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Antiviral activity of C-5 substituted tubercidin analogues.
Bergstrom DE, Brattesani AJ, Ogawa MK, Reddy PA, Schweickert MJ, Balzarini J, De Clercq E. Bergstrom DE, et al. Among authors: de clercq e. J Med Chem. 1984 Mar;27(3):285-92. doi: 10.1021/jm00369a010. J Med Chem. 1984. PMID: 6699874
3'-Spiro nucleosides, a new class of specific human immunodeficiency virus type 1 inhibitors: synthesis and antiviral activity of [2'-5'-bis-O-(tert-butyldimethylsilyl)-beta-D-xylo- and -ribofuranose]-3'-spiro-5"-[4"-amino-1",2"-oxathiole 2",2"-dioxide] (TSAO) pyrimidine nucleosides.
Camarasa MJ, Pérez-Pérez MJ, San-Félix A, Balzarini J, De Clercq E. Camarasa MJ, et al. Among authors: de clercq e. J Med Chem. 1992 Jul 24;35(15):2721-7. doi: 10.1021/jm00093a002. J Med Chem. 1992. PMID: 1495006
TSAO analogues. Stereospecific synthesis and anti-HIV-1 activity of 1-[2',5'-bis-O-(tert-butyldimethylsilyl)-beta-D-ribofuranosyl]-3'-spiro -5''- (4''-amino-1'',2''-oxathiole 2'',2''-dioxide) pyrimidine and pyrimidine-modified nucleosides.
Pérez-Pérez MJ, San-Félix A, Balzarini J, De Clercq E, Camarasa MJ. Pérez-Pérez MJ, et al. Among authors: de clercq e. J Med Chem. 1992 Aug 7;35(16):2988-95. doi: 10.1021/jm00094a009. J Med Chem. 1992. PMID: 1501224
Nucleic acid related compounds. 74. Synthesis and biological activity of 2'(and 3')-deoxy-2'(and 3')-methylenenucleoside analogues that function as mechanism-based inhibitors of S-adenosyl-L-homocysteine hydrolase and/or ribonucleotide reductase.
Robins MJ, Samano V, Zhang W, Balzarini J, De Clercq E, Borchardt RT, Lee Y, Yuan CS. Robins MJ, et al. Among authors: de clercq e. J Med Chem. 1992 Jun 12;35(12):2283-93. doi: 10.1021/jm00090a020. J Med Chem. 1992. PMID: 1613752
2,295 results