Clomesone

Chemical Information
Clomesone is the 2-chloroethyl ester of (methylsulfonyl) methanesulfonic acid with potential antineoplastic effects. Acting as a chloroethylating agent, clomesone induces the formation of DNA interstrand crosslinks in some cell lines, and exhibits antitumor activity in some animal models. Alkylating agents exert cytotoxic and, in some cases, chemotherapeutic effects by transferring alkyl groups to DNA, thereby damaging DNA and interfering with DNA synthesis and cell division. (NCI04)
| CAS Number | 88343-72-0 |
| PubChem CID | 100651 |
| IUPAC Name | 2-chloroethyl methylsulfonylmethanesulfonate |
| Molecular Formula | C4H9ClO5S2 |
| Molecular Weight | 236.7 |
| XLogP | -0.3 |
| Topological Polar Surface Area | 94.3 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 5 |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 304 |
| Property | Value |
|---|---|
| Molecular Weight | 236.7 |
| XLogP3 | -0.3 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 5 |
| Exact Mass | 235.9579934 |
| Monoisotopic Mass | 235.9579934 |
| Topological Polar Surface Area | 94.3 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 304 |
| 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 |
Alternative Products
| Catalog | Name |
|---|---|
| BUP08439-01 | Clomesone |
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