نتایج جستجو برای: luorine compounds

تعداد نتایج: 226641  

Journal: :the iranian journal of pharmaceutical research 0
ali razmi 1- department of pharmacology and toxicology, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran. 2- pharmacology and applied medicine department of medicinal plants research center, institute of medicinal plants, acecr, karaj, iran. afshin zarghi department of medicinal chemistry, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran. sara arfaee department of medicinal chemistry, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran. nima naderi department of pharmacology and toxicology, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran. mehrdad faizi department of pharmacology and toxicology, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran.

chalcone (1,3-diarylprop-2-en-1-one) derivatives have been introduced as selective cyclooxygenase-2 inhibitors. in the present study, anti-nociceptive and anti-inflammatory effects of eight novel compounds were evaluated in male mice and wistar rats by using the writhing and formalin-induced paw edema tests respectively. the activities of the compounds were compared with celecoxib as a referenc...

Journal: :علوم و تکنولوژی پلیمر 0
سعید تقوایی گنجعلی ارسلان بیگ زاده کاظم سبحان منش فرسا فتوحی نصراله مجیدیان

in some special cases, rubber compounds with high amounts of unsaturated elastomer are recommended with organic sulfur donors instead of mineral sulfurs. in this condition, activated sulfur is produced in situ and curingprocess is facilitated without accelerators. organic sulfur donor compounds have low thermal stability and in the vulcanization temperature produce free and activated sulfurs. t...

Journal: Journal of Herbal Drugs 2017
Fatemeh Nejati, Gholamreza Espareh Maryam Jafari

Background and aim: Extraction of natural antioxidant compounds has recently attracted the attention of researchers. Almond is one of the native products of  Iran, which annually during the process of production , large volumes of waste is achieved. The aim of this study is investigating the impact of two parameters (time and ethanol percentage) on the extraction of phenol and ...

Journal: :The Journal of organic chemistry 2008
Ian R Morgan Arife Yazici Stephen G Pyne Brian W Skelton

Pyrido- and pyrrolo[2,3-d]oxazoles can be conveniently prepared in high yield from the Ritter reaction of nitriles and in situ generated chiral cyclic N-acyliminium ions. cis-4-Hydroxy-5-acylaminopyrrolidines and cis-5-hydroxy-6-acylaminopiperidines can be readily obtained by acid hydrolysis of these bicyclic heterocyclic compounds, respectively.

Journal: :Organic & biomolecular chemistry 2010
Tong Wang Xue-Liang Huang Song Ye

Chiral N-heterocyclic carbenes were found to be efficient catalysts for the formal [2+2] cycloaddition reaction of alkyl(aryl)ketenes and nitroso compounds to give the corresponding 1,2-oxazetidin-3-ones in moderate to good yields with high enantioselectivities. Reductive ring-opening of the oxazetidinones give the corresponding α-hydroxy acid derivatives in good yields.

Journal: :iranian journal of pharmaceutical sciences 0
shashikant r. pattan department of pharmaceutical chemistry, pravara rural college of pharmacy, loni, ahemednager, india. prajact kekare department of pharmaceutical chemistry, k. l. e's college of pharmacy belgum, india ashwini patil department of pharmaceutical chemistry, y. b. chavan college of pharmacy aurangabad, india ana nikalje department of pharmaceutical chemistry, y. b. chavan college of pharmacy aurangabad, india bs kittur department of pharmaceutical chemistry, h s k college of pharmacy bagalkot, india

a new series of thiazolidinedione derivatives were synthesized. the structures of these compounds were established by means of ir, 1h-nmr and elemental analysis. all of the compounds were screened for antidiabetic activity on albino rats. most of the compounds showed significant antidiabetic activity when compared with the standard drug glibenclamide.

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