نتایج جستجو برای: methoxymethyl ethers

تعداد نتایج: 7421  

Journal: :The Journal of pharmacology and experimental therapeutics 2002
Jeffery J Anderson Sara P Rao Blake Rowe Darlene R Giracello Greg Holtz Deborah F Chapman Lida Tehrani Margaret J Bradbury Nicholas D P Cosford Mark A Varney

The binding of [3H]methoxymethyl-3-[(2-methyl-1,3-thiazol-4-yl)ethynyl]pyridine (methoxymethyl-MTEP), a potent and selective antagonist for metabotropic glutamate (mGlu)5 receptors, was characterized in rat brain both in vitro and in vivo. Nonspecific binding, as defined with 10 microM 2-methyl-6-(phenylethynyl)-pyridine (MPEP), was less than 10% of total binding in rat brain membranes. The bin...

Journal: :Acta Crystallographica Section E Structure Reports Online 2006

Journal: :Applied and environmental microbiology 1997
M W Fraaije M Pikkemaat W Van Berkel

When Penicillium simplicissimum is grown on veratryl alcohol, anisyl alcohol, or 4-(methoxymethyl)phenol, an intracellular covalent flavin-containing vanillyl-alcohol oxidase is induced. The induction is highest (up to 5% of total protein) during the growth phase. In addition to vanillyl-alcohol oxidase, an intracellular catalase-peroxidase is induced. Induction of vanillyl-alcohol oxidase in P...

Journal: :Molecules 2010
Grazyna Groszek Agata Bajek Agnieszka Bis Agnieszka Nowak-Król Marek Bednarski Agata Siwek Barbara Filipek

The synthesis of (2R,S)-1-(6-methoxy-4-(methoxymethyl)-1H-indol-5-yloxy)-3-(2-(2-methoxyphenoxy)ethylamino)propan-2-ol and (2R,S)-1-(4-methoxy-6-(methoxymethyl)-1H-indol-5-yloxy)-3-(2-(2-methoxyphenoxy)ethylamino)propan-2-ol is described. The compounds were tested for electrographic, antiarrhythmic, hypotensive, and spasmolytic activity, as well as for alpha(1)-, alpha(2)- and beta(1)-adrenocep...

Journal: :The Journal of antibiotics 1992
E Nakayama K Fujimoto S Muramatsu J Ide

In a previous paper3), we reported on the synthesis and the biological activity of 3-methoxymethyl cephalosporin derivatives, one of which, cefpodoxime proxetil (Fig. 1), has been successfully developed as a prodrug for oral use. Our further elaboration for developing orally active cephalosporins has been made in the direction of chemical modification of the C-7 acyl substituent of the 3-methox...

Journal: :Acta Crystallographica Section E Structure Reports Online 2012

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