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European Journal of Medicinal Chemistry
|
September 5, 2020
New indolylarylsulfone non-nucleoside reverse transcriptase inhibitors show low nanomolar inhibition of single and double HIV-1 mutant strains
Marianna Nalli, Jorge I Armijos Rivera, Domiziana Masci, et al.
Journal of Medicinal Chemistry
|
June 20, 2017
Chiral Indolylarylsulfone Non-Nucleoside Reverse Transcriptase Inhibitors as New Potent and Broad Spectrum Anti-HIV-1 Agents
Valeria Famiglini, Giuseppe La Regina, Antonio Coluccia, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
June 9, 2025
Exploring structure-activity relationships of pyrrolyl diketo acid derivatives as non-nucleoside inhibitors of terminal deoxynucleotidyl transferase enzyme
Valentina Noemi Madia, Nadia Garibaldi, Davide Ialongo, et al.
Journal of Medicinal Chemistry
|
November 25, 2014
Indolylarylsulfones carrying a heterocyclic tail as very potent and broad spectrum HIV-1 non-nucleoside reverse transcriptase inhibitors
Valeria Famiglini, Giuseppe La Regina, Antonio Coluccia, et al.
Journal of Medicinal Chemistry
|
November 16, 2019
Multitarget CFTR Modulators Endowed with Multiple Beneficial Side Effects for Cystic Fibrosis Patients: Toward a Simplified Therapeutic Approach †
Sabrina Tassini, Emily Langron, Leen Delang, et al.
International Journal of Molecular Sciences
|
March 6, 2021
A Role for Human DNA Polymerase λ in Alternative Lengthening of Telomeres
Elisa Mentegari, Federica Bertoletti, Miroslava Kissova, et al.
Archiv Der Pharmazie
|
January 28, 2025
Synthesis and biological investigation of peptidomimetic SARS-CoV-2 main protease inhibitors bearing quinoline-based heterocycles at P<sub>3</sub>
Sara Rossi, Graziano Deidda, Lia Fiaschi, et al.
Journal of Medicinal Chemistry
|
December 12, 2018
Effect of α-Methoxy Substitution on the Anti-HIV Activity of Dihydropyrimidin-4(3 H)-ones
Maxim B Nawrozkij, Mariantonietta Forgione, Alexandre S Yablokov, et al.
Journal of Medicinal Chemistry
|
April 30, 2015
Studies on the ATP Binding Site of Fyn Kinase for the Identification of New Inhibitors and Their Evaluation as Potential Agents against Tauopathies and Tumors
Cristina Tintori, Giuseppina La Sala, Giulia Vignaroli, et al.
Journal of Medicinal Chemistry
|
January 16, 2016
Discovery of the First Potent and Selective Inhibitors of Human dCTP Pyrophosphatase 1
Sabin Llona-Minguez, Andreas Höglund, Sylvain A Jacques, et al.
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Search research articles
Search
Showing results (81-90 of 92) with videos related to
Sort By:
Page
of 10
European Journal of Medicinal Chemistry
|
September 5, 2020
New indolylarylsulfone non-nucleoside reverse transcriptase inhibitors show low nanomolar inhibition of single and double HIV-1 mutant strains
Marianna Nalli, Jorge I Armijos Rivera, Domiziana Masci, et al.
Journal of Medicinal Chemistry
|
June 20, 2017
Chiral Indolylarylsulfone Non-Nucleoside Reverse Transcriptase Inhibitors as New Potent and Broad Spectrum Anti-HIV-1 Agents
Valeria Famiglini, Giuseppe La Regina, Antonio Coluccia, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
June 9, 2025
Exploring structure-activity relationships of pyrrolyl diketo acid derivatives as non-nucleoside inhibitors of terminal deoxynucleotidyl transferase enzyme
Valentina Noemi Madia, Nadia Garibaldi, Davide Ialongo, et al.
Journal of Medicinal Chemistry
|
November 25, 2014
Indolylarylsulfones carrying a heterocyclic tail as very potent and broad spectrum HIV-1 non-nucleoside reverse transcriptase inhibitors
Valeria Famiglini, Giuseppe La Regina, Antonio Coluccia, et al.
Journal of Medicinal Chemistry
|
November 16, 2019
Multitarget CFTR Modulators Endowed with Multiple Beneficial Side Effects for Cystic Fibrosis Patients: Toward a Simplified Therapeutic Approach †
Sabrina Tassini, Emily Langron, Leen Delang, et al.
International Journal of Molecular Sciences
|
March 6, 2021
A Role for Human DNA Polymerase λ in Alternative Lengthening of Telomeres
Elisa Mentegari, Federica Bertoletti, Miroslava Kissova, et al.
Archiv Der Pharmazie
|
January 28, 2025
Synthesis and biological investigation of peptidomimetic SARS-CoV-2 main protease inhibitors bearing quinoline-based heterocycles at P<sub>3</sub>
Sara Rossi, Graziano Deidda, Lia Fiaschi, et al.
Journal of Medicinal Chemistry
|
December 12, 2018
Effect of α-Methoxy Substitution on the Anti-HIV Activity of Dihydropyrimidin-4(3 H)-ones
Maxim B Nawrozkij, Mariantonietta Forgione, Alexandre S Yablokov, et al.
Journal of Medicinal Chemistry
|
April 30, 2015
Studies on the ATP Binding Site of Fyn Kinase for the Identification of New Inhibitors and Their Evaluation as Potential Agents against Tauopathies and Tumors
Cristina Tintori, Giuseppina La Sala, Giulia Vignaroli, et al.
Journal of Medicinal Chemistry
|
January 16, 2016
Discovery of the First Potent and Selective Inhibitors of Human dCTP Pyrophosphatase 1
Sabin Llona-Minguez, Andreas Höglund, Sylvain A Jacques, et al.
Page
of 10