddA Bis (SATE) Phosphotriester and 3-Azido-2′,3′- dideoxythymidine Biochem. Pharmacol., 48, 11-14 (1994).
    • (1994) Biochem. Pharmacol. , vol.48 , pp. 11-14
    • Périgaud, C.1    Aubertin, A.M.2    Benzaria, S.3    Pélicano, H.4    Girardet, J.L.5    Maury, G.6    Gosselin, G.7    Kirn, A.8    Imbach, J.L.9
  • 139
    • 0029796002 scopus 로고    scopus 로고
    • Comparison of Cytotoxicity of Mononucleoside Phosphotriester Derivatives Bearing Biolabile Phosphate Protecting Groups in Normal Human Bone Marrow Progenitor Cells
    • Périgaud, C., Girardet, J. L., Lefebvre, I., Xie, M. Y., Aubertin, A. M., Kirn, A., Gosselin, G., Imbach, J. L., and Sommadossi, J. P., Comparison of Cytotoxicity of Mononucleoside Phosphotriester Derivatives Bearing Biolabile Phosphate Protecting Groups in Normal Human Bone Marrow Progenitor Cells. Antiviral Chem. Chemother., 7, 338-345 (1996).
    • (1996) Antiviral Chem. Chemother. , vol.7 , pp. 338-345
    • Périgaud, C.1    Girardet, J.L.2    Lefebvre, I.3    Xie, M.Y.4    Aubertin, A.M.5    Kirn, A.6    Gosselin, G.7    Imbach, J.L.8    Sommadossi, J.P.9
  • 141
    • 0001962580 scopus 로고    scopus 로고
    • Minireview: From the Pronucleotide Concept to the SATE Phosphate Protecting Groups
    • Périgaud, C., Gosselin, G., and Imbach, J. L., Minireview: from the Pronucleotide Concept to the SATE Phosphate Protecting Groups. Curr. Topics in Med. Chem., 2, 15-29 (1997).
    • (1997) Curr. Topics in Med. Chem. , vol.2 , pp. 15-29
    • Périgaud, C.1    Gosselin, G.2    Imbach, J.L.3
  • 145
    • 0027133478 scopus 로고
    • Pharmacokinetics of Famciclovir in Man
    • Pue, M. A. and Benet, L. Z., Pharmacokinetics of Famciclovir in Man. Antiviral Chem. Chemother., 4 (Suppl. 1), 47-55 (1993).
    • (1993) Antiviral Chem. Chemother. , vol.4 , Issue.1 SUPPL. , pp. 47-55
    • Pue, M.A.1    Benet, L.Z.2
  • 147
    • 0018840754 scopus 로고
    • Combined VM-26 and Cytosine Arabinoside in Treatment of Refractory Childhood Lymphocytic Leukemia
    • Rivera, G., Rhomes, J. A., Dahl, G. V., Pratt, C. B., Wood, A., and Avery, T. L., Combined VM-26 and Cytosine Arabinoside in Treatment of Refractory Childhood Lymphocytic Leukemia. Cancer, 45, 1284 (1980).
    • (1980) Cancer , vol.45 , pp. 1284
    • Rivera, G.1    Rhomes, J.A.2    Dahl, G.V.3    Pratt, C.B.4    Wood, A.5    Avery, T.L.6
  • 148
    • 0004215574 scopus 로고
    • Design of Biopharmaceutical Properties through Prodrugs and Analogs
    • Washington DC
    • Roche, E. B., Design of Biopharmaceutical Properties through Prodrugs and Analogs. Academy of Pharmaceutical Sciences Symposium, Washington DC (1977).
    • (1977) Academy of Pharmaceutical Sciences Symposium
    • Roche, E.B.1
  • 149
    • 0029416920 scopus 로고
    • Plasma clearance of an antibody-enzyme conjugate in ADEPT by monoclonal anti-enzyme: Its effect on prodrug activation in vivo
    • Rogers, G. T., Burke, P. J., Shama, S. K., Koodie, R., and Boden, J. A., Plasma clearance of an antibody-enzyme conjugate in ADEPT by monoclonal anti-enzyme: its effect on prodrug activation in vivo. Br. J. Cancer, 72, 1357-1363 (1995).
