Mitobronitol
 | |
| Names | |
|---|---|
| Preferred IUPAC name
1,6-Dibromo-1,6-dideoxy-D-mannitol | |
| Systematic IUPAC name
1,6-Dibromohexane-2,3,4,5-tetrol[1] | |
| Identifiers | |
| ATC code | L01 |
488-41-5 (2S,3S,4S,5S)-2,3,4,5-tetrol  | |
| ChEMBL | ChEMBL161657 ChEMBL447629 |
| ChemSpider | 4063 5145112 (2S,3S,5R)-2,3,5-triol 5145112 (2R,3R,4R,5R)-2,3,4,5-tetrol |
| EC number | 207-676-8 |
| |
| Jmol-3D images | Image |
| KEGG | D02020 |
| MeSH | Mitobronitol |
| PubChem | 4208 44119013 (2R,3R)-2,3-diol 6713087 (2S,3S,5R)-2,3,5-triol 2794952 (2R,3R,4R,5R)-2,3,4,5-tetrol 656655 (2S,3S,4S,5S)-2,3,4,5-tetrol |
| RTECS number | OP2800000 (2RS,3RS,4RS,5RS)-2,3,4,5-tetrol |
| |
| UNII | 5UP30YED7N |
| Properties | |
| Molecular formula |
C6H12Br2O4 |
| Molar mass | 307.97 g·mol−1 |
| Appearance | Colourless crystals |
| log P | −0.226 (2RS,3RS,4RS,5RS)-2,3,4,5-tetrol |
| Acidity (pKa) | 12.609 (2RS,3RS,4RS,5RS)-2,3,4,5-tetrol |
| Basicity (pKb) | 1.388 (2RS,3RS,4RS,5RS)-2,3,4,5-tetrol |
| Related compounds | |
| Related compounds |
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| Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
| Infobox references | |
Mitobronitol (1,6-dibromo-1,6-dideoxy-D-mannitol) is a brominated analog of mannitol. It is an anticancer drug that is classified as an alkylating agent.[2]
References
- ↑ "Mitolactol - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 25 March 2005. Identification. Retrieved 22 June 2012.
- ↑ Mitobronitol, The Centre for Cancer Education
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