aeruginosin 298-A

Known as: aeruginosin 298 A 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2001-2017
01220012017

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2017
2017
The synthesis of the presumed structure of aeruginosin KT608A was accomplished for the first time. The unusual d-diepi-Choi core… (More)
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2013
2013
An aqueous MeOH extract of Microcystis aeruginosa (IL-399) afforded three new protease inhibitors, micropeptin HH978 (1… (More)
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2012
2012
Six new metabolites, micropeptin KT1042, microguanidine KT636, aeruginosins KT608A, KT608B, and KT650, and pseudoaeruginosin… (More)
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2009
2009
Aeruginosins are a family of naturally occurring oligopeptides that share a common bicyclic amino acid core structure. Many… (More)
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2005
2005
[reaction: see text] The design and synthesis of a new core structure, a ring-oxygenated variant of 2-carboxy-6… (More)
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2004
2004
Aeruginosin 298-A was isolated from the freshwater cyanobacterium Microcystis aeruginosa (NIES-298) and is an equipotent thrombin… (More)
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2003
2003
We developed a versatile synthetic process for aeruginosin 298-A as well as several attractive analogues, in which all… (More)
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2003
2003
[structure: see text] The putative structure of the naturally occurring aquatic peptide aeruginosin EI461 has been prepared from… (More)
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2002
2002
Two new trypsin inhibitors, micropeptins EI992 (1) and EI964 (2), and a modified linear peptide aeruginosin EI461 (3) were… (More)
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2001
2001
The first total syntheses of aeruginosin 298-A (1) and aeruginosin 298-B (3) are described. The syntheses of the alternative… (More)
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