نتایج جستجو برای: آمینو 4h

تعداد نتایج: 9055  

Journal: :Organic & biomolecular chemistry 2007
Shujiang Tu Junyong Zhang Runhong Jia Bo Jiang Yan Zhang Hong Jiang

A new reaction of 4-arylidene-3-methylisoxazol-5(4H)-one or 4-arylidene-2-phenyloxazol-5(4H)-one with 2,6-diaminopyrimidin-4(3H)-one is described and a number of new pyrido[2,3-d]pyrimidine-4,7-dione derivatives are synthesized. This protocol has the advantages of good yields, broad substrate scope and simple work-up.

2006
László Szilágyi Tünde Z. Illyés Zoltán Györgydeák György Szabó

3-Arylsubstituted derivatives of 2H,3H,4H,7Hand 1H,2H,3H,4H-[1,2,4]triazolo[4,5a]pyrimidin-4-ones were synthesized from 2-arylidenehydrazino-6-methyl-4-pyrimidones by treatment with acetic anhydride. The structures of the starting compounds and of the isomeric diN-acetylated reaction products were established by NMR.

Journal: :Neuroscience Letters 2013
Diego S. Asnar Camila F. Roncari Laurival A. De Luca Patrícia M. de Paula Débora S.A. Colombari José V. Menani

Bilateral injections of the GABA(A) agonist muscimol into the lateral parabrachial nucleus (LPBN) disrupt satiety and induce strong ingestion of water and 0.3M NaCl in fluid-replete rats by mechanisms not completely clear. In the present study, we investigated the effects of the blockade of central muscarinic cholinergic receptors with atropine injected intracerebroventricularly (i.c.v.) on 0.3...

Journal: :Stroke 2008
Hen Hallevi Nicole R Gonzales Andrew D Barreto Sheryl Martin-Schild Karen C Albright Elizabeth A Noser Kachi Illoh Aslam M Khaja Teresa Allison Miguel A Escobar Hashem M Shaltoni James C Grotta

BACKGROUND AND PURPOSE Recombinant-activated factor VII (rFVIIa) is an investigational treatment for intracerebral hemorrhage (ICH). We have evaluated the drug's treatment effect based on time to treatment. METHODS ICH patients treated up to 4 hours from symptom onset were divided based on time to treatment: <or=3 hours (3H) and 3 to 4 hours (4H). Head CT was done at baseline and 24 hours. Ou...

2003
Masaru Hashimoto Miyoko Matsumoto Shiro Terashima

A model compound bearing the C1–C17 fragment of carzinophilin was synthesized. The synthesis involved coupling reaction of a cyclic thioimidate with the 4H-oxazol-5-one derivative, ring-opening of the 4H-oxazol-5-one to furnish a dehydropeptide system, elaboration of the C1–C6 enolamide, and construction of the aziridine ring as key steps. q 2003 Elsevier Science Ltd. All rights reserved.

Journal: :Organic & biomolecular chemistry 2013
Calum W Muir Alan R Kennedy Joanna M Redmond Allan J B Watson

4H-Quinolizin-4-ones are a unique class of heterocycle with valuable physicochemical properties and which are emerging as key pharmacophores for a range of biological targets. A tandem Horner-Wadsworth-Emmons olefination/cyclisation method has been developed to allow facile access to substituted 4H-quinolizin-4-ones encoded with a range of functional groups.

Journal: :iranian journal of pharmaceutical research 0
afsaneh zonouzi school of chemistry, university college of science, university of tehran, p.o. box 14155-6455, tehran, iran roghieh mirzazadeh school of chemistry, university college of science, university of tehran, p.o. box 14155-6455, tehran, iran maliheh safavi institute of biochemistry and biophysics, department of biochemistry, university of tehran, tehran, iran sussan k ardestani institute of biochemistry and biophysics, department of biochemistry, university of tehran, tehran, iran saeed emami department of medicinal chemistry and pharmaceutical sciences research center, faculty of pharmacy, mazandaran university of medical sciences, sari, iran. alireza foroumadi 1- faculty of pharmacy and pharmaceutical sciences research center, tehran university of medical sciences, tehran, iran. 2- drug design and development research center, tehran university of medical sciences, tehran, iran.

a series of 2-amino-4-(nitroalkyl)-4h-chromene-3-carbonitriles were synthesized by an efficient multicomponent reaction in aqueous media using dbu (1,8-diazabicyclo[5.4.0]undec-7-ene) as a catalyst at room temperature. mild condition, environment friendly procedure and excellent yields are the main advantages of this procedure. the cytotoxic activity of target compounds were evaluated against t...

Journal: :Blood 2005
Wilhelm Woessmann Kathrin Seidemann Georg Mann Martin Zimmermann Birgit Burkhardt Ilske Oschlies Wolf-Dieter Ludwig Thomas Klingebiel Norbert Graf Bernd Gruhn Heribert Juergens Felix Niggli Reza Parwaresch Helmut Gadner Hansjoerg Riehm Martin Schrappe Alfred Reiter

In the Non-Hodgkin Lymphoma-Berlin-Frankfurt-Münster 95 (NHL-BFM95) study, we tested by randomization whether for patients with B-cell neoplasms methotrexate as intravenous infusion over 4 hours (MTX-4h) is not inferior to, but less toxic than, a 24-hour intravenous infusion (MTX-24h). Second, we investigated against the historical control of study NHL-BFM90, whether for patients with moderate ...

ژورنال: :علوم سبزی ها 0
مریم حقیقی استادیار گروه علوم باغبانی دانشگاه صنعتی اصفهان مریم مظفریان کارشناسی علوم باغبانی دانشگاه شیراز

افزایش تقاضا برای محصولات ارگانیک رو به افزایش است؛ آمینو اسید، فرم ارگانیک نیتروژن است که می تواند سبب افزایش رشد و عملکرد گیاهان شود، اما تحقیق جامعی درباره‎ی سبزی های مختلف صورت نگرفته است. این آزمایش به منظور بررسی سطوح مختلف آمینو اسید(صفر، 3، 4 و 6 میلی گرم در لیتر) در قالب طرح کاملاً تصادفی با چهار تکرار در گلخانه دانشگاه صنعتی اصفهان بر دو سبزی مهم گوجه فرنگی و فلفل دلمه ای انجام شد. نتا...

Journal: :iranian chemical communication 2016
mahdieh sadeghpour

a simple, efficient, and high yielding one-pot protocol has been developed for the synthesis of 4h-benzo[b]pyrans scaffolds installing a three-component tandem knoevenagel-cyclocondensation reaction of an aldehyde, malononitrile and dimedone using guanidinium chloride as polyfunctional organocatalyst under solvent-free conditions in high to excellent yields. various aromatic aldehydes were util...

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