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C 1311
Known as:
C-1311
, C1311
National Institutes of Health
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Related topics
Related topics
1 relation
Broader (1)
Aminoacridines
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
DNA-Damaging Imidazoacridinone C-1311 Induces Autophagy followed by Irreversible Growth Arrest and Senescence in Human Lung Cancer Cells
Joanna Polewska
,
Anna Skwarska
,
E. Augustin
,
J. Konopa
Journal of Pharmacology and Experimental…
2013
Corpus ID: 13575601
Imidazoacridinone 5-diethylaminoethylamino-8-hydroxyimidazoacridinone (C-1311) is an antitumor inhibitor of topoisomerase II and…
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2012
2012
Role of Human UDP-Glucuronosyltransferases in the Biotransformation of the Triazoloacridinone and Imidazoacridinone Antitumor Agents C-1305 and C-1311: Highly Selective Substrates for UGT1A10
Barbara Fedejko-Kap
,
S. Bratton
,
M. Finel
,
A. Radomińska-Pandya
,
Z. Mazerska
Drug Metabolism And Disposition
2012
Corpus ID: 5484544
5-Diethylaminoethylamino-8-hydroxyimidazoacridinone, C-1311 (NSC-645809), is an antitumor agent shown to be effective against…
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2011
2011
The Imidazoacridinone Antitumor Drug, C-1311, Is Metabolized by Flavin Monooxygenases but Not by Cytochrome P450s
Agnieszka Potęga
,
E. Dąbrowska
,
+5 authors
Z. Mazerska
Drug Metabolism And Disposition
2011
Corpus ID: 290327
5-Diethylaminoethylamino-8-hydroxyimidazoacridinone (C-1311) is an antitumor agent that is also active against autoimmune…
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2011
2011
Anticancer imidazoacridinone C-1311 inhibits hypoxia-inducible factor-1α (HIF-1α), vascular endothelial growth factor (VEGF) and angiogenesis
J. Paradziej-Łukowicz
,
Anna Skwarska
,
G. Peszyńska-Sularz
,
A. Brillowska-Dąbrowska
,
J. Konopa
Cancer Biology & Therapy
2011
Corpus ID: 39702419
Antitumor imidazoacridinone C-1311 is a DNA-reactive topoisomerase II and FLT3 receptor tyrosine kinase inhibitor. Here, we…
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2008
2008
Phase II trial of C1311, a novel inhibitor of topoisomerase II in advanced breast cancer
R. Capizzi
,
L. Roman
,
+5 authors
P. Fumoleau
2008
Corpus ID: 70960354
1055 Background: C1311 was designed from mitoxantrone to lessen cardiotoxicity. Although an inhibitor of topo II, its locus of…
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2007
2007
Comparative evaluation of C1311 cytotoxic activity and interference with cell cycle progression in a panel of human solid tumour and leukaemia cell lines.
C. De Marco
,
N. Zaffaroni
,
Elizabeth C Comijn
,
A. Tesei
,
W. Zoli
,
G. Peters
International Journal of Oncology
2007
Corpus ID: 25046341
The cytotoxic activity of the imidazoacridinone C1311 was related to its effect on cell cycle progression in 16 human cell lines…
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2006
2006
The imidazoacridinone, C-1311 (Symadex™): The first of a potent new class of FLT3 inhibitors
M. Chau
,
Y. Otake
,
J. Christensen
,
D. Fernandes
,
A. Ajami
2006
Corpus ID: 83984424
B35 Background: C-1311 (Symadex™) is the lead compound in clinical development from a new series of agents, the…
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2005
2005
Compatibility and stability of the novel anti-cancer agent C1311 in infusion devices and its in vitro biocompatibility
M. W. D. den Brok
,
B. Nuijen
,
+4 authors
J. Beijnen
Journal of Oncology Pharmacy Practice
2005
Corpus ID: 26141240
C1311 is the lead compound from the imidazoacridinones, a novel group of rationally designed anti-cancer agents. The compound is…
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2005
2005
Development and validation of an LC-UV method for the quantification and purity determination of the novel anticancer agent C1311 and its pharmaceutical dosage form.
M. W. D. den Brok
,
B. Nuijen
,
M. Hillebrand
,
C. Grieshaber
,
M. D. Harvey
,
J. Beijnen
Journal of Pharmaceutical and Biomedical Analysis
2005
Corpus ID: 2024111
2002
2002
Intercalation of imidazoacridinones to DNA and its relevance to cytotoxic and antitumor activity.
J. Dziegielewski
,
B. Ślusarski
,
A. Konitz
,
A. Składanowski
,
J. Konopa
Biochemical Pharmacology
2002
Corpus ID: 24175786
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