6-Amino-2,4,5-trimethylpyridin-3-ols: A new general synthetic route and antiangiogenic activity
DC Field | Value | Language |
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dc.contributor.author | Kim, Dong-Guk | - |
dc.contributor.author | Kang, Youra | - |
dc.contributor.author | Lee, Hyunji | - |
dc.contributor.author | Lee, Eun Kyung | - |
dc.contributor.author | Tae-gyu Nam | - |
dc.contributor.author | Kim, Jung-Ae | - |
dc.contributor.author | Jeong, Byeong-Seon | - |
dc.date.accessioned | 2021-06-22T23:24:15Z | - |
dc.date.available | 2021-06-22T23:24:15Z | - |
dc.date.created | 2021-01-21 | - |
dc.date.issued | 2014-05 | - |
dc.identifier.issn | 0223-5234 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/22878 | - |
dc.description.abstract | A new synthetic strategy for preparation of a wide range of 6-amino-2,4,5-trimethylpyridin-3-ols from pyridoxine center dot HCl via a six-step sequence has been developed. This approach features an introduction of various amino groups to C(6)-position of 3-benzyloxy-6-bromo-2,4,5-trimethylpyridine (13), a key intermediate, by a Buchwald-Hartwig amination reaction using palladium(0) transition metal, which certainly renders an expanded scope of amino substituents. Some analogs prepared using the methods described here showed high level of antiangiogenic and antitumor activities in chick chorioallantoic membrane (CAM) assay, demonstrating the potential of these new aminopyridinols as antiangiogenic agents. (C) 2014 Elsevier Masson SAS. All rights reserved. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER | - |
dc.title | 6-Amino-2,4,5-trimethylpyridin-3-ols: A new general synthetic route and antiangiogenic activity | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Tae-gyu Nam | - |
dc.identifier.doi | 10.1016/j.ejmech.2014.03.045 | - |
dc.identifier.scopusid | 2-s2.0-84897456629 | - |
dc.identifier.wosid | 000335805400013 | - |
dc.identifier.bibliographicCitation | EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, v.78, pp.126 - 139 | - |
dc.relation.isPartOf | EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY | - |
dc.citation.title | EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY | - |
dc.citation.volume | 78 | - |
dc.citation.startPage | 126 | - |
dc.citation.endPage | 139 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Medicinal | - |
dc.subject.keywordPlus | PALLADIUM-CATALYZED AMINATION | - |
dc.subject.keywordPlus | TYROSINE KINASE INHIBITORS | - |
dc.subject.keywordPlus | ENDOTHELIAL GROWTH-FACTOR | - |
dc.subject.keywordPlus | ARYL HALIDES | - |
dc.subject.keywordPlus | ANGIOGENESIS | - |
dc.subject.keywordPlus | MECHANISM | - |
dc.subject.keywordPlus | ETHERS | - |
dc.subject.keywordAuthor | Aminopyridinol | - |
dc.subject.keywordAuthor | Angiogenesis | - |
dc.subject.keywordAuthor | Antiangiogenic | - |
dc.subject.keywordAuthor | Antitumor | - |
dc.subject.keywordAuthor | Chick chorioallantoic membrane assay | - |
dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S022352341400258X?via%3Dihub | - |
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