Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 230,528,812 papers from all fields of science
Search
Sign In
Create Free Account
GL 331
Known as:
GL-331
, GL331
An epipodophyllotoxin analogue possessing antineoplastic properties. GL331 binds to and inhibits topoisomerase II, resulting in the accumulation of…
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
2 relations
Broader (1)
Etoposide
analogs & derivatives
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2012
2012
Induction of cell cycle arrest by GL331 via triggering an ATM-dependent DNA damage response in HepG2 cells
Ya-jie Wang
,
Xiao-guang Chen
,
Zhiyan Xiao
,
Geng-tao Liu
,
Hua Sun
Journal of Asian natural products research
2012
Corpus ID: 13300271
GL331, a topoisomerase II inhibitor, has been found to trigger DNA damage response (DDR) to induce cell cycle arrest. However…
Expand
2008
2008
[Mechanism of regulation of leptin expression in human lung adenocarcinoma cells by hypoxia inducible factor-1alpha: a preliminary study].
Yan-bei Zhang
,
Ming Fang
,
+4 authors
Rong-Yu Liu
Zhonghua yi xue za zhi
2008
Corpus ID: 24519029
OBJECTIVE To investigate the regulation of leptin expression in human lung adenocarcinoma cells by hypoxia inducible factor-1…
Expand
2006
2006
GL331, a topoisomerase II inhibitor, induces radiosensitization of human glioma cells.
Yun Chen
,
Tzu-Yu Lin
,
Jin-Cherng Chen
,
Hung-Zen Yang
,
S. Tseng
Anticancer Research
2006
Corpus ID: 23180715
BACKGROUND GL331 is a topoisomerase II inhibitor and its effects on cultured human T98G glioma cells were investigated in this…
Expand
2005
2005
Induction of apoptosis and cell cycle arrest in glioma cells by GL331 (a topoisomerase II inhibitor).
Yun Chen
,
Yen-Hao Su
,
Chih-Hsien Wang
,
Jiann-Ming Wu
,
Jin-Cherng Chen
,
S. Tseng
Anticancer Research
2005
Corpus ID: 5687874
BACKGROUND GL331 is a topoisomerase II inhibitor and, in this study, the effects of GL331 upon rat C6 glioma cells were…
Expand
2004
2004
Antitumor agents. Part 235: Novel 4'-ester etoposide analogues as potent DNA topoisomerase II inhibitors with improved therapeutic potential.
Zhiyan Xiao
,
J. R. Vance
,
K. Bastow
,
A. Brossi
,
Hui-Kang Wang
,
K. Lee
Bioorganic & Medicinal Chemistry
2004
Corpus ID: 21886030
2002
2002
Phase II and pharmacokinetic study of GL331 in previously treated Chinese gastric cancer patients
J. Liu
,
L. Chen
,
+10 authors
J. Whang‐Peng
Cancer Chemotherapy and Pharmacology
2002
Corpus ID: 33822430
Abstract.Purpose: A phase II and pharmacokinetic study was designed to assess the efficacy and toxicity profile of an…
Expand
2001
2001
Evaluation of GL331 in combination with paclitaxel: GL331's interference with paclitaxel-induced cell cycle perturbation and apoptosis
Tze-Sing Huang
,
C. Shu
,
Yee Chao
,
Li‐Tzong Chen
Anti-Cancer Drugs
2001
Corpus ID: 25876152
Combination of selecting agents that act on different cellular mechanisms is a common strategy in cancer chemotherapy. GL331 is a…
Expand
2000
2000
In vitro evaluation of GL331's cancer cell killing and apoptosis-inducing activity in combination with other chemotherapeutic agents
Tze-Sing Huang
,
C. Shu
,
Chun-chung Lee
,
Li‐Tzong Chen
,
J. Whang‐Peng
Apoptosis
2000
Corpus ID: 11622831
GL331 is a novel podophyllotoxin-derived compound and is more efficacious than its congener VP-16 in killing several types of…
Expand
1999
1999
Differential in vitro interactions of a series of clinically useful topoisomerase-interacting compounds with the cleavage/religation activity of the human topoisomerase IIalpha and IIbeta isoforms.
B. van Hille
,
D. Perrin
,
B. Hill
Anti-Cancer Drugs
1999
Corpus ID: 35944327
The topoisomerase II (TOP2)-associated DNA cleavage activity and the DNA sequence preference of 20 antitumor drugs, including 15…
Expand
1996
1996
GL331-induced disruption of cyclin B1/CDC 2 complex and inhibition of CDC 2 kinase activity
T-S. Huang
,
W. Yang
,
J. Whang-peng
Apoptosis
1996
Corpus ID: 32091817
GL331, a new homologue of etoposide (VP-16), was developed to cope with the multiple drug resistance occurring in certain…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE