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Mitobronitol

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Mitobronitol
Stereo, skeletal formula of mitobronitol (2S,3S,4S,5S)-2,3,4,5-tetrol
Names
Preferred IUPAC name 1,6-Dibromo-1,6-dideoxy-D-mannitol
Systematic IUPAC name 1,6-Dibromohexane-2,3,4,5-tetrol
Identifiers
CAS Number
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.006.979 Edit this at Wikidata
EC Number
  • 207-676-8
KEGG
MeSH Mitobronitol
PubChem CID
RTECS number
  • OP2800000 (2RS,3RS,4RS,5RS)-2,3,4,5-tetrol
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C6H12Br2O4/c7-1-3(9)5(11)6(12)4(10)2-8/h3-6,9-12H,1-2H2Key: VFKZTMPDYBFSTM-UHFFFAOYSA-N
SMILES
  • OC(CBr)C(O)C(O)C(O)CBr
Properties
Chemical formula C6H12Br2O4
Molar mass 307.966 g·mol
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
Pharmacology
ATC code L01AX01 (WHO)
Related compounds
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 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.

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
Intracellular chemotherapeutic agents / antineoplastic agents (L01)
SPs/MIs
(M phase)
Block microtubule assembly
Block microtubule disassembly
DNA replication
inhibitor
DNA precursors/
antimetabolites
(S phase)
Folic acid
Purine
Pyrimidine
Deoxyribonucleotide
Topoisomerase inhibitors
(S phase)
I
II
II+Intercalation
Crosslinking of DNA
(CCNS)
Alkylating
Platinum-based
Nonclassical
Intercalation
Photosensitizers/PDT
Other
Enzyme inhibitors
Receptor antagonists
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