-
1
-
-
0034966673
-
Antiviral drugs: Current state of the art
-
De Clercq, E. Antiviral drugs: Current state of the art. J. Clin. Virol. 2001, 22, 73-89.
-
(2001)
J. Clin. Virol
, vol.22
, pp. 73-89
-
-
De Clercq, E.1
-
2
-
-
0033165851
-
-
Meyer, P. R.; Matsuura, S. E.; Mian, A. M.; So, A. G.; Scott, W. A. A mechanism of AZT resistance: An increase in nucleotide-dependent primer unblocking by mutant HIV-1 reverse transcriptase. Mol. Cell. 1999, 4, 35-43.
-
Meyer, P. R.; Matsuura, S. E.; Mian, A. M.; So, A. G.; Scott, W. A. A mechanism of AZT resistance: An increase in nucleotide-dependent primer unblocking by mutant HIV-1 reverse transcriptase. Mol. Cell. 1999, 4, 35-43.
-
-
-
-
3
-
-
0032506055
-
Phenotypic mechanism of HIV-1 resistance to 3′-azido-3′- deoxythymidine (AZT): Increased polymerization processivity and enhanced sensitivity to pyrophosphate of the mutant viral reverse transcriptase
-
Arion, D.; Kaushik, N.; McCormick, S.; Borkow, G.; Parniak, M. A. Phenotypic mechanism of HIV-1 resistance to 3′-azido-3′- deoxythymidine (AZT): Increased polymerization processivity and enhanced sensitivity to pyrophosphate of the mutant viral reverse transcriptase. Biochemistry 1998, 37, 15908-15917.
-
(1998)
Biochemistry
, vol.37
, pp. 15908-15917
-
-
Arion, D.1
Kaushik, N.2
McCormick, S.3
Borkow, G.4
Parniak, M.A.5
-
4
-
-
19444384266
-
Molecular Mechanisms of resistance to nucleoside analogue inhibitors of human immunodeficiency virus reverse transcriptase. Drug Des. Rev
-
Menendez-Arias, L.; Matamoros, T.; Deval, J.; Canard, B. Molecular Mechanisms of resistance to nucleoside analogue inhibitors of human immunodeficiency virus reverse transcriptase. Drug Des. Rev.-Online 2005, 2, 101-113.
-
(2005)
Online
, vol.2
, pp. 101-113
-
-
Menendez-Arias, L.1
Matamoros, T.2
Deval, J.3
Canard, B.4
-
5
-
-
0033990454
-
Boranophosphate backbone: A mimic of phosphodiesters, phosphorothioates, and methyl phosphonates
-
Shaw, B. R.; Sergueev, D.; He, K.; Porter, K.; Summers, J.; Sergueeva, Z.; Rait, V. Boranophosphate backbone: A mimic of phosphodiesters, phosphorothioates, and methyl phosphonates. Methods Enzymol 2000, 313, 226-257.
-
(2000)
Methods Enzymol
, vol.313
, pp. 226-257
-
-
Shaw, B.R.1
Sergueev, D.2
He, K.3
Porter, K.4
Summers, J.5
Sergueeva, Z.6
Rait, V.7
-
6
-
-
0026464493
-
Boron neutron capture therapy for cancer, realities and prospects
-
Barth, R. F.; Soloway, A. H.; Fairchild, R. G.; Brugger, R. M. Boron neutron capture therapy for cancer, realities and prospects. Cancer 1992, 70, 2995-3007.
-
(1992)
Cancer
, vol.70
, pp. 2995-3007
-
-
Barth, R.F.1
Soloway, A.H.2
Fairchild, R.G.3
Brugger, R.M.4
-
7
-
-
5444224668
-
Reading, writing, and modulating genetic information with boranophosphate mimics of nucleotides, DNA, and RNA
-
Shaw, B. R.; Dobrikov, M.; Wang, X.; Wan, J.; He, K.; Lin, J. L.; Li, P.; Rait, V.; Sergueeva, Z. A.; Sergueev, D. Reading, writing, and modulating genetic information with boranophosphate mimics of nucleotides, DNA, and RNA. Ann. N. Y. Acad. Sci. 2003, 1002, 12-29.
