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BE 22179
Known as:
Alanine, N-((3-hydroxy-2-quinolinyl)carbonyl)cysteinylglycyl-N-methylcysteinyl-2,3-didehydro-N-methylthio-, bimol. (4-1'),(4'-1)-(thio lactone), cyclic (3-3')-disulfide
, BE-22179
National Institutes of Health
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Related topics
Related topics
2 relations
Broader (2)
Peptides
Topoisomerase II Inhibitors
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2008
2008
Protection by Conformationally Restricted Mobility: First Solid-Phase Synthesis of Triostin[emsp14]A
Judit Tulla-Puche
,
E. Marcucci
,
M. Fermin
,
F. Albericio
2008
Corpus ID: 263442353
Triostin A (Figure 1) belongs to a family of peptide antibiotics produced by marine bacteria. Triostins (A, B, and C) were…
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1994
1994
A new topoisomerase II inhibitor, BE-22179, produced by a streptomycete. I. Producing strain, fermentation, isolation and biological activity.
Hiromasa Okada
,
Hajime Suzuki
,
+5 authors
Daisuke Uemura
Journal of antibiotics (Tokyo. )
1994
Corpus ID: 9297282
A new topoisomerase II inhibitor, designated BE-22179, was isolated from the culture broth of Streptomyces sp. A22179, which…
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1994
1994
Inhibition of Topoisomerase II by a Novel Antitumor Cyclic Depsipeptide, BE‐22179
T. Yoshinari
,
H. Okada
,
+4 authors
A. Okura
Japanese journal of cancer research : Gann
1994
Corpus ID: 8703839
BE‐22179, a novel cyclic depsipeptide antibiotic having two 3‐hydroxyquinoline moieties, inhibited the DNA‐relaxing activity of…
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1972
1972
Cytotoxic compounds. XIV. Reactions of the bismethanesulphonates of 3-arylthiopropane-1,2-diols and of 2-arylthiopropane-1,3-diols with nucleophiles.
M. S. Khan
,
L. N. Owen
Journal of The Chemical Society-perkin…
1972
Corpus ID: 42785306
The products formed in the title reactions have been examined by 1H n.m.r. spectroscopy. The aryl group was p-methoxy-, p…
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