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pubmed-article:14565234pubmed:abstractTextHalogenated 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.lld:pubmed
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pubmed-article:14565234pubmed:authorpubmed-author:KimHea OkHOlld:pubmed
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pubmed-article:14565234pubmed:authorpubmed-author:LeeKang ManKMlld:pubmed
pubmed-article:14565234pubmed:authorpubmed-author:KimJoong...lld:pubmed
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pubmed-article:14565234pubmed:authorpubmed-author:ShinDae...lld:pubmed
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pubmed-article:14565234pubmed:pagination589-92lld:pubmed
pubmed-article:14565234pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:14565234pubmed:articleTitleSynthesis and biological evaluation of halo-neplanocin A as novel mechanism-based inhibitors of S-adenosylhomocysteine hydrolase.lld:pubmed
pubmed-article:14565234pubmed:affiliationCollege of Pharmacy, Ewha Womans University, Seoul, Korea. lakjeong@ewha.ac.krlld:pubmed
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