-
1
-
-
0028560018
-
Therapeutical potential of PMEA as an antiviral drug
-
(a) Naesens, L.; Balzarini, J.; De Clercq, E. Therapeutical potential of PMEA as an antiviral drug. Med. Virol. 1994, 4, 147-159.
-
(1994)
Med. Virol.
, vol.4
, pp. 147-159
-
-
Naesens, L.1
Balzarini, J.2
De Clercq, E.3
-
2
-
-
0025837774
-
Broad-spectrum anti-DNA virus and anti-retrovirus activity of phosphonylmethoxyalkylpurines and -pyrimidines
-
(b) De Clercq, E. Broad-spectrum anti-DNA virus and anti-retrovirus activity of phosphonylmethoxyalkylpurines and -pyrimidines. Biochem. Pharmacol. 1991, 42, 963-972.
-
(1991)
Biochem. Pharmacol.
, vol.42
, pp. 963-972
-
-
De Clercq, E.1
-
3
-
-
0022450584
-
A novel selective broad-spectrum anti-DNA virus agent
-
(c) De Clercq, E.; Holy, A.; Rosenberg, I.; Sakuma, T.; Balzarini, J.; Maudgal, P. C. A novel selective broad-spectrum anti-DNA virus agent. Nature 1986, 323, 464-467.
-
(1986)
Nature
, vol.323
, pp. 464-467
-
-
De Clercq, E.1
Holy, A.2
Rosenberg, I.3
Sakuma, T.4
Balzarini, J.5
Maudgal, P.C.6
-
4
-
-
0035997915
-
Cidofovir in the treatment of poxvirus infections
-
(d) De Clercq, E. Cidofovir in the treatment of poxvirus infections. Antiviral Res. 2002, 55, 1-13.
-
(2002)
Antiviral Res
, vol.55
, pp. 1-13
-
-
De Clercq, E.1
-
5
-
-
33645430256
-
Orally bioavailable acyclic nucleoside phosphonate prodrugs: Adefovir dipivoxil and Ms(POC)PMPA
-
De Clercq E., Ed.; JAI Press: Stamford, CT
-
(e) Arimilli, M. N.; Dougherty, J. P.; Cundy K. C.; Bischofberger, N. Orally bioavailable acyclic nucleoside phosphonate prodrugs: Adefovir dipivoxil and Ms(POC)PMPA. In Advances in Antiviral Drug Design; De Clercq E., Ed.; JAI Press: Stamford, CT, 1999; pp 69-91.
-
(1999)
Advances in Antiviral Drug Design
, pp. 69-91
-
-
Arimilli, M.N.1
Dougherty, J.P.2
Cundy, K.C.3
Bischofberger, N.4
-
6
-
-
0031916651
-
Anti-human immunodeficiency virus activity and cellular metabolism of a potential prodrug of the acyclic nucleoside phosphonate 9-R-(2- phosphonomethoxypropyl)adenine (PMPA), bis(isopropyloxymethylcarbonyl)PMPA
-
(f) Robbins, B. L.; Srinivas, R. V.; Kim, C.; Bischofberger, N.; Fridland, A. Anti-Human Immunodeficiency Virus Activity and Cellular Metabolism of a Potential Prodrug of the Acyclic Nucleoside Phosphonate 9-R-(2-Phosphonomethoxypropyl)adenine (PMPA), Bis(isopropyloxymethylcarbonyl) PMPA. Antimicrob. Agents Chemother. 1998, 42, 612-617.
-
(1998)
Antimicrob. Agents Chemother.
, vol.42
, pp. 612-617
-
-
Robbins, B.L.1
Srinivas, R.V.2
Kim, C.3
Bischofberger, N.4
Fridland, A.5
-
7
-
-
0027440278
-
Metabolism an 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.; Fridland, A. Metabolism an in vitro Antiretroviral Activities of Bis(Pivaloyloxymethyl)-Prodrugs of Acyclic Nucleoside Phosphonates. Antimicrob. Agents Chemother. 1993, 37, 2247-2250.
-
(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
-
8
-
-
0026739035
-
Synthesis and in vitro evaluation of a phosphonate prodrug: Bis(pivaloylosymethyl)9-(2-phosphonylmethoxyethyl)adenine
-
Starrett Jr., J. E.; Tortolani, D. R.; Hitchcock, M. J. M.; Martin, J. C.; Mansuri, M. M. Synthesis and in vitro evaluation of a phosphonate prodrug: bis(pivaloylosymethyl)9-(2-phosphonylmethoxyethyl)adenine. Antiviral Res. 1992, 19, 267-273.
-
(1992)
Antiviral Res.
