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Antiangiogenic activity of 2-formyl-8-hydroxy-quinolinium chloride
K. H. Lam
, K. K.H. Lee
, S. H.L. Kok
, R. S.M. Wong
, F. Y. Lau
, G. Y.M. Cheng
, Wai Yeung WONG
, S. W. Tong
, K. W. Chan
, R. Y.K. Chan
, J. C.O. Tang
*
, C. H. Cheng
, D. K.P. Hau
,
Zhaoxiang BIAN
, R. Gambari
, Chung Hin CHUI
*
Corresponding author for this work
Department of Chemistry
Chinese Medicine - Clinical Division
School of Chinese Medicine
Research output
:
Contribution to journal
›
Journal article
›
peer-review
10
Citations (Scopus)
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Keyphrases
Chloride
100%
Formyl
100%
Antiangiogenic Activity
100%
Quinolinium
100%
Quinoline
33%
Antiangiogenic Agents
33%
Antitumor Therapy
33%
High Stability
16%
Nude Mice
16%
Tumor Growth
16%
Cancer Cells
16%
Pyridine
16%
Hepatocarcinogenesis
16%
Anti-angiogenesis
16%
Antitumor Agents
16%
Compound II
16%
Metastasis
16%
Therapeutic Use
16%
Human Umbilical Vein Endothelial Cells (HUVECs)
16%
Carbon Atom
16%
Diethylnitrosamine
16%
Nitrogen Compounds
16%
New Blood Vessel
16%
Synthetic Compounds
16%
Tumor Volume
16%
Double Ring Structure
16%
Antitumor Treatment
16%
Xenografted Tumor
16%
Working Mechanism
16%
Hep3B
16%
Pharmaceutical Applications
16%
Benzene Ring
16%
Neovascular
16%
Aromatic Nitrogen
16%
Ring-fused
16%
Pharmacology, Toxicology and Pharmaceutical Science
Antiangiogenic
100%
Nude Mouse
25%
Malignant Neoplasm
25%
Tumor Growth
25%
Carcinogenesis
25%
Angiogenesis Inhibitor
25%
Diethylnitrosamine
25%
Nitrogen Derivative
25%
Liver Carcinogenesis
25%
Chemistry
Antiangiogenic
100%
Antitumor
80%
formation
20%
Carbon Atom
20%
Benzene Ring
20%
Nitrogen Compound
20%