101654-29-9Relevant articles and documents
Synthesis of GABA-valproic acid derivatives and evaluation of their anticonvulsant and antioxidant activity
Rekatas, George V.,Tani, Ekaterini,Demopoulos, Vassilis J.,Kourounakis, Panos N.
, p. 393 - 398 (1996)
The synthesis and the anticonvulsant activity of a number of GABA and valproic acid derivatives are reported. The lipophilicity of these compunds and their inhibitory effect on lipid peroxidation were also investigated, in an effort to correlate the anticonvulsant activity with lipophilicity and inhibitory effect on lipid peroxidation. The synthetized compounds exhibited anticonvulsant effects which were stronger for the more lipophilic derivatives. One of the active anticonvulsants showed appreciable antioxidant properties. Finally, a good correlation was found between the experimentally derived (R(M)) and calculated (Σf and log P(SK)) lipophilicity for this series of compounds.
Preparation of substituted cyclopentane and cyclopentene compounds and certain intermediates
-
Page column 11-12, (2008/06/13)
The invention relates to methods for preparing substituted cyclopentene compounds, their intermediates and use as neuraminidase inhibitors.
Substituted 2-arylimino heterocycles and compositions containing them, for use as progesterone receptor binding agents
-
Page column 79, (2010/02/05)
This invention relates to 2-arylimino heterocycles, including 2-arylimino-1,3-thiazolidines, 2-arylimino-2,3,4,5-tetrahydro-1,3-thiazines, 2-arylimino-1,3-thiazolidin-4-ones, 2-arylimino-1,3-thiazolidin-5-ones, and 2-arylimino-1,3-oxazolidines, and their use in modulating progesterone receptor mediated processes, and pharmaceutical compositions for use in such therapies.
Pheromones, 89.- Wittig Syntheses of Alkyl-Branched and Cyclic Analogs of (Z)-5-Decenyl Acetate, the Sex Pheromone of Agrotis segetum (Lepitoptera: Noctuidae)
Albores, Martha,Bestmann, Hans Juergen,Doehla, Bodo,Hirsch, Hans-Ludwig,Roesel, Peter,Vostrowsky, Otto
, p. 231 - 236 (2007/10/02)
By means of (Z)-selective Wittig olefination alkyl-branched and cyclic analogs of (Z)-5-decenyl acetate, the sex pheromone of the turnip moth, Agrotis segetum (Lepidoptera: Noctuidae), have been synthesized. Key Words: Pheromones / (Z)-5-decenyl acetate / Wittig reactions / Agrotis segetum