    • (1995) Br. J. Cancer , vol.72 , pp. 1357-1363
    • Rogers, G.T.1    Burke, P.J.2    Shama, S.K.3    Koodie, R.4    Boden, J.A.5
  • 150
    • 0028799413 scopus 로고
    • Pharmacokinetics of New Antiherpetic Agents
    • Rolan, P., Pharmacokinetics of New Antiherpetic Agents. Clin. Pharmacokinet., 29, 333-340 (1995).
    • (1995) Clin. Pharmacokinet. , vol.29 , pp. 333-340
    • Rolan, P.1
  • 151
    • 0027293527 scopus 로고
    • Deacylation-Reacylation Cycle: A Possible Absorption Mechanism for the Novel Lymphotropic Antitumor Agent Dipalmitoylphosphatidyl-fluorouridine in Rats
    • Sakai, A., Mori, N., Shuto, S., Suzuki, T., Deacylation-Reacylation Cycle: A Possible Absorption Mechanism for the Novel Lymphotropic Antitumor Agent Dipalmitoylphosphatidyl-fluorouridine in Rats. J. Pharm. Sci., 83, 575-578 (1993).
    • (1993) J. Pharm. Sci. , vol.83 , pp. 575-578
    • Sakai, A.1    Mori, N.2    Shuto, S.3    Suzuki, T.4
  • 152
    • 0026524003 scopus 로고
    • Membrane-Permeable Dideoxyuridine 5-Monophosphate Analogue Inhibits Human Immunodeficiency Virus Infection
    • Sastry, J. K., Nehete, P. N., Khan, S., Nowak, B. J., Plunkett, W., Arlinghaus, R. B., and Farquhar, D., Membrane-Permeable Dideoxyuridine 5-Monophosphate Analogue Inhibits Human Immunodeficiency Virus Infection. Mol. Pharmacol., 41, 441-445 (1992).
    • (1992) Mol. Pharmacol. , vol.41 , pp. 441-445
    • Sastry, J.K.1    Nehete, P.N.2    Khan, S.3    Nowak, B.J.4    Plunkett, W.5    Arlinghaus, R.B.6    Farquhar, D.7
  • 153
    • 0025373638 scopus 로고
    • Inactivation and clearance of an anti-CEA carboxypeptidase G2 conjugate in blood after localization in a xenograft model
    • Shama, S. K., Bagshawe, K. D., Burke, P. J., Boden, R. W., and Rogers, G. T., Inactivation and clearance of an anti-CEA carboxypeptidase G2 conjugate in blood after localization in a xenograft model. Br. J. Cancer, 61, 659-662 (1990).
    • (1990) Br. J. Cancer , vol.61 , pp. 659-662
    • Shama, S.K.1    Bagshawe, K.D.2    Burke, P.J.3    Boden, R.W.4    Rogers, G.T.5
  • 155
    • 0028694296 scopus 로고
    • Antibody-directed enzyme prodrug therapy (ADEPT). A three phase study in ovarian tumor xenografts
    • Shama, S. K., Boden, J. A., Springer, C. J., Burke, P. J., and Bagshawe, K. D., Antibody-directed enzyme prodrug therapy (ADEPT). A three phase study in ovarian tumor xenografts. Cell. Biophys., 24, 219-228 (1994).
    • (1994) Cell. Biophys. , vol.24 , pp. 219-228
    • Shama, S.K.1    Boden, J.A.2    Springer, C.J.3    Burke, P.J.4    Bagshawe, K.D.5
  • 156
    • 0033588816 scopus 로고    scopus 로고
    • A phase 1-2 clinical trial of gene therapy for recurrent glioblastoma multiforme by tumor transduction with herpes simplex thymidine kinase gene followed by ganciclovir
    • Shand, N., Weber, F., Mariani, L., Bernstein, M., Gianella-Borradori, A., Long, Z., Sorensen, A. G., and Barbier, N., A phase 1-2 clinical trial of gene therapy for recurrent glioblastoma multiforme by tumor transduction with herpes simplex thymidine kinase gene followed by ganciclovir. Hum. Gene Ther., 10, 2325-2335 (1999).
