Synthesis, characterization and cytotoxic activity of diorganotin (IV) complexes with 4H-pyrido[1,2-a]pyrimidin-4-one derivatives
β Scribed by Talal A.K. Al-Allaf; Redha I.H. Al-Bayati; Luay J. Rashan; Rula F. Khuzaie
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 376 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0268-2605
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β¦ Synopsis
The coordination behaviour of the diorganotin(1V) compounds R,SnCI, (where R = Me, Ph) with 4Hpyrido [ 1,2-a] pyrimidin-4-one derivatives (L) has been described. The complexes R,SnCI,. L obtained have been characterized physicochemically and spectroscopically. The pyrimidin-Cone ligands were found to coordinate with R,SnCl, species in a monodentate fashion, mainly via the oxygen atom of the 4-one group or possibly via the nitrogen atom of the -C=N linkage (the less sterically hindered nitrogen of the pyrimidine derivative) to give pentacoordinate tin complexes. Of the complexes selected to be screened against five tumour cell lines, some exhibited significant in uitro activity.
π SIMILAR VOLUMES
The compounds [SnR 2 X 2 (MBIm)] (MBIm = Nmethyl-2,2Π-bisimidazole; R = Me, Et, Bu, Ph; X = Cl or Br) have been synthesized and characterized by IR, Raman, MΓΆssbauer and NMR spectroscopy, and their capacity to inhibit tumour cell division has been assayed. Measurements of conductivity in acetonitril
## Abstract As part of our ongoing research effort to develop new antimitotic agents based on the recently reported pyrimido[4,5β__c__]quinolineβ1(2__H__)βone ring skeleton, we were interested in identifying structural elements that contribute to the cytotoxicity of this class of compounds. The eff