dehydroapratoxin A

Known as: dehydro-apratoxin A 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2004-2018
012320042018

Papers overview

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2016
2016
In this research, the synthesis, biological evaluation, and conformational analysis of an apratoxin C oxazoline analog (3) have… (More)
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2016
2016
An efficient method for asymmetric synthesis of apratoxin E 2 is described in this report. The chiral lactone 8, recycled from… (More)
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2016
2016
Apratoxin E provided the inspiration for the design of apratoxin A/E hybrids under preclinical development. Through total… (More)
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2014
2014
This paper describes the synthetic studies conducted on a marine natural product, cyclodepsipeptide apratoxin A. Total synthesis… (More)
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2014
2014
Total synthesis of apratoxin C, a cyanobacterial cyclodepsipeptide with highly potent cytotoxicity against some cancer cell lines… (More)
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2012
2012
The first asymmetric total synthesis of the marine natural product apratoxin D, a highly potent inhibitor of H-460 human lung… (More)
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2008
2008
Cancer cell toxicity-guided fractionation of extracts of the Papua New Guinea marine cyanobacteria Lyngbya majuscula and Lyngbya… (More)
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2008
2008
A collection of the marine cyanobacterium Lyngbya bouillonii from Guam afforded apratoxin E (1), a new peptide-polyketide hybrid… (More)
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2004
2004
A total synthesis of apratoxin A was developed. Apratoxin A, isolated from Lyngbya spp. cyanobacteria, is representative of a… (More)
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