References
- Palomino , E. , Meltsner , B. R. , Kessel , D. and Horwitz , P. J. 1990 . Synthesis and in vitro evaluation of some modified 4-thiopyrmidine nucleoside for prevention or reversal of AIDS-associated neurological disorders. . J. Med. Chem. , 33 : 33 – 258 .
- Wang , E.-C. , Chen , H.-Y. and Tzeng , C.-C. 1994 . Acyclic nucleosides: Synthesis of 1-[1-hydroxy-2-propoxy) methyl] thymine, 6-azathymine, uracil, and 6-azauracil as potential antiviral agents. . Nucleosides and Nucleotides , 13 : 13 – 1201 .
- Cohen , J. 1998 . Exploring how to get at-and eradicate-hidden HIV. . Science , 279 : 279 – 1854 .
- Tsai , C. , Johnson , M. , Nicholson , V. and Naim , M. 1987 . A topological approach to molecular similarity analysis and its application. . Studies in Physical and Theoretical Chemistry , 51 : 51 – 231 .
- Herdewijn , P. and De Clercq , E. 1990 . “ Dideoxynucleoside analogoues as inhibitors of HIV replication. ” . In Design of Anti-AIDS Drugs , Edited by: De Clercq , E. 141 – 174 . New York, , USA : Elsevier Science Publishers B.V. .
- Nasr , M. , Cradock , J. and Johnston , M. 1992 . Computer-assisted structure-activity correlations of halodideoxynucleoside analogs as potential anti-HIV drugs. . AIDS Research and Human Retroviruses , 8 : 8 – 135 .
- Durand , P. J. 1996 . “ An Improved Program for Toplogical Similarity Analysis of Molecules. Masters Thesis ” . 261 Kent, Ohio, , USA : Kent State University .
- Nasr , M. and Turk , S. 1993 . “ Structure-actvity correlations of 2′,3′-dideoxy- and 2′,3′-dihydro-2′, 3′-dideoxypyrimidine nucleosides as potential anti-HIV agents. ” . In Nucleosides and Nucleotides as Antitumor and Antiviral Agents , Edited by: Chu , C. K. and Baker , D. C. 203 – 217 . New York : Plenum Press .
- Balzarini , J. and De Clercq , E. 1990 . “ Acyclic and carbocyclic nucleoside analogues as inhibitors of HIV replication. ” . In Design of Anti-AIDS Drugs , Edited by: De Clercq , E. 175 – 194 . New York, , USA : Elsevier Science Publishers B.V. .
- Charvet , A. S. , Camplo , M. , Faury , P. , Graciet , J.-C. , Mourier , N. , Chermann , J.-C. and Kraus , J.-L. 1994 . Inhibition of human immunodeficiency virus Type 1 replication by phosphonoformate- and phosphonoactetae-2′,3′-thiacytidine Conjugates. . J. Med. Chem. , 37 : 37 – 2216 .
- Camarasa , M. J. , Perez-Perez , M.-J. , San-Felix , A. , Balzarini , J. and De Clercq , E. 1992 . 3′-Spiro nucleosides, a new class of specific human immunodeficiency virus type I inhibitors: Synthesis and antiviral activity of [2′,5′-Bis-O-(tert-butyldimethylsilyl)-β-D-xylo- and -ribofuranose]-3′-spiro-5″-[4″-amino-1″,2″-oxathiole 2″,2″-Dioxide] (TSAO) pyrimidine nucleosides. . J. Med. Chem. , 35 : 35 – 2721 .
- Hayashi , S. , Phadatare , S. , Zemlicka , J. , Matsukura , M. , Mitsuya , H. and Broder , S. 1988 . Adenallene and cytallene: Acyclic nucleoside analogues that inhibit replication and cytopathic effect of human immunodeficiency virus . in vitro. Proc. Natl. Acad. Sci. USA , 85 : 85 – 6127 .
- Hopfinger , A. J. 1980 . A QSAR investigation of dihydrofolate reductase inhibition by baker triazines based upon molecular shape analysis. . J. Amer. Chem. , 102 : 102 – 7196 .