نتایج جستجو برای: thiazol

تعداد نتایج: 902  

Journal: :Molecules 2016
Yasmeen Gull Nasir Rasool Mnaza Noreen Ataf Ali Altaf Syed Ghulam Musharraf Muhammad Zubair Faiz-Ul-Hassan Nasim Asma Yaqoob Vincenzo DeFeo Muhammad Zia-Ul-Haq

A new series of N-(6-arylbenzo[d]thiazol-2-yl)acetamides were synthesized by C-C coupling methodology in the presence of Pd(0) using various aryl boronic pinacol ester/acids. The newly synthesized compounds were evaluated for various biological activities like antioxidant, haemolytic, antibacterial and urease inhibition. In bioassays these compounds were found to have moderate to good activitie...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2002
Ralph A Stearns Randy R Miller Wei Tang Gloria Y Kwei Frank S Tang Robert J Mathvink Elizabeth M Naylor Dawn Chitty Vincent J Colandrea Ann E Weber Adria E Colletti John R Strauss Carol Ann Keohane William P Feeney Susan A Iliff Shuet-Hing Lee Chiu

The pharmacokinetics and oral bioavailability of (R)-N-[4-[2-[[2-hydroxy-2-(pyridin-3-yl)ethyl]amino]ethyl]phenyl]-4-[4-[4-(trifluoromethylphenyl]thiazol-2-yl]benzenesulfonamide (1), a 3-pyridyl thiazole benzenesulfonamide beta3-adrenergic receptor agonist, were investigated in rats, dogs, and monkeys. Systemic clearance was higher in rats (approximately 30 ml/min/kg) than in dogs and monkeys (...

Journal: :Acta Crystallographica Section E Structure Reports Online 2009

Journal: :Acta Crystallographica Section E Structure Reports Online 2009

Journal: :Journal of chemical research 2023

In this study, a series of 4-(3-benzylbenzo[ d]thiazol-2(3 H)-ylidene)-cyclohexa-2,5-dien-1-one derivatives are efficiently synthesized in excellent yields by reactions 2-chlorobenzothiazole, benzyl bromides, and phenols acetonitrile under reflux catalyst-free conditions the presence triethylamine for 2 h. The structures products characterized NMR, IR, EI-MS, elemental analyses.

Journal: :Molecules 2010
Mykhaylo V Vovk Oleksandr M Pinchuk Andrij O Tolmachov Andrei A Gakh

The title compounds, (4-trifluoromethoxyphenyl)-2,5-dimethyl-3-(2-R-thiazol-4-yl)-1H-pyrroles, were prepared in four steps starting from commercially available 4-trifluoromethoxyaniline. The pyrrole (second ring) was added in one step using the Paal-Knorr method. The thiazole (third ring) was added in three steps using chloroacylation with chloroacetonitrile followed by heterocyclization with t...

2015
Carl J. Mallia Lukas Englert Gary C. Walter Ian R. Baxendale

This short note describes the synthesis of the title compound through spontaneous aerobic oxidation of ethyl 2-phenyl-2-(thiazol-2-yl)acetate. Due to the prevalence of such functional motifs in biologically active substances, we believe the oxidation encountered highlights an important degradation pathway worthy of note.

2016
Shuai Qiu Choon-Hong Tan Zhiyong Jiang

A dipeptide-based urea-amide tertiary amine (DP-UAA) was shown to be an effective Brønsted base catalyst for the first asymmetric annulation reaction between 5H-thiazol-4-ones and N-itaconimides. High levels of enantioselectivity (up to 99% ee) and diastereoselectivity (>19:1 dr) were obtained for a series of spirocyclic 1,4-sulfur-bridged piperidinone-based succinimides.

Journal: :Inorganic chemistry communications 2016
Shayna Sandhaus Rosella Taylor Tiffany Edwards Alexis Huddleston Ykeysha Wooten Ramaiyer Venkatraman Ralph T Weber Antonio González-Sarrías Patrick M Martin Patrice Cagle Yuk-Ching Tse-Dinh Stephen J Beebe Navindra Seeram Alvin A Holder

A novel complex, [Cu(acetylethTSC)Cl]Cl•0.25C2H5OH 1 (where acetylethTSC = (E)-N-ethyl-2-[1-(thiazol-2-yl)ethylidene]hydrazinecarbothioamide), was shown to have anti-proliferative activity against various colon and aggressive breast cancer cell lines. In vitro studies showed that complex 1 acted as a poison inhibitor of human topoisomerase IIα, which may account for the observed anti-cancer eff...

Journal: :Molecules 2010
J Mikael Hillgren Markus K Dahlgren Tam M To Mikael Elofsson

A focused library of [4-(2-hydroxyphenyl)thiazol-2-yl]methanones was prepared in a four-step synthesis with the aim to obtain potent inhibitors of type III secretion in Gram-negative bacteria. The compounds are potential bioisosteres of salicylidene acylhydrazides that are a known class of type III secretion inhibitors.

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