A substituted 3,4-dihydropyrimidinone derivative (compound D22) prevents inflammation mediated neurotoxicity; role in microglial activation in BV-2 cells
DC Field | Value | Language |
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dc.contributor.author | Kwon, Oh Wook | - |
dc.contributor.author | Moon, Eunjung | - |
dc.contributor.author | Chari, Murugulla A. | - |
dc.contributor.author | Kim, Tae Woo | - |
dc.contributor.author | Kim, Ae-jung | - |
dc.contributor.author | Lee, Pyeongjae | - |
dc.contributor.author | Ahn, Kwang-Hyun | - |
dc.contributor.author | Kim, Sun Yeou | - |
dc.date.available | 2020-02-29T05:44:46Z | - |
dc.date.created | 2020-02-06 | - |
dc.date.issued | 2012-08-15 | - |
dc.identifier.issn | 0960-894X | - |
dc.identifier.uri | https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/16230 | - |
dc.description.abstract | A novel synthetic 3,4-dihydropyrimidinone derivative, compound D22(ethyl 6-methyl-4-(3-phenoxyphenyl)-2-thioxo-3,4-dihydropyrimidine-5-carboxylate), was found to exert anti-inflammatory properties in lipopolysaccharide-stimulated microglial BV-2 cells. Compound D22 reduced the pro-inflammatory factors such as nitric oxide, prostaglandin E-2, tumor necrosis factor-alpha and interleukin-1 beta. Moreover, it suppressed the expressions of inducible NO synthase and cyclooxygenase-2. Compound D22 inhibited the activation of mitogen-activated protein kinases. When compound D22-conditioned media from BV-2 cells were applied to N2a cells, neuronal cell death was inhibited via suppression of caspase-3 activation and regulation of Bcl-2 and Bax proteins expression. These results suggest that compound D22 may be useful for treating neurodegenerative diseases related with neuroinflammation. Crown Copyright (c) 2012 Published by Elsevier Ltd. All rights reserved. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | - |
dc.relation.isPartOf | BIOORGANIC & MEDICINAL CHEMISTRY LETTERS | - |
dc.subject | NITRIC-OXIDE | - |
dc.subject | IN-VITRO | - |
dc.subject | DISEASE | - |
dc.subject | APOPTOSIS | - |
dc.subject | CYTOKINES | - |
dc.subject | RESPONSES | - |
dc.subject | INJURY | - |
dc.subject | AGENTS | - |
dc.subject | DEATH | - |
dc.subject | UREA | - |
dc.title | A substituted 3,4-dihydropyrimidinone derivative (compound D22) prevents inflammation mediated neurotoxicity; role in microglial activation in BV-2 cells | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.description.journalClass | 1 | - |
dc.identifier.wosid | 000306962800008 | - |
dc.identifier.doi | 10.1016/j.bmcl.2012.06.082 | - |
dc.identifier.bibliographicCitation | BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.22, no.16, pp.5199 - 5203 | - |
dc.identifier.scopusid | 2-s2.0-84864400412 | - |
dc.citation.endPage | 5203 | - |
dc.citation.startPage | 5199 | - |
dc.citation.title | BIOORGANIC & MEDICINAL CHEMISTRY LETTERS | - |
dc.citation.volume | 22 | - |
dc.citation.number | 16 | - |
dc.contributor.affiliatedAuthor | Kim, Sun Yeou | - |
dc.type.docType | Article | - |
dc.subject.keywordAuthor | DHPM | - |
dc.subject.keywordAuthor | Ethyl 6-methyl-4-(3-phenoxyphenyl)-2-thioxo-3,4-dihydropyrimidine-5-carboxylate | - |
dc.subject.keywordAuthor | Neuroinflammation | - |
dc.subject.keywordAuthor | Neuroprotection | - |
dc.subject.keywordAuthor | Microglia | - |
dc.subject.keywordPlus | NITRIC-OXIDE | - |
dc.subject.keywordPlus | IN-VITRO | - |
dc.subject.keywordPlus | DISEASE | - |
dc.subject.keywordPlus | APOPTOSIS | - |
dc.subject.keywordPlus | CYTOKINES | - |
dc.subject.keywordPlus | RESPONSES | - |
dc.subject.keywordPlus | INJURY | - |
dc.subject.keywordPlus | AGENTS | - |
dc.subject.keywordPlus | DEATH | - |
dc.subject.keywordPlus | UREA | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Medicinal | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
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