-
(2003)
Ann. N. Y. Acad. Sci
, vol.1002
, pp. 12-29
-
-
Shaw, B.R.1
Dobrikov, M.2
Wang, X.3
Wan, J.4
He, K.5
Lin, J.L.6
Li, P.7
Rait, V.8
Sergueeva, Z.A.9
Sergueev, D.10
-
8
-
-
20244364115
-
Synthesis of 2′,3′-dideoxynucleoside 5′-α-P-borano- β,γ-(difluoromethylene)triphosphates and their inhibition of HIV-1 reverse transcriptase
-
Boyle, N. A.; Rajwanshi, V. K.; Prhavc, M.; Wang, G.; Fagan, P.; Chen, F.; Ewing, G. J.; Brooks, J. L.; Hurd, T.; Leeds, J. M.; Bruice, T. W.; Cook, P. D. Synthesis of 2′,3′-dideoxynucleoside 5′-α-P-borano- β,γ-(difluoromethylene)triphosphates and their inhibition of HIV-1 reverse transcriptase. J. Med. Chem. 2005, 48, 2695-2700.
-
(2005)
J. Med. Chem
, vol.48
, pp. 2695-2700
-
-
Boyle, N.A.1
Rajwanshi, V.K.2
Prhavc, M.3
Wang, G.4
Fagan, P.5
Chen, F.6
Ewing, G.J.7
Brooks, J.L.8
Hurd, T.9
Leeds, J.M.10
Bruice, T.W.11
Cook, P.D.12
-
9
-
-
0034679569
-
Structural basis for activation of alpha-boranophosphate nucleotide analogues targeting drug-resistant reverse transcriptase
-
Meyer, P.; Schneider, B.; Sarfati, S.; Deville-Bonne, D.; Guerreiro, C.; Boretto, J.; Janin, J.; Veron, M.; Canard, B. Structural basis for activation of alpha-boranophosphate nucleotide analogues targeting drug-resistant reverse transcriptase. EMBO J. 2000, 19, 3520-3529.
-
(2000)
EMBO J
, vol.19
, pp. 3520-3529
-
-
Meyer, P.1
Schneider, B.2
Sarfati, S.3
Deville-Bonne, D.4
Guerreiro, C.5
Boretto, J.6
Janin, J.7
Veron, M.8
Canard, B.9
-
10
-
-
0036829992
-
The molecular mechanism of multidrug resistance by the Q151M human immunodeficiency virus type 1 reverse transcriptase and its suppression using alpha-boranophosphate nucleotide analogues
-
Deval, J.; Selmi, B.; Boretto, J.; Egloff, M. P.; Guerreiro, C.; Sarfati, S.; Canard, B. The molecular mechanism of multidrug resistance by the Q151M human immunodeficiency virus type 1 reverse transcriptase and its suppression using alpha-boranophosphate nucleotide analogues. J. Biol. Chem. 2002, 277, 42097-42104.
-
(2002)
J. Biol. Chem
, vol.277
, pp. 42097-42104
-
-
Deval, J.1
Selmi, B.2
Boretto, J.3
Egloff, M.P.4
Guerreiro, C.5
Sarfati, S.6
Canard, B.7
-
11
-
-
13544271167
-
Mechanistic insights into the suppression of drug resistance by human immunodeficiency virus type 1 reverse transcriptase using alpha-boranophosphate nucleoside analogs
-
Deval, J.; Alvarez, K.; Selmi, B.; Bermond, M.; Boretto, J.; Guerreiro, C.; Mulard, L.; Canard, B. Mechanistic insights into the suppression of drug resistance by human immunodeficiency virus type 1 reverse transcriptase using alpha-boranophosphate nucleoside analogs. J. Biol. Chem. 2005, 280, 3838-3846.
-
(2005)
J. Biol. Chem
, vol.280
, pp. 3838-3846
-
-
Deval, J.1
Alvarez, K.2
Selmi, B.3
Bermond, M.4
Boretto, J.5
Guerreiro, C.6
Mulard, L.7
Canard, B.8
-
12
-
-
26644475653
-
Borano-nucleotides: New analogues to circumvent HIV-1RT-mediated nucleoside drugs resistance
-
Alvarez, K.; Deval, J.; Selmi, B.; Barral, K.; Boretto, J.; Guerreiro, C.; Mulard, L.; Sarfati, S.; Canard, B. Borano-nucleotides: New analogues to circumvent HIV-1RT-mediated nucleoside drugs resistance. Nucleosides, Nucleotides Nucleic Acids 2005, 24, 419-422.
