نتایج جستجو برای: biological inhibitors

تعداد نتایج: 638840  

2013
Marek Bajda Anna Więckowska Michalina Hebda Natalia Guzior Christoph A. Sotriffer Barbara Malawska

Cholinesterases are important biological targets responsible for regulation of cholinergic transmission, and their inhibitors are used for the treatment of Alzheimer's disease. To design new cholinesterase inhibitors, of different structure-based design strategies was followed, including the modification of compounds from a previously developed library and a fragment-based design approach. This...

Journal: :iranian journal of pharmaceutical research 0
afshin zarghi shahid beheshti univ. med. sci. iman sabakhi department of medicinal chemistry, school of pharmacy, shahid beheshti university of medical sciences vigen topuzyan the scientific thechnological centre of organic and pharmaceutical chemistry nasraal. mnjoyan institute of fine organic chemistry, yerevan, armenia. zahra hajimahdi department of medicinal chemistry, school of pharmacy, shahid beheshti university of medical sciences bahram daraei department of toxicology, faculty of medical sciences, tarbiat modares university hadi arefi department of medicinal chemistry, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran.

as a continuous research for discovery of new cox-2 inhibitors, chemical synthesis, in vitro biological activity and molecular docking study of anew group of 1,4-dihydropyridine (dhp) derivatives were presented. novel synthesized compounds possessing a cox-2 so2me pharmacophore at the para position of c-4 phenyl ring, different hydrophobic groups (r1) at c-2 position and alkoxycarbonyl groups (...

Kaolin-SO3H as a new solid acid is prepared via reaction of kaolin and chlorosulfonic acid. This natural based catalyst is very inexpensive and easy available. Imidazoles are an important class of heterocycles being the core fragment of different natural products and biological systems such as anti-allergic, anti-inflammatory, analgesic, antifungal, antimycotic, antibiotic, antiulcerative, anti...

Journal: :Journal of medicinal chemistry 2009
Ugo Chiacchio Luisa Borrello Lia Crispino Antonio Rescifina Pedro Merino Beatrice Macchi Emanuela Balestrieri Antonio Mastino Anna Piperno Giovanni Romeo

3'-Deoxy-4'-azaribonucleosides (15a-d) were synthesized starting from the commercially available (4R)-trans-4-hydroxy-l-proline 7. From biological evaluations, 15b and 15d emerged as potent inhibitors of HCV replication on a replicon assay. These findings demonstrate that synthesized pyrrolidine nucleosides represent a new template for antiviral or other biological studies and could be consider...

As a continuous research for discovery of new COX-2 inhibitors, chemical synthesis, in vitro biological activity and molecular docking study of anew group of 1,4-dihydropyridine (DHP) derivatives were presented. Novel synthesized compounds possessing a COX-2 SO2Me pharmacophore at the para position of C-4 phenyl ring, different hydrophobic groups (R1) at C-2 position and alkoxycarbonyl groups (...

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