نتایج جستجو برای: chalcones

تعداد نتایج: 1021  

2014
Dragana D. Bozic Marina Milenkovic Branka Ivkovic Ivana Cirkovic

Biofilm formation and adherence of bacteria to host tissue are one of the most important virulence factors of methicillin-resistant strains of Staphylococcus aureus (MRSA). The number of resistant strains is seriously increasing during the past years and bacteria have become resistant, not only to methicillin, but also to other commonly used antistaphylococcal antibiotics. There is a great need...

2012
Ewelina Szliszka Dagmara Jaworska Małgorzata Kłósek Zenon P. Czuba Wojciech Król

Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) induces apoptosis in cancer cells without toxicity to normal cells. TRAIL binds to death receptors, TRAIL-R1 (DR4) and TRAIL-R2 (DR5) expressed on cancer cell surface and activates apoptotic pathways. Endogenous TRAIL plays an important role in immune surveillance and defense against cancer cells. However, as more tumor cells are r...

Journal: :The Journal of antimicrobial chemotherapy 2015
Nívea Pereira de Sá Patrícia Silva Cisalpino Luciana de Carvalho Tavares Leandro Espíndola Moacir Geraldo Pizzolatti Patrícia Campi Santos Talles Prosperi de Paula Carlos Augusto Rosa Daniele da Glória de Souza Daniel Assis Santos Susana Johann

BACKGROUND Chalcones are an important class of natural compounds that have been widely applied as synthons in synthetic organic chemistry and possess diverse and interesting biological properties. METHODS We conducted tests with the synthetic substances 6-quinolinyl N-oxide chalcones 4c and 4e to determine their antifungal activity against several isolates of Paracoccidioides spp. and their a...

2014
Siham Abdelrahmane Lahsasni Faeza Hamad Al Korbi Nabilah Abdel-Aziz Aljaber

BACKGROUND Chalcone, an important intermediate of flavonoid synthetic pathway, has been shown to exhibit diverse biological and pharmacological activities such as anti- cancer, antioxidant, anti-inflammatory, etc. RESULTS In this study, a novel series of chalcones fatty acid esters 5b-e and 6b-e have been synthesized via the reaction of the respective chalcones with either palmitic or stearic...

2017
Nisha Sharma

Chemically chalcones are 1,3–diphenyl-2-propene-1-one, containing dual aromatic rings which are linked to each other via carbon bridge system enveloping keto-ethylenic core structure. Owing to the presence of conjugated double bond and electron dense aromatic ring system, the molecule possesses less redox potential; thus greater probability for characteristic electron transfer reactions. Natura...

Journal: :Antimicrobial agents and chemotherapy 2001
M Chen L Zhai S B Christensen T G Theander A Kharazmi

Our previous studies have shown that chalcones exhibit potent antileishmanial and antimalarial activities in vitro and in vivo. Preliminary studies showed that these compounds destroyed the ultrastructure of Leishmania parasite mitochondria and inhibited the respiration and the activity of mitochondrial dehydrogenases of Leishmania parasites. The present study was designed to further investigat...

Journal: :European journal of medicinal chemistry 2012
Tânia R Mielcke Alessandra Mascarello Eduardo Filippi-Chiela Rafael F Zanin Guido Lenz Paulo César Leal Louise Domeneghini Chiaradia Rosendo A Yunes Ricardo J Nunes Ana M O Battastini Fernanda B Morrone Maria M Campos

Gliomas are the most common and devastating tumors of the central nervous system (CNS). Many pieces of evidence point out the relevance of natural compounds for cancer therapy and prevention, including chalcones. In the present study, eight synthetic quinoxaline-derived chalcones, structurally based on the selective PI3Kγ inhibitor AS605240, were evaluated for anti-proliferative activity and vi...

امامی, سعید, میرزایی, حسن, کیقبادی, مسعود,

Cancer is a complex and life-threatening disease involving uncontrollable cell proliferation, evading apoptosis, and metastasis. Despite recent developments in cancer chemotherapy, there are no effective broad spectrum anticancer agents that could selectively target cancer cells. Thus, designing and discovering new efficient and selective anticancer agents are urgent needs. It is important that...

2017
Nirav M. Shah Hitendra S. Joshi

Some new pyrimido[1,2-a]benzimidazole derivatives were synthesized by reacting 2-amino benzimidazole and chalcones in n-butanol at reflux temperature. In our present study we have used various heterocyclic chalcones derived from furfural and substituted acetophenones. All synthesized compounds were characterized by IR, 1 H NMR and Mass spectroscopy. All synthesized compounds were screened for t...

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