cyanonaphthyridinomycin

Known as: 4,6-Methano-5H-benz(h)oxazolo(3,2-a)pyrazino(3,2,1-de)(1,5)naphthyridine-7-carbonitrile, 1,2,3a,4,4a,6,7,9,10,13,13b,13c-dodecahydro-9-(hydroxymethyl)-11-methoxy-5,12-dimethyl-10,13-dioxo-, (3aS-(3aalpha,4alpha,4abeta,6alpha,7beta,9alpha,13bbeta,13cbeta))-, cyanocycline A 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1982-2011
01219822011

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2011
2011
A full account of our [C + NC + CC] coupling approach to the naphthyridinomycin family of natural products is presented… (More)
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Review
2008
Review
2008
In this tutorial review, which should be of general interest to synthetic organic chemists at large, recent progress in the total… (More)
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1991
1991
Cyanocycline A was found to have a pKa of 6.6. Protonation of N14 was established by 1H NMR spectroscopy. In strongly acidic… (More)
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1985
1985
The characteristics of the in vitro interaction of cyanonaphthyridinomycin (CYANO) with DNA are described. Unlike… (More)
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1983
1983
Cyanocycline A was cytotoxic against Meth A cells in vitro, and also showed marked activity against the same cell line grown as… (More)
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1982
1982
A new antibiotic, cyanocycline A, was isolated from the fermentation broth of Streptomyces flavogriseus strain No. 49, a soil… (More)
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