نتایج جستجو برای: thiazol

تعداد نتایج: 902  

Journal: :Acta Crystallographica Section E Structure Reports Online 2013

Journal: :Acta Crystallographica Section E Structure Reports Online 2013

Journal: :Polycyclic Aromatic Compounds 2022

A highly efficient one-pot three-component protocol was devised for the synthesis of novel derivatives ((phenylethlidene)hydrazinyl)thiazol-4(5H)one by reaction acetophenone derivatives, ethyl chloroacetate and thiosemicarbazide, in ethanol at room temperature presence copper supported hydroxyapatite-encapsulated-γ-Fe2O3 (γ-Fe2O3@HAp@CPTMS@AT@Cu(ӀI)) as new magnetically recyclable heterogeneous...

2016
Anna Kats Maria Norgård Zenebech Wondimu Catalin Koro Hernán Concha Quezada Göran Andersson Tülay Yucel-Lindberg

Periodontitis is characterized by chronic inflammation and osteoclast-mediated bone loss regulated by the receptor activator of nuclear factor-κB (RANK), RANK ligand (RANKL) and osteoprotegerin (OPG). The aim of this study was to investigate the effect of aminothiazoles targeting prostaglandin E synthase-1 (mPGES-1) on RANKL- and lipopolysaccharide (LPS)-mediated osteoclastogenesis and prostagl...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2012
Maria G Beconi Dawn Yates Kathryn Lyons Kim Matthews Steve Clifton Tania Mead Michael Prime Dirk Winkler Catherine O'Connell Daryl Walter Leticia Toledo-Sherman Ignacio Munoz-Sanjuan Celia Dominguez

Understanding whether regulation of tryptophan metabolites can ameliorate neurodegeneration is of high interest to investigators. A recent publication describes 3,4-dimethoxy-N-(4-(3-nitrophenyl)-5-(piperidin-1-ylmethyl)thiazol-2-yl)benzenesulfonamide (JM6) as a novel prodrug for the kynurenine 3-monooxygenase (KMO) inhibitor 3,4-dimethoxy-N-(4-(3-nitrophenyl)thiazol-2-yl)benzenesulfonamide (Ro...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2013
Amit S Kalgutkar Tim F Ryder Gregory S Walker Suvi T M Orr Shawn Cabral Theunis C Goosen Kimberly Lapham Heather Eng

The current study examined the bioactivation potential of ghrelin receptor inverse agonists, 1-{2-[2-chloro-4-(2H-1,2,3-triazol-2-yl)benzyl]-2,7-diazaspiro[3.5]nonan-7-yl}-2-(imidazo[2,1-b]thiazol-6-yl)ethanone (1) and 1-{2-[2-chloro-4-(2H-1,2,3-triazol-2-yl)benzyl]-2,7-diazaspiro[3.5]nonan-7-yl}-2-(2-methylimidazo[2,1-b]thiazol-6-yl)ethanone (2), containing a fused imidazo[2,1-b]thiazole motif...

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