, vol.19
, pp. 267-273
-
-
Starrett Jr., J.E.1
Tortolani, D.R.2
Hitchcock, M.J.M.3
Martin, J.C.4
Mansuri, M.M.5
-
9
-
-
0029731207
-
Synthesis, in vitro antiviral evaluation, and stability studies of bis(S-acyl-2-thioethyl) ester derivatives of 9-(2-phosphonometoxy)ethyladenine (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.; Gosselin, G. Synthesis, in vitro antiviral evaluation, and stability studies of bis(S-acyl-2-thioethyl) ester derivatives of 9-(2-phosphonometoxy)ethyladenine (PMEA) as potential PMEA prodrugs with improved oral bioavailability. J. Med. Chem. 1996, 39, 4958-4965.
-
(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
-
10
-
-
0036595701
-
CycloSal-pronucleotides - Design of chemical trojan horses
-
(a) Meier, C. CycloSal-pronucleotides - design of chemical trojan horses. Mini Rev. Med. Chem. 2002, 2, 219-234.
-
(2002)
Mini Rev. Med. Chem.
, vol.2
, pp. 219-234
-
-
Meier, C.1
-
11
-
-
3042561444
-
Lock-in-cycloSal-pronucleotides - A new generation of chemical trojan horses
-
(b) Meier, C.; Ruppel, M.; Vukadinovic, D.; Balzarini, J. "Lock-in"-cycloSal-pronucleotides - a new generation of chemical trojan horses. Mini Rev. Med. Chem. 2004, 4, 383-394.
-
(2004)
Mini Rev. Med. Chem.
, vol.4
, pp. 383-394
-
-
Meier, C.1
Ruppel, M.2
Vukadinovic, D.3
Balzarini, J.4
-
12
-
-
24344433696
-
CycloSal-pronucleotides - Design of the concept, chemistry and antiviral acticity
-
De Clercq, E., Ed.; JAI Press: Stamford, CT
-
(c) Meier, C. CycloSal-pronucleotides - design of the concept, chemistry and antiviral acticity. In Advances in Antiviral Drug Design; De Clercq, E., Ed.; JAI Press: Stamford, CT, 2004; Vol. 4, pp 147-213.
-
(2004)
Advances in Antiviral Drug Design
, vol.4
, pp. 147-213
-
-
Meier, C.1
-
13
-
-
0032560234
-
CycloSal-2′,3′-dideoxy-2′,3′-didehydrothymidine monophosphate (cycloSal-d4TMP): Synthesis and antiviral evaluation of a new d4TMP delivery system
-
(a) Meier, C.; Lorey, M.; De Clercq, E.; Balzarini, J. CycloSal-2′,3′-dideoxy-2′,3′-didehydrothymidine monophosphate (cycloSal-d4TMP): Synthesis and antiviral evaluation of a new d4TMP delivery system. J. Med. Chem. 1998, 41, 1417-1427.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 1417-1427
-
-
Meier, C.1
Lorey, M.2
De Clercq, E.3
Balzarini, J.4
-
14
-
-
0346732153
-
3,5-Tert-butyl-6-fluoro-cycloSal-d4TMP - A pronucleotide with a highly optimized masking group
-
(b) Ducho, C.; Wendicke, S.; Görbig, U.; Balzarini, J.; Meier, C. 3,5-tert-Butyl-6-fluoro-cycloSal-d4TMP - a pronucleotide with a highly optimized masking group. Eur. J. Org. Chem. 2003, 4786-4791.
-
(2003)
Eur. J. Org. Chem.
, pp. 4786-4791
-
-
Ducho, C.1
Wendicke, S.2
Görbig, U.3
Balzarini, J.4
Meier, C.5
-
15
-
-
0037038326
-
CycloSal-BVDUMP pronucleotides - How to convert an anti-EBV-inactive nucleoside analogue into a bioactive compound
-
Meier, C.; Lomp, A.; Meerbach, A.; P. Wutzier, P. CycloSal-BVDUMP pronucleotides - How to convert an anti-EBV-inactive nucleoside analogue into a bioactive compound. J. Med. Chem. 2002, 45, 5157-5172.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 5157-5172
-
-
Meier, C.1
Lomp, A.2
Meerbach, A.3
Wutzier, P.P.4
-
16
-
-
1542785031
-
Second generation of cycloSal-pronucleotides with esterase-cleavable sites - The "lock-in"-concept
-
Meier, C.; Ruppel, M.; Vukadinovic, D.; Balzarini, J. Second generation of cycloSal-pronucleotides with esterase-cleavable sites - the "lock-in"-concept. Nucl., Nucl., Nucleic Acids 2004, 89-115.
-
(2004)
Nucl., Nucl., Nucleic Acids
, pp. 89-115
-
-
Meier, C.1
Ruppel, M.2
Vukadinovic, D.3
Balzarini, J.4
-
17
-
-
0027433373
-
Intracellular delivery of nucleoside monophosphates through a reductase-mediated activation process
-
Puech, F.; Gosselin, G.; Lefebvre, I.; Pompom, A.; Aubertin, A.-M.; Kim, A.; Imbach, J.-L. Intracellular delivery of nucleoside monophosphates through a reductase-mediated activation process. Antiviral Res. 1993, 22, 155-174.
