327037-11-6Relevant articles and documents
OXAZOLIDINONE DERIVATIVES AS PPAR LIGANDS
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Paragraph 0149; 0158, (2016/06/28)
The present invention relates to a family of differently substituted oxazolidinones and to the pharmaceutically acceptable salts, esters, prodrugs, tautomers, solvates and hydrates thereof, which show affinity for the alpha and gamma subtypes of the perox
Design, synthesis, and biological evaluation of a series of lavendustin A analogues that inhibit EGFR and Syk tyrosine kinases, as well as tubulin polymerization
Mu,Coffing,Riese II,Geahlen,Verdier-Pinard,Hamel,Johnson,Cushman
, p. 441 - 452 (2007/10/03)
A series of N-alkylamide analogues of the lavendustin A pharmacophore were synthesized and tested for inhibitiofi of the epidermal growth factor receptor (EGFR) protein tyrosine kinase and the nonreceptor protein tyrosine kinase Syk. Although several comp