Page last updated: 2024-08-24

tsao-t and r 82150

tsao-t has been researched along with r 82150 in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Balzarini, J; Camarasa, MJ; De Clercq, E; Pérez-Pérez, MJ; San-Félix, A	1
Anné, J; Balzarini, J; Camarasa, MJ; De Clercq, E; Desmyter, J; Jonckheere, H; Taymans, JM; Velázquez, S	1

Other Studies

2 other study(ies) available for tsao-t and r 82150

Article	Year
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] ( Journal of medicinal chemistry, 1992, Jul-24, Volume: 35, Issue:15 Topics: Antiviral Agents; Cells, Cultured; HIV-1; HIV-2; Humans; Molecular Structure; Pyrimidine Nucleosides; Simian Immunodeficiency Virus; Tumor Cells, Cultured; Virus Replication	1992
Resistance of HIV-1 reverse transcriptase against [2',5'-bis-O-(tert-butyldimethylsilyl)-3'-spiro-5''-(4''-amino-1'',2''- oxathiole-2'',2''-dioxide)] (TSAO) derivatives is determined by the mutation Glu138-->Lys on the p51 subunit. The Journal of biological chemistry, 1994, Oct-14, Volume: 269, Issue:41 Topics: Antiviral Agents; Base Sequence; Benzodiazepines; Binding Sites; Deoxyguanine Nucleotides; Dideoxynucleotides; Drug Resistance; Escherichia coli; HIV Reverse Transcriptase; Imidazoles; Molecular Sequence Data; Mutagenesis, Site-Directed; Mutation; Protein Conformation; Recombinant Proteins; Reverse Transcriptase Inhibitors; RNA-Directed DNA Polymerase; Sequence Analysis, DNA; Spiro Compounds; Thymidine; Uridine	1994

Article

Year

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] (

Journal of medicinal chemistry, 1992, Jul-24, Volume: 35, Issue:15

Topics: Antiviral Agents; Cells, Cultured; HIV-1; HIV-2; Humans; Molecular Structure; Pyrimidine Nucleosides; Simian Immunodeficiency Virus; Tumor Cells, Cultured; Virus Replication

1992

Resistance of HIV-1 reverse transcriptase against [2',5'-bis-O-(tert-butyldimethylsilyl)-3'-spiro-5''-(4''-amino-1'',2''- oxathiole-2'',2''-dioxide)] (TSAO) derivatives is determined by the mutation Glu138-->Lys on the p51 subunit.

The Journal of biological chemistry, 1994, Oct-14, Volume: 269, Issue:41

Topics: Antiviral Agents; Base Sequence; Benzodiazepines; Binding Sites; Deoxyguanine Nucleotides; Dideoxynucleotides; Drug Resistance; Escherichia coli; HIV Reverse Transcriptase; Imidazoles; Molecular Sequence Data; Mutagenesis, Site-Directed; Mutation; Protein Conformation; Recombinant Proteins; Reverse Transcriptase Inhibitors; RNA-Directed DNA Polymerase; Sequence Analysis, DNA; Spiro Compounds; Thymidine; Uridine

1994