Luca Gambini

Affiliations: 
2015-2016 Chemistry University of California, Riverside, Riverside, CA, United States 
Google:
"Luca Gambini"
Mean distance: (not calculated yet)
 
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Baggio C, Udompholkul P, Gambini L, et al. (2022) Targefrin: A Potent Agent Targeting the Ligand Binding Domain of EphA2. Journal of Medicinal Chemistry
Udompholkul P, Baggio C, Gambini L, et al. (2021) Lysine Covalent Antagonists of Melanoma Inhibitors of Apoptosis Protein. Journal of Medicinal Chemistry. 64: 16147-16158
Udompholkul P, Baggio C, Gambini L, et al. (2021) Effective Tumor Targeting by EphA2-Agonist-Biotin-Streptavidin Conjugates. Molecules (Basel, Switzerland). 26
Gambini L, Udompholkul P, Baggio C, et al. (2021) Design, Synthesis, and Structural Characterization of Lysine Covalent BH3 Peptides Targeting Mcl-1. Journal of Medicinal Chemistry. 64: 4903-4912
Gambini L, Udompholkul P, Salem AF, et al. (2020) Stability and cell permeability of sulfonyl fluorides in the design  of Lys-covalent antagonists of protein-protein interactions. Chemmedchem
Barile E, Baggio C, Gambini L, et al. (2020) Potential Therapeutic Targeting of Coronavirus Spike Glycoprotein Priming. Molecules (Basel, Switzerland). 25
Salem AF, Gambini L, Udompholkul P, et al. (2020) Therapeutic Targeting of Pancreatic Cancer via EphA2 Dimeric Agonistic Agents. Pharmaceuticals (Basel, Switzerland). 13
Baggio C, Udompholkul P, Gambini L, et al. (2020) N-locking stabilization of covalent helical peptides: Application to Bfl-1 antagonists. Chemical Biology & Drug Design
Baggio C, Udompholkul P, Gambini L, et al. (2019) Aryl-fluorosulfate-based Lysine Covalent pan-Inhibitors of Apoptosis Proteins (IAP) Antagonists with Cellular Efficacy. Journal of Medicinal Chemistry
Gambini L, Baggio C, Udompholkul P, et al. (2019) Covalent Inhibitors of Protein-Protein Interactions Targeting Lysine, Tyrosine, or Histidine Residues. Journal of Medicinal Chemistry
See more...