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Open Access Articles- Top Results for Mitobronitol

Mitobronitol

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Mitobronitol
Stereo, skeletal formula of mitobronitol (2S,3S,4S,5S)-2,3,4,5-tetrol
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Preferred IUPAC name
1,6-Dibromo-1,6-dideoxy-D-mannitol[citation needed]
Systematic IUPAC name
1,6-Dibromohexane-2,3,4,5-tetrol[1]
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ATC code L01AX01
488-41-5 (2S,3S,4S,5S)-2,3,4,5-tetrol 7pxY
ChEMBL ChEMBL161657 7pxY
ChEMBL447629 7pxY
ChemSpider 4063 7pxY
5145112 (2S,3S,5R)-2,3,5-triol 7pxY
5145112 (2R,3R,4R,5R)-2,3,4,5-tetrol 7pxY
EC number 207-676-8
Jmol-3D images Image
KEGG D02020 7pxY
MeSH Mitobronitol
PubChem Template:Chembox PubChem/formatTemplate:Chembox PubChem/formatTemplate:Chembox PubChem/formatTemplate:Chembox PubChem/formatTemplate:Chembox PubChem/format
RTECS number OP2800000 (2RS,3RS,4RS,5RS)-2,3,4,5-tetrol
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This page is a soft redirect. Properties

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C6H12Br2O4
Molar mass Lua error in Module:Math at line 495: attempt to index field 'ParserFunctions' (a nil value). 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
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Related compounds
Except where otherwise noted, 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

  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

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