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CA1P
Known as:
1,2-Benzenediol, 3-methoxy-6-((1Z)-2-(3,4,5-trimethoxyphenyl)ethenyl)-, 1,2-bis(dihydrogen Phosphate)
, Combretastatin A-1 bis(phosphate)
, Combretastatin A1 diphosphate
The diphosphate prodrug of the stilbenoid combretastatin A1, originally isolated from the plant Combretum caffrum, with vascular-disrupting and…
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National Institutes of Health
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Related topics
Related topics
3 relations
Microtubule Process
NCIt Antineoplastic Agent Terminology
Oxi 4503
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2013
Review
2013
Design of combretastatin A-4 analogs as tubulin targeted vascular disrupting agent with special emphasis on their cis-restricted isomers.
H. Rajak
,
P. Dewangan
,
+5 authors
A. Dixit
Current pharmaceutical design
2013
Corpus ID: 36591347
Tubulin protein is a highly imperative and feasible goal for anticancer drug discovery. Hundreds of naturally occurring, semi…
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Highly Cited
2010
Highly Cited
2010
Design, synthesis, and biological evaluations of 2,5-diaryl-2,3-dihydro-1,3,4-oxadiazoline analogs of combretastatin-A4.
Lauren Lee
,
Lyda M Robb
,
+8 authors
Moses Lee
Journal of Medicinal Chemistry
2010
Corpus ID: 207238822
A total of 24 novel 2,5-diaryl-1,3,4-oxadiazoline analogs of combretastatin A-4 (CA-4, 1) were designed, synthesized, and…
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Highly Cited
2006
Highly Cited
2006
Interaction of 4-arylcoumarin analogues of combretastatins with microtubule network of HBL100 cells and binding to tubulin.
Catherine Rappl
,
P. Barbier
,
+6 authors
V. Peyrot
Biochemistry
2006
Corpus ID: 30691317
The synthesis of different 4-arylcoumarin analogues of combretastatin A-4 led to the identification of two new compounds (1 and 2…
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Highly Cited
2006
Highly Cited
2006
Combretastatin CA-4 and combretastatin derivative induce mitotic catastrophe dependent on spindle checkpoint and caspase-3 activation in non-small cell lung cancer cells
I. Vitale
,
A. Antoccia
,
+5 authors
C. Tanzarella
Apoptosis
2006
Corpus ID: 23898499
Combretastatin A-4 (CA-4), a natural stilbenoid isolated from Combretum caffrum, is a new vascular targeting agent (VTA) known…
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Highly Cited
2005
Highly Cited
2005
Synthesis and cytotoxicity of epoxide and pyrazole analogs of the combretastatins.
Regan M. LeBlanc
,
J. Dickson
,
+8 authors
Moses Lee
Bioorganic & Medicinal Chemistry
2005
Corpus ID: 25863293
2005
2005
Combretastatin A-4 resistance in H460 human lung carcinoma demonstrates distinctive alterations in beta-tubulin isotype expression.
H. Wehbe
,
C. Kearney
,
K. Pinney
Anticancer Research
2005
Corpus ID: 29494864
Tubulin isotype distribution may play a role in the development of anti-cancer anti-tubulin drug resistance as well as in drug…
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Highly Cited
2004
Highly Cited
2004
The tubulin-binding agent combretastatin A-4-phosphate arrests endothelial cells in mitosis and induces mitotic cell death.
C. Kanthou
,
O. Greco
,
+4 authors
G. Tozer
American Journal of Pathology
2004
Corpus ID: 2078868
Highly Cited
2001
Highly Cited
2001
Comparative effects of combretastatin A-4 disodium phosphate and 5,6-dimethylxanthenone-4-acetic acid on blood perfusion in a murine tumour and normal tissues.
Rumi Murata
,
Jens Overgaard
,
M. Horsman
International Journal of Radiation Biology
2001
Corpus ID: 23709867
PURPOSE To compare the ability of combretastatin A-4 disodium phosphate (CA4DP) and 5,6-dimethylxanthenone-4-acetic acid (DMXAA…
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Highly Cited
1999
Highly Cited
1999
Evaluation of Antivascular and Antimitotic Effects of Tubulin Binding Agents in Solid Tumor Therapy
Y. Nihei
,
Manabu Suzuki
,
+6 authors
Yasufumi Sato
Japanese journal of cancer research : Gann
1999
Corpus ID: 13724831
Tubulin binding agents (TBAs) reduce tumor perfusion and inhibit mitosis of tumor cells in solid tumors, but it is not clear…
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Highly Cited
1997
Highly Cited
1997
Antitumor agents. 174. 2',3',4',5,6,7-Substituted 2-phenyl-1,8-naphthyridin-4-ones: their synthesis, cytotoxicity, and inhibition of tubulin polymerization.
K. Chen
,
S. Kuo
,
+4 authors
K. Lee
Journal of Medicinal Chemistry
1997
Corpus ID: 39561923
Two series of 2',3',4',5,6,7-substituted 2-phenyl-1,8-naphthyridin-4-ones and 2-phenylpyrido[1,2-alpha]pyrimidin-4-ones have been…
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