Liothyronine (sodium)

Chemical Information
Liothyronine sodium is the sodium salt of liothyronine. Thought to be more active than levothyroxine and with a rapid (few hours) onset and short duration of action, liothyronine sodium is used in the treatment of hypothyroidism, particularly in cases of hypothyroid coma. It contains a 3,3',5-triiodo-L-thyroninate.
| CAS Number | 55-06-1 |
| PubChem CID | 23666110 |
| IUPAC Name | sodium (2S)-2-amino-3-[4-(4-hydroxy-3-iodophenoxy)-3,5-diiodophenyl]propanoate |
| Molecular Formula | C15H11I3NNaO4 |
| Molecular Weight | 672.95 |
| Topological Polar Surface Area | 95.6 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 5 |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 408 |
| Property | Value |
|---|---|
| Molecular Weight | 672.95 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 5 |
| Exact Mass | 672.7720 |
| Monoisotopic Mass | 672.7720 |
| Topological Polar Surface Area | 95.6 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 408 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 2 |
| Compound Is Canonicalized | Yes |
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