نتایج جستجو برای: anticancer agent

تعداد نتایج: 284103  

2012
Khairul Islam Shaikh M Mohsin Ali Mele Jesmin Jahan Ara Khanam

OBJECTIVE Benzophenone semicarbazone (BSC) was synthesized and characterized to identify compounds with anticancer activities. METHODS Anticancer activities were studied against Ehrlich Ascites Carcinoma (EAC) cells in Swiss albino mice by monitoring parameters such as tumor weight measurement, survival time of tumor bearing mice, tumor cell growth inhibition, and so on. Some hematological pa...

Journal: :Biological & pharmaceutical bulletin 2008
Sumio Matzno Yuka Yamaguchi Takeshi Akiyoshi Toshikatsu Nakabayashi Kenji Matsuyama

The possibility of vitamin K3 (VK3) as an anticancer agent was assessed. VK3 dose-dependently diminished the cell viability (measured as esterase activity) with IC50 of 13.7 microM and Hill coefficient of 3.1 in Hep G2 cells. It also decreased the population of S phase and arrested cell cycle in the G2/M phase in a dose-dependent manner. G2/M arrest was regulated by the increment of cyclin A/cd...

2015
S. Supraja P. Arumugam

Silver nanoparticles were synthesized using Cynodon dactylon leaf extract and this study demonstrates the efficacy of biologically synthesized Silver nanoparticles (AgNPs) as anticancer and antibacterial agent. Anticancer activity of the biologically synthesized silver nanoparticles was studied using HEpG-2 cell line. The AgNPs showed dose-dependent cytotoxicity against HEpG-2 cells. Antimicrob...

2015
XIAOjIN SONG YAMING LI HANwEN ZHANG QIFENG YANG

Trametes robiniophila Murr. (Huaier) is a sandy beige mushroom found on the trunks of trees and has been widely used in traditional Chinese medicine (TCM) for ~1,600 years. The anticancer effects of Huaier have attracted increasing worldwide interest in recent years. Accumulating evidence suggests that the anticancer mechanism of Huaier may be associated with various biological activities, such...

Journal: :Molecules 2014
Yong-An Yang Wen-Jian Tang Xin Zhang Ji-Wen Yuan Xin-Hua Liu Hai-Liang Zhu

Glycyrrhizin (GA) analogs in the form of 3-glucuronides and 18-epimers were synthesized and their anticancer activities were evaluated. Alkaline isomerization of monoglucuronides is reported. In vitro and in vivo studies showed that glycyrrhetinic acid monoglucuronides (GAMGs) displayed higher anticancer activities than those of bisglucuronide GA analogs, while anticancer activity of the 18α-ep...

2012
Sarfaraj Hussain Sheeba Fareed Saba Ansari Sajid khan

Various active anticancer agents are derived from plants and terrestrial microorganisms. Isolation of C-nucleosides from the Caribbean sponge, Cryptotheca crypta, four decades ago, provided the basis for the synthesis of cytarabine, the first marine derived anticancer agent to be developed for clinical use. Cytarabine is currently used in the routine treatment of patients with leukaemia and lym...

Journal: :Jordan Journal of Pharmaceutical Sciences 2022

Cancer is a fatal disease that causes around 9 million deaths annually in developing and developed countries worldwide. Recently, natural products as alternatives for chemical agents have become growing area of interest. Essential oils (EOs) are secondary metabolites the plant, with wide range bioactivities, such anticancer effect. The present systematic review attempts to collect document rece...

Journal: :Organic & biomolecular chemistry 2015
Yuanzhen Xu Jianjun Chen Ya Li Shoujiao Peng Xueyan Gu Meng Sun Kun Gao Jianguo Fang

A novel anticancer prodrug compound 1, which was designed to be triggered by thiols and release the chemotherapeutic agent mechlorethamine, was successfully prepared and evaluated for the first time. The activation of compound 1 was determined by NMR analysis and denaturing alkaline agarose gel electrophoresis. A fluorescence image and comet assay indicated that the inducible reactivity of 1 co...

Journal: :Molecules 2016
Yang Li Ling Feng Zhi-Fang Song Hai-Bei Li Qi-Yong Huai

A total of forty novel glycyrrhetinic acid (GA) derivatives were designed and synthesized. The cytotoxic activity of the novel compounds was tested against two human breast cancer cell lines (MCF-7, MDA-MB-231) in vitro by the MTT method. The evaluation results revealed that, in comparison with GA, compound 42 shows the most promising anticancer activity (IC50 1.88 ± 0.20 and 1.37 ± 0.18 µM for...

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