Mitozolomide

Chemical compound
  • none
Identifiers
  • 3-(2-chloroethyl)-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide
CAS Number
  • 85622-95-3 checkY
PubChem CID
  • 71766
ChemSpider
  • 64805 ☒N
UNII
  • E3U7286V3W
ChEMBL
  • ChEMBL435951 ☒N
CompTox Dashboard (EPA)
  • DTXSID40234862 Edit this at Wikidata
ECHA InfoCard100.079.921 Edit this at WikidataChemical and physical dataFormulaC7H7ClN6O2Molar mass242.62 g·mol−13D model (JSmol)
  • Interactive image
  • NC(=O)c1ncn2C(=O)N(CCCl)\N=N/c12
InChI
  • InChI=1S/C7H7ClN6O2/c8-1-2-14-7(16)13-3-10-4(5(9)15)6(13)11-12-14/h3H,1-2H2,(H2,9,15) ☒N
  • Key:QXYYYPFGTSJXNS-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Mitozolomide (INN) is an antineoplastic. It is an imidazotetrazine derivative.

Development of mitozolomide was discontinued during Phase II clinical trials after it was found to cause severe and unpredictable bone marrow suppression.[1] Temozolomide, which has been in clinical use since 1999, is a less toxic analogue of mitozolomide.[2]

References

  1. ^ Fairbairn LJ, Chinnasamy N, Lashford LS, Chinnasamy D, Rafferty JA (February 2000). "Enhancing hemopoietic drug resistance: a rationale for reconsidering the clinical use of mitozolomide" (PDF). Cancer Gene Ther. 7 (2): 233–9. doi:10.1038/sj.cgt.7700120. PMID 10770631. S2CID 2597751.
  2. ^ Newlands ES, Blackledge GR, Slack JA, et al. (February 1992). "Phase I trial of temozolomide (CCRG 81045: M&B 39831: NSC 362856)". Br J Cancer. 65 (2): 287–91. doi:10.1038/bjc.1992.57. PMC 1977719. PMID 1739631.
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