Recent Advances of SHP2 Inhibitors in Cancer Therapy: Current Development and Clinical Application | Journal of Medicinal Chemistry
Development of M1 mAChR Allosteric and Bitopic Ligands: Prospective Therapeutics for the Treatment of Cognitive Deficits | ACS Chemical Neuroscience
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Sialidase Inhibitors with Different Mechanisms | Journal of Medicinal Chemistry
Inhibition of mutant RAS-RAF interaction by mimicking structural and dynamic properties of phosphorylated RAS | eLife
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Discovery of the Potent and Selective M1 PAM-Agonist N-[(3R,4S)-3-Hydroxytetrahydro-2H-pyran-4-yl]-5-methyl-4-[4-(1,3-thiazol-4-yl)benzyl]pyridine-2-carboxamide (PF-06767832): Evaluation of Efficacy and Cholinergic Side Effects | Journal of Medicinal ...
Inhibition of mutant RAS-RAF interaction by mimicking structural and dynamic properties of phosphorylated RAS | eLife
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Complexation of Ln3+ Ions with Cyclam Dipicolinates: A Small Bridge that Makes Huge Differences in Structure, Equilibrium, and Kinetic Properties | Inorganic Chemistry
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The Communicator_Ed.2_v.50_2022_2023 by The Communicator - Issuu
Inhibition of mutant RAS-RAF interaction by mimicking structural and dynamic properties of phosphorylated RAS | eLife
Development of M1 mAChR Allosteric and Bitopic Ligands: Prospective Therapeutics for the Treatment of Cognitive Deficits | ACS Chemical Neuroscience
The CIC-ERF co-deletion underlies fusion-independent activation of ETS family member, ETV1, to drive prostate cancer progression | eLife
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Surface Probing by Fragment-Based Screening and Computational Methods Identifies Ligandable Pockets on the von Hippel–Lindau (VHL) E3 Ubiquitin Ligase | Journal of Medicinal Chemistry
World Development Report 2022 by World Bank Publications - Issuu
