Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 노분조 | * |
dc.date.accessioned | 2016-08-28T10:08:17Z | - |
dc.date.available | 2016-08-28T10:08:17Z | - |
dc.date.issued | 2012 | * |
dc.identifier.issn | 0968-0896 | * |
dc.identifier.other | OAK-8904 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/222752 | - |
dc.description.abstract | Six β-carboline alkaloids (1-6) of the eudistomin Y class were isolated from the Korean ascidian Synoicum sp. These compounds were chemically converted to a known compound, eudistomin Y 1 (7) and six new derivatives, designated eudistomins Y 8-Y 13 (8-13). Several of these natural and synthetic compounds exhibited moderate to significant antimicrobial activity, weak cytotoxic activity, and inhibitory activities toward sortase A, isocitrate lyase, and Na +/K +-ATPase. Structure-activity relationships were also deduced. © 2012 Elsevier Ltd. All rights reserved. | * |
dc.language | English | * |
dc.title | Beta-carboline alkaloids derived from the ascidian Synoicum sp. | * |
dc.type | Article | * |
dc.relation.issue | 13 | * |
dc.relation.volume | 20 | * |
dc.relation.index | SCI | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | 4082 | * |
dc.relation.lastpage | 4087 | * |
dc.relation.journaltitle | Bioorganic and Medicinal Chemistry | * |
dc.identifier.doi | 10.1016/j.bmc.2012.05.002 | * |
dc.identifier.wosid | WOS:000305279700014 | * |
dc.identifier.scopusid | 2-s2.0-84862164208 | * |
dc.author.google | Won T.H. | * |
dc.author.google | Jeon J.-E. | * |
dc.author.google | Lee S.-H. | * |
dc.author.google | Rho B.J. | * |
dc.author.google | Oh K.-B. | * |
dc.author.google | Shin J. | * |
dc.contributor.scopusid | 노분조(7006330628;55251197500) | * |
dc.date.modifydate | 20240423081003 | * |