نتایج جستجو برای: 3 functionalized imidazoles

تعداد نتایج: 1832131  

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2006
Zhuohan Zhang Xiaoying Yang Yuan Zhang Bin Zeng Shujing Wang Tianhui Zhu Richard B S Roden Yongsheng Chen Rongcun Yang

PURPOSE To determine whether -CONH-(CH(2))(6)-NH(3)(+)Cl(-) functionalized single-walled carbon nanotubes (SWNT) carrying complexed small interfering RNA (siRNA) can enter into tumor cells, wherein they release the siRNA to silence the targeted gene. EXPERIMENTAL DESIGN -CONH-(CH(2))(6)-NH(3)(+)Cl(-) was used to mediate the conjugation of telomerase reverse transcriptase (TERT) siRNA to SWNTs...

Journal: :journal of particle science and technology 0
zinat gordi department of chemistry, payame noor university, tehran, iran. mohammad vazan department of chemistry, payame noor university, tehran, iran.

a series of tri- and tetra- substituted imidazoles were synthesized from benzyl, aldehyde and ammonium acetate in the presence of zeolite as an ecofriendly reusable catalyst under microwave irradiation in the absence of solvent. the yields are high to excellent and the use of microwave irradiation reduces reaction times to few minute.

Journal: :Chemical communications 2014
Hiroshi Taneda Kiyofumi Inamoto Yoshinori Kondo

The efficient synthesis of functionalized enamines including β-enaminoesters was effectively accomplished by the direct condensation of functionalized sp(3) carbanions such as acetates with formamides using in situ generated HMDS base from catalytic cesium fluoride and stoichiometric tristrimethylsilylamine.

Organic-inorganic hybrid mesoporous materials such as amino functionalized silica (SBA-Pr-NH2) have received considerable attention due to their basic catalytic applications and adsorption functions. In this work, we investigated the efficient role of SBA-Pr-NH2 as a heterogeneous nano catalyst in the synthesis of 9,10-diaryl-7H-benzo[d,e]imidazo[2,1-a]isoquinolin-7-one derivatives. Application...

Journal: :Antimicrobial agents and chemotherapy 1979
I J Sud D L Chou D S Feingold

The presence of free fatty acids in liposome model membranes sensitizes these membranes to the action of the imidazole antifungals, clotrimazole, micronazole, and sulconazole. Unsaturation of the fatty acids is an important variable; the effect of linoleic and oleic acids is much greater than that of stearic acid. The imidazoles differ somewhat in action, with clotrimazole potency greatest both...

Journal: :The journal of physical chemistry. B 2010
Dmitry Lipkind Chatchawat Plienrasri James S Chickos

The vaporization enthalpies of 1-methyl-, 1-ethyl-, 1-phenyl-, and 1-benzylimidazole, 1-methyl- and 1-phenylpyrazole, and trans-azobenzene are evaluated by correlation-gas chromatography (C-GC) using a variety of azines and diazines as standards. The vaporization enthalpies obtained by C-GC when compared to literature values are approximately 14 kJ·mol(-1) smaller for the imidazoles and 6 kJ·mo...

A. Bamoniri, S. Rohani

A general synthetic route to the synthesis of imidazoles has been developed using nano SbCl5/SiO2 under solvent-free conditions. The multi-component reactions of aldehydes, benzil and ammonium acetate were carried out to afford some trisubstituted imidazole derivatives. This method provides several advantages like simple work-up, environmentally benign, and shorter reaction times along wi...

Journal: :Chemical communications 2009
Patrick S Bäuerlein Ismael Arenas Gonzalez Jarno J M Weemers Martin Lutz Anthony L Spek Dieter Vogt Christian Müller

8-Hydroxy-6-methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine was formed selectively in high yields from N-(beta-methallyl)imidazole by a tandem hydroformylation-cyclization sequence, representing a novel one-pot catalytic synthesis of bicyclic imidazole derivatives.

2009
Praveen Kumar Suryadevara Srinivas Olepu Jeffrey W. Lockman Junko Ohkanda Mandana Karimi Christophe L. M. J. Verlinde James M. Kraus Jan Schoepe Wesley C. Van Voorhis Andrew D. Hamilton Frederick S. Buckner Michael H. Gelb

We report structure-activity studies of a large number of dialkyl imidazoles as inhibitors of Trypanosoma cruzi lanosterol-14R-demethylase (L14DM). The compounds have a simple structure compared to posaconazole, another L14DM inhibitor that is an anti-Chagas drug candidate. Several compounds display potency for killing T. cruzi amastigotes in vitro with values of EC50 in the 0.4-10 nM range. Tw...

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