ACS Medicinal Chemistry Letters · 2017 · 86 citations · 29 references
PharmacyMedicinal ChemistryPharmacologyDrug DiscoveryEnzymologyMolecular PharmacologyEnzyme InhibitionStructure-activity Relationship AnalysisChemical Enzyme InhibitorsEnzyme Inhibition ScreeningEnzyme Inhibitor DiscoveryEnzyme Inhibitor SynthesisInhibitor ClassificationInhibitor ScreeningLysyl Oxidase Inhibition
Two series of novel LOXL2 enzyme inhibitors are described: benzylamines substituted with electron withdrawing groups at the para -position and 2-substituted pyridine-4-ylmethanamines. The most potent compound, (2-chloropyridin-4-yl)methanamine 20 (hLOXL2 IC 50 = 126 nM), was shown to be selective for LOXL2 over LOX and three other amine oxidases (MAO-A, MAO-B, and SSAO). Compound 20 is the first published small molecule inhibitor selective for LOXL2 over LOX.
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Elastic fiber homeostasis requires lysyl oxidase–like 1 protein
Xiaoqing Liu, Yun Zhao, Jiangang Gao et al. · Nature Genetics · 2004 · 659 citations
S.R. Pinnell, George R. Martin · Proceedings of the National Academy of Sciences · 1968 · 496 citations · Full text