نتایج جستجو برای: adrafinil analogues

تعداد نتایج: 28279  

Journal: :Bioorganic & Medicinal Chemistry Letters 2015

Journal: :Annals of internal medicine 2008
Rehan Qayyum Shari Bolen Nisa Maruthur Leonard Feldman Lisa M Wilson Spyridon S Marinopoulos Padmini Ranasinghe Muhammed Amer Eric B Bass

BACKGROUND Evidence comparing premixed insulin analogues (a mixture of rapid-acting and intermediate-acting insulin analogues) with other antidiabetic agents is urgently required to guide appropriate therapy. PURPOSE To summarize the English-language literature on the effectiveness and safety of premixed insulin analogues compared with other antidiabetic agents in adults with type 2 diabetes....

Journal: :Cancer research 1989
M Kamiwatari Y Nagata H Kikuchi A Yoshimura T Sumizawa N Shudo R Sakoda K Seto S Akiyama

Ten synthetic dihydropyridine analogues were investigated for their ability to reverse drug resistance in a multidrug-resistant human carcinoma cell line, KB-Cl. Four dihydropyridine analogues completely reversed the resistance, three lowered the resistance, and three had little effect. The radioactive photoactive dihydropyridine calcium channel blocker, [3H]azidopine, photolabels P-glycoprotei...

Journal: :The Biochemical journal 2002
John L A Mitchell Aviva Leyser Michelle S Holtorff Jill S Bates Benjamin Frydman Aldonia L Valasinas Venodhar K Reddy Laurence J Marton

The polyamines spermidine and spermine and their diamine precursor putrescine are essential for mammalian cell growth and viability, and strategies are sought for reducing polyamine levels in order to inhibit cancer growth. Several structural analogues of the polyamines have been found to decrease natural polyamine levels and inhibit cell growth, probably by stimulating normal feedback mechanis...

Journal: :The Journal of biological chemistry 1959
B M ANDERSON N O KAPLAN

It has been previously shown (l-3) that the nicotinamide moiety of diphosphopyridine nucleotide can be replaced by other pyridine bases without the loss of the coenzyme function. The observation that both the 3-acetylpyridine and pyridine-3aldehyde analogues of diphosphopyridine nucleotide function as coensymes with various dehydrogenases (3) indicated that the amide group on DPN was not essent...

Journal: :The Journal of organic chemistry 2012
Jae Chul Lee Subhashree Francis Dinah Dutta Vijayalaxmi Gupta Yan Yang Jin-Yi Zhu Joseph S Tash Ernst Schönbrunn Gunda I Georg

Eight- and four-membered analogues of N-butyldeoxynojirimycin (NB-DNJ), a reversible male contraceptive in mice, were prepared and tested. A chiral pool approach was used for the synthesis of the target compounds. Key steps for the synthesis of the eight-membered analogues involve ring-closing metathesis and Sharpless asymmetric dihydroxylation and for the four-membered analogues Sharpless epox...

Journal: :The Biochemical journal 2008
Mohamed El Khattabi Maarten L van Roosmalen Dennis Jager Heidi Metselaar Hjalmar Permentier Kees Leenhouts Jaap Broos

Incorporation of Trp (tryptophan) analogues into a protein may facilitate its structural analysis by spectroscopic techniques. Development of a biological system for the biosynthetic incorpor-ation of such analogues into proteins is of considerable importance. The Gram-negative Escherichia coli is the only prokaryotic expression host regularly used for the incorporation of Trp analogues into re...

2010
Seergazhi G. Srivatsan Anupam A. Sawant

Numerous biophysical tools based on fluorescence have been developed to advance the understanding of RNA–nucleic acid, RNA–protein, and RNA–small molecule inter actions. In this regard, fluorescent ribonucleoside analogues that are sensitive to their local environment provide sensitive probes for investigating RNA structure, dynamics, and recognition. Most of these analogues closely resemble th...

Journal: :The Biochemical journal 1990
A Morgan R D Burgoyne

The effect of GTP analogues on catecholamine secretion and [3H]arachidonic acid release from digitonin-permeabilized adrenal chromaffin cells was examined. Several GTP analogues stimulated Ca2(+)-independent exocytosis, with the order of efficacy being XTP greater than ITP greater than guanosine 5'-[beta gamma-imido]triphosphate (p[NH]ppG) greater than guanosine 5'-[gamma-thio]triphosphate (GTP...

Journal: :Nucleic acids research 2004
Martin Zacharias Joachim W Engels

Chemically modified bases are frequently used to stabilize nucleic acids, to study the driving forces for nucleic acid structure formation and to tune DNA and RNA hybridization conditions. In particular, fluorobenzene and fluorobenzimidazole base analogues can act as universal bases able to pair with any natural base and to stabilize RNA duplex formation. Although these base analogues are compa...

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