Drug intelligence / Profile preview

C-1311

Development stage
Discontinued
Lead developer
University of Bradford
Modality
Small Molecules
Administration
Intravenous
01

Overview

C-1311 is a synthetic **imidazoacridinone derivative** developed as an anti-tumor agent. It acts primarily as a DNA-damaging agent through **intercalation/alkylation**, causing DNA strand breaks by inhibiting DNA topoisomerase II, and halting cancer cell proliferation. C-1311 also acts as a **FLT3 (Fms-like tyrosine kinase 3) inhibitor** and mitosis inhibitor, with additional activities such as inhibition of receptor kinases (notably FLT3), cytochrome P450 1A2 and 3A4 isoenzymes, and angiogenesis via the HIF-1α/VEGF pathway. It was investigated in clinical trials for multiple cancers (AML, breast, colorectal, lymphoid), but development has been discontinued. The drug induces p53-dependent senescence in non-cancerous cells and mitotic catastrophe/apoptosis especially in p53-deficient cancer cells. It also has radiosensitizing properties.[1][2][3][4][5]

Brand names
SymadexSymadex Pathfinder
Other names
ImidacrineImidazoloacridine
02

Targets

AR (Adrenergic receptors)HIF1A (Hypoxia-inducible factor 1-alpha)CYP1A2 (Cytochrome P450 1A2)CYP3A4 (Cytochrome P450 3A4)DNATOP2A (DNA topoisomerase II)FLT3-ITD (Fms-like tyrosine kinase 3 with internal tandem duplication)

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