نتایج جستجو برای: guanyl hydrazones

تعداد نتایج: 1752  

Journal: :journal of sciences islamic republic of iran 0
n.b patel

substituted schiff bases (hydrazones) 5a-j have been prepared from the starting material 2-chloro pyridine-3-carboxylic acid 1 by a sequence of reactions like reaction with 2-amino-6-nitro benzothiazole (ullamann condensation), thionyl chloride, hydrazine hydrate and different aromatic aldehydes. on cyclocondensation of 5a-j with thioglycolic acid in dry 1,4-dioxane furnished desired compounds ...

Journal: :Chemical communications 2006
Béatrice Quiclet-Sire Samir Z Zard

The reaction of hydrazones with iodine/base leads to diazo intermediates that can be trapped by an internal alkene or alkyne.

Journal: :The Journal of biological chemistry 1982
J F Krall S C Leshon M Frolich N Jamgotchian S G Korenman

Particulate adenylate cyclase preparations from rat uterine smooth muscle had a single class of [3H]guanyl-5'-yl imidodiphosphate ([3H]GMP.P(NH)P)-binding sites with all of the properties of the guanyl nucleotide-requiring enzyme activation sites (N) which couple hormone receptors and catalytic subunits. These sites bound the radioligand in a reversible manner at low temperature (less than 2 de...

Journal: :Antimicrobial agents and chemotherapy 2016
Souvik Sarkar Asim A Siddiqui Shubhra J Saha Rudranil De Somnath Mazumder Chinmoy Banerjee Mohd S Iqbal Shiladitya Nag Susanta Adhikari Uday Bandyopadhyay

We synthesized a new series of conjugated hydrazones that were found to be active against malaria parasite in vitro, as well as in vivo in a murine model. These hydrazones concentration-dependently chelated free iron and offered antimalarial activity. Upon screening of the synthesized hydrazones, compound 5f was found to be the most active iron chelator, as well as antiplasmodial. Compound 5f a...

Journal: :Cancer research 2011
Siyuan Song Tania Christova Stephen Perusini Solmaz Alizadeh Ren-Yue Bao Bryan W Miller Rose Hurren Yulia Jitkova Marcela Gronda Methvin Isaac Babu Joseph Ratheesh Subramaniam Ahmed Aman Anh Chau Donna E Hogge Scott J Weir James Kasper Aaron D Schimmer Rima Al-awar Jeff L Wrana Liliana Attisano

Excessive signaling from the Wnt pathway is associated with numerous human cancers. Using a high throughput screen designed to detect inhibitors of Wnt/β-catenin signaling, we identified a series of acyl hydrazones that act downstream of the β-catenin destruction complex to inhibit both Wnt-induced and cancer-associated constitutive Wnt signaling via destabilization of β-catenin. We found that ...

Journal: :Physical chemistry chemical physics : PCCP 2011
Diana Cheshmedzhieva Plamena Ivanova Stanimir Stoyanov Donka Tasheva Mashenka Dimitrova Ivaylo Ivanov Sonia Ilieva

Absorption and fluorescence spectra in acetonitrile for a series of substituted aryl hydrazones of N-hexyl-1,8-naphthalimide are studied with the aim of potential application of the compounds for enzyme activity localization. The influence of the substituents on the spectral characteristics has been evaluated. The absorption and fluorescence energies of substituted aryl-1,8-naphthalimide hydraz...

Journal: :Journal of bacteriology 2012
Kosuke Taniyama Hideomi Itoh Atsushi Takuwa Yasuyuki Sasaki Shunsuke Yajima Masanori Toyofuku Nobuhiko Nomura Naoki Takaya

Hydrazones are natural and synthetic compounds containing a C=N-N moiety. Here we found that the opportunistic pathogen Pseudomonas aeruginosa PAO1 produced NAD(+)- or NADP(+)-dependent hydrazone dehydrogenase (HDH), which converts hydrazones to the corresponding hydrazides and acids rather than to the simple hydrolytic product aldehydes. Gene cloning indicated that the HDH is part of the group...

Journal: :Chemical communications 2014
Guojing Ji Xi Wang Songnan Zhang Yan Xu Yuxuan Ye Ming Li Yan Zhang Jianbo Wang

A mild and efficient method for the synthesis of 3-trifluoromethylpyrazoles has been established via trifluoromethylation/cyclization of α,β-alkynic hydrazones using a hypervalent iodine reagent under transition-metal-free conditions.

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