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mitindomide
Known as:
3a,3b,4,4a,7a,8a,8b-octahydro-4,8-ethenopyrrolo(3',4':3,4)cyclobut(1,2-f)isoindole-1,3,5,7(2H,6H)-tetrone
, 4, 8-Ethenopyrrolo[3',4':3,4]cyclobut[1,2-f]isoindole-1,3,5,7(2H, 6H)tetrone, octahydro-
, tricyclo(4.2.2.0(2,5))dec-9-ene-3,4,7,8-tetracarboxylic acid diimide
A bisdioxopiperazines analog with antineoplastic activity. Mitinomide inhibits topoisomerase II and slowly promotes DNA-interstrand cross-linking…
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National Institutes of Health
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Related topics
Related topics
3 relations
Broader (1)
Isoindoles
NCIt Antineoplastic Agent Terminology
Narrower (1)
NSC 284356
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Theoretical investigation on the structure and performance of N, N′-azobis-polynitrodiazoles
Mei Jing
,
Huarong Li
,
+4 authors
Yigang Huang
Journal of Molecular Modeling
2014
Corpus ID: 21154122
Six novel high energy density compounds of N, N′-azobis-polynitrodiazoles were designed. Their optimized geometric and electronic…
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2008
2008
Determination of Biomedicine Resource of Benzene/Ethanol Extractives of Flesh Eucalyptus Urophydis Chips by Py-GC/MS
Peng Wan-xi
,
Wu Yi-qiang
,
Z. Dang-quan
,
Wu Shu-bin
,
Tan Yang
International Conferences on Biomedical and…
2008
Corpus ID: 44002615
The extractives of Eucalyptus urophydis wood consumes more bleaching agents which seriously affect the quality of pulp and paper…
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2003
2003
Probing the role of linker substituents in bisdioxopiperazine analogs for activity against wild-type and mutant human topoisomerase II alpha.
A. Renodon-Cornière
,
Tina K. Sorensen
,
+4 authors
L. Jensen
Molecular Pharmacology
2003
Corpus ID: 8398443
The bisdioxopiperazines are catalytic inhibitors of eukaryotic type II DNA topoisomerases capable of trapping these enzymes as a…
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1997
1997
Mitindomide is a catalytic inhibitor of DNA topoisomerase II that acts at the bisdioxopiperazine binding site.
B. Hasinoff
,
A. M. Creighton
,
H. Kozłowska
,
P. Thampatty
,
W. Allan
,
J. Yalowich
Molecular Pharmacology
1997
Corpus ID: 11048075
The antitumor drug mitindomide (NSC 284356) was shown to inhibit the decatenation activity of human and Chinese hamster ovary…
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1991
1991
METHOD OF SYNTHESIS OF (-)1β-ETHYL-1α-(HYDROXYMETHYL)-1,2,3,4,6,7,12,a-OCTAHYDRO- INDOLE(2,3-A)QUINOLIZINE (VARIANTS), 1-ETHYL-1-(HYDROXYMETHYL)- 1,2,3,4,6,7-HEXAHYDRO-12H-INDOLE(2,3-A)QUINOLIZINE…
Крайдль Янош
,
Цибула Ласло
,
+4 authors
Ногради Каталин
1991
Corpus ID: 103909857
FIELD: organic chemistry. SUBSTANCE: method of synthesis of (-)1β-ethyl-1α-(hydroxymethyl)-1,2,3,4,6,7,12,12b, a-octa…
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1987
1987
Stability indicating assay for fetindomide (NSC 373965), a potential prodrug of mitindomide (NSC 284356), employing high-performance liquid chromatography.
K. Umprayn
,
V. Stella
,
C. Riley
Journal of Pharmaceutical and Biomedical Analysis
1987
Corpus ID: 32674019
1986
1986
Synthesis of congeners and prodrugs of the benzene maleimide photoadduct mitindomide as potential antitumor agents. 2.
H. Deutsch
,
L. Gelbaum
,
+4 authors
L. Zalkow
Journal of Medicinal Chemistry
1986
Corpus ID: 25380532
Potential prodrugs of the highly insoluble, diimide antitumor agent mitindomide (1b) were synthesized by several different…
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