Uramustine

Chemical compound
  • L01AD08 (WHO)
Pharmacokinetic dataProtein binding5%ExcretionRenalIdentifiers
  • 5-[bis(2-Chloroethyl)amino]-1H-pyrimidine-2,4-dione
CAS Number
  • 66-75-1 checkY
PubChem CID
  • 6194
IUPHAR/BPS
  • 7621
DrugBank
  • DB00791 ☒N
ChemSpider
  • 5959 ☒N
UNII
  • W7KQ46GJ8U
KEGG
  • D06265 checkY
ChEMBL
  • ChEMBL1488 ☒N
CompTox Dashboard (EPA)
  • DTXSID8026270 Edit this at Wikidata
ECHA InfoCard100.000.574 Edit this at WikidataChemical and physical dataFormulaC8H11Cl2N3O2Molar mass252.10 g·mol−13D model (JSmol)
  • Interactive image
  • O=C1C(\N(CCCl)CCCl)=C/NC(=O)N1
InChI
  • InChI=1S/C8H11Cl2N3O2/c9-1-3-13(4-2-10)6-5-11-8(15)12-7(6)14/h5H,1-4H2,(H2,11,12,14,15) ☒N
  • Key:IDPUKCWIGUEADI-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Uramustine (INN) or uracil mustard is a chemotherapy drug which belongs to the class of alkylating agents.[1] It is used in lymphatic malignancies such as non-Hodgkin's lymphoma. It works by damaging DNA, primarily in cancer cells that preferentially take up the uracil due to their need to make nucleic acids during their rapid cycles of cell division. The DNA damage leads to apoptosis of the affected cells. Bone marrow suppression and nausea are the main side effects.

Chemically it is a derivative of nitrogen mustard and uracil.

References

  1. ^ Ghorani-Azam A, Balali-Mood M (2015). "Clinical pharmacology and toxicology of mustard compounds.". In Balali-Mood M, Abdollahi M (eds.). Basic and clinical toxicology of mustard compounds. Cham: Springer. p. 74. ISBN 978-3-319-23874-6.


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SPs/MIs
(M phase)
Block microtubule assembly
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DNA replication
inhibitor
DNA precursors/
antimetabolites
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Folic acid
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Topoisomerase inhibitors
(S phase)
I
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II+Intercalation
Crosslinking of DNA
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Alkylating
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