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Epothilones
Known as:
Epothilon
, Epothilone
, Epothilones [Chemical/Ingredient]
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A class of compounds isolated from the myxobacterium Sorangium cellulosum. Similar to taxanes, epothilone compounds induce microtubule polymerization…
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National Institutes of Health
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Related topics
Related topics
29 relations
Narrower (17)
(S)-14-methoxyepothilone
12,13-desoxyepothilone F
BMS 310705
BMS-748285
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Broader (3)
Antineoplastic Agents
Thiazoles
Tubulin Modulators
In Blood
Negative Regulation of Microtubule Depolymerization
Process of secretion
agonists
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2008
Highly Cited
2008
STX140 Is Efficacious In vitro and In vivo in Taxane-Resistant Breast Carcinoma Cells
S. Newman
,
P. Foster
,
+9 authors
A. Purohit
Clinical Cancer Research
2008
Corpus ID: 7316791
Purpose: The aim of these studies was to characterize the action of STX140 in a P-glycoprotein–overexpressing tumor cell line…
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Review
2008
Review
2008
The Epothilones: Translating from the Laboratory to the Clinic
James J. Lee
,
S. Swain
Clinical Cancer Research
2008
Corpus ID: 18829404
The epothilones are macrolide compounds that have been shown to stabilize microtubules. The epothilones are strong promoters of…
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Review
2005
Review
2005
Recent developments in the chemical biology of epothilones.
K. Altmann
Current pharmaceutical design
2005
Corpus ID: 28709690
Epothilones A and B are naturally occurring microtubule-stabilizers, which inhibit the growth of human cancer cells in vitro at…
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Highly Cited
2004
Highly Cited
2004
The merger of natural product synthesis and medicinal chemistry: on the chemistry and chemical biology of epothilones.
K. Altmann
Organic and biomolecular chemistry
2004
Corpus ID: 11589920
Based on epothilones as powerful natural product leads several promising new anticancer agents have emerged through concerted…
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Highly Cited
2002
Highly Cited
2002
Highly concise routes to epothilones: the total synthesis and evaluation of epothilone 490.
Kaustav Biswas
,
Hong Lin
,
+7 authors
S. Danishefsky
Journal of the American Chemical Society
2002
Corpus ID: 33276066
A concise modular laboratory construction of the epothilone class of promising antitumor agents has been accomplished. For the…
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Review
2002
Review
2002
The role of new agents in the treatment of non-small cell lung cancer.
Linda E. Bröker
,
G. Giaccone
European Journal of Cancer
2002
Corpus ID: 26249719
Review
2001
Review
2001
Recent developments in the chemistry, biology and medicine of the epothilones.
K. Nicolaou
,
A. Ritzén
,
K. Namoto
Chemical Communications
2001
Corpus ID: 19117380
The epothilones have occupied center stage on the scenes of total synthesis, chemical biology and medicine for the last five…
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2001
2001
Total synthesis of epothilones B and D.
R. Taylor
,
Yue Chen
Organic Letters
2001
Corpus ID: 29431061
[reaction: see text] A highly convergent total synthesis of the natural products epothilone B and D is described. The route is…
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Highly Cited
2000
Highly Cited
2000
Total syntheses of epothilones B and D.
Johann Mulzer
,
A. Mantoulidis
,
Elisabeth Öhler
Journal of Organic Chemistry
2000
Corpus ID: 1672504
Total syntheses of the microtubule stabilizing antitumor drugs epothilone B and D are described, starting from optically pure (S…
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Highly Cited
1998
Highly Cited
1998
Directed evolution of an esterase for the stereoselective resolution of a key intermediate in the synthesis of epothilones.
U. Bornscheuer
,
J. Altenbuchner
,
H. Meyer
Biotechnology and Bioengineering
1998
Corpus ID: 28589425
The directed evolution of an esterase from Pseudomonas fluorescens using the mutator strain Epicurian coli XL1-Red was…
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