Merbarone

Chemical Information
Merbarone is a nonsedating derivative of thiobarbituric acid and a novel catalytic topoisomerase II inhibitor with antineoplastic activity. Merbarone interferes with DNA replication via binding directly to topoisomerase II at a domain that maybe shared by other topoisomerase II cleavage-enhancing agents, ex., etoposide. Its mechanism of action appears to be a novel one, since merbarone does not intercalate DNA nor stabilize DNA-topoisomerase II cleavable complexes.
| CAS Number | 97534-21-9 |
| PubChem CID | 4990817 |
| IUPAC Name | 4,6-dioxo-N-phenyl-2-sulfanylidene-1,3-diazinane-5-carboxamide |
| Molecular Formula | C11H9N3O3S |
| Molecular Weight | 263.27 |
| XLogP | 0.1 |
| Topological Polar Surface Area | 119 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 2 |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 384 |
| Property | Value |
|---|---|
| Molecular Weight | 263.27 |
| XLogP3 | 0.1 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 2 |
| Exact Mass | 263.03646233 |
| Monoisotopic Mass | 263.03646233 |
| Topological Polar Surface Area | 119 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 384 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
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