Jump to content

Chlorozotocin

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by DePiep (talk | contribs) at 15:41, 2 April 2016 (Remove redundant parameters InChI, InChIKey (StdInChI, StdInChIKey are used). See Talk (via AWB script)). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Chlorozotocin
Structural formula of chlorozotocin
Space-filling model of the chlorozotocin molecule
Clinical data
ATC code
  • none
Identifiers
  • 1-(2-Chloroethyl)-1-nitroso-3-[(2R,3R,4S,5R)-3,4,5,6-tetrahydroxy-1-oxohexan-2-yl]urea
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC9H16ClN3O7
Molar mass313.69 g/mol g·mol−1
3D model (JSmol)
  • ClCCN(N=O)C(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)[C@H](O)CO
  • InChI=1S/C9H16ClN3O7/c10-1-2-13(12-20)9(19)11-5(3-14)7(17)8(18)6(16)4-15/h3,5-8,15-18H,1-2,4H2,(H,11,19)/t5-,6+,7+,8+/m0/s1 ☒N
  • Key:MKQWTWSXVILIKJ-LXGUWJNJSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Chlorozotocin is a nitrosourea. It is used for cancer therapy.[citation needed]

It is an analogue of streptozotocin.[1]

References

  1. ^ Wolfe, M. Michael (2006). Therapy of digestive disorders. Elsevier Health Sciences. pp. 477–. ISBN 978-1-4160-0317-5. Retrieved 31 July 2011.