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Volumn 8, Issue 6, 2013, Pages 556-564

Prodrug strategies for improved efficacy of nucleoside antiviral inhibitors

Author keywords

adenovirus; antiviral agents; hepatitis B virus; hepatitis C virus; herpes simplex virus; HIV; nucleoside antiviral agents; prodrugs

Indexed keywords

2' DEOXY 2' FLUORO 2' METHYLCYTIDINE; ACICLOVIR; AMDOXOVIR; AMVIR; ANTIVIRUS AGENT; CIDOFOVIR; CIDOFOVIR 3 HEXADECYLOXYPROPYL ESTER; FAMCICLOVIR; MERICITABINE; NUCLEOSIDE ANTIVIRAL INHIBITOR; PENCICLOVIR; PRODRUG; SOFOSBUVIR; TENOFOVIR; TENOFOVIR 3 HEXADECYLOXYPROPYL ESTER; TENOFOVIR ALAFENAMIDE; UNCLASSIFIED DRUG; VALACICLOVIR;

EID: 84886096395     PISSN: 1746630X     EISSN: 17466318     Source Type: Journal    
DOI: 10.1097/COH.0000000000000007     Document Type: Review
Times cited : (15)

References (65)
  • 1
    • 23444445718 scopus 로고    scopus 로고
    • Antiviral drug discovery and development: Where chemistrymeets with biomedicine
    • De Clercq E. Antiviral drug discovery and development: where chemistrymeets with biomedicine. Antiviral Res 2005; 67:56-75.
    • (2005) Antiviral Res , vol.67 , pp. 56-75
    • De Clercq, E.1
  • 2
    • 33747100570 scopus 로고    scopus 로고
    • Pharmacology of current and promising nucleosides for the treatment of human immunodeficiency viruses
    • Schinazi RF, Hernandez-Santiago BI, Hurwitz SJ. Pharmacology of current and promising nucleosides for the treatment of human immunodeficiency viruses. Antiviral Res 2006; 71:322-334.
    • (2006) Antiviral Res , vol.71 , pp. 322-334
    • Schinazi, R.F.1    Hernandez-Santiago, B.I.2    Hurwitz, S.J.3
  • 3
    • 0025136741 scopus 로고
    • Broad-spectrum antiviral activity of carbodine, the carbocyclic analogue of cytidine
    • De Clercq E, Bernaerts R, Shealy YF, Montgomery JA. Broad-spectrum antiviral activity of carbodine, the carbocyclic analogue of cytidine. Biochem Pharmacol 1990; 39:319-325.
    • (1990) Biochem Pharmacol , vol.39 , pp. 319-325
    • De Clercq, E.1    Bernaerts, R.2    Shealy, Y.F.3    Montgomery, J.A.4
  • 4
    • 84872565980 scopus 로고    scopus 로고
    • Comparative effectiveness of antiviral treatment for hepatitis C virus infection in adults: A systematic review
    • Chou R, Hartung D, Rahman B, et al. Comparative effectiveness of antiviral treatment for hepatitis C virus infection in adults: a systematic review. Ann Intern Med 2013; 158:114-123.
    • (2013) Ann Intern Med , vol.158 , pp. 114-123
    • Chou, R.1    Hartung, D.2    Rahman, B.3
  • 5
    • 81855168414 scopus 로고    scopus 로고
    • Nucleoside/nucleotide analogues in the treatment of chronic hepatitis B
    • Fung J, Lai CL, Seto WK, Yuen MF. Nucleoside/nucleotide analogues in the treatment of chronic hepatitis B. J Antimicrob Chemother 2011; 66:2715-2725.
    • (2011) J Antimicrob Chemother , vol.66 , pp. 2715-2725
    • Fung, J.1    Lai, C.L.2    Seto, W.K.3    Yuen, M.F.4
  • 6
    • 73549088038 scopus 로고    scopus 로고
    • Nucleoside and nucleotide HIV reverse transcriptase inhibitors: 25 years after zidovudine
    • Cihlar T, Ray AS. Nucleoside and nucleotide HIV reverse transcriptase inhibitors: 25 years after zidovudine. Antiviral Res 2010; 85:39-58.
