نتایج جستجو برای: 123 triazol

تعداد نتایج: 19970  

آزادبخت , آزاده, دریکوند, زهره , عباسی , امیر رضا , مرسلی, علی ,

4-(4H-1,2,4-Triazol-4-yl)phenol (compound I) as a triazol aromatic compound was obtained by the reaction diformylhydrazineand p-aminophenol in dimethylformamide (DMF) under hydrothermal condition. The crystal structure of this compound was determined by FT-IR spectroscopy, NMR, elemental analysis and single crystal X-ray diffraction method. Crystallographic data for I was collected at 298 K. Th...

Journal: :Molbank 2023

The reaction of 1-(5-methyl-1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)ethan-1-one (1) with excess hydroxylamine hydrochloride (2 mole equivalents) in dry ethanol afforded (E)-1-(5-methyl-1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)ethan-1-one oxime (2) 86% yield. structure the new heterocycle 2 was confirmed using nuclear magnetic resonance spectroscopy, single crystal X-ray and elemental analysis.

Journal: :Symmetry 2022

Four carbanion monosubstituted 4’-aryl-1,2,4-triazol-1-ium-4-R2-phenacylids, used as precursors in obtaining new heterocyclic compounds, and their corresponding derivatives belonging to the C2v point group of symmetry were studied by computational means dimethylformamide (DMF) solutions compared with isolated state. The changes computed parameters induced solvent those molecules analyzed this p...

Journal: :Molecules 2012
Reginaldo G Lima-Neto Nery N M Cavalcante Rajendra M Srivastava Francisco J B Mendonça Junior Almir G Wanderley Rejane P Neves Janaína V dos Anjos

1,2,3-Triazoles have been extensively studied as compounds possessing important biological activities. In this work, we describe the synthesis of ten 2-(1-aryl-1H-1,2,3-triazol-4-yl)propan-2-ols via copper catalyzed azide alkyne cycloaddition (CuAAc or click chemistry). Next the in vitro antifungal activity of these ten compounds was evaluated using the microdilution broth method against 42 iso...

Journal: :Zeitschrift für anorganische und allgemeine Chemie 2021

Two potentially tripodal ligands, tris(1-phenyl-1H-1,2,3-triazol-4-yl)phosphine oxide (OP(1,2,3Tz1?Ph)3) and tris(1-benzyl-1H-1,2,3-triazol-4-yl)phosphine (OP(1,2,3Tz1?benz)3), were used in reactions with [Re(CO)5Br] (NEt4)2[Tc(CO)3Cl3]. While the formation of rhenium complexes bidentate tridentate coordinated phosphine oxides was observed, for technetium only cationic OP(1,2,3Tz1?R) ligands is...

Journal: :Molbank 2022

A reaction of equimolar equivalents 2-naphthaldehyde (1) and 1-(5-methyl-1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)ethan-1-one (2) in ethanolic sodium hydroxide at 20 °C for 4 h gave (E)-1-(5-methyl-1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl)-3-(naphthalen-2-yl)prop-2-en-1-one (3) 92% yield. Nuclear magnetic resonance spectroscopy single-crystal X-ray diffraction were used to establish the structure...

Journal: :Molbank 2023

The new polyheterocyclic compound, 2-benzyl-7-(4-chlorophenyl)-3-morpholino-6-((1-phenyl-1H-1,2,3-triazol-4-yl)methyl)-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-5-one, was synthesized by a sequential combination of 4-chlorobenzaldehyde, (1-phenyl-1H-1,2,3-triazol-4-yl)methanamine, 2-isocyano-1-morpholino-3-phenylpropan-1-one, and maleic anhydride under microwave-assisted one-pot process [Ugi-Zhu/aza...

Journal: :The Journal of pharmacology and experimental therapeutics 2011
Koji Matsumoto Ken Okamoto Naoki Ashizawa Takeshi Nishino

4-[5-(Pyridin-4-yl)-1H-1,2,4-triazol-3-yl]pyridine-2-carbonitrile (FYX-051) is a potent inhibitor of bovine milk xanthine oxidoreductase (XOR). Steady-state kinetics study showed that it initially behaved as a competitive-type inhibitor with a K(i) value of 5.7 × 10(-9) M, then after a few minutes it formed a tight complex with XOR via a Mo-oxygen-carbon atom covalent linkage, as reported previ...

Journal: :Berichte der deutschen chemischen Gesellschaft 1892

2016
Supriyo Saha Dilipkumar Pal Sushil Kumar

Purpose: To design and develop a new series of histone deacetylase inhibitors (FP1 FP12) and evaluate their inhibitory activity against hydroxyacetamide (HDAC) enzyme mixture-derived HeLa cervical carcinoma cell and MCF-7. Methods: The designed molecules (FP1 FP12) were docked using AUTODOCK 1.4.6. FP3 and FP8 showed higher interaction comparable to the prototypical HDACI. The designed series o...

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