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Focher

Showing results (91-100 of 100) with videos related to

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Methods and Findings in Experimental and Clinical Pharmacology|September 1, 1989
Nucleoside analogs as non-substrate inhibitors of herpes simplex viruses thymidine kinaseF Focher, D Sandoli, C Hildebrand, et al.
Anticancer Research|September 1, 1986
DNA polymerases and DNA topoisomerases as targets for the development of anticancer drugsS Spadari, G Pedrali-Noy, F Focher, et al.
Chemical Biology & Drug Design|August 6, 2015
Site-directed Mutagenesis of Key Residues Unveiled a Novel Allosteric Site on Human Adenosine Kinase for Pyrrolobenzoxa(thia)zepinone Non-Nucleoside InhibitorsLida Savi, Margherita Brindisi, Gloria Alfano, 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 enzymesA Verri, F Focher, R J Duncombe, et al.
Antiviral Chemistry & Chemotherapy|October 15, 2015
Prodrugs of herpes simplex thymidine kinase inhibitorsMilka Yanachkova, Wei-Chu Xu, Sofya Dvoskin, et al.
Antiviral Chemistry & Chemotherapy|October 30, 2003
Design and synthesis of phosphonoacetic acid (PPA) ester and amide bioisosters of ribofuranosylnucleoside diphosphates as potential ribonucleotide reductase inhibitors and evaluation of their enzyme inhibitory, cytostatic and antiviral activityStefano Manfredini, Nicola Solaroli, Angela Angusti, et al.
Antimicrobial Agents and Chemotherapy|April 18, 2007
Sensitivity of monkey B virus (Cercopithecine herpesvirus 1) to antiviral drugs: role of thymidine kinase in antiviral activities of substrate analogs and acyclonucleosidesFederico Focher, Andrea Lossani, Annalisa Verri, et al.
Bioorganic & Medicinal Chemistry Letters|June 4, 2011
Enantioselective binding of second generation pyrrolobenzoxazepinones to the catalytic ternary complex of HIV-1 RT wild-type and L100I and K103N drug resistant mutantsStefania Butini, Sandra Gemma, Margherita Brindisi, et al.
European Journal of Medicinal Chemistry|July 10, 2017
First dual AK/GSK-3β inhibitors endowed with antioxidant properties as multifunctional, potential neuroprotective agentsSimone Brogi, Anna Ramunno, Lida Savi, et al.
Journal of Medicinal Chemistry|February 16, 2011
Non-nucleoside inhibitors of human adenosine kinase: synthesis, molecular modeling, and biological studiesStefania Butini, Sandra Gemma, Margherita Brindisi, et al.
Pageof 10

Showing results (91-100 of 100) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 100 results.
Methods and Findings in Experimental and Clinical Pharmacology|September 1, 1989
Nucleoside analogs as non-substrate inhibitors of herpes simplex viruses thymidine kinaseF Focher, D Sandoli, C Hildebrand, et al.
Anticancer Research|September 1, 1986
DNA polymerases and DNA topoisomerases as targets for the development of anticancer drugsS Spadari, G Pedrali-Noy, F Focher, et al.
Chemical Biology & Drug Design|August 6, 2015
Site-directed Mutagenesis of Key Residues Unveiled a Novel Allosteric Site on Human Adenosine Kinase for Pyrrolobenzoxa(thia)zepinone Non-Nucleoside InhibitorsLida Savi, Margherita Brindisi, Gloria Alfano, 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 enzymesA Verri, F Focher, R J Duncombe, et al.
Antiviral Chemistry & Chemotherapy|October 15, 2015
Prodrugs of herpes simplex thymidine kinase inhibitorsMilka Yanachkova, Wei-Chu Xu, Sofya Dvoskin, et al.
Antiviral Chemistry & Chemotherapy|October 30, 2003
Design and synthesis of phosphonoacetic acid (PPA) ester and amide bioisosters of ribofuranosylnucleoside diphosphates as potential ribonucleotide reductase inhibitors and evaluation of their enzyme inhibitory, cytostatic and antiviral activityStefano Manfredini, Nicola Solaroli, Angela Angusti, et al.
Antimicrobial Agents and Chemotherapy|April 18, 2007
Sensitivity of monkey B virus (Cercopithecine herpesvirus 1) to antiviral drugs: role of thymidine kinase in antiviral activities of substrate analogs and acyclonucleosidesFederico Focher, Andrea Lossani, Annalisa Verri, et al.
Bioorganic & Medicinal Chemistry Letters|June 4, 2011
Enantioselective binding of second generation pyrrolobenzoxazepinones to the catalytic ternary complex of HIV-1 RT wild-type and L100I and K103N drug resistant mutantsStefania Butini, Sandra Gemma, Margherita Brindisi, et al.
European Journal of Medicinal Chemistry|July 10, 2017
First dual AK/GSK-3β inhibitors endowed with antioxidant properties as multifunctional, potential neuroprotective agentsSimone Brogi, Anna Ramunno, Lida Savi, et al.
Journal of Medicinal Chemistry|February 16, 2011
Non-nucleoside inhibitors of human adenosine kinase: synthesis, molecular modeling, and biological studiesStefania Butini, Sandra Gemma, Margherita Brindisi, et al.
Pageof 10