    • (2010) Antiviral Res , vol.85 , pp. 39-58
    • Cihlar, T.1    Ray, A.S.2
  • 7
    • 0344845009 scopus 로고    scopus 로고
    • Complex patterns of viral load decay under antiretroviral therapy: Influence of pharmacokinetics and intracellular delay
    • Dixit NM, Perelson AS. Complex patterns of viral load decay under antiretroviral therapy: influence of pharmacokinetics and intracellular delay. J Theor Biol 2004; 226:95-109.
    • (2004) J Theor Biol , vol.226 , pp. 95-109
    • Dixit, N.M.1    Perelson, A.S.2
  • 8
    • 41349110928 scopus 로고    scopus 로고
    • Development of a population simulation model for HIV monotherapy virological outcomes using lamivudine
    • Hurwitz SJ, Asif G, Schinazi RF. Development of a population simulation model for HIV monotherapy virological outcomes using lamivudine. Antivir Chem Chemother 2007; 18:329-341.
    • (2007) Antivir Chem Chemother , vol.18 , pp. 329-341
    • Hurwitz, S.J.1    Asif, G.2    Schinazi, R.F.3
  • 9
    • 58949084496 scopus 로고    scopus 로고
    • Modeling complex decay profiles of hepatitis B virus during antiviral therapy
    • Dahari H, Shudo E, Ribeiro RM, Perelson AS. Modeling complex decay profiles of hepatitis B virus during antiviral therapy. Hepatology 2009; 49:32-38.
    • (2009) Hepatology , vol.49 , pp. 32-38
    • Dahari, H.1    Shudo, E.2    Ribeiro, R.M.3    Perelson, A.S.4
  • 10
    • 84883247224 scopus 로고    scopus 로고
    • Mathematical analysis of multiscale models for hepatitis C virus dynamics under therapy with direct-acting antiviral agents
    • Rong L, Perelson AS. Mathematical analysis of multiscale models for hepatitis C virus dynamics under therapy with direct-acting antiviral agents. Math Biosci 2013; 245:22-30.
    • (2013) Math Biosci , Issue.245 , pp. 22-30
    • Rong, L.1    Perelson, A.S.2
  • 11
    • 84873095350 scopus 로고    scopus 로고
    • Practical considerations for developing nucleoside reverse transcriptase inhibitors
    • Hurwitz SJ, Schinazi RF. Practical considerations for developing nucleoside reverse transcriptase inhibitors. Drug Discov Today Technol 2012; 9:e183-e193.
    • (2012) Drug Discov Today Technol , vol.9
    • Hurwitz, S.J.1    Schinazi, R.F.2
  • 12
    • 80054862874 scopus 로고    scopus 로고
    • Application of kinase bypass strategies to nucleoside antivirals
    • Ray AS, Hostetler KY. Application of kinase bypass strategies to nucleoside antivirals. Antiviral Res 2011; 92:277-291.
    • (2011) Antiviral Res , vol.92 , pp. 277-291
    • Ray, A.S.1    Hostetler, K.Y.2
  • 13
    • 0025552679 scopus 로고
    • Biochemical pharmacology of acyclic nucleotide analogues
    • Bronson JJ, Ho HT, De Boeck H, et al. Biochemical pharmacology of acyclic nucleotide analogues. Ann N Y Acad Sci 1990; 616:398-407.
    • (1990) Ann N y Acad Sci , vol.616 , pp. 398-407
    • Bronson, J.J.1    Ho, H.T.2    De Boeck, H.3
  • 14
    • 1242340323 scopus 로고    scopus 로고
    • The ABCs of solute carriers: Physiological, pathological and therapeutic implications of human membrane transport proteinsIntroduction
    • Hediger MA, Romero MF, Peng JB, et al. The ABCs of solute carriers: physiological, pathological and therapeutic implications of human membrane transport proteinsIntroduction. Pflugers Arch 2004; 447:465-468.
    • (2004) Pflugers Arch , vol.447 , pp. 465-468
    • Hediger, M.A.1    Romero, M.F.2    Peng, J.B.3
  • 15
    • 65649111235 scopus 로고    scopus 로고
    • Strategies to increase the oral bioavailability of nucleoside analogs
    • Lalanne M, Andrieux K, Couvreur P. Strategies to increase the oral bioavailability of nucleoside analogs. Curr Med Chem 2009; 16:1391-1399.
