A Perspective on the Development of c-Jun N-terminal Kinase Inhibitors as Therapeutics for Alzheimer's Disease: Investigating Structure through Docking Studies
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Cho, Hyunwook | - |
dc.contributor.author | Hah, Jung-Mi | - |
dc.date.accessioned | 2022-07-18T01:31:44Z | - |
dc.date.available | 2022-07-18T01:31:44Z | - |
dc.date.issued | 2021-10 | - |
dc.identifier.issn | 2227-9059 | - |
dc.identifier.issn | 2227-9059 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/108185 | - |
dc.description.abstract | c-Jun N-terminal kinase (JNK) plays an important role in cell death caused by various stimuli. Because the isoform JNK3 is mainly expressed in the brain, it is believed to play a pivotal role in various neurodegenerative diseases, including Alzheimer's disease (AD) and Parkinson's disease (PD), which still lack plausible therapeutics. To develop a novel and selective JNK3 inhibitor, we conducted a decadal review (2011 to 2021) of published articles on JNK inhibitors, particularly those focusing on a structural perspective and docking insights. We observed the structures of three isoforms of JNK, namely holo-proteins and co-crystal structures, with JNK3 inhibitors and summarized the significant structural aspects of selective JNK3 inhibitors as AD therapeutics.</p> | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | MDPI | - |
dc.title | A Perspective on the Development of c-Jun N-terminal Kinase Inhibitors as Therapeutics for Alzheimer's Disease: Investigating Structure through Docking Studies | - |
dc.type | Article | - |
dc.publisher.location | 스위스 | - |
dc.identifier.doi | 10.3390/biomedicines9101431 | - |
dc.identifier.scopusid | 2-s2.0-85117300398 | - |
dc.identifier.wosid | 000714589400001 | - |
dc.identifier.bibliographicCitation | BIOMEDICINES, v.9, no.10 | - |
dc.citation.title | BIOMEDICINES | - |
dc.citation.volume | 9 | - |
dc.citation.number | 10 | - |
dc.type.docType | Review | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Research & Experimental Medicine | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Medicine, Research & Experimental | - |
dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
dc.subject.keywordPlus | CRYSTAL-STRUCTURE | - |
dc.subject.keywordPlus | PROTEIN-KINASE | - |
dc.subject.keywordPlus | JNK INHIBITOR | - |
dc.subject.keywordPlus | OPTIMIZATION | - |
dc.subject.keywordPlus | ACTIVATION | - |
dc.subject.keywordPlus | DISCOVERY | - |
dc.subject.keywordPlus | DESIGN | - |
dc.subject.keywordPlus | POTENT | - |
dc.subject.keywordPlus | PHOSPHORYLATION | - |
dc.subject.keywordPlus | SELECTIVITY | - |
dc.subject.keywordAuthor | Alzheimer's disease | - |
dc.subject.keywordAuthor | c-Jun N-terminal kinase | - |
dc.subject.keywordAuthor | small-molecule protein kinase inhibitor | - |
dc.subject.keywordAuthor | JNK3 | - |
dc.subject.keywordAuthor | selectivity | - |
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