Naphthoquinones: A continuing source for discovery of therapeutic antineoplastic agents.

about

Naphthoquinones: A continuing source for discovery of therapeutic antineoplastic agents.

Item

http://www.wikidata.org/entity/Q46262914

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-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

2017年學術文章

@zh-hant

name

Naphthoquinones: A continuing source for discovery of therapeutic antineoplastic agents.

@en

Naphthoquinones: A continuing source for discovery of therapeutic antineoplastic agents.

@nl

type

Item

label

Naphthoquinones: A continuing source for discovery of therapeutic antineoplastic agents.

@en

Naphthoquinones: A continuing source for discovery of therapeutic antineoplastic agents.

@nl

prefLabel

Naphthoquinones: A continuing source for discovery of therapeutic antineoplastic agents.

@en

Naphthoquinones: A continuing source for discovery of therapeutic antineoplastic agents.

@nl

P1476

Naphthoquinones: A continuing source for discovery of therapeutic antineoplastic agents

@en

P2093

Cheng-Yi Tang

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

Han-Yue Qiu

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

Hong-Yan Lin

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

P2860

Targeting DNA topoisomerase II in cancer chemotherapy

Anti-Cancer Stem-like Cell Compounds in Clinical Development - An Overview and Critical Appraisal

Drugging topoisomerases: lessons and challenges

The STATs of cancer--new molecular targets come of age

Stat3 as an oncogene

Topoisomerase I inhibitors: camptothecins and beyond

Anthracyclines: molecular advances and pharmacologic developments in antitumor activity and cardiotoxicity

Targeting hypoxia in cancer therapy

Reactive oxygen species, antioxidants, and the mammalian thioredoxin system

5-hydroxy-2-methyl-1,4-naphthoquinone, a vitamin K3 analogue, suppresses STAT3 activation pathway through induction of protein tyrosine phosphatase, SHP-1: potential role in chemosensitization.

P304

681-690

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

P31

scholarly article

P356

10.1111/CBDD.13141

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

P433

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

P478

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

P50

Peng-Fei Wang

Yong-Hua Yang

Hai-Liang Zhu

P577

2017-11-28T00:00:00Z

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

P698

29130595

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