18 eredmény a kulcsszóra: 'human cancer cell lines'
falciparum 3D7 Parasites, HCMV, and Various Human Breast and Cervical Cancer Cell Lines. EC 50
N/A
Various extracts of these plants were screened for their cytotoxicity against five human cancer cell lines: urinary bladder cancer (EJ-138), liver hepatocellular carcinoma
N/A
Certain C-16 modified derivatives display outstanding cell growth-inhibitory action against a range of human adherent cancer cell lines 2.. The microwave assisted
N/A
Compounds 1–5 were tested for their antiproliferative activ- ities on a diverse set of tumor cell lines including a panel of human breast cancer cell lines (MCF-7, T47D, MDA-MB-231
N/A
Ruthenium and osmium analogs showed a striking difference in antiproliferative activity in three human cancer cell lines A549 nonsmall cell lung carcinoma, CH1 ovarian carcinoma
N/A
In order to screen the cancer cell-specific antiproliferative effect of the synthesized D-ring-fused steroidal 5-aminopyrazoles (6a–h), various human cancerous cell lines, namely
N/A
Four new compounds were prepared and studied for their in vitro antitumor activity against four gynecological human cancer cell lines including HeLa and SiHa
N/A
EtOH extract with weak antiproliferative effect on different animal and human cancer cell lines and remarkable antimicrobial activity against Escherichia coli, Bacillus cereus,
N/A
The antiproliferative properties of the prepared analogs were determined in vitro against a panel of human adherent cancer cell lines 40 including HeLa (cervix
N/A
The antiproliferative activities of the structurally related steroidal pyrazol-5'-ones and their deacetylated analogs were screened on three human adherent breast cancer cell
N/A
The cytotoxic properties of the prepared compounds were determined in human adherent gynecological cancer cell lines by the
N/A
However, derivatives containing one substituted p-quinol ring showed promising antiproliferative activities against di ff erent human cancer cell lines, and this was observed
N/A
However, derivatives containing one substituted p-quinol ring showed promising antiproliferative activities against di ff erent human cancer cell lines, and this was observed
N/A
In this study, the cytotoxicity of n-hexane, dichloromethane (DCM) and methanol (MeOH) extracts of the leaves and tubers of AA were studied against EJ138 (human bladder
N/A
mAb, Monoclonal antibody; MCF-7, Michigan Cancer Foundation-7 breast-cancer cell line; MDA-MB-231, Breast-cancer cell line; NSCLC, Non-small cell lung cancer; OEC- M1, Human
N/A
Copper( II ) complexes and corresponding TSCs were tested for cytotoxicity against a panel of human cancer cell lines includ- ing breast adenocarcinoma MCF7, ovarian carcinoma
N/A
The antiproliferative activities of the newly synthesised brominated and phosphonated compounds against a panel of human cancer cell lines (A2780, MCF-7, MDA-MB 231) were
N/A