نتایج جستجو برای: urease inhibitory

تعداد نتایج: 131739  

Journal: :Chemical & pharmaceutical bulletin 2002
Shinichi Uesato Yuichiro Hashimoto Masaru Nishino Yasuo Nagaoka Hiroshi Kuwajima

In order to seek a urease inhibitor more potent than hydroxyurea (1), its alkyl- or phenyl-substituted derivatives were synthesized and evaluated for their effect on the jack bean urease. Of 16 compounds tested, m-methyl- (10) and m-methoxy-phenyl substituted hydroxyurea (13) showed the most potent inhibitory activities against the enzyme.

Journal: :iranian journal of pharmaceutical research 0
mahmood biglar tehran university of medical sciences hessameddin sufi department of medicinal chemistry, faculty of pharmacy and medicinal plants research center, tehran university of medical sciences, tehran, iran. kowsar bagherzadeh department of medicinal chemistry, faculty of pharmacy and medicinal plants research center, tehran university of medical sciences, tehran, iran faraz mojab school of pharmacy, shaheed beheshty university of medical sciences, tehran, iran.

infection with helicobacter pyloriis the most common cause of stomach and duodenal ulcers. about more than 80 % of people are infected with h. pylori in developing countries. h. pyloriuses urease enzyme product “ammonia” in order to neutralize and protect itself from the stomach acidic condition and urease enzyme activity has been shown to be essential to the colonization of h. pylori. inhibito...

Infection with Helicobacter pyloriis the most common cause of stomach and duodenal ulcers. About more than 80 % of people are infected with H. pylori in developing countries. H. pyloriuses urease enzyme product “ammonia” in order to neutralize and protect itself from the stomach acidic condition and urease enzyme activity has been shown to be essential to the colonization of H. pylori. Inhibito...

فرشته جبل عاملی, , فریدون ملک زاده, ,

In Vivo, after administration of treatment, concentrations of anti‌microbial agents will reduce to sub-inhibitory levels (sub-MIC) and may therefore affect the properties of target bacteria. The purpose of the present study was to investigate the in vitro effect of sub-minimum inhibitory concentrations (sub-MIC) of ampicillin, gentamicin and nalidixin acid on morphology, growth, ammonium produc...

2018
Xinming Yang Mohamad Koohi-Moghadam Runming Wang Yuen-Yan Chang Patrick C. Y. Woo Junwen Wang Hongyan Li Hongzhe Sun

Urease as a potential target of antimicrobial drugs has received considerable attention given its versatile roles in microbial infection. Development of effective urease inhibitors, however, is a significant challenge due to the deeply buried active site and highly specific substrate of a bacterial urease. Conventionally, urease inhibitors are designed by either targeting the active site or mim...

Journal: :Journal of biochemistry 1975
K Kobashi S Takebe N Terashima J Hase

Hydroxamic acids have been reported to be potent and specific inhibitors of urease (EC 3.5.1.5) activity of plant and bacterial origin. The present investigation was performed on the inhibitory effect of hydroxamic acid derivatives of naturally occurring amino acids on the urease activity of the Jack Bean and the alimentary tracts of rats. Methionine-hydroxamic acid was the most powerful inhi...

2014
Mahmood Biglar Hessameddin Sufi Kowsar Bagherzadeh Massoud Amanlou Faraz Mojab

Infection with Helicobacter pyloriis the most common cause of stomach and duodenal ulcers. About more than 80 % of people are infected with H. pylori in developing countries. H. pylori uses urease enzyme product "ammonia" in order to neutralize and protect itself from the stomach acidic condition and urease enzyme activity has been shown to be essential to the colonization of H. pylori. Inhibit...

Journal: :iranian journal of pharmaceutical research 0
ghodsi mohammadi sakineh faramarzi alzahra university shima asadi alzahra university massoud amanlou tehran university

sulfonic acid functionalized sba-15 (sba-pr-so3h) with pore size 6 nm as an efficient heterogeneous nanoporous solid acid catalyst exhibited good catalytic activity in the biginelli-like reaction in the synthesis of spiroheterobicyclic rings with good yield and good recyclability. spiro-pyrimidinethiones/spiro-pyrimidinones-barbituric acid derivatives were synthesized in a simple and efficient ...

Journal: :Journal of environmental quality 2005
C W Ingram M S Coyne D W Williams

Diazinon [O,O-diethyl O-2-isopropyl-6-methyl(pyrimidine-4-yl) phosphorothioate] and imidacloprid [1-(1-[6-chloro-3-pyridinyl]methyl)-N-nitro-2-imidazolidinimine] are applied to lawns for insect control simultaneously with nitrogenous fertilizers such as urea, but their potential effect on urease activity and nitrogen availability in turfgrass management has not been evaluated. Urease activity i...

Journal: :DARU Journal of Pharmaceutical Sciences 2013

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