نتایج جستجو برای: chalcones

تعداد نتایج: 1021  

Journal: :Pathogens 2021

Trypanosomiasis and leishmaniasis are a group of neglected parasitic diseases caused by several species parasites belonging to the family Trypansomatida. The present study investigated antitrypanosomal antileishmanial activity chalcones flavanones from Polygonum salicifolium, which grows in wetlands Iraq. phytochemical evaluation plant yielded two chalcones, 2′,4′-dimethoxy-6′-hydroxychalcone 2...

Journal: :Molecules 2012
Suvitha Syam Siddig Ibrahim Abdelwahab Mohammed Ali Al-Mamary Syam Mohan

Several chalcones were synthesized and their in vitro cytotoxicity against various human cell lines, including human breast adenocarcinoma cell line MCF-7, human lung adenocarcinoma cell line A549, human prostate cancer cell line PC3, human adenocarcinoma cell line HT-29 (colorectal cancer) and human normal liver cell line WRL-68 was evaluated. Most of the compounds being active cytotoxic agent...

Journal: :Revista Colombiana de Ciencias Químico-Farmacéuticas 2018

2010
Jing Peng Huifen Xu Zhe Li Yuyan Zhang Jianzhang Wu

The title compound, C(16)H(12)F(3)NO, a derivative of biologically active chalcones, comprises two benzene rings and a central -CH=CH-C(=O)- unit. The dihedral angle between the two rings is 10.9 (1)° and the mol-ecule adopts an E configuration about the central olefinic bond. The crystal structure is stabilized by inter-molecular N-H⋯O and N-H⋯N hydrogen bonds.

2011
MANISH S. BHATIA PRAFULLA B. CHOUDHARI KUNDAN B. INGALE BANDU E. ZAREKAR

New 2,4-disubstituted 1,5-benzodiazepine derivatives containing different functional groups have been synthesized and screened for their antibacterial activity. The 2,4-disubstituted 1,5benzodiazepine derivatives were synthesized by reacting substituted chalcones synthesized using aldol condensation with o-phenylenediamine. QSAR studies of synthesized derivatives were performed. QSAR equation s...

1999
P.G. Latha M.N.S. Nayar

The seeds of Psoralea corylifolia Linn. (Fabaceae) have been used extensively as a remedy for leucoderma and Vitiligo. A number of compounds have been isolated from the seeds like furocoumarins, chalcones, flavonoids, terpenoids etc.. We have reported the cytotoxic and antitumour properties of the hexane extract of the seeds of P.corylifolia. The present investigation reports the identification...

Journal: :Journal of pharmaceutical and biopharmaceutical research 2022

The chalcones (E)-3-(4-chlorophenyl)-1-phenyl-2-propen-1-one (4-CL) and (E)-3-(3,4-dimethoxyphenyl)-1-phenyl-2 -propen-1-one (DMF) are versatile easily synthesized into low-cost compounds that have a wide spectrum of biological activities. In this study, the cytotoxic, genotoxic modulatory activities 4-CL DMF were evaluated using Ames test mouse micronucleus assay. results revealed both did not...

2015
Markella Konstantinidou Panayiotis A. Koutentis

Within the framework of our attempts to synthesize pleiotropic anti-inflammatory agents, we have synthesized some chalcones and their corresponding 3,4-pyrrolyl derivatives. Chalcones constitute a class of compounds with high biological impact. They are known for a number of biological activities, including anti-inflammatory and free radical scavenging activities. They inhibit several enzymes i...

Journal: :European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences 2006
Xiang Wu Edward R T Tiekink Iouri Kostetski Nikolai Kocherginsky Agnes L C Tan Soo Beng Khoo Prapon Wilairat Mei-Lin Go

A series of ferrocenyl chalcones were synthesized and evaluated in vitro against Plasmodium falciparum (K1) in a [3H] hypoxanthine uptake assay. Appropriate size, electronic, lipophilic and electrochemical parameters were determined for QSAR analysis. The results showed that the location of ferrocene influenced the ease of oxidation of Fe2+ in ferrocene and the polarity of the carbonyl linkage....

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