N-Substituted piperazinyl quinolones as potential cytotoxic agents: structure-activity relationships study.

N-Substituted piperazinyl quinolones as potential cytotoxic agents: structure-activity relationships study.

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http://www.wikidata.org/entity/Q40004467
Characterization of Abcc4 gene amplification in stepwise-selected mouse J774 macrophages resistant to the topoisomerase II inhibitor ciprofloxacinPiperonal ciprofloxacin hydrazone induces growth arrest and apoptosis of human hepatocarcinoma SMMC-7721 cells.Synthesis and cytotoxic activity of some 2-amino-4-aryl-3-cyano-7-(dimethylamino)-4H-chromenes.Novel N-2-(Furyl)-2-(chlorobenzyloxyimino) Ethyl Piperazinyl Quinolones: Synthesis, Cytotoxic Evaluation and Structure-Activity Relationship.Trimethoxy-benzaldehyde levofloxacin hydrazone inducing the growth arrest and apoptosis of human hepatocarcinoma cells.Medicinal potential of ciprofloxacin and its derivatives.Study of the cytotoxic/toxic potential of the novel anticancer selenodiazoloquinolone on fibroblast cells and 3D skin model.Synthesis, cytotoxicity and mechanistic evaluation of 4-oxoquinoline-3-carboxamide derivatives: finding new potential anticancer drugs.
P2860

N-Substituted piperazinyl quinolones as potential cytotoxic agents: structure-activity relationships study.

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http://www.wikidata.org/entity/Q40004467
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
N-Substituted piperazinyl quin ...... -activity relationships study.
@en
type
label
N-Substituted piperazinyl quin ...... -activity relationships study.
@en
prefLabel
N-Substituted piperazinyl quin ...... -activity relationships study.
@en
P1433
P1476
P2093
P304
P31
P356
P433
P478
P50
P577
P698
P921
P356
P1433
P1476
N-Substituted piperazinyl quin ...... -activity relationships study.
@en
P2093
P304
P31
P356
10.1016/J.BIOPHA.2008.01.016
P433
P478
P50
P577
P698
P921