نتایج جستجو برای: pyrimidine derivative

تعداد نتایج: 73261  

Journal: :Indian Journal of Pharmaceutical Education and Research 2023

Abstract: Background: Search for the better anti-cancer agents become central part many research teams as current drugs in use suffer lack of specificity to cancer targets. Design and development target specific increase potency safety drugs. Materials Methods: Current intends develop a novel series pyrimidine derivatives owing potential scaffold. In multicomponent reaction approach, 4,5-disubs...

Journal: : 2021

A series of substituted chalcones and pyrimidine derivatives on their base was synthesized. Obtained compounds were tested for antimicrobial activity ability to increase known substances. Pyrimidine products shown good against Staphylococcus aureus Candida tropicalis. These also could modified polyguanidines aureus.

Journal: :the iranian journal of pharmaceutical research 0
nan jiang college of pharmacy, yanbian university, no. 977, park road, yanji, jilin, 133002, china. xian-qing deng college of pharmacy, yanbian university, no. 977, park road, yanji, jilin, 133002, china. fu-nan li department of pharmacy, medical college of xiamen university, no. 168, daxue rd, xiamen, fujian, 361005, china. zhe-shan quan college of pharmacy, yanbian university, no. 977, park road, yanji, jilin, 133002, china.

considerable interest has been focused on the triazole structure, which has been known to possess a broad spectrum of biological activities such as antitumor, anti-inflammatory, antimicrobial, antiviral, and anticonvulsant activities. before this, several heterocyclic compounds containing triazole were synthesized that had shown considerable anticonvulsant activity. as part of our continuous re...

T3P/DMSO is shown to be an effective and mild reagent for the one-pot synthesis of furo[2,3-d]pyrimidine-2,4(1H,3H)-diones from a variety of alcohols. Alcohols are oxidized in situ to aldehydes under mild conditions, which undergo a three-component reaction with N,N'-dimethylbarbituric acid and various isocyanides to afford furo[2,3-d]pyrimidine-2,4(1H,3H)-diones in good yields.

There has been special interest in the chemistry of quinolone and pyrimidine derivatives due to their diverse biological activities such as anticonvulsant, anti-malarial agents, antibacterial, antiviral, cytostatic, antithelemintic, antigenotoxic, anti-cancer agents. These compounds are also used as targeting delayed-type hypersensivity and anti-convulsant agents. As a part of our research work...

Journal: :iranian chemical communication 0
hojat veisi department of chemistry, payame noor university, po box 19395-4697 tehran, iran abbas maleki department of chemistry, payame noor university, po box 19395-4697 tehran, iran yasaman farokhzad department of chemistry, payame noor university, po box 19395-4697 tehran, iran

an electroorganic reaction for the synthesis of 7-amino-2, 4-dioxo-5-phenyl-2,3,4,5-tetrahydro-1h-pyrano[2, 3-d] pyrimidine-6-carbonitrile and ethyl-7-amino-2, 4-dioxo-5-phenyl-2,3,4,5-tetrahydro-1h-pyrano[2, 3-d] pyrimidine-6-carboxylate derivatives are described, using an electrogenerated base of the anion of malonitrile or ethylcyanoacetate. this one-pot, three-component condensation of an a...

Journal: :iranian journal of pharmaceutical research 0
akbar mobinikhaledi department of chemistry, faculty of science, arak university, arak 38156-8-8349, iran behvar asghari department of plant production and breeding engineering, faculty of engineering and technology, imam khomeini international university, qazvin, iran mahsa jabbarpour department of chemistry, faculty of science, arak university, arak 38156-8-8349, iran.

in an endeavor to find a novel series of antihyperglycemic agents, new benzimidazole and pyrimidine derivatives were successfully synthesized efficiently in high yield with high purity, starting from amino acids in the presence of phosphorus oxychloride (pocl3). the synthesized compounds were identified by 1h-nmr, 13c-nmr, ft-ir spectroscopic techniques and elemental analysis. all products were...

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