    • (1999) Hum. Gene Ther. , vol.10 , pp. 2325-2335
    • Shand, N.1    Weber, F.2    Mariani, L.3    Bernstein, M.4    Gianella-Borradori, A.5    Long, Z.6    Sorensen, A.G.7    Barbier, N.8
  • 157
    • 0027518914 scopus 로고
    • Synthesis and Anti-HIV Activity of Prodrugs of Azidothymidine
    • Sharma, A. P., Ollapally, A. P., and Lee, H. J., Synthesis and Anti-HIV Activity of Prodrugs of Azidothymidine. Antiviral Chem. Chemother., 4, 93-96 (1993).
    • (1993) Antiviral Chem. Chemother. , vol.4 , pp. 93-96
    • Sharma, A.P.1    Ollapally, A.P.2    Lee, H.J.3
  • 158
    • 0021871027 scopus 로고
    • Purification and properties of carboxypeptidase G2 from Pseudomonas sp. strain RS-16. Use of a novel triazine dye affinity method
    • Sherwood, R., Melton, R., Alwan, S., and Hughes, P., Purification and properties of carboxypeptidase G2 from Pseudomonas sp. strain RS-16. Use of a novel triazine dye affinity method. Eur. J. Biochem., 148, 447-453 (1985).
    • (1985) Eur. J. Biochem. , vol.148 , pp. 447-453
    • Sherwood, R.1    Melton, R.2    Alwan, S.3    Hughes, P.4
  • 159
    • 0034640040 scopus 로고    scopus 로고
    • Estrogen and progestin, lipoprotein (a), and the risk of recurrent coronary heart disease events after menopause
    • Shlipak, M. G., Simon, J. A., Vittinghoff, E., Lin, F., Barrett-Conner, E., Knopp, R. H., Levy, R. I., and Hulley, S. B., Estrogen and progestin, lipoprotein (a), and the risk of recurrent coronary heart disease events after menopause. JAMA, 283, 1845-1852 (2000).
    • (2000) JAMA , vol.283 , pp. 1845-1852
    • Shlipak, M.G.1    Simon, J.A.2    Vittinghoff, E.3    Lin, F.4    Barrett-Conner, E.5    Knopp, R.H.6    Levy, R.I.7    Hulley, S.B.8
  • 160
    • 0026538901 scopus 로고
    • New Neplanocin Analogues II. Enzymatic One-Step Synthesis and Antitumor Activity of 6′-(3-sn-Phosphatidyl)Neplanocin a Derivatives
    • Shuto, S., Itoh, H., Obara, T., Nakagami, K., Yaso, M., Yaginuma, S., Tsujino, M., and Saito, T. New Neplanocin Analogues II. Enzymatic One-Step Synthesis and Antitumor Activity of 6′-(3-sn-Phosphatidyl)Neplanocin a Derivatives. Nucleosides & Nucleotides, 11, 437-446 (1992).
    • (1992) Nucleosides & Nucleotides , vol.11 , pp. 437-446
    • Shuto, S.1    Itoh, H.2    Obara, T.3    Nakagami, K.4    Yaso, M.5    Yaginuma, S.6    Tsujino, M.7    Saito, T.8
  • 161
    • 0023838866 scopus 로고
    • A Facile Enzymatic Synthesis of 5′-(3-sn-Phosphatidyl)nucleosides and Their Antileukemic Activities
    • Shuto, S., Itoh, H.; Ueda, S., Imamura, S., Fukukawa, K., Tsujino, M., Matsuda, A., and Ueda, T., A Facile Enzymatic Synthesis of 5′-(3-sn- Phosphatidyl)nucleosides and Their Antileukemic Activities. Chem. Pharm. Bull., 36, 209-217 (1988).
    • (1988) Chem. Pharm. Bull. , vol.36 , pp. 209-217
    • Shuto, S.1    Itoh, H.2    Ueda, S.3    Imamura, S.4    Fukukawa, K.5    Tsujino, M.6    Matsuda, A.7    Ueda, T.8
  • 162
    • 0033048195 scopus 로고    scopus 로고
    • The Presence of Substituents on the Aryl Moiety of the Aryl Phosphoramidate Derivative of d4T Enhances Anti-HIV Efficacy in Cell Culture: A Structure-Activity Relationship
    • Siddiqui, A. Q., Ballatore, C., McGuigan, C., De Clerq, E., and Balzarini, J., The Presence of Substituents on the Aryl Moiety of the Aryl Phosphoramidate Derivative of d4T Enhances Anti-HIV Efficacy in Cell Culture: A Structure-Activity Relationship. J. Med. Chem., 42, 393-399 (1999).
