capuramycin

Known as: beta-D-Allofuranuronamide, 1-deoxy-5-O-(4-deoxy-N-(hexahydro-2-oxo-1H-azepin-3-yl)-alpha-L-erythro-hex-4-enopyranuronamidosyl)-1-(3,4-dihydro-2,4-dioxo-1(2H)-pyrimidinyl)-3-O-methyl-, (S)- 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1986-2017
012319862017

Papers overview

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2013
2013
Capuramycin and its congeners are considered to be important lead molecules for the development of a new drug for multidrug… (More)
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2010
2010
OBJECTIVES To determine antibacterial activity of capuramycin analogues SQ997, SQ922, SQ641 and RKS2244 against several non… (More)
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2010
2010
Capuramycin-related compounds, including A-500359s and A-503083s, are nucleoside antibiotics that inhibit the enzyme bacterial… (More)
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2009
2009
A concise total synthesis of capuramycin (1), a promising preclinical TB drug lead, is achieved by high-yield formations of the… (More)
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2009
2009
New delivery vehicles and routes of delivery were developed for the capuramycin analogue SQ641. While this compound has… (More)
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2008
2008
Translocase I inhibitor compounds derived from capuramycin demonstrated rapid bactericidal activity against several different… (More)
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2004
2004
OBJECTIVES The antimycobacterial activities of RS-112997, RS-124922 and RS-118641, three capuramycin analogues that inhibit… (More)
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2003
2003
Acylated derivatives of capuramycin and A-500359A were synthesized and tested for antimycobacterial activity. Compound 20 having… (More)
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2003
2003
Capuramycin analogues with a variety of substituents in place of the azepan-2-one moiety were synthesized from A-500359E and were… (More)
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1986
1986
A new antibiotic capuramycin was isolated from the culture filtrate of Streptomyces griseus 446-S3 by adsorption and partition… (More)
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