    • (2009) Curr Med Chem , vol.16 , pp. 1391-1399
    • Lalanne, M.1    Andrieux, K.2    Couvreur, P.3
  • 16
    • 79851489459 scopus 로고    scopus 로고
    • The role of intestinal carboxylesterase in the oral absorption of prodrugs
    • Imai T, Ohura K. The role of intestinal carboxylesterase in the oral absorption of prodrugs. Curr Drug Metab 2010; 11:793-805.
    • Curr Drug Metab , vol.2010 , Issue.11 , pp. 793-805
    • Imai, T.1    Ohura, K.2
  • 17
    • 0029062086 scopus 로고
    • Valaciclovir compared with acyclovir for improved therapy for herpes zoster in immunocompetent adults
    • Beutner KR, Friedman DJ, Forszpaniak C, et al. Valaciclovir compared with acyclovir for improved therapy for herpes zoster in immunocompetent adults. Antimicrob Agents Chemother 1995; 39:1546-1553.
    • (1995) Antimicrob Agents Chemother , vol.39 , pp. 1546-1553
    • Beutner, K.R.1    Friedman, D.J.2    Forszpaniak, C.3
  • 18
    • 0029113580 scopus 로고
    • Famciclovir for the treatment of acute herpes zoster: Effects on acute disease and postherpetic neuralgia. A randomized, double-blind, placebo-controlled trial
    • Tyring S, Barbarash RA, Nahlik JE, et al. Famciclovir for the treatment of acute herpes zoster: effects on acute disease and postherpetic neuralgia. A randomized, double-blind, placebo-controlled trial. Collaborative Famciclovir Herpes Zoster Study Group. Ann Intern Med 1995; 123:89-96.
    • (1995) Collaborative Famciclovir Herpes Zoster Study Group. Ann Intern Med , vol.123 , pp. 89-96
    • Tyring, S.1    Barbarash, R.A.2    Nahlik, J.E.3
  • 19
    • 0029993960 scopus 로고    scopus 로고
    • The clinical pharmacokinetics of famciclovir
    • Gill KS, Wood MJ. The clinical pharmacokinetics of famciclovir. Clin Pharmacokinet 1996; 31:1-8.
    • (1996) Clin Pharmacokinet , vol.31 , pp. 1-8
    • Gill, K.S.1    Wood, M.J.2
  • 20
    • 30344486584 scopus 로고    scopus 로고
    • Antiviral prodrugs: The development of successful prodrug strategies for antiviral chemotherapy
    • De Clercq E, Field HJ. Antiviral prodrugs: the development of successful prodrug strategies for antiviral chemotherapy. Br J Pharmacol 2006; 147:1-11.
    • (2006) Br J Pharmacol , vol.147 , pp. 1-11
    • De Clercq, E.1    Field, H.J.2
  • 21
    • 84860317044 scopus 로고    scopus 로고
    • Antivirals for management of herpes zoster including ophthalmicus: A systematic review of high-quality randomized controlled trials
    • McDonald EM, de Kock J, Ram FSF. Antivirals for management of herpes zoster including ophthalmicus: a systematic review of high-quality randomized controlled trials. Antivir Ther 2012; 17:255-264.
    • (2012) Antivir Ther , Issue.17 , pp. 255-264
    • McDonald, E.M.1    De Kock, J.2    Fsf, R.3
  • 22
    • 0030199335 scopus 로고    scopus 로고
    • Famciclovir, from the bench to the patient: A comprehensive review of preclinical data
    • Bacon TH. Famciclovir, from the bench to the patient: a comprehensive review of preclinical data. Int J Antimicrob Agents 1996; 7:119-134.
    • (1996) Int J Antimicrob Agents , vol.7 , pp. 119-134
    • Bacon, T.H.1
  • 23
    • 0030840879 scopus 로고    scopus 로고
    • Vitro oxidation of famciclovir and 6-deoxypenciclovir by aldehyde oxidase from human, guinea pig, rabbit, and rat liver
    • Rashidi MR, Smith JA, Clarke SE, Beedham C. In vitro oxidation of famciclovir and 6-deoxypenciclovir by aldehyde oxidase from human, guinea pig, rabbit, and rat liver. Drug Metab Dispos 1997; 25:805-813.
