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Triethylenemelamine

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Triethylenemelamine
Clinical data
ATC code
  • None
Identifiers
  • 2,4,6-Tris(aziridin-1-yl)-1,3,5-triazine
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.000.076Edit this at Wikidata
Chemical and physical data
FormulaC9H12N6
Molar mass204.237 g·mol−1
3D model (JSmol)
  • C1CN1c2nc(nc(n2)N3CC3)N4CC4
  • InChI=1S/C9H12N6/c1-2-13(1)7-10-8(14-3-4-14)12-9(11-7)15-5-6-15/h1-6H2 ☒N
  • Key:IUCJMVBFZDHPDX-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Triethylenemelamine (abbreviatedTEM, also calledTretamine) is a drug used inchemotherapy.[1]

It can causechromatid aberrations in cell models.[2]

See also

[edit]

References

[edit]
  1. ^Wong JR, Morton LM, Tucker MA, Abramson DH, Seddon JM, Sampson JN, Kleinerman RA (October 2014)."Risk of subsequent malignant neoplasms in long-term hereditary retinoblastoma survivors after chemotherapy and radiotherapy".Journal of Clinical Oncology.32 (29):3284–3290.doi:10.1200/JCO.2013.54.7844.PMC 4178525.PMID 25185089.
  2. ^Luippold HE, Gooch PC, Brewen JG (February 1978)."The production of chromosome aberrations in various mammalian cells by triethylenemelamine".Genetics.88 (2):317–326.doi:10.1093/genetics/88.2.317.PMC 1213803.PMID 565312.
SPs/MIs
(M phase)
Blockmicrotubule 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
Other/ungrouped
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