-
(2005)
Nucleosides, Nucleotides Nucleic Acids
, vol.24
, pp. 419-422
-
-
Alvarez, K.1
Deval, J.2
Selmi, B.3
Barral, K.4
Boretto, J.5
Guerreiro, C.6
Mulard, L.7
Sarfati, S.8
Canard, B.9
-
13
-
-
0026020310
-
Intracellular metabolism and mechanism of anti-retrovirus action of 9-(2-phosphonylmethoxyethyl)adenine, a potent anti-human immunodeficiency virus compound
-
Balzarini, J.; Hao, Z.; Herdewijn, P.; Johns, D. G.; De Clercq, E. Intracellular metabolism and mechanism of anti-retrovirus action of 9-(2-phosphonylmethoxyethyl)adenine, a potent anti-human immunodeficiency virus compound. Proc. Natl. Acad. Sci. U.S.A. 1991, 88, 1499-1503.
-
(1991)
Proc. Natl. Acad. Sci. U.S.A
, vol.88
, pp. 1499-1503
-
-
Balzarini, J.1
Hao, Z.2
Herdewijn, P.3
Johns, D.G.4
De Clercq, E.5
-
14
-
-
0032538456
-
Selective inhibition of HIV-1 reverse transcriptase by an antiviral inhibitor, (R)-9-(2-phosphonyl-methoxypropyl) adenine
-
Suo, Z.; Johnson, K. A. Selective inhibition of HIV-1 reverse transcriptase by an antiviral inhibitor, (R)-9-(2-phosphonyl-methoxypropyl) adenine. J. Biol. Chem. 1998, 273, 27250-27258.
-
(1998)
J. Biol. Chem
, vol.273
, pp. 27250-27258
-
-
Suo, Z.1
Johnson, K.A.2
-
15
-
-
0345138983
-
Phosphonomethoxyalkyl analogues of nucleotides
-
Holy, A. Phosphonomethoxyalkyl analogues of nucleotides. Curr. Pharm. Des. 2003, 9, 2567-2592.
-
(2003)
Curr. Pharm. Des
, vol.9
, pp. 2567-2592
-
-
Holy, A.1
-
16
-
-
27844455955
-
Acyclic nucleoside phosphonates: A key class of antiviral drugs
-
De Clercq, E.; Holy, A. Acyclic nucleoside phosphonates: A key class of antiviral drugs. Nat. Rev. Drug Discovery 2005, 4, 928-940.
-
(2005)
Nat. Rev. Drug Discovery
, vol.4
, pp. 928-940
-
-
De Clercq, E.1
Holy, A.2
-
17
-
-
0142126681
-
Clinical potential of the acyclic nucleoside phosphonates cidofovir, adefovir, and tenofovir in treatment of DNA virus and retrovirus infections
-
De Clercq, E. Clinical potential of the acyclic nucleoside phosphonates cidofovir, adefovir, and tenofovir in treatment of DNA virus and retrovirus infections. Clin. Microbiol. Rev. 2003, 16, 569-596.
-
(2003)
Clin. Microbiol. Rev
, vol.16
, pp. 569-596
-
-
De Clercq, E.1
-
18
-
-
0346502201
-
Gateways to clinical trials
-
Bayes, M.; Rabasseda, X.; Prous, J. R. Gateways to clinical trials. Methods Find. Exp. Clin. Pharmacol. 2003, 25, 53-76.
-
(2003)
Methods Find. Exp. Clin. Pharmacol
, vol.25
, pp. 53-76
-
-
Bayes, M.1
Rabasseda, X.2
Prous, J.R.3
-
19
-
-
0034850922
-
Borane-amine complexes-Versatile reagents in the chemistry of nucleic acids and their analogs
-
Sergueeva, Z. A.; Sergueev, D. S.; Shaw, B. R. Borane-amine complexes-Versatile reagents in the chemistry of nucleic acids and their analogs. Nucleosides, Nucleotides Nucleic Acids 2001, 20, 941-945.