    • (1997) Drug Metab Dispos , vol.25 , pp. 805-813
    • Rashidi, M.R.1    Smith, J.A.2    Clarke, S.E.3    Beedham, C.4
  • 24
    • 0028832926 scopus 로고
    • Role of aldehyde oxidase in the in vitro conversion of famciclovir to penciclovir in human liver
    • Clarke SE, Harrell AW, Chenery RJ. Role of aldehyde oxidase in the in vitro conversion of famciclovir to penciclovir in human liver. Drug Metab Dispos 1995; 23:251-254.
    • (1995) Drug Metab Dispos , vol.23 , pp. 251-254
    • Clarke, S.E.1    Harrell, A.W.2    Chenery, R.J.3
  • 25
    • 0027146271 scopus 로고
    • Use of isotopically chiral [40 -13C]famciclovir and 13C NMR to identify the chiral monoacetylated intermediates in the conversion of famciclovir to penciclovir by human intestinal wall extract
    • Vere Hodge RA, Darlison SJ, Readshaw SA. Use of isotopically chiral [40 -13C]famciclovir and 13C NMR to identify the chiral monoacetylated intermediates in the conversion of famciclovir to penciclovir by human intestinal wall extract. Chirality 1993; 5:577-582.
    • (1993) Chirality , vol.5 , pp. 577-582
    • Vere Hodge, R.A.1    Darlison, S.J.2    Readshaw, S.A.3
  • 26
    • 0031916247 scopus 로고    scopus 로고
    • Pharmacokinetics and bioavailability of the antihuman immunodeficiency virus nucleotide analog 9-[(R)-2-(phosphonomethoxy) propyl]adenine (PMPA) in dogs
    • Cundy KC, Sueoka C, Lynch GR, et al. Pharmacokinetics and bioavailability of the antihuman immunodeficiency virus nucleotide analog 9-[(R)-2- (phosphonomethoxy) propyl]adenine (PMPA) in dogs. Antimicrob Agents Chemother 1998; 42:687-690.
    • (1998) Antimicrob Agents Chemother , vol.42 , pp. 687-690
    • Cundy, K.C.1    Sueoka, C.2    Lynch, G.R.3
  • 27
    • 0031430945 scopus 로고    scopus 로고
    • Metabolism and pharmacokinetics of novel oral prodrugs of 9-[(R)-2-(phosphonomethoxy)propyl]adenine (PMPA) in dogs
    • Shaw JP, Sueoko CM, Oliyai R, et al. Metabolism and pharmacokinetics of novel oral prodrugs of 9-[(R)-2-(phosphonomethoxy)propyl]adenine (PMPA) in dogs. Pharm Res 1997; 14:1824-1829.
    • (1997) Pharm Res , vol.14 , pp. 1824-1829
    • Shaw, J.P.1    Sueoko, C.M.2    Oliyai, R.3
  • 28
    • 0031863214 scopus 로고    scopus 로고
    • Antiretroviral efficacy and pharmacokinetics of oral bis(isopropyloxycarbonyloxymethyl)-9-(2-phosphonylmethoxypropyl) adenine in mice
    • Naesens L, Bischofberger N, Augustijns P, et al. Antiretroviral efficacy and pharmacokinetics of oral bis(isopropyloxycarbonyloxymethyl)-9-(2- phosphonylmethoxypropyl) adenine in mice. Antimicrob Agents Chemother 1998; 42:1568-1573.
    • (1998) Antimicrob Agents Chemother , vol.42 , pp. 1568-1573
    • Naesens, L.1    Bischofberger, N.2    Augustijns, P.3
  • 29
    • 77149177021 scopus 로고    scopus 로고
    • Lack of pharmacokinetic interaction between amdoxovir and reduced- and standard-dose zidovudine in HIV-1- infected individuals
    • Hurwitz SJ, Asif G, Fromentin E, et al. Lack of pharmacokinetic interaction between amdoxovir and reduced- and standard-dose zidovudine in HIV-1- infected individuals. Antimicrob Agents Chemother 2010; 54:1248-1255.
    • Antimicrob Agents Chemother , vol.2010 , Issue.54 , pp. 1248-1255
    • Hurwitz, S.J.1    Asif, G.2    Fromentin, E.3
  • 30
    • 67349157073 scopus 로고    scopus 로고
    • Alkoxyalkyl prodrugs of acyclic nucleoside phosphonates enhance oral antiviral activity and reduce toxicity: Current state of the art
    • Epub 2009/05/09
    • Hostetler KY. Alkoxyalkyl prodrugs of acyclic nucleoside phosphonates enhance oral antiviral activity and reduce toxicity: current state of the art. Antiviral Res 2009; 82:A84-A98; Epub 2009/05/09..
