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dc.contributor.author정낙신-
dc.date.accessioned2017-01-05T02:01:17Z-
dc.date.available2017-01-05T02:01:17Z-
dc.date.issued2003-
dc.identifier.issn1525-7770-
dc.identifier.otherOAK-1624-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/233700-
dc.description.abstractHalogenated analogues of neplanocin A were synthesized from the key intermediate 1, among which fluoro-neplanocin A was found to be novel mechanism-based irreversible inhibitor of S-Adenosylhomocysteine hydrolase.-
dc.languageEnglish-
dc.titleSynthesis and biological evaluation of halo-neplanocin A as novel mechanism-based inhibitors of S-Adenosylhomocysteine hydrolase-
dc.typeConference Paper-
dc.relation.issue5-8-
dc.relation.volume22-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage589-
dc.relation.lastpage592-
dc.relation.journaltitleNucleosides, Nucleotides and Nucleic Acids-
dc.identifier.doi10.1081/NCN-120021961-
dc.identifier.wosidWOS:000185439200010-
dc.identifier.scopusid2-s2.0-0141425747-
dc.author.googleJeong L.S.-
dc.author.googleMoon H.R.-
dc.author.googlePark J.G.-
dc.author.googleShin D.H.-
dc.author.googleChoi W.J.-
dc.author.googleLee K.M.-
dc.author.googleKim H.O.-
dc.author.googleChun M.W.-
dc.author.googleKim H.-D.-
dc.author.googleKim J.H.-
dc.contributor.scopusid정낙신(16028528200)-
dc.date.modifydate20211210153610-
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약학대학 > 약학과 > Journal papers
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