Weight | 364.358 g/mol |
---|---|
Formula | C16H20N4O6 |
Hydrogen Acceptors | 8 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 6 |
diaziquone (57998-68-2)
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- Metabolism of Diaziquone by NAD(P)H:(Quinone Acceptor) Oxidoreductase (DT-Diaphorase): Role in Diaziquone-induced DNA Damage and Cytotoxicity in Human Colon Carcinoma Cells (Cancer Research, 1990)
- Mechanisms of DNA Strand Breakage and Interstrand Cross-Linking by Diaziridinylbenzoquinone (Diaziquone) in Isolated Nuclei from Human Cells (Cancer Research, 1984)
- DNA Cross-Linking Responses of Human Malignant Glioma Cell Strains to Chloroethylnitrosoureas, Cisplatin, and Diaziquone (Cancer Research, 1987)
- Inhibition of cellular thioredoxin reductase by diaziquone and doxorubicin: Relationship to the inhibition of cell proliferation and decreased ribonucleotide reductase activity (Biochemical Pharmacology, 1992)
- DNA Strand Scission and Cross-Linking by Diaziridinylbenzoquinone (Diaziquone) in Human Cells and Relation to Cell Killing (Cancer Research, 1984)
- Phase I/II trial and pharmacokinetics of intrathecal diaziquone in refractory meningeal malignancies. (Journal of Clinical Oncology, 1992)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCOC(=O)NC1=C(C(=O)C(=C(C1=O)N2CC2)NC(=O)OCC)N3CC3
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InChIKeyWVYXNIXAMZOZFK-UHFFFAOYSA-N
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