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Antibiotics (Basel, Switzerland)
|
November 27, 2024
Enhancing Antibacterial Efficacy: Combining Novel Bacterial Topoisomerase Inhibitors with Efflux Pump Inhibitors and Other Agents Against Gram-Negative Bacteria
Maša Zorman, Maja Kokot, Irena Zdovc, et al.
Journal of Medicinal Chemistry
|
May 20, 2011
Structure-based design of a new series of D-glutamic acid based inhibitors of bacterial UDP-N-acetylmuramoyl-L-alanine:D-glutamate ligase (MurD)
Tihomir Tomasić, Nace Zidar, Roman Sink, et al.
Pharmaceutics
|
December 30, 2020
Hybrid Inhibitors of DNA Gyrase A and B: Design, Synthesis and Evaluation
Martina Durcik, Žiga Skok, Janez Ilaš, et al.
Biochemical Pharmacology
|
June 19, 2012
MurD enzymes from different bacteria: evaluation of inhibitors
Hélène Barreteau, Izidor Sosič, Samo Turk, et al.
European Journal of Medicinal Chemistry
|
October 4, 2011
New 5-benzylidenethiazolidin-4-one inhibitors of bacterial MurD ligase: design, synthesis, crystal structures, and biological evaluation
Nace Zidar, Tihomir Tomašić, Roman Šink, et al.
ACS Medicinal Chemistry Letters
|
June 6, 2014
Dual Inhibitor of MurD and MurE Ligases from Escherichia coli and Staphylococcus aureus
Tihomir Tomašić, Roman Sink, Nace Zidar, et al.
Bioorganic Chemistry
|
August 12, 2019
Searching new structural scaffolds for BRAF inhibitors. An integrative study using theoretical and experimental techniques
Ludmila E Campos, Francisco M Garibotto, Emilio Angelina, et al.
European Journal of Medicinal Chemistry
|
May 21, 2018
New N-phenylpyrrolamide DNA gyrase B inhibitors: Optimization of efficacy and antibacterial activity
Martina Durcik, Denise Lovison, Žiga Skok, et al.
Chemmedchem
|
December 22, 2009
5-Benzylidenethiazolidin-4-ones as multitarget inhibitors of bacterial Mur ligases
Tihomir Tomasić, Nace Zidar, Andreja Kovac, et al.
Bioorganic Chemistry
|
October 12, 2024
First dual inhibitors of human topoisomerase IIα and Hsp90 C-terminal domain inhibit the growth of Ewing sarcoma in vitro and in vivo
Jaka Dernovšek, Dunja Urbančič, Živa Zajec, et al.
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of 8
Search research articles
Search
Showing results (51-60 of 78) with videos related to
Sort By:
Page
of 8
Antibiotics (Basel, Switzerland)
|
November 27, 2024
Enhancing Antibacterial Efficacy: Combining Novel Bacterial Topoisomerase Inhibitors with Efflux Pump Inhibitors and Other Agents Against Gram-Negative Bacteria
Maša Zorman, Maja Kokot, Irena Zdovc, et al.
Journal of Medicinal Chemistry
|
May 20, 2011
Structure-based design of a new series of D-glutamic acid based inhibitors of bacterial UDP-N-acetylmuramoyl-L-alanine:D-glutamate ligase (MurD)
Tihomir Tomasić, Nace Zidar, Roman Sink, et al.
Pharmaceutics
|
December 30, 2020
Hybrid Inhibitors of DNA Gyrase A and B: Design, Synthesis and Evaluation
Martina Durcik, Žiga Skok, Janez Ilaš, et al.
Biochemical Pharmacology
|
June 19, 2012
MurD enzymes from different bacteria: evaluation of inhibitors
Hélène Barreteau, Izidor Sosič, Samo Turk, et al.
European Journal of Medicinal Chemistry
|
October 4, 2011
New 5-benzylidenethiazolidin-4-one inhibitors of bacterial MurD ligase: design, synthesis, crystal structures, and biological evaluation
Nace Zidar, Tihomir Tomašić, Roman Šink, et al.
ACS Medicinal Chemistry Letters
|
June 6, 2014
Dual Inhibitor of MurD and MurE Ligases from Escherichia coli and Staphylococcus aureus
Tihomir Tomašić, Roman Sink, Nace Zidar, et al.
Bioorganic Chemistry
|
August 12, 2019
Searching new structural scaffolds for BRAF inhibitors. An integrative study using theoretical and experimental techniques
Ludmila E Campos, Francisco M Garibotto, Emilio Angelina, et al.
European Journal of Medicinal Chemistry
|
May 21, 2018
New N-phenylpyrrolamide DNA gyrase B inhibitors: Optimization of efficacy and antibacterial activity
Martina Durcik, Denise Lovison, Žiga Skok, et al.
Chemmedchem
|
December 22, 2009
5-Benzylidenethiazolidin-4-ones as multitarget inhibitors of bacterial Mur ligases
Tihomir Tomasić, Nace Zidar, Andreja Kovac, et al.
Bioorganic Chemistry
|
October 12, 2024
First dual inhibitors of human topoisomerase IIα and Hsp90 C-terminal domain inhibit the growth of Ewing sarcoma in vitro and in vivo
Jaka Dernovšek, Dunja Urbančič, Živa Zajec, et al.
Page
of 8