Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 오세관 | * |
dc.date.accessioned | 2016-11-30T02:11:30Z | - |
dc.date.available | 2016-11-30T02:11:30Z | - |
dc.date.issued | 2008 | * |
dc.identifier.issn | 1747-0277 | * |
dc.identifier.other | OAK-5227 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/232906 | - |
dc.description.abstract | A simple synthesis involving a key coupling reaction and biological activity of N-protected cyclopropylethylcarbamates (18-21) are described. The key fragments are amine·HCl salt (13) and acids (16 and 17) which were smoothly coupled by using 2-(7-aza-1H-benzotriazol-1-yl)-1,1,3,3- tetramethyluroniumhexafluorophosphate in high yield. We have found that the in vitro growth inhibitory potency of new compound 19 exhibited good histone deacetylase activity. © 2008 The Authors. | * |
dc.language | English | * |
dc.title | Synthesis, structural characterization and biological evaluation of N-protected cyclopropylethylcarbamates as potential histone deacetylase inhibitor | * |
dc.type | Article | * |
dc.relation.issue | 6 | * |
dc.relation.volume | 72 | * |
dc.relation.index | SCI | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | 592 | * |
dc.relation.lastpage | 595 | * |
dc.relation.journaltitle | Chemical Biology and Drug Design | * |
dc.identifier.doi | 10.1111/j.1747-0285.2008.00743.x | * |
dc.identifier.wosid | WOS:000261117500014 | * |
dc.identifier.scopusid | 2-s2.0-56649086401 | * |
dc.author.google | Jung J.-C. | * |
dc.author.google | Moon H.-I. | * |
dc.author.google | Oh S. | * |
dc.contributor.scopusid | 오세관(7404103757) | * |
dc.date.modifydate | 20240118133340 | * |