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Journal of Medicinal Chemistry
|
October 30, 1992
L-thymidine is phosphorylated by herpes simplex virus type 1 thymidine kinase and inhibits viral growth
S Spadari, G Maga, F Focher, et al.
Nucleosides & Nucleotides
|
August 26, 1998
Some 6-aza-5-substituted-2'-deoxyuridines show potent and selective inhibition of herpes simplex virus type 1 thymidine kinase
I Basnak, M Sun, T A Hamor, et al.
Antiviral Research
|
April 1, 1985
In vivo distribution and activity of aphidicolin on dividing and quiescent cells
S Spadari, F Focher, C Kuenzle, et al.
Bioorganic & Medicinal Chemistry
|
June 27, 2001
5-(Trifluoromethyl)-beta-l-2'-deoxyuridine, the L-enantiomer of trifluorothymidine: stereospecific synthesis and antiherpetic evaluations
R Salvetti, A Marchand, M Pregnolato, et al.
Anticancer Research
|
September 1, 1986
DNA polymerases and DNA topoisomerases as targets for the development of anticancer drugs
S Spadari, G Pedrali-Noy, F Focher, et al.
The Biochemical Journal
|
October 12, 2000
Anti-(herpes simplex virus) activity of 4'-thio-2'-deoxyuridines: a biochemical investigation for viral and cellular target enzymes
A Verri, F Focher, R J Duncombe, et al.
European Journal of Biochemistry
|
August 17, 1990
Revised nomenclature for eukaryotic DNA polymerases
P M Burgers, R A Bambara, J L Campbell, et al.
Antiviral Chemistry & Chemotherapy
|
May 20, 2000
Non-nucleoside HIV-1 reverse transcriptase inhibitors: synthesis and biological evaluation of novel quinoxalinylethylpyridylthioureas as potent antiviral agents
G Campiani, M Fabbrini, E Morelli, et al.
The Journal of Biological Chemistry
|
September 27, 2001
The stereoselective targeting of a specific enzyme-substrate complex is the molecular mechanism for the synergic inhibition of HIV-1 reverse transcriptase by (R)-(-)-PPO464: a novel generation of nonnucleoside inhibitors
G Maga, A Ramunno, V Nacci, et al.
Journal of Medicinal Chemistry
|
November 2, 1999
Pyrrolobenzoxazepinone derivatives as non-nucleoside HIV-1 RT inhibitors: further structure-activity relationship studies and identification of more potent broad-spectrum HIV-1 RT inhibitors with antiviral activity
G Campiani, E Morelli, M Fabbrini, et al.
Page
of 15
Search research articles
Search
Showing results (131-140 of 141) with videos related to
Sort By:
Page
of 15
Journal of Medicinal Chemistry
|
October 30, 1992
L-thymidine is phosphorylated by herpes simplex virus type 1 thymidine kinase and inhibits viral growth
S Spadari, G Maga, F Focher, et al.
Nucleosides & Nucleotides
|
August 26, 1998
Some 6-aza-5-substituted-2'-deoxyuridines show potent and selective inhibition of herpes simplex virus type 1 thymidine kinase
I Basnak, M Sun, T A Hamor, et al.
Antiviral Research
|
April 1, 1985
In vivo distribution and activity of aphidicolin on dividing and quiescent cells
S Spadari, F Focher, C Kuenzle, et al.
Bioorganic & Medicinal Chemistry
|
June 27, 2001
5-(Trifluoromethyl)-beta-l-2'-deoxyuridine, the L-enantiomer of trifluorothymidine: stereospecific synthesis and antiherpetic evaluations
R Salvetti, A Marchand, M Pregnolato, et al.
Anticancer Research
|
September 1, 1986
DNA polymerases and DNA topoisomerases as targets for the development of anticancer drugs
S Spadari, G Pedrali-Noy, F Focher, et al.
The Biochemical Journal
|
October 12, 2000
Anti-(herpes simplex virus) activity of 4'-thio-2'-deoxyuridines: a biochemical investigation for viral and cellular target enzymes
A Verri, F Focher, R J Duncombe, et al.
European Journal of Biochemistry
|
August 17, 1990
Revised nomenclature for eukaryotic DNA polymerases
P M Burgers, R A Bambara, J L Campbell, et al.
Antiviral Chemistry & Chemotherapy
|
May 20, 2000
Non-nucleoside HIV-1 reverse transcriptase inhibitors: synthesis and biological evaluation of novel quinoxalinylethylpyridylthioureas as potent antiviral agents
G Campiani, M Fabbrini, E Morelli, et al.
The Journal of Biological Chemistry
|
September 27, 2001
The stereoselective targeting of a specific enzyme-substrate complex is the molecular mechanism for the synergic inhibition of HIV-1 reverse transcriptase by (R)-(-)-PPO464: a novel generation of nonnucleoside inhibitors
G Maga, A Ramunno, V Nacci, et al.
Journal of Medicinal Chemistry
|
November 2, 1999
Pyrrolobenzoxazepinone derivatives as non-nucleoside HIV-1 RT inhibitors: further structure-activity relationship studies and identification of more potent broad-spectrum HIV-1 RT inhibitors with antiviral activity
G Campiani, E Morelli, M Fabbrini, et al.
Page
of 15