74067-99-5Relevant articles and documents
A new group of oxime carbamates as reversible inhibitors of fatty acid amide hydrolase
Gattinoni, Sonia,Simone, Chiara De,Dallavalle, Sabrina,Fezza, Filomena,Nannei, Raffaella,Battista, Natalia,Minetti, Patrizia,Quattrociocchi, Gianandrea,Caprioli, Antonio,Borsini, Franco,Cabri, Walter,Penco, Sergio,Merlini, Lucio,MacCarrone, Mauro
supporting information; experimental part, p. 4406 - 4411 (2010/10/02)
A series of oxime carbamates have been identified as potent inhibitors of fatty acid amide hydrolase (FAAH), an important regulatory enzyme of the endocannabinoid signaling system. Kinetic analysis indicates that they behave as non-competitive, reversible
Properties of the Liquid Crystals Formed by Ceratin Azomethines Derived from 4-Cycloalkylanilines and from 4-Cycloalkylbenzaldehydes
Brown, J. W.,Byron, D. J.,Southcott, M.,Wilson, R. C.,Guillon, D.,et al.
, p. 37 - 52 (2007/10/02)
The liquid crystal behaviour of four homologous series of azomethines related to the nO.m series but containing a cycloalkyl group, is reported and discussed.Many of these compounds show extensive smectic polymorphism, one member of the nO.c6 series giving rise to five smectic polymorphic modofications for which phase type assignments have been made by thermal optical microscopy.Keywords: smectic polymorphism, azomethines, cycloalkyl derivatives