    • (1999) J. Med. Chem. , vol.42 , pp. 393-399
    • Siddiqui, A.Q.1    Ballatore, C.2    McGuigan, C.3    De Clerq, E.4    Balzarini, J.5
  • 163
    • 0031194865 scopus 로고    scopus 로고
    • Construction, expression, and activities of L49-sFv b-lactamase, a single-chain antibody fusion protein for anticancer prodrug activation
    • Siemers, N. O., Kerr, D. E., Yarnold, S., Stebbins, M., Vrudhula, V. M., Hellstrom, I., Hellstrom, K. E., and Senter, P. D., Construction, expression, and activities of L49-sFv b-lactamase, a single-chain antibody fusion protein for anticancer prodrug activation. Bioconjug. Chem., 8, 510-519 (1997).
    • (1997) Bioconjug. Chem. , vol.8 , pp. 510-519
    • Siemers, N.O.1    Kerr, D.E.2    Yarnold, S.3    Stebbins, M.4    Vrudhula, V.M.5    Hellstrom, I.6    Hellstrom, K.E.7    Senter, P.D.8
  • 165
    • 0019465972 scopus 로고
    • Anti-inflammatory activity of acid ester derivatives of prednisolone
    • Soliman, M. R. I., and Lee, H. J., Anti-inflammatory activity of acid ester derivatives of prednisolone. Res. Comm. Chem. Path. Pharm., 33(2), 357-360 (1981).
    • (1981) Res. Comm. Chem. Path. Pharm. , vol.33 , Issue.2 , pp. 357-360
    • Soliman, M.R.I.1    Lee, H.J.2
  • 166
    • 0030589523 scopus 로고    scopus 로고
    • Gene-directed enzyme prodrug therapy (GDEPT): Choice of prodrugs
    • Springer, C. J. and Niculescu-Duvaz, I., Gene-directed enzyme prodrug therapy (GDEPT): choice of prodrugs. Adv. Drug Deliv. Rev., 22, 351-364 (1996).
    • (1996) Adv. Drug Deliv. Rev. , vol.22 , pp. 351-364
    • Springer, C.J.1    Niculescu-Duvaz, I.2
  • 167
    • 0029621825 scopus 로고
    • Optimization of alkylating agent prodrugs derived from phenol nad aniline mustards: A new clincal candidate prodrug (ZD 2767) for antibody-directed enzyme prodrug therapy (ADEPT)
    • Springer, C. J., Dowell, R., Burke, P. J., Hadley, E., Davies, D. H., Blakey, D. C., Melton, R. G., and Niculescu-Duvaz, I., Optimization of alkylating agent prodrugs derived from phenol nad aniline mustards: a new clincal candidate prodrug (ZD 2767) for antibody-directed enzyme prodrug therapy (ADEPT). J. Med. Chem., 38, 5051-5065 (1995).
    • (1995) J. Med. Chem. , vol.38 , pp. 5051-5065
    • Springer, C.J.1    Dowell, R.2    Burke, P.J.3    Hadley, E.4    Davies, D.H.5    Blakey, D.C.6    Melton, R.G.7    Niculescu-Duvaz, I.8
  • 168
    • 0027440278 scopus 로고
    • Metabolism and in Vitro Antiretroviral Activities of Bis(Pivaloyloxymethyl) Prodrugs of Acyclic Nucleoside Phosphonates
    • Srinivas, R. V., Robbins, B. L., Connelly, M. C., Gong, Y.-F., Bischofberger, N., and Fridland, A., Metabolism and In Vitro Antiretroviral Activities of Bis(Pivaloyloxymethyl) Prodrugs of Acyclic Nucleoside Phosphonates. Antimicrob. Agents Chemother., 37, 2247-2250 (1993).
