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Nitrosourea

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Nitrosourea
Skeletal formula of a minor tautomer of nitrosourea
Skeletal formula of a minor tautomer of nitrosourea
Ball and stick model a minor tautomer of nitrosourea
Ball and stick model a minor tautomer of nitrosourea
Names
IUPAC name Nitrosourea
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/CH3N3O2/c2-1(5)3-4-6/h(H3,2,3,5,6)Key: OSTGTTZJOCZWJG-UHFFFAOYSA-N
SMILES
  • NC(=O)N=NO
  • C(=O)(N)NN=O
Properties
Chemical formula CH3N3O2
Molar mass 89.054 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Nitrosourea is both the name of a molecule, and a class of compounds that include a nitroso (R-NO) group and a urea.

Examples

Examples include:

Nitrosourea compounds are DNA alkylating agents and are often used in chemotherapy. They are lipophilic and thus can cross the blood–brain barrier, making them useful in the treatment of brain tumors such as glioblastoma multiforme.

Side effects

Some nitrosoureas (e.g. lomustine) have been associated with the development of interstitial lung disease.

References

  1. "Antineop". Archived from the original on 2009-03-07. Retrieved 2009-01-24.
  2. Takimoto CH, Calvo E. "Principles of oncologic pharmacotherapy". in Pazdur R, Wagman LD, Camphausen KA, Hoskins WJ (Eds) Cancer management: a multidisciplinary approach. 11 ed. 2008.
  3. Tucci E, Verdiani P, Di Carlo S, Sforza V (1986). "Lomustine (CCNU)-induced pulmonary fibrosis". Tumori. 72 (1): 95–8. doi:10.1177/030089168607200114. PMID 3952821. S2CID 33327504.

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