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Antibiotics (Basel, Switzerland)|August 29, 2024
Targeting <i>N</i>-Acetylglucosaminidase in <i>Staphylococcus aureus</i> with Iminosugar InhibitorsJanja Sluga, Tihomir Tomašič, Marko Anderluh, et al.
ACS Medicinal Chemistry Letters|August 14, 2024
Galectin-8N-Selective 4-Halophenylphthalazinone-Galactals Double π-Stack in a Unique PocketSjors van Klaveren, Mujtaba Hassan, Maria Håkansson, et al.
ACS Medicinal Chemistry Letters|November 19, 2021
Structure-Guided Design of d-Galactal Derivatives with High Affinity and Selectivity for the Galectin-8 N-Terminal DomainMujtaba Hassan, Floriane Baussière, Samo Guzelj, et al.
Nature Communications|January 9, 2021
Potent DNA gyrase inhibitors bind asymmetrically to their target using symmetrical bifurcated halogen bondsAnja Kolarič, Thomas Germe, Martina Hrast, et al.
Bioorganic Chemistry|February 23, 2021
Combining cross-coupling reaction and Knoevenagel condensation in the synthesis of glyco-BODIPY probes for DC-SIGN super-resolution bioimagingGiacomo Biagiotti, Edvin Purić, Iztok Urbančič, et al.
Chemmedchem|October 6, 2021
Selective Monovalent Galectin-8 Ligands Based on 3-LactoylgalactosideBenedetta Girardi, Martina Manna, Sjors Van Klaveren, et al.
Molecules (Basel, Switzerland)|March 26, 2022
Discovery of a New Drug-like Series of OGT Inhibitors by Virtual ScreeningElena M Loi, Tihomir Tomašič, Cyril Balsollier, et al.
European Journal of Medicinal Chemistry|January 12, 2005
Design and synthesis of novel platelet fibrinogen receptor antagonists with 2H-1,4-benzoxazine-3(4H)-one scaffold. A systematic studyMarko Anderluh, Jozko Cesar, Petra Stefanic, et al.
Elife|November 3, 2016
<i>TP53</i> exon-6 truncating mutations produce separation of function isoforms with pro-tumorigenic functionsNitin H Shirole, Debjani Pal, Edward R Kastenhuber, et al.
Communications Chemistry|February 24, 2025
Nanomolar inhibitor of the galectin-8 N-terminal domain binds via a non-canonical cation-π interactionEdvin Purić, Mujtaba Hassan, Fredrik Sjövall, et al.
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