<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kanno T</submitter><funding>the Japan Science and Technology Agency</funding><pagination>e0186227</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5633190</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(10)</volume><pubmed_abstract>Therapeutic agents to the central nervous system (CNS) need to be efficiently delivered to the target site of action at appropriate therapeutic levels. However, a limited number of effective drugs for the treatment of neurological diseases has been developed thus far. Further, the pharmacological mechanisms by which such therapeutic agents can protect neurons from cell death have not been fully understood. We have previously reported the novel small-molecule compound, 2-[mesityl(methyl)amino]-N-[4-(pyridin-2-yl)-1H-imidazol-2-yl] acetamide trihydrochloride (WN1316), as a unique neuroprotectant against oxidative injury and a highly promising remedy for the treatment of amyotrophic lateral sclerosis (ALS). One of the remarkable characteristics of WN1316 is that its efficacious doses in ALS m</pubmed_abstract><journal>PloS one</journal><pubmed_title>A novel function of N-linked glycoproteins, alpha-2-HS-glycoprotein and hemopexin: Implications for small molecule compound-mediated neuroprotection.</pubmed_title><pmcid>PMC5633190</pmcid><funding_grant_id>Adaptable and Seamless Technology Transfer Program through Target-driven R&amp;amp;D (A-STEP)</funding_grant_id><pubmed_authors>Kanno T</pubmed_authors><pubmed_authors>Hadano S</pubmed_authors><pubmed_authors>Tanaka K</pubmed_authors><pubmed_authors>Ikeda JE</pubmed_authors><pubmed_authors>Yasutake K</pubmed_authors></additional><is_claimable>false</is_claimable><name>A novel function of N-linked glycoproteins, alpha-2-HS-glycoprotein and hemopexin: Implications for small molecule compound-mediated neuroprotection.</name><description>Therapeutic agents to the central nervous system (CNS) need to be efficiently delivered to the target site of action at appropriate therapeutic levels. However, a limited number of effective drugs for the treatment of neurological diseases has been developed thus far. Further, the pharmacological mechanisms by which such therapeutic agents can protect neurons from cell death have not been fully understood. We have previously reported the novel small-molecule compound, 2-[mesityl(methyl)amino]-N-[4-(pyridin-2-yl)-1H-imidazol-2-yl] acetamide trihydrochloride (WN1316), as a unique neuroprotectant against oxidative injury and a highly promising remedy for the treatment of amyotrophic lateral sclerosis (ALS). One of the remarkable characteristics of WN1316 is that its efficacious doses in ALS m</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017</publication><modification>2025-04-27T03:58:14.419Z</modification><creation>2019-03-27T02:58:30Z</creation></dates><accession>S-EPMC5633190</accession><cross_references><pubmed>29016670</pubmed><doi>10.1371/journal.pone.0186227</doi></cross_references></HashMap>