Search research articles
Contact Us
Filters
Showing results (81-90 of 104) with videos related to
Page
of 11
Sort By:
Nature
|
March 11, 2020
An open-source drug discovery platform enables ultra-large virtual screens
Christoph Gorgulla, Andras Boeszoermenyi, Zi-Fu Wang, et al.
Molecules (Basel, Switzerland)
|
January 28, 2026
Click Chemistry-Enabled Parallel Synthesis of <i>N</i>-Acyl Sulfonamides and Their Evaluation as Carbonic Anhydrase Inhibitors
Oleksii V Gavrylenko, Bohdan V Vashchenko, Vasyl Naumchyk, et al.
Journal of Medicinal Chemistry
|
June 11, 2026
First Structure-Activity-Relationship Study of Potent G2A Antagonists
Victor Hernandez-Olmos, Jan Heering, Felix F Lillich, et al.
Nature
|
December 9, 2021
Structures of the σ<sub>2</sub> receptor enable docking for bioactive ligand discovery
Assaf Alon, Jiankun Lyu, Joao M Braz, et al.
Nature Communications
|
December 9, 2025
Ultra-large virtual screening unveils potent agonists of the neuromodulatory orphan receptor GPR139
Israel Cabeza de Vaca, Boris Trapkov, Ling Shen, et al.
Biorxiv : the Preprint Server for Biology
|
March 27, 2026
Library docking for Cannabinoid-2 Receptor ligands
Moira M Rachman, Christos Iliopoulos-Tsoutsouvas, Michael D Sacco, et al.
Nature
|
February 11, 2020
Virtual discovery of melatonin receptor ligands to modulate circadian rhythms
Reed M Stein, Hye Jin Kang, John D McCorvy, et al.
Nature Communications
|
December 6, 2023
Docking for EP4R antagonists active against inflammatory pain
Stefan Gahbauer, Chelsea DeLeon, Joao M Braz, et al.
Nature
|
December 16, 2021
Synthon-based ligand discovery in virtual libraries of over 11 billion compounds
Arman A Sadybekov, Anastasiia V Sadybekov, Yongfeng Liu, et al.
Communications Chemistry
|
August 1, 2025
A bottom-up approach to find lead compounds in expansive chemical spaces
Álvaro Serrano-Morrás, Andrea Bertran-Mostazo, Marina Miñarro-Lleonar, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 104) with videos related to
Sort By:
Page
of 11
Nature
|
March 11, 2020
An open-source drug discovery platform enables ultra-large virtual screens
Christoph Gorgulla, Andras Boeszoermenyi, Zi-Fu Wang, et al.
Molecules (Basel, Switzerland)
|
January 28, 2026
Click Chemistry-Enabled Parallel Synthesis of <i>N</i>-Acyl Sulfonamides and Their Evaluation as Carbonic Anhydrase Inhibitors
Oleksii V Gavrylenko, Bohdan V Vashchenko, Vasyl Naumchyk, et al.
Journal of Medicinal Chemistry
|
June 11, 2026
First Structure-Activity-Relationship Study of Potent G2A Antagonists
Victor Hernandez-Olmos, Jan Heering, Felix F Lillich, et al.
Nature
|
December 9, 2021
Structures of the σ<sub>2</sub> receptor enable docking for bioactive ligand discovery
Assaf Alon, Jiankun Lyu, Joao M Braz, et al.
Nature Communications
|
December 9, 2025
Ultra-large virtual screening unveils potent agonists of the neuromodulatory orphan receptor GPR139
Israel Cabeza de Vaca, Boris Trapkov, Ling Shen, et al.
Biorxiv : the Preprint Server for Biology
|
March 27, 2026
Library docking for Cannabinoid-2 Receptor ligands
Moira M Rachman, Christos Iliopoulos-Tsoutsouvas, Michael D Sacco, et al.
Nature
|
February 11, 2020
Virtual discovery of melatonin receptor ligands to modulate circadian rhythms
Reed M Stein, Hye Jin Kang, John D McCorvy, et al.
Nature Communications
|
December 6, 2023
Docking for EP4R antagonists active against inflammatory pain
Stefan Gahbauer, Chelsea DeLeon, Joao M Braz, et al.
Nature
|
December 16, 2021
Synthon-based ligand discovery in virtual libraries of over 11 billion compounds
Arman A Sadybekov, Anastasiia V Sadybekov, Yongfeng Liu, et al.
Communications Chemistry
|
August 1, 2025
A bottom-up approach to find lead compounds in expansive chemical spaces
Álvaro Serrano-Morrás, Andrea Bertran-Mostazo, Marina Miñarro-Lleonar, et al.
Page
of 11