    • (2009) Antiviral Res , vol.82
    • Hostetler, K.Y.1
  • 32
    • 84860188140 scopus 로고    scopus 로고
    • First pharmacokinetic and safety study in humans of the novel lipid antiviral conjugate CMX001, a broadspectrum oral drug active against double-stranded DNA viruses
    • Painter W, Robertson A, Trost LC, et al. First pharmacokinetic and safety study in humans of the novel lipid antiviral conjugate CMX001, a broadspectrum oral drug active against double-stranded DNA viruses. Antimicrob Agents Chemother 2012; 56:2726-2734.
    • (2012) Antimicrob Agents Chemother , vol.56 , pp. 2726-2734
    • Painter, W.1    Robertson, A.2    Trost, L.C.3
  • 34
    • 78049375232 scopus 로고    scopus 로고
    • Mechanism of activation of PSI-7851 and its diastereoisomer PSI-7977
    • Murakami E, Tolstykh T, Bao H, et al. Mechanism of activation of PSI-7851 and its diastereoisomer PSI-7977. J Biol Chem 2010; 285:34337-34347.
    • J Biol Chem , vol.2010 , Issue.285 , pp. 34337-34347
    • Murakami, E.1    Tolstykh, T.2    Bao, H.3
  • 35
    • 38649112300 scopus 로고    scopus 로고
    • The mechanism of action of beta-D-20- deoxy-20-fluoro-20-C-methylcytidme involves a second metabolic pathway leading to beta-D-20-deoxy-2-fluoro-20-C- methyluridine 50-triphosphate, a potent inhibitor of the hepatitis C virus RNA-dependent RNA polymerase
    • Murakami E, Niu CR, Bao HY, et al. The mechanism of action of beta-D-20- deoxy-20-fluoro-20-C-methylcytidme involves a second metabolic pathway leading to beta-D-20-deoxy-2-fluoro-20-C-methyluridine 50-triphosphate, a potent inhibitor of the hepatitis C virus RNA-dependent RNA polymerase. Antimicrob Agents Chemother 2008; 52:458-464.
    • (2008) Antimicrob Agents Chemother , vol.52 , pp. 458-464
    • Murakami, E.1    Niu, C.R.2    Bao, H.Y.3
  • 36
    • 35648968189 scopus 로고    scopus 로고
    • Characterization of the metabolic activation of hepatitis C virus nucleoside inhibitor beta-D-2 0-deoxy-2 0-fluoro-2 0-Cmethylcytidine (PSI-6130) and identification of a novel active 5 0-triphosphate species
    • Ma H, Jiang WR, Robledo N, et al. Characterization of the metabolic activation of hepatitis C virus nucleoside inhibitor beta-D-2 0-deoxy-2 0-fluoro-2 0-Cmethylcytidine (PSI-6130) and identification of a novel active 5 0-triphosphate species. J Biol Chem 2007; 282:29812-29820.
    • (2007) J Biol Chem , vol.282 , pp. 29812-29820
    • Ma, H.1    Jiang, W.R.2    Robledo, N.3
  • 37
    • 67649415182 scopus 로고    scopus 로고
    • Mechanistic basis of using body size and maturation to predict clearance in humans
    • Anderson BJ, Holford NH. Mechanistic basis of using body size and maturation to predict clearance in humans. Drug Metab Pharmacokinet 2009; 24:25-36.
    • (2009) Drug Metab Pharmacokinet , vol.24 , pp. 25-36
    • Anderson, B.J.1    Holford, N.H.2
  • 38
    • 84865484675 scopus 로고    scopus 로고
    • Comprehensive assessment of human pharmacokinetic prediction based on in vivo animal pharmacokinetic data, part 2: Clearance
    • Lombardo F, Waters NJ, Argikar UA, et al. Comprehensive assessment of human pharmacokinetic prediction based on in vivo animal pharmacokinetic data, part 2: clearance. J Clin Pharmacol 2013; 53:178-191.