    • (1993) Antimicrob. Agents Chemother. , vol.37 , pp. 2247-2250
    • Srinivas, R.V.1    Robbins, B.L.2    Connelly, M.C.3    Gong, Y.-F.4    Bischofberger, N.5    Fridland, A.6
  • 169
    • 0028306517 scopus 로고
    • Synthesis, Oral Bioavailability Determination, and in Vitro Evaluation of Prodrugs of the Antiviral Agent 9-[2-(Phosphonomehtoxy)-ethyl]adenine (PMEA)
    • Starrett, J. E., Jr., Tortolani, D. R., Russel, J., Hitchcock, M. J. M., Whiterock, V., Martin, J. C., and Mansuri, M. M., Synthesis, Oral Bioavailability Determination, and In Vitro Evaluation of Prodrugs of the Antiviral Agent 9-[2-(Phosphonomehtoxy)-ethyl]adenine (PMEA). J. Med. Chem., 37, 1857-1864 (1994).
    • (1994) J. Med. Chem. , vol.37 , pp. 1857-1864
    • Starrett Jr., J.E.1    Tortolani, D.R.2    Russel, J.3    Hitchcock, M.J.M.4    Whiterock, V.5    Martin, J.C.6    Mansuri, M.M.7
  • 170
    • 0034688260 scopus 로고    scopus 로고
    • Regressions of established breast carcinoma xenografts by carboxypeptidase G2 suicide gene therapy and the prodrug CMDA are due to a bystander effect
    • Stribbling, S. M., Friedlos, F., Martin, J., Davies, L., Spooner, R. A., Marais, R., and Springer, C. J., Regressions of established breast carcinoma xenografts by carboxypeptidase G2 suicide gene therapy and the prodrug CMDA are due to a bystander effect. Hm. Gene Ther., 11, 258-292 (2000).
    • (2000) Hm. Gene Ther. , vol.11 , pp. 258-292
    • Stribbling, S.M.1    Friedlos, F.2    Martin, J.3    Davies, L.4    Spooner, R.A.5    Marais, R.6    Springer, C.J.7
  • 171
    • 0032835577 scopus 로고    scopus 로고
    • Examination of local anti-inflammatory activities of new steroids, hemisuccinyl methyl glycolates
    • Suzuki, T., Sato, E., Tada, H., and Tojima, Y., Examination of local anti-inflammatory activities of new steroids, hemisuccinyl methyl glycolates. Biol. Pharm. Bull., 22(8), 816-821 (1999a).
    • (1999) Biol. Pharm. Bull. , vol.22 , Issue.8 , pp. 816-821
    • Suzuki, T.1    Sato, E.2    Tada, H.3    Tojima, Y.4
  • 172
    • 0032916089 scopus 로고    scopus 로고
    • Examination on biological activities and fates of new steroids, steroid-17-yl methyl glycolates derivatives
    • Suzuki, T., Tada, H., Sato, E., and Tojima, Y., Examination on biological activities and fates of new steroids, steroid-17-yl methyl glycolates derivatives. Tohoku J. Exptl. Med., 187(2), 127-140 (1999b).
    • (1999) Tohoku J. Exptl. Med. , vol.187 , Issue.2 , pp. 127-140
    • Suzuki, T.1    Tada, H.2    Sato, E.3    Tojima, Y.4
  • 173
    • 0032560235 scopus 로고    scopus 로고
    • Therapeutic effects of monoclonal antibody-b-lactamase conjugates in combination with a nitrogen mustard anticacer prodrug in models of human renal cell carcinoma
    • Svensson, H. P., Frank, I. S., Berry, K. K., and Senter, P. D., Therapeutic effects of monoclonal antibody-b-lactamase conjugates in combination with a nitrogen mustard anticacer prodrug in models of human renal cell carcinoma. J. Med. Chem., 41, 1507-1512 (1998).
    • (1998) J. Med. Chem. , vol.41 , pp. 1507-1512
    • Svensson, H.P.1    Frank, I.S.2    Berry, K.K.3    Senter, P.D.4
  • 174
    • 0026826545 scopus 로고
    • Monoclonal antibody-b-lactamase conjugates for the activation of a cephalosporin mustard prodrug
    • Svensson, H. P., Kadow, J. F., Vrudhula, V. M., Wallace, P. M. and Senter, P. D., Monoclonal antibody-b-lactamase conjugates for the activation of a cephalosporin mustard prodrug. Bioconjug. Chem., 3, 176-181 (1992).
