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fosbretabulin
Known as:
1-(3,4,5-Trimethoxyphenyl)-2-(3'-hydroxy-4'-methoxyphenyl)ethene
, Combretastatin A-4 Phosphate
, Combretastatin A-4
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A water-soluble prodrug derived from the African bush willow (Combretum caffrum) with antineoplastic activity. Fosbretabulin is dephosphorylated to…
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National Institutes of Health
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Related topics
Related topics
10 relations
Broader (2)
Antineoplastic Agents, Phytogenic
Stilbenes
Narrower (3)
CRC 87-09
combretastatin A-4 disodium phosphate
combretastatin A4 phosphate
Fosbretabulin Tromethamine
Microtubule Process
NCIt Antineoplastic Agent Terminology
deoxycombretastatin A-4
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
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
2008
Highly Cited
2008
Novel A-ring and B-ring modified combretastatin A-4 (CA-4) analogues endowed with interesting cytotoxic activity.
D. Simoni
,
R. Romagnoli
,
+10 authors
C. Pisano
Journal of Medicinal Chemistry
2008
Corpus ID: 42196513
A novel class of combretastatins, modified at A-ring or both A- and B-rings, mainly by replacement with benzofuran or benzo[b…
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2007
2007
Combretastatin A4-Induced Differential Cytotoxicity and Reduced Metastatic Ability by Inhibition of AKT Function in Human Gastric Cancer Cells
Heng‐Liang Lin
,
S. Chiou
,
+7 authors
C. Chi
Journal of Pharmacology and Experimental…
2007
Corpus ID: 15545482
Combretastatin A4 (CA4) is a drug that targets tumor vasculature to inhibit angiogenesis. Whether CA4 has a direct effect on…
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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
2001
2001
Antimitotic and cell growth inhibitory properties of combretastatin A-4-like ethers.
Nicholas J. Lawrence
,
David Rennison
,
Meiki Woo
,
Alan T. McGown
,
J. Hadfield
Bioorganic & Medicinal Chemistry Letters
2001
Corpus ID: 45897020
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
1999
Highly Cited
1999
A Novel Combretastatin A‐4 Derivative, AC‐7700, Shows Marked Antitumor Activity against Advanced Solid Tumors and Orthotopically Transplanted Tumors
Y. Nihei
,
Y. Suga
,
+11 authors
T. Tsuruo
Japanese journal of cancer research : Gann
1999
Corpus ID: 13717321
AC‐7700, a novel combretastatin A‐4 derivative, suppresses the growth of solid tumors by inhibiting tumor perfusion. We evaluated…
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Highly Cited
1998
Highly Cited
1998
Induction of apoptosis in proliferating human endothelial cells by the tumor-specific antiangiogenesis agent combretastatin A-4.
S. Iyer
,
Chaplin Dj
,
D. Rosenthal
,
Boulares Ah
,
Lu‐Yuan Li
,
M. Smulson
Cancer Research
1998
Corpus ID: 14197720
The antiangiogenic, tubulin-binding drug combretastatin A-4 exhibits a selective toxicity for proliferating endothelial cells in…
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Highly Cited
1996
Highly Cited
1996
Computational and molecular modeling evaluation of the structural basis for tubulin polymerization inhibition by colchicine site agents.
E. ter Haar
,
H. Rosenkranz
,
E. Hamel
,
B. Day
Bioorganic & Medicinal Chemistry
1996
Corpus ID: 28389805
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