    • (2013) J Clin Pharmacol , Issue.53 , pp. 178-191
    • Lombardo, F.1    Waters, N.J.2    Argikar, U.A.3
  • 39
    • 84866369227 scopus 로고    scopus 로고
    • Comparative assessment of in vitro-in vivo extrapolation methods used for predicting hepatic metabolic clearance of drugs
    • Poulin P, Hop CE, Ho Q, et al. Comparative assessment of in vitro-in vivo extrapolation methods used for predicting hepatic metabolic clearance of drugs. J Pharm Sci 2012; 101:4308-4326.
    • (2012) J Pharm Sci , Issue.101 , pp. 4308-4326
    • Poulin, P.1    Hop, C.E.2    Ho, Q.3
  • 40
    • 58149142515 scopus 로고    scopus 로고
    • Database for physiologically based pharmacokinetic (PBPK) modeling: Physiological data for healthy and health-impaired elderly
    • Thompson CM, Johns DO, Sonawane B, et al. Database for physiologically based pharmacokinetic (PBPK) modeling: physiological data for healthy and health-impaired elderly. J Toxicol Environ Health B Crit Rev 2009; 12:1-24.
    • (2009) J Toxicol Environ Health B Crit Rev , vol.12 , pp. 1-24
    • Thompson, C.M.1    Johns, D.O.2    Sonawane, B.3
  • 41
    • 84862619047 scopus 로고    scopus 로고
    • Physiologically based pharmacokinetics joined with in vitro-in vivo extrapolation of ADME: A marriage under the arch of systems pharmacology
    • Rostami-Hodjegan A. Physiologically based pharmacokinetics joined with in vitro-in vivo extrapolation of ADME: a marriage under the arch of systems pharmacology. Clin Pharmacol Ther 2012; 92:50-61.
    • (2012) Clin Pharmacol Ther , vol.92 , pp. 50-61
    • Rostami-Hodjegan, A.1
  • 42
    • 84877074929 scopus 로고    scopus 로고
    • Dose selection based on physiologically based pharmacokinetic (PBPK) approaches
    • Jones HM, Mayawala K, Poulin P. Dose selection based on physiologically based pharmacokinetic (PBPK) approaches. AAPS J 2013; 15:377-387.
    • (2013) AAPS J , vol.15 , pp. 377-387
    • Jones, H.M.1    Mayawala, K.2    Poulin, P.3
  • 43
    • 84896269353 scopus 로고    scopus 로고
    • Discovery of the first C-nucleoside HCV polymerase inhibitor (GS-6620) with demonstrated antiviral response in HCV infected patients
    • Epub ahead of print. GS-6620 had variable pharmacokinetics and efficacy in humans despite reproducible pharmacokinetics in dogs
    • Cho A, Zhang L, Xu J, et al. Discovery of the first C-nucleoside HCV polymerase inhibitor (GS-6620) with demonstrated antiviral response in HCV infected patients. J Med Chem 2013; Epub ahead of print. GS-6620 had variable pharmacokinetics and efficacy in humans despite reproducible pharmacokinetics in dogs.
    • (2013) J Med Chem
    • Cho, A.1    Zhang, L.2    Xu, J.3
  • 44
    • 18244398917 scopus 로고    scopus 로고
    • Selective intracellular activation of a novel prodrug of the human immunodeficiency virus reverse transcriptase inhibitor tenofovir leads to preferential distribution and accumulation in lymphatic tissue
    • Lee WA, He GX, Eisenberg E, et al. Selective intracellular activation of a novel prodrug of the human immunodeficiency virus reverse transcriptase inhibitor tenofovir leads to preferential distribution and accumulation in lymphatic tissue. Antimicrob Agents Chemother 2005; 49:1898-1906.
    • (2005) Antimicrob Agents Chemother , vol.49 , pp. 1898-1906
    • Lee, W.A.1    He, G.X.2    Eisenberg, E.3
  • 45
    • 45749091322 scopus 로고    scopus 로고
    • Activation of 9-[(R)-2-[[(S)-[[(S)-1-(Isopropoxycarbonyl) ethyl]amino] phenoxyphosphinyl]-methoxy]propyl]adenine (GS-7340) and other tenofovir phosphonamidate prodrugs by human proteases
    • Birkus G, Kutty N, He GX, et al. Activation of 9-[(R)-2-[[(S)-[[(S)-1- (Isopropoxycarbonyl) ethyl]amino] phenoxyphosphinyl]-methoxy]propyl]adenine (GS-7340) and other tenofovir phosphonamidate prodrugs by human proteases. Mol Pharmacol 2008; 74:92-100.
