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WIN 53338

Known as: Isoxazole, 5-(5-(2-chloro-4-(4,5-dihydro-2-oxazolyl)phenoxy)pentyl)-3-methyl-, WIN-53338, WIN53338 
National Institutes of Health

Papers overview

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2020
2020
In this work, the first application of 3,5-dimethyl-4-nitroisoxazole as a vinylogous pronucleophile in the allylic–allylic… 
2015
2015
Exchange proteins directly activated by cAMP (EPAC) as guanine nucleotide exchange factors mediate the effects of the pivotal… 
2013
2013
The invention discloses an isoxazole norcantharidin derivative, and a preparation method and an application thereof. The… 
2012
2012
A new series of isoxazole derivatives, N-phenyl-5-carboxamidyl isoxazoles, was investigated for their anticancer activity with… 
1998
1998
Abstract Glutamate-mediated excitotoxicity plays an important role in the degeneration of nigrostriatal dopamine (DA) neurons… 
1995
1995
Compounds that activate neuronal nicotinic acetylcholine receptors (nAChRs) may have potential benefit in the treatment of… 
1993
1993
The effects of the anti picornaviral drug WIN 54954 (5-(5-(2.6-dichloro-4-(4.5-dihydro-2-oxazolyl)phenoxy)pentyl)-3-me thyl… 
1966
1966
Summary U-10387 (S-carboxy-3-methyl-isoxazole) was shown to increase glucose-1-C14 oxidation and depress release of FFA by…