Hycanthone

Chemical Information
Hycanthone is a thioxanthen-9-one compound having a hydroxymethyl substituent at the 1-position and a 2-[(diethylamino)ethyl]amino substituent at the 4-position. It was formerly used (particularly as the monomethanesulfonic acid salt) as a schistosomicide for individual or mass treatement of infection with Schistosoma haematobium and S. mansoni, but due to its toxicity and concern about possible carcinogenicity, it has been replaced by other drugs such as praziquantel. It has a role as a mutagen and a schistosomicide drug. It is functionally related to a lucanthone. It is a conjugate base of a hycanthone(1+).
| CAS Number | 3105-97-3 |
| PubChem CID | 3634 |
| IUPAC Name | 1-[2-(diethylamino)ethylamino]-4-(hydroxymethyl)thioxanthen-9-one |
| Molecular Formula | C20H24N2O2S |
| Molecular Weight | 356.5 |
| XLogP | 2.7 |
| Topological Polar Surface Area | 77.9 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 7 |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 443 |
| Property | Value |
|---|---|
| Molecular Weight | 356.5 |
| XLogP3 | 2.7 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 7 |
| Exact Mass | 356.15584919 |
| Monoisotopic Mass | 356.15584919 |
| Topological Polar Surface Area | 77.9 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 443 |
| 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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