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12 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Design and synthesis of potent substrate-based inhibitors of the Trypanosoma cruzi dihydroorotate dehydrogenase.EBI
Nagasaki University
Synthesis, resolution, and biological evaluation of atropisomeric (aR)- and (aS)-16-methyllamellarins N: unique effects of the axial chirality on the selectivity of protein kinases inhibition.EBI
Nagasaki University
Synthesis and characterization of [¹²¿?¿I]2-iodo N-[(S)-{(S)-1-methylpiperidin-2-yl}(phenyl)methyl]3-trifluoromethyl-benzamide as novel imaging probe for glycine transporter 1.EBI
Nagasaki University
Novel benzofuran derivatives for PET imaging of beta-amyloid plaques in Alzheimer's disease brains.EBI
Nagasaki University
Radioiodinated flavones for in vivo imaging of beta-amyloid plaques in the brain.EBI
Nagasaki University
Synthesis and evaluation of azalamellarin N and its A-ring-modified analogues as non-covalent inhibitors of the EGFR T790M/L858R mutant.EBI
Nagasaki University
Synthesis and evaluation of a radioiodinated 4,6-diaryl-3-cyano-2-pyridinone derivative as a survivin targeting SPECT probe for tumor imaging.EBI
Nagasaki University
Synthesis and biological evaluation of radioiodinated quinacrine-based derivatives for SPECT imaging of Aβ plaques.EBI
Nagasaki University
Synthesis, structure-activity relationships, and mechanism of action of anti-HIV-1 lamellarin α 20-sulfate analogues.EBI
Nagasaki University
Synthesis and structure-activity relationship study of lamellarin derivatives.EBI
Nagasaki University
Design and synthesis of estrogen receptor ligands with a 4-heterocycle-4-phenylheptane skeleton.EBI
Nagasaki University
Design, synthesis, and evaluation of A-ring-modified lamellarin N analogues as noncovalent inhibitors of the EGFR T790M/L858R mutant.EBI
Nagasaki University