-
(2001)
Nucleosides, Nucleotides Nucleic Acids
, vol.20
, pp. 941-945
-
-
Sergueeva, Z.A.1
Sergueev, D.S.2
Shaw, B.R.3
-
20
-
-
0032560927
-
H-phosphonate approach for solid-phase synthesis of oligodeoxyribonucleoside boranophosphates and their characterization
-
Sergueev, D. S.; Ramsay Shaw, B. H-phosphonate approach for solid-phase synthesis of oligodeoxyribonucleoside boranophosphates and their characterization. J. Am. Chem. Soc. 1998, 120, 9417-9427.
-
(1998)
J. Am. Chem. Soc
, vol.120
, pp. 9417-9427
-
-
Sergueev, D.S.1
Ramsay Shaw, B.2
-
21
-
-
0035950081
-
Design, synthesis, and biological evaluation of novel nucleoside and nucleotide analogues as agents against DNA viruses and/or retrovirases
-
Hakimelahi, G. H.; Ly, T. W.; Moosavi-Movahedi, A. A.; Jain, M. L.; Zakerinia, M.; Davari, H.; Mei, H.-C.; Sambaiah, T.; Moshfegh, A. A.; Hakimelahi, S. Design, synthesis, and biological evaluation of novel nucleoside and nucleotide analogues as agents against DNA viruses and/or retrovirases. J. Med. Chem. 2001, 44, 3710-3720.
-
(2001)
J. Med. Chem
, vol.44
, pp. 3710-3720
-
-
Hakimelahi, G.H.1
Ly, T.W.2
Moosavi-Movahedi, A.A.3
Jain, M.L.4
Zakerinia, M.5
Davari, H.6
Mei, H.-C.7
Sambaiah, T.8
Moshfegh, A.A.9
Hakimelahi, S.10
-
22
-
-
0032473894
-
Practical synthesis of the anti-HIV drug, PMPA
-
Schultze, L. M.; Chapman, H. H.; Dubree, N. J. P.; Jones, R. J.; Kent, K. M.; Lee, T. T.; Louie, M. S.; Postich, M. J.; Prisbe, E. J.; Pohloff, J. C.; Yu, R. H. Practical synthesis of the anti-HIV drug, PMPA. Tetrahedron Lett. 1998, 39, 1853-1856.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 1853-1856
-
-
Schultze, L.M.1
Chapman, H.H.2
Dubree, N.J.P.3
Jones, R.J.4
Kent, K.M.5
Lee, T.T.6
Louie, M.S.7
Postich, M.J.8
Prisbe, E.J.9
Pohloff, J.C.10
Yu, R.H.11
-
23
-
-
0036420227
-
Synthesis, kinetics, and molecular docking of novel 9-(2-hydroxypropyl)purine nucleoside analogs as ligands of herpesviral thymidine kinases
-
Pospisil, P.; Pilger, B. D.; Marveggio, S.; Schelling, P.; Wurth, C.; Scapozza, L.; Folkers, G. Synthesis, kinetics, and molecular docking of novel 9-(2-hydroxypropyl)purine nucleoside analogs as ligands of herpesviral thymidine kinases. Helv. Chim. Acta 2002, 85, 3237-3250.
-
(2002)
Helv. Chim. Acta
, vol.85
, pp. 3237-3250
-
-
Pospisil, P.1
Pilger, B.D.2
Marveggio, S.3
Schelling, P.4
Wurth, C.5
Scapozza, L.6
Folkers, G.7
-
24
-
-
37049069402
-
Synthesis and biological activity of the diphosphorylphosphonate derivatives of (+)-cis-9-(4′-hydroxycyclopent-2′-enyl)guanine and (-)-cis-9-(4′-hydroxycyclopent-2′-enyl)guanine
-
Merlo, V.; Roberts, S. M.; Storer, R.; Bethell, R. C. Synthesis and biological activity of the diphosphorylphosphonate derivatives of (+)-cis-9-(4′-hydroxycyclopent-2′-enyl)guanine and (-)-cis-9-(4′-hydroxycyclopent-2′-enyl)guanine. J. Chem. Soc., Perkin Trans, 1 1994, 11, 1477-1481.
