Mitobronitol

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Mitobronitol
Stereo, skeletal formula of mitobronitol (2S,3S,4S,5S)-2,3,4,5-tetrol
Identifiers
CAS number 488-41-5 (2S,3S,4S,5S)-2,3,4,5-tetrol YesY
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
ChemSpider 4063 YesY, 5145112 (2S,3S,5R)-2,3,5-triol YesY, 5145112 (2R,3R,4R,5R)-2,3,4,5-tetrol YesY
UNII 5UP30YED7N YesY
EC number 207-676-8
KEGG D02020 YesY
MeSH Mitobronitol
ChEMBL CHEMBL161657 YesY, CHEMBL447629 YesY
RTECS number OP2800000 (2RS,3RS,4RS,5RS)-2,3,4,5-tetrol
ATC code L01AX01
Jmol-3D images Image 1
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
Except where noted otherwise, data are 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[edit]

  1. ^ "Mitolactol - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 25 March 2005. Identification. Retrieved 22 June 2012. 
  2. ^ Mitobronitol, The Centre for Cancer Education