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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
17
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pubmed:dateCreated |
2003-11-12
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pubmed:abstractText |
Capuramycin analogues with a variety of substituents in place of the azepan-2-one moiety were synthesized from A-500359E and were tested for their translocase I inhibitory activity and in vitro antimycobacterial activity. Phenyl-type moieties were found to be effective substituents for capuramycin analogues.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0960-894X
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pubmed:author |
pubmed-author:AbeTomomiT,
pubmed-author:DaigoMakikoM,
pubmed-author:FukuokaTakashiT,
pubmed-author:FurukawaMiyukiM,
pubmed-author:HarasakiTamakoT,
pubmed-author:HotodaHitoshiH,
pubmed-author:InukaiMasatoshiM,
pubmed-author:IshiiMichiko MiyazawaMM,
pubmed-author:KakutaMasayoM,
pubmed-author:KanekoMasakatsuM,
pubmed-author:MiyakoshiShun-ichiS,
pubmed-author:MuramatsuYasunoriY,
pubmed-author:MurayamaKazuhiroK,
pubmed-author:OhyaSatoshiS,
pubmed-author:TakatsuToshioT,
pubmed-author:UtsuiYukioY
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pubmed:issnType |
Print
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|
pubmed:day |
1
|
|
pubmed:volume |
13
|
|
pubmed:owner |
NLM
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|
pubmed:authorsComplete |
Y
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pubmed:pagination |
2829-32
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
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pubmed:year |
2003
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pubmed:articleTitle |
Synthesis and antimycobacterial activity of capuramycin analogues. Part 1: substitution of the azepan-2-one moiety of capuramycin.
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pubmed:affiliation |
Exploratory Chemistry Research Laboratories, Sankyo Co., Ltd., Tokyo, Japan. hotoda@hq.sankyo.co.jp
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pubmed:publicationType |
Journal Article
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