Intercalation of a Zn(II) complex containing ciprofloxacin drug between DNA base pairs.

about

Intercalation of a Zn(II) complex containing ciprofloxacin drug between DNA base pairs.

Item

http://www.wikidata.org/entity/Q49553791

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Intercalation of a Zn

@nl

Intercalation of a Zn(II) complex containing ciprofloxacin drug between DNA base pairs.

@en

type

Item

label

Intercalation of a Zn

@nl

Intercalation of a Zn(II) complex containing ciprofloxacin drug between DNA base pairs.

@en

prefLabel

Intercalation of a Zn

@nl

Intercalation of a Zn(II) complex containing ciprofloxacin drug between DNA base pairs.

@en

P1476

Intercalation of a Zn(II) complex containing ciprofloxacin drug between DNA base pairs.

@en

P2093

Ali Ashraf Asadian

http://www.w3.org/2001/XMLSchema#string

Mryam Mahdavi

http://www.w3.org/2001/XMLSchema#string

Nahid Shahabadi

http://www.w3.org/2001/XMLSchema#string

P2860

Designed sequence-specific minor groove ligands

Bacterial topoisomerase inhibitors: quinolone and pyridone antibacterial agents

The design of new molecular "light switches" for DNA.

Zinc(II), cadmium(II) and mercury(II) complexes of the vitamin B1 antagonist oxythiamine.

Synthesis, structural characterization and antimicrobial activities of 12 zinc(II) complexes with four thiosemicarbazone and two semicarbazone ligands.

Replacement of ParC alpha4 helix with that of GyrA increases the stability and cytotoxicity of topoisomerase IV-quinolone-DNA ternary complexes.

In vitro activity of sparfloxacin compared with those of five other quinolones

Overcoming the immortality of tumour cells by telomere and telomerase based cancer therapeutics--current status and future prospects.

Zinc(II) complexes with potent cyclin-dependent kinase inhibitors derived from 6-benzylaminopurine: synthesis, characterization, X-ray structures and biological activity.

Isothiazoloquinolones containing functionalized aromatic hydrocarbons at the 7-position: synthesis and in vitro activity of a series of potent antibacterial agents with diminished cytotoxicity in human cells.

P304

676-689

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1080/15257770.2017.1388394

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2017-11-29T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

29185900

http://www.w3.org/2001/XMLSchema#string