Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

// request.cf · coarse context

A page that knows where it met you.

Only coarse request metadata is shown. This demo does not display or persist visitor IP addresses.

Country
US
Cloudflare location
CMH
Connection
HTTP/2
Language
Not provided

Ray ID: a22a7f76d86d386c

Jump to content

// Workers AI · dad joke modeWhy did Triethylenemelamine go to therapy? It had a bonding issue.

From Wikipedia, the free encyclopedia
(Redirected from Tretamine)
Triethylenemelamine
Clinical data
ATC code
  • None
Identifiers
  • 2,4,6-Tris(aziridin-1-yl)-1,3,5-triazine
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.000.076 Edit 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 X markN
  • Key:IUCJMVBFZDHPDX-UHFFFAOYSA-N X markN
 X markNcheckY (what is this?)  (verify)

Triethylenemelamine (abbreviated TEM, also called Tretamine) is a drug used in chemotherapy.[1]

It is a mutagenic chemical because it is an alkylating antineoplastic agent, a trifunctional alkylating agent that has three reactive groups that enable it to bind covalently to DNA at three distinct sites. As a result, TEM can cause chromatid aberrations in cell models.[2] It was one of the first compounds used for chemical mutagenesis in laboratory mice, with the impact on mutagenesis measured by the specific-locus test by Bruce Cattanach.[3]

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.
  3. Cattanach, B. M. (1966). "Chemically induced mutations in mice". Mutation Research. 3 (4): 346–353. doi:10.1016/0027-5107(66)90041-8. PMID 5969214.