نتایج جستجو برای: 3 dihydro 1h phenothiazine 45ah one

تعداد نتایج: 3441519  

Journal: :Acta Crystallographica Section E Structure Reports Online 2012

2013
Alaa A. El-Tombary

In the present investigation, some new pyrazolo[3,4-d]pyrimidin-4(5H)-one derivatives (7-12) as well as fused pyrazolo[3',4':4,5]pyrimido[1,2-b]pyridazin-4(1H)-one (14-16) and 7,8,9,10-tetrahydropyrazolo[3',4':4,5]pyrimido[1,2-b]-cinnolin-4(1H)-one (17) ring systems were synthesized using the starting compound 5-amino-6-methyl-1-phenyl-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one (5). The stru...

Journal: :Acta Crystallographica Section E Structure Reports Online 2011

Journal: :Molecules 2008
Muzaffer Alkan Haydar Yüksek Ozlem Gürsoy-Kol Mustafa Calapoğlu

3-Alkyl(aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones 2a-g reacted with 4-diethylaminobenzaldehyde to afford the corresponding 3-alkyl(aryl)-4-(4-diethyl-aminobenzylidenamino)-4,5-dihydro-1H-1,2,4-triazol-5-ones 3a-g. The acetylation reactions of compounds 3a-e were investigated and compounds 4a-e were thus obtained. The new compounds were characterized using IR, (1)H-NMR, (13)C-NMR, UV and...

2015
Ola Fjellström Sibel Akkaya Hans-Georg Beisel Per-Olof Eriksson Karl Erixon David Gustafsson Ulrik Jurva Daiwu Kang David Karis Wolfgang Knecht Viveca Nerme Ingemar Nilsson Thomas Olsson Alma Redzic Robert Roth Jenny Sandmark Anna Tigerström Linda Öster

Activated factor XI (FXIa) inhibitors are anticipated to combine anticoagulant and profibrinolytic effects with a low bleeding risk. This motivated a structure aided fragment based lead generation campaign to create novel FXIa inhibitor leads. A virtual screen, based on docking experiments, was performed to generate a FXIa targeted fragment library for an NMR screen that resulted in the identif...

Journal: :Molecules 2016
Malose J Mphahlele Tebogo A Khoza Peaceful Mabeta

Herein we describe the synthesis and evaluation of a series of novel 2,3-dihydro-1H-pyrrolo[3,2,1-ij]quinazolin-1-ones for in vitro cytotoxicity against three human cancer cell lines as well as for potential antimalarial activity against the chloroquine-sensitive strain 3D7 of Plasmodium falciparum. The title compounds were prepared via PdCl₂-mediated endo-dig cyclization of 2-aryl-8-(arylethyn...

2013
Agnieszka A. Kaczor Urszula Kijkowska-Murak Kalevi Pihlaja Jari Sinkkonen Waldemar Wysocki Zbigniew Karczmarzyk Dariusz Matosiuk

ABSTRACT The pseudo-Michael reaction of 1-aryl-4,5-dihydro-1H-imidazol-2-amines with ethyl 2-cyano-3-methoxyprop-2-enoate (ethyl ethoxymethylenecyanoacetate) is investigated. At -10 °C reaction takes place on the exocyclic nitrogen atom, giving exclusively ethyl esters of 2-cyano-3-[(1-phenyl-4,5-dihydro-1H-imidazol-2-yl)amino]prop-2-enoic acid. The formation of isomeric enamines which may be a...

Journal: :Acta pharmaceutica 2012
Eman M Flefel Randa E Abdel-Mageid Waled A Tantawy Mohamed A Ali Abd El-Galil E Amr

1 3-[2-(4-Bromphenyl)hydrazono]-5-phenyl-furan-2(3H)-one () was used for preparation of some novel pyrazole, pyridazinone, oxadiazole, triazole, thiazolidine and thioxopyrimidine derivatives. Some of the prepared products were tested for anti-avian influenza virus activity and revealed promising antiviral activity against H5N1 virus [A/Chicken/Egypt/1/20 % (H5N1)] by determination of both E...

Journal: :Molecules 2010
Abdullah M Asiri Salman A Khan

A series of 1,5-dimethyl-2-phenyl-1,2-dihydro-3H-pyrazol-3-one-containing Schiff bases were synthesized, characterized and screened for their antibacterial activities. The structures of the synthesized compounds were established by spectroscopic (FT-IR, ¹H-NMR, ¹³C-NMR, MS) and elemental analyses. The anti-bacterial activities (with MIC values) of compounds were evaluated. The anti-bacterial sc...

Journal: :Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 2007
L M T Frija I D Reva A Gómez-Zavaglia M L S Cristiano R Fausto

The photochemistry and molecular structure of 1-phenyl-4-allyl-tetrazolone (PAT) was studied by FT-IR matrix isolation spectroscopy and DFT(B3LYP)/6-311++G(d,p) calculations. The spectrum of matrix-isolated PAT monomers agrees well with the sum spectrum of three conformers predicted theoretically. UV irradiation (lambda > 235 nm) of matrix-isolated PAT induces three types of photofragmentation:...

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