    • (2008) Mol Pharmacol , vol.74 , pp. 92-100
    • Birkus, G.1    Kutty, N.2    He, G.X.3
  • 48
    • 84886093851 scopus 로고    scopus 로고
    • Resistance to tenofovir-based regimens during treatment failure of subtype C HIV-1 in South Africa
    • Epub 2013/06/12
    • Hoffmann CJ, Ledwaba J, Li JF, et al. Resistance to tenofovir-based regimens during treatment failure of subtype C HIV-1 in South Africa. Antivir Ther 2013; Epub 2013/06/12.
    • (2013) Antivir Ther
    • Hoffmann, C.J.1    Ledwaba, J.2    Li, J.F.3
  • 49
    • 57049172088 scopus 로고    scopus 로고
    • Development of an optimized dose for coformulation of zidovudine with drugs that select for the K65R mutation using a population pharmacokinetic and enzyme kinetic simulation model
    • Hurwitz SJ, Asif G, Kivel NM, Schinazi RF. Development of an optimized dose for coformulation of zidovudine with drugs that select for the K65R mutation using a population pharmacokinetic and enzyme kinetic simulation model. Antimicrob Agents Chemother 2008; 52:4241-4250.
    • (2008) Antimicrob Agents Chemother , vol.52 , pp. 4241-4250
    • Hurwitz, S.J.1    Asif, G.2    Kivel, N.M.3    Schinazi, R.F.4
  • 50
    • 84879236151 scopus 로고    scopus 로고
    • Hypersusceptibility mechanism of tenofovir-resistant HIV to EFdA
    • Michailidis E, Ryan EM, Hachiya A, et al. Hypersusceptibility mechanism of tenofovir-resistant HIV to EFdA. Retrovirol 2013; 10:65.
    • (2013) Retrovirol , Issue.10 , pp. 65
    • Michailidis, E.1    Ryan, E.M.2    Hachiya, A.3
  • 54
    • 34948857943 scopus 로고    scopus 로고
    • Evaluation of hexadecyloxypropyl-9- R-[2-(Phosphonomethoxy)propyl]- adenine, CMX157, as a potential treatment for human immunodeficiency virus type 1 and hepatitis B virus infections
    • Painter GR, Almond MR, Trost LC, et al. Evaluation of hexadecyloxypropyl-9- R-[2-(Phosphonomethoxy)propyl]-adenine, CMX157, as a potential treatment for human immunodeficiency virus type 1 and hepatitis B virus infections. Antimicrob Agents Chemother 2007; 51:3505-3509.
    • (2007) Antimicrob Agents Chemother , vol.51 , pp. 3505-3509
    • Painter, G.R.1    Almond, M.R.2    Trost, L.C.3
  • 56
    • 78349234678 scopus 로고    scopus 로고
    • Efficacy of CMX001 against herpes simplex virus infections in mice and correlations with drug distribution studies
    • Quenelle DC, Lampert B, Collins DJ, et al. Efficacy of CMX001 against herpes simplex virus infections in mice and correlations with drug distribution studies. J Infect Dis 2010; 202:1492-1499.
    • (2010) J Infect Dis , vol.202 , pp. 1492-1499
    • Quenelle, D.C.1    Lampert, B.2    Collins, D.J.3
  • 57
    • 35848968505 scopus 로고    scopus 로고
    • Synergistic efficacy of the combination of ST-246 with CMX001 against orthopoxviruses
    • Quenelle DC, Prichard MN, Keith KA, et al. Synergistic efficacy of the combination of ST-246 with CMX001 against orthopoxviruses. Antimicrob Agents Chemother 2007; 51:4118-4124.
    • (2007) Antimicrob Agents Chemother , vol.51 , pp. 4118-4124
    • Quenelle, D.C.1    Prichard, M.N.2    Keith, K.A.3
  • 58
    • 84859872029 scopus 로고    scopus 로고
    • Safety and efficacy of CMX001 as salvage therapy for severe adenovirus infections in immunocompromised patients
    • Florescu DF, Pergam SA, Neely MN, et al. Safety and efficacy of CMX001 as salvage therapy for severe adenovirus infections in immunocompromised patients. Biol Blood Marrow Transplant 2012; 18:731-738.