-
(1993)
Antiviral Res
, vol.22
, pp. 155-174
-
-
Puech, F.1
Gosselin, G.2
Lefebvre, I.3
Pompom, A.4
Aubertin, A.-M.5
Kim, A.6
Imbach, J.-L.7
-
19
-
-
0028925262
-
Synthesis and in vivo evaluation of prodrugs of 9-[2-(phosphonomethoxy) ethoxy]adenine
-
(b) Serafinowska, H. T.; Ashton, A. J.; Bailey, S.; Harnden, M. R.; Jackson, S. M.; Sutton, D. Synthesis and in vivo evaluation of prodrugs of 9-[2-(phosphonomethoxy)ethoxy]adenine. J. Med. Chem. 1995, 38, 1372-1379.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 1372-1379
-
-
Serafinowska, H.T.1
Ashton, A.J.2
Bailey, S.3
Harnden, M.R.4
Jackson, S.M.5
Sutton, D.6
-
20
-
-
11144357250
-
450 3A-activated prodrugs (HepDirect prodrugs) useful for targeting phosph(on)ate-based drugs to the liver
-
450 3A-activated prodrugs (HepDirect prodrugs) useful for targeting phosph(on)ate-based drugs to the liver. J. Am. Chem. Soc. 2004, 126, 5154-5163.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 5154-5163
-
-
Erion, M.D.1
Reddy, K.R.2
Boyer, S.H.3
Matelich, M.C.4
Gomez-Galeno, J.5
Lemus, R.H.6
Ugarkar, B.G.7
Colby, T.J.8
Schanzer, J.9
Poelje, P.D.10
-
21
-
-
0024520447
-
Estimation of the lipophilicity of anti-HIV nucleoside analogues by determination of the partition coefficient and retention time on a LiChrosphere 60 RP-8 HPLC column
-
Balzarini, J.; Cools, J. M.; De Clercq, E. Estimation of the lipophilicity of anti-HIV nucleoside analogues by determination of the partition coefficient and retention time on a LiChrosphere 60 RP-8 HPLC column. Biochem. Biophys. Res. Commun. 1989, 158, 413-422.
-
(1989)
Biochem. Biophys. Res. Commun.
, vol.158
, pp. 413-422
-
-
Balzarini, J.1
Cools, J.M.2
De Clercq, E.3
-
22
-
-
0033789009
-
Cyclosaligenyl-2′,3′-didehydro-2′,3′- dideoxythymidine monophosphate: Efficient intracellular delivery of d4TMP
-
(a) Balzarini, J.; Aquaro, S.; Knispel, T.; Rampazzo, C.; Bianchi, V.; Perno, C.-F.; De Clercq, E.; Meier, C. Cyclosaligenyl-2′,3′- didehydro-2′,3′-dideoxythymidine monophosphate: Efficient intracellular delivery of d4TMP. Mol. Pharmacol. 2000, 58, 928-935.
-
(2000)
Mol. Pharmacol.
, vol.58
, pp. 928-935
-
-
Balzarini, J.1
Aquaro, S.2
Knispel, T.3
Rampazzo, C.4
Bianchi, V.5
Perno, C.-F.6
De Clercq, E.7
Meier, C.8
-
23
-
-
0032731244
-
Intracellular metabolism of cycloSaligenyl 3′-azido-2′, 3′-dideoxythymidine monophosphate, a prodrug of 3′-azido-2′, 3′-dideoxythymidine (Zidovudine)
-
(b) Balzarini, J.; Naesens, L.; Aquaro, S.; Knispel, T.; Perno, C.-F.; De Clercq, E.; Meier, C. Intracellular metabolism of cycloSaligenyl 3′-azido-2′,3′-dideoxythymidine monophosphate, a prodrug of 3′-azido-2′,3′-dideoxythymidine (Zidovudine). Mol. Pharmacol. 1999, 56, 1354-1361.
-
(1999)
Mol. Pharmacol.
, vol.56
, pp. 1354-1361
-
-
Balzarini, J.1
Naesens, L.2
Aquaro, S.3
Knispel, T.4
Perno, C.-F.5
De Clercq, E.6
Meier, C.7
-
24
-
-
11744329951
-
Mechanisms of nucleophilic substitution in phosphate esters
-
Cox, Jr., J. R.; Ramsay, B. Mechanisms of nucleophilic substitution in phosphate esters. Chem. Rev. 1964, 64, 317-352.
-
(1964)
Chem. Rev.
