نتایج جستجو برای: analogues

تعداد نتایج: 28274  

Journal: :iranian journal of pharmaceutical research 0
f hadizadeh mr jaafari a samiei a mostafavirad e mohammadian

four conformationally restricted analogues of pentamidine were prepared. then, different concentrations (0.039, 0.078, 0.156, 0.312 and 0.625 mg/ml) of each compound and two positive controls (amphotericin b and pentamidine, 0.625 mg/ml), one negative control (culture medium) and one solvent control (dmso) were prepared and placed in 24-well plates containing 50000 parasite per well. promastigo...

Farzin Hadizadeh, Hadi Shakeri Mohammad Ali Ghafuri Mohammad Reza Saberi Mohsen Imenshahidi Ramin Sakhtianchi Seyedeh Toktam Ziaee Somieh Hajian Zohreh Badieyan

Objective(s) In recent years highly selective COX-2inhibitors were withdrawn from the market because of an increased risk of cardiovascular complications. In this study we were looking for potent compounds with moderate selectivity for cox-2. So, four analogues of 4, 5-diaryl-2-(2-alkylthio-5-imidazolyl) imidazole derivatives were synthesized and their anti-inflammatory and anti-nociceptive ac...

F Hadizadeh H Hosseinzadeh M Seifi SH Kazemi VS Motamed-Shariaty

Moclobemide is a selective and reversible monoamine oxidase-A inhibitor, which is used as an antidepressant. Three moclobemide analogues were synthesized by replacing moclobemide phenyl ring with substituted imidazoles. So, N-[(4-morpholinyl) ethyl)]-1-benzyl-2-(alkylthio)-1H-imidazole-5-carboxamides (7a-c) were synthesized and studied for the antidepressant activity using forced swimming test ...

Journal: :iranian journal of chemistry and chemical engineering (ijcce) 2010
babak heidary alizadeh mohsen vosooghi mehdi khoobi azita javidnia fatemeh panah,

chromanone derivatives demonstrate remarkable cytotoxity against a varieties of cancer cell lines. novel 9-[hydroxy(substitutedphenyl)methyl]-2,2-dimethyl-2,3,8,9- tetrahydro-4h,10h-pyrano[2,3-f]chromene-4,10-diones as glyasperin analogues were synthesized in four steps from known 4-chromone 1. the key step was the preparation of chromane dione 5a by regioselective intramolecular cyclization re...

Journal: :journal of physical & theoretical chemistry 2009
z. bayat j. movaffagh

it is important to determine whether a candidate molecule is capable of penetrating the plasma-brain barrier indrug discovery and development. the aim of this paper is to establish a predictive model for plasma-brainbarrier penetration using simple descriptors the usefulness of the quantum chemical descriptors, calculated atthe level of the dft and he theories using 6-310* basis set for qsar st...

Journal: :journal of sciences, islamic republic of iran 2015
m.j. taghizadeh a. javidan o. hosseinchi

a new magnetic nanocatalyst has been prepared using immobilization of vanadate onto aminopropyl functionalized sio2/fe3o4(vo3-/nh3+-sio2/fe3o4). the obtained magnetic catalyst was characterized by ft-ir, xrd, vsm and sem techniques and used for sulfoxidation of sulfide compounds to the correspondingsulfoxides in presence of h2o2 as oxidant at room temperature. the optimum of reaction conditions...

اسدالهی, اقباله, اونیل, پروفسور پال, خسروی, افرا,

Background and Objective: Resistance to chloroquine (CQ) in Plasmodium falciparum malaria has become a major health concern in the developing countries. This problem has prompted investigators for finding alternative antimalarials that may be effective against resistant strains. Amodiaquine (AQ) is an antimalarial which is effective against many chloroquine-resistant strains of P. falciparum. H...

Aazr Tahghighi, Arezoo Rafiee Parhizgar

Antimalarial drugs with the 4-aminoquinoline scaffold such as the important drugs, chloroquine (CQ) and amodiaquine (AQ), have been used to prevent and treat malaria for many years. The importance of these drugs is related to their simple usage, high efficacy, affordability, and cost-effectiveness of their synthesis. In recent years, with the spread of parasite resistance to CQ and cross-resist...

Journal: :iranian journal of pharmaceutical research 0
f hadizadeh h hosseinzadeh vs motamed-shariaty m seifi sh kazemi

moclobemide is a selective and reversible monoamine oxidase-a inhibitor, which is used as an antidepressant. three moclobemide analogues were synthesized by replacing moclobemide phenyl ring with substituted imidazoles. so, n-[(4-morpholinyl) ethyl)]-1-benzyl-2-(alkylthio)-1h-imidazole-5-carboxamides (7a-c) were synthesized and studied for the antidepressant activity using forced swimming test ...

F Hadizadeh H Hosseinzadeh M Seifi SH Kazemi VS Motamed-Shariaty

Moclobemide is a selective and reversible monoamine oxidase-A inhibitor, which is used as an antidepressant. Three moclobemide analogues were synthesized by replacing moclobemide phenyl ring with substituted imidazoles. So, N-[(4-morpholinyl) ethyl)]-1-benzyl-2-(alkylthio)-1H-imidazole-5-carboxamides (7a-c) were synthesized and studied for the antidepressant activity using forced swimming test ...

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