    • (1992) Bioconjug. Chem. , vol.3 , pp. 176-181
    • Svensson, H.P.1    Kadow, J.F.2    Vrudhula, V.M.3    Wallace, P.M.4    Senter, P.D.5
  • 176
    • 0023915671 scopus 로고
    • AIDS Dementia: Synthesis and Properties of a Derivative of 3-Azido-3-Deoxythymidine (AZT) That May Become Locked in the Central Nervous System
    • Terrence, P. F., Kinjo, J. E., Lesiak, K., Balazarine, J., and De Clerq, E., AIDS Dementia: Synthesis and Properties of a Derivative of 3-Azido-3-Deoxythymidine (AZT) That May Become Locked in the Central Nervous System. FEBS Lett., 234, 135 (1988).
    • (1988) FEBS Lett. , vol.234 , pp. 135
    • Terrence, P.F.1    Kinjo, J.E.2    Lesiak, K.3    Balazarine, J.4    De Clerq, E.5
  • 177
    • 0029878187 scopus 로고    scopus 로고
    • Anti-inflammatory and antishock water-soluble polyesters of glucocorticoids with low level systemic toxicity
    • Timofeevski, S. L., Panarin, E. F., Vinogradov, O. L., and Nezhentsev, M. V., Anti-inflammatory and antishock water-soluble polyesters of glucocorticoids with low level systemic toxicity. Pharm. Res., 13(3), 476-480 (1996).
    • (1996) Pharm. Res. , vol.13 , Issue.3 , pp. 476-480
    • Timofeevski, S.L.1    Panarin, E.F.2    Vinogradov, O.L.3    Nezhentsev, M.V.4
  • 178
    • 0023694012 scopus 로고
    • Liposomal Sustained-Release Delivery Systems for Intravenous Injection. IV. Antitumor Activity of Newly Synthesized Lipophilic 1-β-D- Arabinofuranosylcytosine Prodrug-Bearing Liposomes
    • Tokunaga, Y., Iwasa, T., Fujisaki, J., Sawai, S., and Kagayama, A., Liposomal Sustained-Release Delivery Systems for Intravenous Injection. IV. Antitumor Activity of Newly Synthesized Lipophilic 1-β-D- Arabinofuranosylcytosine Prodrug-Bearing Liposomes. Chem. Pharm. Bull., 36, 3574-3583 (1988a).
    • (1988) Chem. Pharm. Bull. , vol.36 , pp. 3574-3583
    • Tokunaga, Y.1    Iwasa, T.2    Fujisaki, J.3    Sawai, S.4    Kagayama, A.5
  • 179
    • 0023729153 scopus 로고
    • Liposomal Sustained-Release Delivery Systems for IntravenousInjection. III. AntitumorActivity of Lipophilic Mitomycin C Prodrug Bearing Liposomes
    • Tokunaga, Y., Iwasa, T., Fujisaki, J., Sawai, S., and Kagayama, A., Liposomal Sustained-Release Delivery Systems for IntravenousInjection. III. AntitumorActivity of Lipophilic Mitomycin C Prodrug Bearing Liposomes. Chem. Pharm. Bull., 36, 3565 (1988b).
    • (1988) Chem. Pharm. Bull. , vol.36 , pp. 3565
    • Tokunaga, Y.1    Iwasa, T.2    Fujisaki, J.3    Sawai, S.4    Kagayama, A.5
  • 180
    • 0031941292 scopus 로고    scopus 로고
    • Regional 'prodrug' gene therapy: Intravenous administration of an adenoviral vector expressing the E. coli cytosine deaminase gene and systemic administration of 5-fluorocytosine suppresses growth of hepatic metastasis of colon carcinoma
    • Topf, N., Worgall, N. R., Hackett, N. R., and Crystal, R. G., Regional 'prodrug' gene therapy: intravenous administration of an adenoviral vector expressing the E. coli cytosine deaminase gene and systemic administration of 5-fluorocytosine suppresses growth of hepatic metastasis of colon carcinoma. Gene Ther., 5, 507-513 (1998).
    • (1998) Gene Ther. , vol.5 , pp. 507-513
    • Topf, N.1    Worgall, N.R.2    Hackett, N.R.3    Crystal, R.G.4
  • 181
    • 0027395053 scopus 로고
    • Synthesis and Pharmacokinetics of a Dihydropyridine Chemical Delivery System for the Antiimmunodeficiency Virus Agent Dideoxycytidine
    • Torrence, P. F., Kinjo, J., Khamnei, S., and Greig, N. H., Synthesis and Pharmacokinetics of a Dihydropyridine Chemical Delivery System for the Antiimmunodeficiency Virus Agent Dideoxycytidine. J. Med. Chem., 36, 529-537 (1993).