, vol.64
, pp. 317-352
-
-
Cox Jr., J.R.1
Ramsay, B.2
-
25
-
-
0011216501
-
The hydrolysis of phosphonate esters
-
Hudson, R. F.; Keay, L. The hydrolysis of phosphonate esters. J. Chem. Soc. 1956, 2463-2469.
-
(1956)
J. Chem. Soc.
, pp. 2463-2469
-
-
Hudson, R.F.1
Keay, L.2
-
26
-
-
33845278824
-
Rates and mechanisms of hydrolysis of esters of phosphorous acid
-
Westheimer, F. H.; Huang, S.; Covitz, F. Rates and mechanisms of hydrolysis of esters of phosphorous acid. J. Am. Chem. Soc. 1988, 110, 181-185.
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 181-185
-
-
Westheimer, F.H.1
Huang, S.2
Covitz, F.3
-
27
-
-
0141607488
-
CycloSal-d4TMP pronucleotides - Structural variations, mechanistic insights and antiviral activity
-
Meier, C.; Renze, J.; Ducho, C.; Balzarini, J. CycloSal-d4TMP pronucleotides - Structural variations, mechanistic insights and antiviral activity. Curr. Top. Med. Chem. 2002, 2, 1111-1121.
-
(2002)
Curr. Top. Med. Chem.
, vol.2
, pp. 1111-1121
-
-
Meier, C.1
Renze, J.2
Ducho, C.3
Balzarini, J.4
-
28
-
-
0035938424
-
Synthesis and evaluation of novel amidate prodrugs of PMEA and PMPA
-
Balatore, C.; McGuigan, C.; De Clercq, E.; Balzarini, J. Synthesis and evaluation of novel amidate prodrugs of PMEA and PMPA. Bioorg. Med. Chem. Lett. 2001, 11, 1053-1056.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 1053-1056
-
-
Balatore, C.1
McGuigan, C.2
De Clercq, E.3
Balzarini, J.4
-
29
-
-
0141537114
-
Noninhibition of acetylcholinesterase by cycloSal-nucleotides
-
Ducho, C.; Balzarini, J.; Meier, C. Noninhibition of acetylcholinesterase by cycloSal-nucleotides. Nucl., Nucl., Nucleic Acids 2003, 22, 841-843.
-
(2003)
Nucl., Nucl., Nucleic Acids
, vol.22
, pp. 841-843
-
-
Ducho, C.1
Balzarini, J.2
Meier, C.3
-
30
-
-
2442717713
-
Interaction of eycloSal-pronucleotides with cholinesterases from different origins - A structure-activity relationship
-
Meier, C.; Ducho, C.; Görbig, U.; Esnouf, R.; Balzarini, J. Interaction of eycloSal-pronucleotides with cholinesterases from different origins - A structure-activity relationship. J. Med. Chem. 2004, 47, 2839-2852.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 2839-2852
-
-
Meier, C.1
Ducho, C.2
Görbig, U.3
Esnouf, R.4
Balzarini, J.5
-
31
-
-
0001153009
-
Synthesis of 9-[2-(phosphonylmethoxy)-ethyl]adenine and related compounds
-
Holy, A.; Rosenberg, I. Synthesis of 9-[2-(phosphonylmethoxy)-ethyl] adenine and related compounds. Collect. Czech. Chem. Commun. 1987, 52, 2801-2809.
-
(1987)
Collect. Czech. Chem. Commun.
, vol.52
, pp. 2801-2809
-
-
Holy, A.1
Rosenberg, I.2
-
32
-
-
0024373015
-
Synthesis and antiviral activity of the nucleotide analogue (S)-1-[3-hydroxy-2-(phosphonylmethoxy)propyl]-cytosine
-
Bronson, J. J.; Ghazzouli, I., Hitchcock, M. J. M.; Webb, R. R., II.; Martin, J. C. Synthesis and antiviral activity of the nucleotide analogue (S)-1-[3-hydroxy-2-(phosphonylmethoxy)propyl]-cytosine. J. Med Chem. 1989, 32, 1457-1463.
-
(1989)
J. Med Chem.
, vol.32
, pp. 1457-1463
-
-
Bronson, J.J.1
Ghazzouli, I.2
Hitchcock, M.J.M.3
Webb II, R.R.4
Martin, J.C.5
-
33
-
-
0021237243
-
Detection, isolation, and continuous production of cytopathic retroviruses (HTLV-III) from patients with AIDS and pre-AIDS
-
Popovic, M.; Sarngadharan, M. G.; Read, E.; Gallo, R. C. Detection, Isolation, and continuous production of cytopathic retroviruses (HTLV-III) from patients with AIDS and pre-AIDS. Science 1984, 224, 497-500.
-
(1984)
Science
, vol.224
, pp. 497-500
-
-
Popovic, M.1
Sarngadharan, M.G.2
Read, E.3
Gallo, R.C.4
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