-
1
-
-
0023194835
-
Phosphonylmethyl analogs of nucleotides and their derivatives: Chemistry and biology
-
Holy, A. Phosphonylmethyl analogs of nucleotides and their derivatives: Chemistry and biology. Nucleosides Nucleotides 1987, 6(1&2), 147-155.
-
(1987)
Nucleosides Nucleotides
, vol.6
, Issue.1-2
, pp. 147-155
-
-
Holy, A.1
-
2
-
-
0025247710
-
Acyclic purine phosphonate analogues as antiviral agents. Synthesis and structure-activity relationships
-
Kim, C.U.; Luh, B.Y.; Misco, P.F.; Bronson, J.J.; Hitchcock, M.J.M.; Ghazzouli, I.; Martin, J.C. Acyclic purine phosphonate analogues as antiviral agents. Synthesis and structure-activity relationships. J. Med. Chem. 1990, 33, 1207-1213.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 1207-1213
-
-
Kim, C.U.1
Luh, B.Y.2
Misco, P.F.3
Bronson, J.J.4
Hitchcock, M.J.M.5
Ghazzouli, I.6
Martin, J.C.7
-
3
-
-
0025781479
-
Activity of acyclic nucleoside phosphonate analogues against human immunodeficiency virus in monocyte/macrophages and peripheral blood lymphocytes
-
Balzarini, J.; Perno, C.F.; Schols, D.; De Clercq, E. Activity of acyclic nucleoside phosphonate analogues against human immunodeficiency virus in monocyte/macrophages and peripheral blood lymphocytes. Biochem. Biophys. Res. Commun. 1991, 178, 329-335.
-
(1991)
Biochem. Biophys. Res. Commun.
, vol.178
, pp. 329-335
-
-
Balzarini, J.1
Perno, C.F.2
Schols, D.3
De Clercq, E.4
-
4
-
-
0022450584
-
A novel selective broad-spectrum anti-DNA virus agent
-
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
-
5
-
-
0030778137
-
Therapeutic potential of HPMPC (cidofovir), PMEA (adefovir) and related acyclic nucleoside phosphonate analogues as broad-spectrum antiviral agents
-
Naesens, L.; De Clercq, E. Therapeutic potential of HPMPC (cidofovir), PMEA (adefovir) and related acyclic nucleoside phosphonate analogues as broad-spectrum antiviral agents. Nucleosides Nucleotides 1997, 16, 983-992.
-
(1997)
Nucleosides Nucleotides
, vol.16
, pp. 983-992
-
-
Naesens, L.1
De Clercq, E.2
-
6
-
-
0029989972
-
Activity of the (R)-enantiomers of 9-(2-phosphonyl-methoxypropyl)adenine and 9-(2-phosphonyl-methoxypropyl)-2,6-diaminopurine against human immunodeficiency virus in different human cell systems
-
Balzarini, J.; Aquaro, S.; Perno, C.-F.; Holy, A.; De Clercq, E. Activity of the (R)-enantiomers of 9-(2-phosphonyl-methoxypropyl)adenine and 9-(2-phosphonyl-methoxypropyl)-2,6-diaminopurine against human immunodeficiency virus in different human cell systems. Biochem. Biophys. Res. Commun. 1996, 219, 337-341.
-
(1996)
Biochem. Biophys. Res. Commun.
, vol.219
, pp. 337-341
-
-
Balzarini, J.1
Aquaro, S.2
Perno, C.-F.3
Holy, A.4
De Clercq, E.5
-
7
-
-
0026675873
-
Synthesis of racemic carboacyclonucleosides derived from butane-1,4-diol and hexane-1,6-diol
-
Perbost, M.; Lucas, M.; Chavis, C.; Imbach, J.-L. Synthesis of racemic carboacyclonucleosides derived from butane-1,4-diol and hexane-1,6-diol. Nucleosides Nucleotides 1992, 11(8), 1489-1505.
-
(1992)
Nucleosides Nucleotides
, vol.11
, Issue.8
, pp. 1489-1505
-
-
Perbost, M.1
Lucas, M.2
Chavis, C.3
Imbach, J.-L.4
-
8
-
-
0026672490
-
An expeditious synthesis of homochiral (R) 2-(9-purinyl)butane-1,4-diols from (S) butane-1,2,4-triol
-
Perbost, M.; Lucas, M.; Chavis, C.; Imbach, J.-L. An expeditious synthesis of homochiral (R) 2-(9-purinyl)butane-1,4-diols from (S) butane-1,2,4-triol. Nucleosides Nucleotides 1992, 11(8), 1529-1537.