    • (2012) Biol Blood Marrow Transplant , vol.18 , pp. 731-738
    • Florescu, D.F.1    Pergam, S.A.2    Neely, M.N.3
  • 59
    • 32044474268 scopus 로고    scopus 로고
    • Synthesis and antiviral activity of 2-deoxy-2-fluoro-2-C-methyl purine nucleosides as inhibitors of hepatitis C virus RNA replication
    • Clark JL, Mason JC, Hollecker L, et al. Synthesis and antiviral activity of 2-deoxy-2-fluoro-2-C-methyl purine nucleosides as inhibitors of hepatitis C virus RNA replication. Bioorg Med Chem Lett 2006; 16:1712-1715.
    • (2006) Bioorg Med Chem Lett , vol.16 , pp. 1712-1715
    • Clark, J.L.1    Mason, J.C.2    Hollecker, L.3
  • 60
    • 84861655785 scopus 로고    scopus 로고
    • Resistance to mericitabine, a nucleoside analogue inhibitor of HCV RNA-dependent RNA polymerase
    • Pawlotsky JM, Najera I, Jacobson I. Resistance to mericitabine, a nucleoside analogue inhibitor of HCV RNA-dependent RNA polymerase. Antivir Ther 2012; 17:411-423.
    • (2012) Antivir Ther , vol.17 , pp. 411-423
    • Pawlotsky, J.M.1    Najera, I.2    Jacobson, I.3
  • 61
    • 33846589710 scopus 로고    scopus 로고
    • Mechanism of activation of beta-D-2- deoxy-2-fluoro-2-C-methylcytidine and inhibition of hepatitis C virus NS5B RNA polymerase
    • Murakami E, Bao HY, Ramesh M, et al. Mechanism of activation of beta-D-2- deoxy-2-fluoro-2-C-methylcytidine and inhibition of hepatitis C virus NS5B RNA polymerase. Antimicrob Agents Chemother 2007; 51:503-509.
    • (2007) Antimicrob Agents Chemother , vol.51 , pp. 503-509
    • Murakami, E.1    Bao, H.Y.2    Ramesh, M.3
  • 62
    • 84877730954 scopus 로고    scopus 로고
    • Sofosbuvir for previously untreated chronic hepatitis C infection
    • Lawitz E, Mangia A, Wyles D, et al. Sofosbuvir for previously untreated chronic hepatitis C infection. N Engl J Med 2013; 368:1878-1887.
    • (2013) N Engl J Med , vol.368 , pp. 1878-1887
    • Lawitz, E.1    Mangia, A.2    Wyles, D.3
  • 63
    • 84877739274 scopus 로고    scopus 로고
    • Sofosbuvir for hepatitis C genotype 2 or 3 in patients without treatment options
    • Jacobson IM, Gordon SC, Kowdley KV, et al. Sofosbuvir for hepatitis C genotype 2 or 3 in patients without treatment options. N Engl J Med 2013; 368:1867-1877.
    • (2013) N Engl J Med , vol.368 , pp. 1867-1877
    • Jacobson, I.M.1    Gordon, S.C.2    Kowdley, K.V.3
  • 64
    • 84878976866 scopus 로고    scopus 로고
    • Sofosbuvir with pegylated interferon alfa-2a and ribavirin for treatment-naive patients with hepatitis C genotype-1 infection (ATOMIC): An open-label, randomised, multicentre phase 2 trial
    • Kowdley KV, Lawitz E, Crespo I, et al. Sofosbuvir with pegylated interferon alfa-2a and ribavirin for treatment-naive patients with hepatitis C genotype-1 infection (ATOMIC): an open-label, randomised, multicentre phase 2 trial. Lancet 2013; 381:2100-2107.
    • (2013) Lancet , vol.381 , pp. 2100-2107
    • Kowdley, K.V.1    Lawitz, E.2    Crespo, I.3
  • 65
    • 84871814966 scopus 로고    scopus 로고
    • Nucleotide polymerase inhibitor sofosbuvir plus ribavirin for hepatitis C
    • Gane EJ, Stedman CA, Hyland RH, et al. Nucleotide polymerase inhibitor sofosbuvir plus ribavirin for hepatitis C. N Engl J Med 2013; 368:34-44.
    • (2013) N Engl J Med , vol.368 , pp. 34-44
    • Gane, E.J.1    Stedman, C.A.2    Hyland, R.H.3


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