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BE 10988
Known as:
4-Thiazolecarboxamide, 2-(5-amino-4,7-dihydro-1-methyl-4,7-dioxo-1H-indol-3-yl)-
, BE-10988
National Institutes of Health
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Related topics
Related topics
2 relations
Broader (2)
Thiazoles
Topoisomerase II Inhibitors
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Synthesis and antiproliferative activity of substituted 3[2-(1H-indol-3-yl)- 1,3-thiazol-4-yl]-1H-pyrrolo[3,2-b]pyridines, marine alkaloid nortopsentin analogues.
A. Carbone
,
M. Pennati
,
+9 authors
P. Diana
Current Medicinal Chemistry
2014
Corpus ID: 27865178
A large number of indolyl-4-azaindolyl thiazoles, nortopsentin analogues, were conveniently synthesized. The antiproliferative…
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2011
2011
Identification and quantitation of a benzoylindole (2-methoxyphenyl)(1-pentyl-1H-indol-3-yl)methanone and a naphthoylindole 1-(5-fluoropentyl-1H-indol-3-yl)- (naphthalene-1-yl)methanone (AM-2201…
J. Nakajima
,
Misako Takahashi
,
+5 authors
Tomoko Hamano
2011
Corpus ID: 55942954
During our careful surveillance of unregulated drugs in January to February 2011, we found two new compounds used as adulterants…
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Review
2009
Review
2009
Evolution of camalexin and structurally related indolic compounds.
Thomas Rauhut
,
E. Glawischnig
Phytochemistry
2009
Corpus ID: 25085686
2008
2008
Biosynthetic origin of BE-10988 in Streptomyces sp. BA10988.
Thomas Rauhut
,
P. Spiteller
,
W. Eisenreich
,
M. Spiteller
,
E. Glawischnig
Journal of Organic Chemistry
2008
Corpus ID: 31044189
The biosynthetic origin of the tumor-inhibitory derivative, BE-10988, was studied in Streptomyces sp . BA10988 by…
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1991
1991
A new topoisomerase-II inhibitor, BE-10988, produced by a streptomycete. I. Taxonomy, fermentation, isolation and characterization.
H. Oka
,
T. Yoshinari
,
+7 authors
Y. Shizuri
Journal of antibiotics (Tokyo. )
1991
Corpus ID: 31773726
A new topoisomerase inhibitor, BE-10988, was isolated from the culture broth of a strain of actinomycetes. The producing strain…
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