17626-82-3Relevant articles and documents
Substituted heterocyclic analogs as selective COX-2 inhibitors in the flosulide class
Ouimet, Nathalie,Chan, Chi-Chung,Charleson, Stella,Claveau, David,Gordon, Robert,Guay, Daniel,Chun-Sing, Li,Ouellet, Marc,Percival, David M.,Riendeau, Denis,Wong, Elizabeth,Zamboni, Robert,Prasit, Petpiboon
, p. 151 - 156 (1999)
Substituted heterocyclic analogs in the Flosulide class were investigated as potential selective cyclooxygenase-2 inhibitors. 6-(4-Ethyl- 2-thiazolylthio)-5-methanesulfonamido-3H-isobenzofuran-1-one 14 was found to be the optimal compound in the series wi
CARBACEPHEM β-LACTAM ANTIBIOTICS
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Page/Page column 88, (2010/04/06)
Carbacephem -lactam antibiotics having structure (I) are disclosed, including stereoisomers, pharmaceutically acceptable salts, esters and prodrugs thereof, wherein Ar1, Ar2, R1 and R2 are as defined herein. The compounds are useful for the treatment of bacterial infections, in particular those caused by methicillin-resistant Staphylococcus spp.
SYNTHESIS AND REACTIONS OF NEW VINYL ISOTHIOCYANATES
Banert, Klaus,Groth, Stefan,Hueckstaedt, Holger,Vrobel, Kai
, p. 323 - 324 (2007/10/02)
New vinyl isothiocyanates, which can be prepared from easily accessible thiocyanates by sigmatropic shifts, show unusually high reactivity used for the synthesis of heterocyclic sulfur compounds.