    • (1993) J. Med. Chem. , vol.36 , pp. 529-537
    • Torrence, P.F.1    Kinjo, J.2    Khamnei, S.3    Greig, N.H.4
  • 182
    • 0032213438 scopus 로고    scopus 로고
    • Enhancement of the herpes simplex virus thymidine kinase ganciclovir bystander effect and its antitumor efficacy in vivo by pharmacologic manipulation of gap junctions
    • Touraine, R. L., Vahanian, N., Ramsey and W. J., Blaese, R. M., Enhancement of the herpes simplex virus thymidine kinase ganciclovir bystander effect and its antitumor efficacy in vivo by pharmacologic manipulation of gap junctions. Hum. Gene Ther., 9, 2385-2391 (1998).
    • (1998) Hum. Gene Ther. , vol.9 , pp. 2385-2391
    • Touraine, R.L.1    Vahanian, N.2    Ramsey, W.J.3    Blaese, R.M.4
  • 185
    • 0014514458 scopus 로고
    • Distribution of 1-β-D-Arabinofuranosylcytosine, Cytidine and Deoxycytidine in Mice Bearing ara-C Sensitive and Resistant P815 Neoplasms
    • Uchida, K., Krieis, W., Distribution of 1-β-D- Arabinofuranosylcytosine, Cytidine and Deoxycytidine in Mice Bearing ara-C Sensitive and Resistant P815 Neoplasms. Biochem. Pharmacol., 18, 1115 (1969).
    • (1969) Biochem. Pharmacol. , vol.18 , pp. 1115
    • Uchida, K.1    Krieis, W.2
  • 186
    • 0029953984 scopus 로고    scopus 로고
    • Decomposition Pathways and in vitro HIV Inhibitory Effects of IsoddA Pronucleotides: Toward a Rational Approach for Intracellular Delivery of Nucleoside 5-Monophosphates
    • Valette, G., Pompon, A., Giradet, J. L., Gosselin, G., Périgaud, C., Gosselin, G., and Imbach, J. L., Decomposition Pathways and in vitro HIV Inhibitory Effects of IsoddA Pronucleotides: Toward a Rational Approach for Intracellular Delivery of Nucleoside 5-Monophosphates. J. Med. Chem., 39, 1981-1990 (1996).
    • (1996) J. Med. Chem. , vol.39 , pp. 1981-1990
    • Valette, G.1    Pompon, A.2    Giradet, J.L.3    Gosselin, G.4    Périgaud, C.5    Gosselin, G.6    Imbach, J.L.7
  • 188
    • 0024416237 scopus 로고
    • Selection of an Oral Prodrug (BRL 42810; Famciclovir) for the Antiherpesvirus Agent BRL 39123 [9-(4-Hydroxy-3-hydroxymethylbut-1-yl)guanine; Penciclovir]
    • Vere Hodge, R. A., Sutton, D., Boyd, M. R., Harnden, M. R., and Jarvest, R. L., Selection of an Oral Prodrug (BRL 42810; Famciclovir) for the Antiherpesvirus Agent BRL 39123 [9-(4-Hydroxy-3-hydroxymethylbut-1-yl)guanine; Penciclovir]. Antimicrob. Agents Chemother., 33, 1765-1773 (1989).
    • (1989) Antimicrob. Agents Chemother. , vol.33 , pp. 1765-1773
    • Vere Hodge, R.A.1    Sutton, D.2    Boyd, M.R.3    Harnden, M.R.4    Jarvest, R.L.5
  • 189
    • 0027655158 scopus 로고
    • Antitumor activities of a cephalosporin prodrug combination with monoclonal antibody-b-lactamase conjugates
    • Vrudhula, V. M., Svensson, H. P., Kennedy, K. A., Senter, P. D., and Wallace, P. M., Antitumor activities of a cephalosporin prodrug combination with monoclonal antibody-b-lactamase conjugates. Bioconjug. Chem., 4, 334-340 (1993).