-
(1994)
J. Chem. Soc., Perkin Trans, 1
, vol.11
, pp. 1477-1481
-
-
Merlo, V.1
Roberts, S.M.2
Storer, R.3
Bethell, R.C.4
-
25
-
-
0034647731
-
Synthesis of acyclic nucleoside and nucleotide analogues from amino acids: A convenient approach to a PMEA-PMPA hybrid
-
Jeffery, A. L.; Kim, J.-H.; Wiemer, D. F. Synthesis of acyclic nucleoside and nucleotide analogues from amino acids: A convenient approach to a PMEA-PMPA hybrid. Tetrahedron 2000, 56, 5077-5083.
-
(2000)
Tetrahedron
, vol.56
, pp. 5077-5083
-
-
Jeffery, A.L.1
Kim, J.-H.2
Wiemer, D.F.3
-
26
-
-
0000976107
-
A facile synthesis of 1,2-bis-(phosphino)benzene and related alkylated species
-
Kyba, E. P.; Liu, S.-T.; Harris, R. L. A facile synthesis of 1,2-bis-(phosphino)benzene and related alkylated species. Organometallics 1983, 2, 1877-1879.
-
(1983)
Organometallics
, vol.2
, pp. 1877-1879
-
-
Kyba, E.P.1
Liu, S.-T.2
Harris, R.L.3
-
27
-
-
0037102984
-
User-friendly' primary phosphines and an arsine: Synthesis and characterization of new air-stable ligands incorporating the ferrocenyl group
-
Henderson, W.; Alley, S. R. 'User-friendly' primary phosphines and an arsine: Synthesis and characterization of new air-stable ligands incorporating the ferrocenyl group. J. Organomet. Chem. 2002, 656, 120-128.
-
(2002)
J. Organomet. Chem
, vol.656
, pp. 120-128
-
-
Henderson, W.1
Alley, S.R.2
-
29
-
-
0000241132
-
Synthesis and structural-analysis of 5-deoxy-5-C-(hydroxyphosphinyl)-xylopyranose and 5-deoxy-5-C-(hydroxyphosphinyl) -glucopyranose
-
Yamamoto, H.; Hanaya, T.; Kawamoto, H.; Inokawa, S.; Yamashita, M.; Armour, M.-A.; Nakashima, T. T. Synthesis and structural-analysis of 5-deoxy-5-C-(hydroxyphosphinyl)-xylopyranose and 5-deoxy-5-C-(hydroxyphosphinyl) -glucopyranose. J. Org. Chem. 1985, 50, 3516-3521.
-
(1985)
J. Org. Chem
, vol.50
, pp. 3516-3521
-
-
Yamamoto, H.1
Hanaya, T.2
Kawamoto, H.3
Inokawa, S.4
Yamashita, M.5
Armour, M.-A.6
Nakashima, T.T.7
-
30
-
-
21844497893
-
2R′ in the side-chain-donor-functionalized amphiphiles
-
2R′ in the side-chain-donor-functionalized amphiphiles. Z. Naturforsh., B: Chem. Sci. 1994, 49, 1511-1524.
-
(1994)
Z. Naturforsh., B: Chem. Sci
, vol.49
, pp. 1511-1524
-
-
Brauer, D.J.1
Fischer, J.2
Kucken, S.3
Langhans, K.P.4
Stelzer, O.5
-
31
-
-
0032563846
-
A convenient method for phosphorylation involving a facile oxidation of H-phosphonate monoesters via bis(trimethylsilyl) phosphites
-
Wada, T.; Mochizuki, A.; Sato, Y.; Sekine, M. A convenient method for phosphorylation involving a facile oxidation of H-phosphonate monoesters via bis(trimethylsilyl) phosphites. Tetrahedron Lett. 1998, 39, 7123-7126.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 7123-7126
-
-
Wada, T.1
Mochizuki, A.2
Sato, Y.3
Sekine, M.4
-
32
-
-
0034733632
-
Boranophosphate diesters as stable synthetic analogues of 1-O-glycosylphosphates
-
Prosperi, D.; Panza, L.; Poletti, L.; Lay, L. Boranophosphate diesters as stable synthetic analogues of 1-O-glycosylphosphates. Tetrahedron 2000, 56, 4811-4815.