-
(1992)
Nucleosides Nucleotides
, vol.11
, Issue.8
, pp. 1529-1537
-
-
Perbost, M.1
Lucas, M.2
Chavis, C.3
Imbach, J.-L.4
-
9
-
-
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
-
10
-
-
34250393768
-
Analogs of purine nucleosides and purine mono- and polynucleotides. II. Substituted α-(9-purinyl)-γ-butyrolactones
-
Giller, S.A.; Getsova, I.N.; Goncharova, I.N.; Petrulyanis, L.N.; Mironova, L.I.; Nazarova, G.F.; Bruk, E.I. Analogs of purine nucleosides and purine mono- and polynucleotides. II. Substituted α-(9-purinyl)-γ- butyrolactones. Chem. Heterocycl. Compd. U.S.S.R. 1974, 10, 1477-1480.
-
(1974)
Chem. Heterocycl. Compd. U.S.S.R.
, vol.10
, pp. 1477-1480
-
-
Giller, S.A.1
Getsova, I.N.2
Goncharova, I.N.3
Petrulyanis, L.N.4
Mironova, L.I.5
Nazarova, G.F.6
Bruk, E.I.7
-
11
-
-
0023138871
-
Synthesis of (-)-talaromycins A and B
-
Mori, K.; Ikunaka, M. Synthesis of (-)-talaromycins A and B. Tetrahedron 1987, 43, 45-58.
-
(1987)
Tetrahedron
, vol.43
, pp. 45-58
-
-
Mori, K.1
Ikunaka, M.2
-
12
-
-
0030597014
-
Synthesis and antiviral activity of acyclic analogues of 1,5-anhydrohexitol nucleosides using Mitsunobu reaction
-
Hossain, N.; Rozenski, J.; De Clercq, E.; Herdewijn, P. Synthesis and antiviral activity of acyclic analogues of 1,5-anhydrohexitol nucleosides using Mitsunobu reaction. Tetrahedron 1996, 52(43), 13655-13670.
-
(1996)
Tetrahedron
, vol.52
, Issue.43
, pp. 13655-13670
-
-
Hossain, N.1
Rozenski, J.2
De Clercq, E.3
Herdewijn, P.4
-
13
-
-
0001171156
-
Purine nucleosides. VIII. Reinvestigation of the position of glycosidation in certain synthetic "7"-substituted 6-dimethylaminopurine nucleosides related to puromycin
-
Townsend, L.B.; Robins, R.K.; Loeppky, R.N.; Leonard, N.J. Purine nucleosides. VIII. Reinvestigation of the position of glycosidation in certain synthetic "7"-substituted 6-dimethylaminopurine nucleosides related to puromycin. J. Am. Chem. Soc. 1964, 86, 5320-5325.
-
(1964)
J. Am. Chem. Soc.
, vol.86
, pp. 5320-5325
-
-
Townsend, L.B.1
Robins, R.K.2
Loeppky, R.N.3
Leonard, N.J.4
-
14
-
-
0037809239
-
Inhibition of hepatitis C virus RNA replication by 2′-modified nucleoside analogs
-
Carroll, S.S.; Tomassini, J.E.; Bosserman, M.; Getty, K.; Stahlhut, M.W.; Eldrup, A.B.; Bhat, B.; Hall, D.; Simcoe, A.L.; LaFemina, R.; Rutkowski, C.A.; Wolanski, B.; Yang, Z.; Migliaccio, G.; De Francesco, R.; Kuo, L.C.; MacCoss, M.; Olsen, D.B. Inhibition of hepatitis C virus RNA replication by 2′-modified nucleoside analogs. J. Biol. Chem. 2003, 278, 11979-11984.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 11979-11984
-
-
Carroll, S.S.1
Tomassini, J.E.2
Bosserman, M.3
Getty, K.4
Stahlhut, M.W.5
Eldrup, A.B.6
Bhat, B.7
Hall, D.8
Simcoe, A.L.9
LaFemina, R.10
Rutkowski, C.A.11
Wolanski, B.12
Yang, Z.13
Migliaccio, G.14
De Francesco, R.15
Kuo, L.C.16
MacCoss, M.17
Olsen, D.B.18
|