نتایج جستجو برای: nitrophenyl

تعداد نتایج: 3814  

Journal: :Molbank 2022

Reaction of equimolar equivalents 1-(5-methyl-1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)ethan-1-one (1) and N-phenylhydrazinecarbothioamide (2) in boiling ethanol containing a catalytic amount concentrated hydrochloric acid for 4 h gave (Z)-2-(1-(5-methyl-1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)ethylidene)-N-phenylhydrazine-1-carbothioamide (3) with 88% yield. The structure 3 was established usin...

Journal: :Journal of The Serbian Chemical Society 2021

A number of 1,4-dihydropyridine derivatives (9a?d, 10a?d and 11a?d) were designed synthesized by the reaction 1,3,4-oxadiazole-5-thiones 1,2,4-triazole-5-thiones to 2,6-dibromomethyl-3,5-diethoxycarbonyl-4-(3- -nitrophenyl)-1,4-dihydropyridine. The compounds characterized using FT-IR, 1H-NMR, 13C-NMR spectral data, ESI-MS elemental analysis. cytotoxicity was evaluated in human breast cancer (MC...

Journal: :Molbank 2022

5-Phenyl-furan-2-carboxylic acids have emerged as a new, promising class of antimycobacterial agents that the ability to interfere with iron homeostasis. Considering lack structural data on these compounds, we analyzed crystal fluorinated ester derivative 5-(4-nitrophenyl)furan-2-carboxylic acid, one most potent candidates in series. Here, describe preparation methyl 5-(2-fluoro-4-nitrophenyl)f...

Journal: :Applied and environmental microbiology 1996
E Margolles-Clark M Tenkanen T Nakari-Setälä M Penttilä

A cDNA expression library of Trichoderma reesei RutC-30 was constructed in the yeast Saccharomyces cerevisiae. Two genes, abf1 and bxl1, were isolated by screening the yeast library for extracellular alpha-L-arabinofuranosidase activity with the substrate p-nitrophenyl-alpha-L-arabinofuranoside. The genes abf1 and bxl1 encode 500 and 758 amino acids, respectively, including the signal sequences...

Journal: :The Biochemical journal 1960
D E BLAND

activated the p-nitrophenyl acetateand p-nitrophenyl butyrate-hydrolysing activity of sheep serum at a significantly slower rate than it did the paraoxon-hydrolysing activity. From this and supporting evidence involving theKm for hydrolysis activity of sheep, rabbit and hog sera and of purified paraoxonase towards p-nitrophenyl acetate, it was concluded that a new esterase hydrolysing pnitrophe...

Journal: :The Journal of biological chemistry 2008
Oksana Lockridge Weihua Xue Andrea Gaydess Hasmik Grigoryan Shi-Jian Ding Lawrence M Schopfer Steven H Hinrichs Patrick Masson

Human albumin is thought to hydrolyze esters because multiple equivalents of product are formed for each equivalent of albumin. Esterase activity with p-nitrophenyl acetate has been attributed to turnover at tyrosine 411. However, p-nitrophenyl acetate creates multiple, stable, acetylated adducts, a property contrary to turnover. Our goal was to identify residues that become acetylated by p-nit...

Journal: :Anais Da Academia Brasileira De Ciencias 2022

Lipases are biocatalysts that may have distinct biochemical characteristics depending on the source. The combination of lipases from different sources with complementary is a viable strategy for increasing enzymatic activity. In this study, fungal (Aspergillus niger 01 - CBMAI 2084) and plant (orange frit – orange peel fragment) were analyzed separately together in concentrations. addition, we ...

Journal: :Zeitschrift fur Naturforschung. C, Journal of biosciences 2010
Filiz Susuz Alanyali Merve Arici Oge Artagan Ilhan Işikdağ Yusuf Ozkay

The mutagenicities of 2,2'-(di-3-hydroxyphenyl)-1H,1H'-[5,5']-bisbenzimidazole, 2,2'-(di-4-hydroxyphenyl)-1H,1H'-[5,5']-bisbenzimidazole, 2,2'-(di-3-methoxyphenyl)-1H,1H'-[5,5']-bisbenzimidazole, 2,2'-bis-(4-nitrophenyl)-1H,1H'-[5,5']-bisbenzimidazole, 2,2'-bis-(3-nitrophenyl)-1H,1H'-[5,5']-bisbenzimidazole, 2,2'-bis-(4-methylphenyl)-1H,1H'-[5,5']-bisbenzimidazole, 2,2'-(di-4-methoxyphenyl)-1H,...

Journal: :Acta Crystallographica Section E Structure Reports Online 2012

Journal: :The Journal of biological chemistry 1967
H Neumann L Boross E Katchalski

Alkaline phosphatase from Escherichia coli catalyzes the hydrolysis of S-substituted monoesters of phosphorothioic acid of the type RSP03Naz (R = -CH2CH2NH2,-CH2CHzNHCOCH3,-CH,COOH, or -CH2CHzCOOCzH~), at the S-P bond, to yield orthophosphate and the corresponding thioalcohols. The rate of enzymic hydrolysis of cysteamine S-phosphate was measured at different pH values and substrate concentrati...

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