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• W2023362218 endingPage "1359" @default.
• W2023362218 startingPage "1348" @default.
• W2023362218 abstract "Paraplegia is caused by injuries of the central nervous system (CNS) and especially young people suffer from these severe consequences as, for example, the loss of motor functions. The lack of repair of the injured nerve strands originates from the inhibitory environment for axon regeneration in the CNS. Specific inhibitory proteins block the regrowth of nerve roots. One of these neurite outgrowth inhibitors is the myelin-associated glycoprotein (MAG), which is a member of the Siglec family (sialic acid-binding immunoglobulin-like lectin). In previous studies, we identified potent small molecule MAG antagonists. In this communication, we report new neuraminic acid derivatives modified in the 4- and 5-position, and the influence of various structural modifications on their kinetic and thermodynamic binding properties." @default.
• W2023362218 created "2016-06-24" @default.
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• W2023362218 date "2010-07-01" @default.
• W2023362218 modified "2023-10-16" @default.
• W2023362218 title "Kinetic and thermodynamic properties of MAG antagonists" @default.
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• W2023362218 doi "https://doi.org/10.1016/j.carres.2010.03.010" @default.
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