Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 이강만 | * |
dc.contributor.author | 정낙신 | * |
dc.contributor.author | 최선 | * |
dc.date.accessioned | 2016-08-28T12:08:45Z | - |
dc.date.available | 2016-08-28T12:08:45Z | - |
dc.date.issued | 2007 | * |
dc.identifier.issn | 0960-894X | * |
dc.identifier.other | OAK-4213 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/219889 | - |
dc.description.abstract | 5′-Deoxy-5′-ureidoadenosine was designed and synthesized as a potent inhibitor of S-adenosylhomocysteine hydrolase (SAH), in which 5′-ureido group acted as multiple hydrogen bonding donor in binding with active site residues of SAH in the molecular modeling study. © 2007. | * |
dc.language | English | * |
dc.title | Design, synthesis, and molecular modeling studies of 5′-deoxy-5′-ureidoadenosine: 5′-ureido group as multiple hydrogen bonding donor in the active site of S-adenosylhomocysteine hydrolase | * |
dc.type | Article | * |
dc.relation.issue | 16 | * |
dc.relation.volume | 17 | * |
dc.relation.index | SCI | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | 4456 | * |
dc.relation.lastpage | 4459 | * |
dc.relation.journaltitle | Bioorganic and Medicinal Chemistry Letters | * |
dc.identifier.doi | 10.1016/j.bmcl.2007.06.013 | * |
dc.identifier.wosid | WOS:000248877800010 | * |
dc.identifier.scopusid | 2-s2.0-34447302305 | * |
dc.author.google | Wang T. | * |
dc.author.google | Lee H.J. | * |
dc.author.google | Tosh D.K. | * |
dc.author.google | Kim H.O. | * |
dc.author.google | Pal S. | * |
dc.author.google | Choi S. | * |
dc.author.google | Lee Y. | * |
dc.author.google | Moon H.R. | * |
dc.author.google | Zhao L.X. | * |
dc.author.google | Lee K.M. | * |
dc.author.google | Jeong L.S. | * |
dc.contributor.scopusid | 이강만(7501506362) | * |
dc.contributor.scopusid | 정낙신(16028528200) | * |
dc.contributor.scopusid | 최선(8659831000) | * |
dc.date.modifydate | 20240305081003 | * |