4-Hydroxycyclophosphamide

Chemical compound
4-Hydroxycyclophosphamide
Identifiers
  • 2-[bis(2-Chloroethyl)amino]-4-hydroxy-2H1,3,2-oxazaphosphinan-2-one
CAS Number
  • 40277-05-2 ☒N
PubChem CID
  • 99735
ChemSpider
  • 90110 ☒N
UNII
  • 1XBF4E50HS
ChEMBL
  • ChEMBL731 ☒N
CompTox Dashboard (EPA)
  • DTXSID90960669 Edit this at Wikidata
Chemical and physical data
FormulaC7H15Cl2N2O3P
Molar mass277.08 g·mol−1
3D model (JSmol)
  • Interactive image
  • OC1CCOP(=O)(N1)N(CCCl)CCCl
InChI
  • InChI=1S/C7H15Cl2N2O3P/c8-2-4-11(5-3-9)15(13)10-7(12)1-6-14-15/h7,12H,1-6H2,(H,10,13) ☒N
  • Key:RANONBLIHMVXAJ-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

4-Hydroxycyclophosphamide is in the class of oxazaphosphorine compounds, and is the main, active metabolite of cyclophosphamide and of mafosfamide after they partially metabolized by cytochrome P450. It is then partially tautomerized into aldophosphamide, which, in turn, easily enters live cells and then is partially detoxified into inactive carboxycyclophosphamide by the enzyme ALDH, but partially is hydrolyzed by another cell's enzyme phosphatase to the two directly cytotoxic metabolites - phosphoramide mustard and acrolein.[1]

References

  1. ^ Ludeman SM (August 1999). "The chemistry of the metabolites of cyclophosphamide". Current Pharmaceutical Design. 5 (8): 627–43. doi:10.2174/1381612805666230110215458. PMID 10469895.
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