Mitobronitol
Names
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]
Identifiers
CAS Number
488-41-5 (2S ,3S ,4S ,5S )-2,3,4,5-tetrol Y
3D model (JSmol)
ChEMBL
ChEMBL161657 Y ChEMBL447629 Y
ChemSpider
4063 Y 5145112 (2S ,3S ,5R )-2,3,5-triol Y 5145112 (2R ,3R ,4R ,5R )-2,3,4,5-tetrol Y
ECHA InfoCard
100.006.979
EC Number
KEGG
D02020 Y
MeSH
Mitobronitol
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 Y
DTXSID3048158 DTXSID7022918, DTXSID3048158
InChI=1S/C6H12Br2O4/c7-1-3(9)5(11)6(12)4(10)2-8/h3-6,9-12H,1-2H2
Y Key: VFKZTMPDYBFSTM-UHFFFAOYSA-N
Y
Properties
Chemical formula
C 6 H 12 Br 2 O 4
Molar mass
307.966 g·mol−1
Appearance
Colourless crystals
log P
−0.226 (2RS ,3RS ,4RS ,5RS )-2,3,4,5-tetrol
Acidity (pK a )
12.609 (2RS ,3RS ,4RS ,5RS )-2,3,4,5-tetrol
Basicity (pK b )
1.388 (2RS ,3RS ,4RS ,5RS )-2,3,4,5-tetrol
Pharmacology
ATC code
L01AX01 (WHO )
Related compounds
Related compounds
1,2-Dibromopropane 1,3-Dibromopropane 1,2,3-Tribromopropane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound
Mitobronitol (1,6-dibromo-1,6-dideoxy-D -mannitol ) is a brominated analog of mannitol. It is an anticancer drug that is also classified as an alkylating agent.[2]
^ "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
Last Update: 2024-01-05T21:33:58Z
Mitobronitol (1,6-dibromo-1,6-dideoxy-D-mannitol) is a brominated analog of mannitol. It is an anticancer drug that is also classified as an alkylating...
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Last Update: 2024-01-10T23:18:23Z
reactivity can be put to good use, for instance in the anti-cancer drug mitobronitol . A number of synthetic corticosteroids exist bearing a fluorohydrin motif...
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