Semicarbazone
From Wikipedia, the free encyclopedia
Semicarbazone | |
---|---|
Image:Semicarbazone.png | |
Systematic name | Semicarbazone |
Chemical formula | R2C=NNHC(=O)NH2 |
Molecular mass | xx.xx g/mol |
Density | x.xxx g/cm³ |
Melting point | xx.x °C |
Boiling point | xx.x °C |
CAS number | [xx-xx-xx] |
SMILES | xxxxx |
Disclaimer and references |
In organic chemistry, semicarbazone is a derivative of semicarbazide which contains an additional ketone functional group. Their structure is R2C=NNHC(=O)NH2. A 'thiosemicarbazone' contains a sulfur thio atom (sulfur) in lieu of the ketonic oygen. Both semicarbazones and thiosemicarbazones are known to have anti-viral and anti-cancer activity, usually mediated through binding to copper or iron in cells.
[edit] See also
- Semicarbazide
- Carbazone
- Carbazide
[edit] External links
- Overview at uni.edu
- Diagram at uic.edu
- "Kinetic vs. Equilibrium Control in Semicarbazone Formation", at msu.edu
- Description of derivatives at dcccd.edu
- Compounds Containing a N-CO-N-N or More Complex Group