4.7 Article

Small Molecules Selectively Targeting Sigma-1 Receptor for the Treatment of Neurological Diseases

期刊

JOURNAL OF MEDICINAL CHEMISTRY
卷 63, 期 24, 页码 15187-15217

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jmedchem.0c01192

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资金

  1. National Natural Science Foundation of China [81703330, 81773702, 81973334]
  2. Natural Science Foundation of Jiangsu Province [BK20170347]
  3. Priority Academic Program Development of the Jiangsu Higher Education Institutes (PAPD)
  4. Jiangsu Key Laboratory of Neuropsychiatric Diseases [BM2013003]
  5. Distinguished Chair Endowment Fund at UTMB
  6. National Institutes of Health (NIH) National Research Service Award (NRSA) [F31 DA04551]

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The sigma-1 (sigma(1)) receptor, an enigmatic protein originally classified as an opioid receptor subtype, is now understood to possess unique structural and functional features of its own and play critical roles to widely impact signaling transduction by interacting with receptors, ion channels, lipids, and kinases. The sigma(1) receptor is implicated in modulating learning, memory, emotion, sensory systems, neuronal development, and cognition and accordingly is now an actively pursued drug target for various neurological and neuropsychiatric disorders. Evaluation of the five selective sigma(1) receptor drug candidates (pridopidine, ANAVEX2-73, SA4503, S1RA, and T-817MA) that have entered clinical trials has shown that reaching clinical approval remains an evasive and important goal. This review provides up-to-date information on the selective targeting of sigma(1) receptors, including their history, function, reported crystal structures, and roles in neurological diseases, as well as a useful collation of new chemical entities as sigma(1) selective orthosteric ligands or allosteric modulators.

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