-
(2000)
Tetrahedron
, vol.56
, pp. 4811-4815
-
-
Prosperi, D.1
Panza, L.2
Poletti, L.3
Lay, L.4
-
33
-
-
0033931669
-
Individual isomers of dinucleoside boranophosphates as synthons for incorporation into oligonucleotides: Synthesis and configurational assignment
-
Sergueeva, Z. A.; Sergueev, D. S.; Ribeiro, A. A.; Summers, J. S.; Ramsay Shaw, B. Individual isomers of dinucleoside boranophosphates as synthons for incorporation into oligonucleotides: Synthesis and configurational assignment. Helv. Chim. Acta 2000, 83, 1377-1391.
-
(2000)
Helv. Chim. Acta
, vol.83
, pp. 1377-1391
-
-
Sergueeva, Z.A.1
Sergueev, D.S.2
Ribeiro, A.A.3
Summers, J.S.4
Ramsay Shaw, B.5
-
34
-
-
0034852138
-
Synthesis of oligonucleoside boranophosphates via an H-phosphonate method without nucleobase protection
-
Sergueev, D. S.; Sergueeva, Z. A.; Shaw, B. R. Synthesis of oligonucleoside boranophosphates via an H-phosphonate method without nucleobase protection. Nucleosides, Nucleotides Nucleic Acids 2001, 20, 789-795.
-
(2001)
Nucleosides, Nucleotides Nucleic Acids
, vol.20
, pp. 789-795
-
-
Sergueev, D.S.1
Sergueeva, Z.A.2
Shaw, B.R.3
-
36
-
-
0029731207
-
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.; Pelicano, 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-(phosphonomethoxy)ethyl)adenine (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
Pelicano, H.2
Johnson, R.3
Maury, G.4
Imbach, J.L.5
Aubertin, A.M.6
Obert, G.7
Gosselin, G.8
-
37
-
-
0027433373
-
Intracellular delivery of nucleoside monophosphates through a reductase-mediated activation process
-
Puech, F.; Gosselin, G.; Lefebvre, I.; Pompon, A.; Aubertin, A. M.; Kirn, 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
Pompon, A.4
Aubertin, A.M.5
Kirn, A.6
Imbach, J.L.7
-
38
-
-
84989418323
-
Vinyl compounds and other monomers containing heterocyclic moieties of nucleic acids
-
Imoto, M.; Takemoto, K. Vinyl compounds and other monomers containing heterocyclic moieties of nucleic acids. Synthesis 1970, 2, 173-179.
-
(1970)
Synthesis
, vol.2
, pp. 173-179
-
-
Imoto, M.1
Takemoto, K.2
-
39
-
-
0014109153
-
Enzyme inhibitors. 18. Studies on the stereoselectivity of inhibition of adenosine deaminase by DL-, D-, and L-9-(2-hydroxypropyl)adenine
-
Schaeffer, H. J.; Vince, R. Enzyme inhibitors. 18. Studies on the stereoselectivity of inhibition of adenosine deaminase by DL-, D-, and L-9-(2-hydroxypropyl)adenine. J. Med. Chem. 1967, 10, 689-691.
-
(1967)
J. Med. Chem
, vol.10
, pp. 689-691
-
-
Schaeffer, H.J.1
Vince, R.2
-
40
-
-
21844508105
-
Synthesis of 9-(2-phosphinomethoxyethyl)adenine and related compounds
-
Alexander, P.; Holy, A.; Masojidkova, M. Synthesis of 9-(2-phosphinomethoxyethyl)adenine and related compounds. Collect. Czech. Chem. Commun. 1994, 59, 1870-1878.
-
(1994)
Collect. Czech. Chem. Commun
, vol.59
, pp. 1870-1878
-
-
Alexander, P.1
Holy, A.2
Masojidkova, M.3
-
41
-
-
0033780046
-
Human immunodeficiency virus type 1 spinoculation enhances infection through virus binding
-
O'Doherty, U.; Swiggard, W. J.; Malim, M. H. Human immunodeficiency virus type 1 spinoculation enhances infection through virus binding. J. Virol. 2000, 74, 10074-10080.
-
(2000)
J. Virol
, vol.74
, pp. 10074-10080
-
-
O'Doherty, U.1
Swiggard, W.J.2
Malim, M.H.3
|