    • (1993) Bioconjug. Chem. , vol.4 , pp. 334-340
    • Vrudhula, V.M.1    Svensson, H.P.2    Kennedy, K.A.3    Senter, P.D.4    Wallace, P.M.5
  • 191
    • 0033067561 scopus 로고    scopus 로고
    • Involvement of Fas (CD95/APO-1) and Fas ligand in apoptosis induced by ganciclovir treatment of tumor cells transduced with herpes simplex virus thymidine kinase
    • Wei, S. J., Chao, Y., Shih, Y. L., Yang, D. M., Hung, Y. M., and Yang, W. K., Involvement of Fas (CD95/APO-1) and Fas ligand in apoptosis induced by ganciclovir treatment of tumor cells transduced with herpes simplex virus thymidine kinase. Gene Ther., 6, 420-431 (1999).
    • (1999) Gene Ther. , vol.6 , pp. 420-431
    • Wei, S.J.1    Chao, Y.2    Shih, Y.L.3    Yang, D.M.4    Hung, Y.M.5    Yang, W.K.6
  • 192
    • 0027117028 scopus 로고
    • Acyclovir: A Decade Later
    • Whitley, R. J. and Gnann, J. W., Acyclovir: A Decade Later. N. Engl. J. Med., 327, 782-788 (1992).
    • (1992) N. Engl. J. Med. , vol.327 , pp. 782-788
    • Whitley, R.J.1    Gnann, J.W.2
  • 193
    • 0028805850 scopus 로고
    • Phosphatidyl-2′,3′-dideoxy-3′-thiacytidine: Synthesis and Antiviral Activity in Hepatitis Band HIV-1 Infected Cells
    • Xie, H., Voronkov, M., Liotta, D. C., Korba, B. A., Schinazi, R. F., Richman, D. D., Hostetler, K. Y., Phosphatidyl-2′,3′-dideoxy- 3′-thiacytidine: Synthesis and Antiviral Activity in Hepatitis Band HIV-1 Infected Cells. Antiviral Res., 28, 113-120 (1995).
    • (1995) Antiviral Res. , vol.28 , pp. 113-120
    • Xie, H.1    Voronkov, M.2    Liotta, D.C.3    Korba, B.A.4    Schinazi, R.F.5    Richman, D.D.6    Hostetler, K.Y.7
  • 194
    • 0029156073 scopus 로고
    • Steroidal anti-inflammatory antedrugs: Synthesis and pharmacological evaluation of 16α-alkoxycarbonyl-17-deoxyprednisolone derivatives
    • Yoon, K.-J., Khalil, M. A., Kwon, T. Choi, S.-J., and Lee, H. J., Steroidal anti-inflammatory antedrugs: synthesis and pharmacological evaluation of 16α-alkoxycarbonyl-17-deoxyprednisolone derivatives. Steroids, 60, 445-451 (1995).
    • (1995) Steroids , vol.60 , pp. 445-451
    • Yoon, K.-J.1    Khalil, M.A.2    Kwon, T.3    Choi, S.-J.4    Lee, H.J.5
  • 195
    • 0033988325 scopus 로고    scopus 로고
    • Novel steroid spiro enones: Consideration of prednisolone derivatives with diethyl oxalate
    • You, Z., Heiman, A. S., Chen, M., and Lee, H. J., Novel steroid spiro enones: Consideration of prednisolone derivatives with diethyl oxalate. Steroids, 65, 109-115 (2000).
    • (2000) Steroids , vol.65 , pp. 109-115
    • You, Z.1    Heiman, A.S.2    Chen, M.3    Lee, H.J.4
  • 196
    • 0028970020 scopus 로고
    • Suppression of the Mattox rearrangement of 16α-cyanoprednisolones in acid: Synthesis of methyl 16α-prednisolone carboxylates
    • You, Z., Khalil, M. A., Ko, D.-H., and Lee, H. J., Suppression of the Mattox rearrangement of 16α-cyanoprednisolones in acid: synthesis of methyl 16α-prednisolone carboxylates. Tetrahedron Lett., 36(19), 3303-3306 (1995).
    • (1995) Tetrahedron Lett. , vol.36 , Issue.19 , pp. 3303-3306
    • You, Z.1    Khalil, M.A.2    Ko, D.-H.3    Lee, H.J.4


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