نتایج جستجو برای: 3 nitro 4 hydroxypyridine

تعداد نتایج: 2487398  

2011
Yan-Jun Hou Xin-Min Li Wen-Yi Chu Zhi-Zhong Sun

The title compound, C(14)H(10)F(3)NO(3), was prepared by a palladium-catalysed Suzuki-Miyaura coupling reaction. The dihedral angle between the nitro group and its parent benzene ring is 66.85 (19)° while the dihedral angle between the two benzene rings is 49.98 (9)°. The CF(3) group is disordered over two sets of sites with occupancies of 0.457 (8) and 0.543 (8).

Journal: :Acta biochimica Polonica 2008
Przemysław Szczeciński Diana Lamparska Adam Gryff-Keller Wanda Gradowska

Organic extracts of six urine samples from children treated with nitisinone, a medicine against tyrosinemia type I, were investigated by (1)H and (19)F NMR spectroscopy. The presence of unchanged 2-[2-nitro-4-(trifluoromethyl)benzoyl]cyclohexane-1,3-dione (NTBC), 6-hydroxy-2-[2-nitro-4-(trifluoromethyl)benzoyl]cyclohexane-1,3-dione (NTBC-OH) and 2-nitro-4-trifluoromethylbenzoic acid (NTFA) as w...

Journal: :research in pharmaceutical sciences 0
m mohammadpour a sadeghi a fassihi l saghaei a movahedian m rostami

a series of ortho -hydroxypyridine-4-ones were prepared in high yields and evaluated for antioxidant and iron chelating activities. n 1 -h hydroxypyridinones va , vb , and ve were the best radical scavengers in dpph free radical scavenging assay. compound vb was proved to be the most potent compound in hydrogen peroxide scavenging assay. all of the synthesized compounds had very close chelating...

Journal: :iranian journal of pharmaceutical research 0
arvind kumar singh kamla nehru institute of management and technology, faculty of pharmacy, sultanpur up, india. m. lohani integral university luck now, uttarpradesh india. r. parthsarthy kamla nehru institute of management and technology, faculty of pharmacy, sultanpur up, india.

a series of five-membered heterocyclic rings were synthesized by the reaction between benzoyl chloride and various chlolro-nitro-benzoyl chlorides and semi carbazide to form (c1-c7) compounds and was tested for their anti-inflammatory activity determined by rat-paw-oedema method. all the synthesis compounds have been characterized by 1hnmr, ir and mass spectral data. the compounds were purified...

1999
Konstantinos D. Zissis Richard G. Brereton Samantha Dunkerley Richard E.A. Escott

A series of two-way diode array chromatograms were recorded at 0.1±0.5% and 1±5% of 3-hydroxypyridine impurity coeluting with 2-hydroxypyridine, recorded at pH 4.9 (good resolution) and 5.0 (poor resolution). Four methods for PLS calibration, namely, using summed spectral pro®les, summed elution pro®les, unfolded three-way PLS and true three-way PLS were applied to the datasets, both using auto...

Journal: :Acta Crystallographica Section E Structure Reports Online 2012

Journal: :Acta pharmaceutica 2013
Priya V Frank Mahesha Manjunatha Poojary Naral Damodara Chandrashekhar Chikkanna

3 Starting from 2-methyl-4-nitro-imidazole, new 5-(2-methyl- 4-nitro-1-imidazomethyl)-1,3,4-oxadiazole-2-thione () was synthesized and was subjected to Mannich reaction with appropriate amines to yield a new series of 3-substituted aminomethyl-5-(2-methyl-4-nitro-1-imidazomethyl)- 1,3,4-oxadiazole-2-thiones (4a-j). The structure of the title compounds was elucidated by elemental analysis and sp...

2006
Sang Geon Kim Raymond F. Novak

The metabolism of 3-hydroxyp)ridine, a significant constituent of tobacco smoke, to 2,5-dihydroxypyridine has been characterized in he patic microsomes and in the reconstituted enzyme system using purified forms of P450. The redox cycling activity of the metabolite and its ability to damage DNA in vitro have been examined. Pyridine-induced microsomes, which contain elevated levels of P4SOIIE1 (...

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