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iodinated azido-leukotriene D4

Known as: (125)I-azido-LTD4 
National Institutes of Health

Papers overview

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2014
2014
Iminosugars, by virtue of their structural resemblance to monosaccharides, are among the most potent inhibitors of glycosidases… 
2013
2013
Site-specific functionalization of proteins by bioorthogonal modification offers a convenient pathway to create, modify, and… 
2012
2012
The prevalence of obesity has increased significantly in recent years, but no succeful treatment for it has been found yet. Among… 
2010
2010
DMXAA (5,6-dimethylxanthenone-4-acetic acid) is in late stages of clinical development as a tumor vascular disrupting agent. The… 
2009
2009
Objective:To synthetize 2’,3’-azido-2’,3’-seconucleoside analogues,and to determine the potential antiviral activity.Methods:The… 
2001
2001
Some 1,2- and 1,3-diacyl glycerols (with acyl groups as stearyl, oleyl, linoleyl, or stearolyl) were synthesized by conventional… 
1986
1986
Desensitization of the leukocyte beta-receptor system has been associated with a functional uncoupling of the components of the… 
1984
1984
Oligoribonucleotide derivatives containing the photoactivated arylazidogroup at 5'-end of the oligonucleotide fragment [2-(N-2,4… 
1983
1983
Azido nitrophenylaminoacetyl [125I]iodo derivative of toxin II from Centruroides suffusus suffusus, a beta-toxin, and azido…