The Cell Viability Rate of LNCaP, PC-3, MCF-7 and MDA-MB-231.

NIAID Data Ecosystem2026-03-09 收录

抗癌药物细胞毒性评估

癌细胞活力分析

数据链接：

https://figshare.com/articles/dataset/The_Cell_Viability_Rate_of_LNCaP_PC-3_MCF-7_and_MDA-MB-231_/3895884 数据链接链接失效反馈

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资源简介：

The Cell Viability Rate of LNCaP, PC-3, MCF-7 and MDA-MB-231.

创建时间：

2016-07-14

File S1 - Compound A398, a Novel Podophyllotoxin Analogue: Cytotoxicity and Induction of Apoptosis in Human Leukemia Cells

白血病细胞凋亡诱导

抗癌药物细胞毒性评估

Combined file of supporting figures. Figure S1. Induction of apoptosis in HL-60 lineage. Cells were treated with derivative A398 (4, 6 and 8 µM) or with Etoposide (5 µM) for 1 h (A), 3 h (B) or 6 h (C

NIAID Data Ecosystem80

The inhibitory rates on the SGC-7901 cells treated with TSN or 5-FU for different time

胃癌细胞药物抑制

抗癌药物细胞毒性评估

Supplementary data 1. The SGC-7901 cells were seeded on plates filled with RPMI1640 medium at a density of 1×104 cells/well in 96-well plates, and cultivated for 24 h to make them adhere on plates, an

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Mixed Ternary Mononuclear Copper(II) Complexes Based on Valproic Acid with 1,10-Phenanthroline and 2,2'-Bipyridine Ligands: DNA Interaction and Cytotoxicity in V79 Cells

金属配合物-DNA相互作用

抗癌药物细胞毒性评估

This paper reports the DNA interaction and cytotoxicity of binary and ternary copper(II) complexes of valproic acid with phenanthroline or bipyridine and the complementary characterization of Cu(Valp)

Figshare2019-03-01 更新20

Cytotoxic activity of FWGP.

抗癌药物细胞毒性评估

肿瘤细胞系药物敏感性

FWGP was assessed for cytotoxic potential in a panel of human cancer cell lines. IC50s were calculated from dose-response (growth inhibition) curves.

NIAID Data Ecosystem60

Physicochemical and in vitro cytotoxicity evaluation of polymeric drugs for combination cancer therapy

抗癌药物细胞毒性评估

药物递送系统

Platinum-based drugs are potent anticancer drugs and are effective for the treatment of various cancers. However, they are limited pharmacologically due to toxic side effects, drug resistance and poor

Taylor & Francis Group2020-09-22 更新20

The Cell Viability Rate of LNCaP, PC-3, MCF-7 and MDA-MB-231.

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