6533b838fe1ef96bd12a483b
RESEARCH PRODUCT
Synthesis and characterization of complexes of trialkyl- and triarylphosphine gold(I) with thiolated purines and pyrimidines. A class of bifunctional compounds with potential antitumor activity.
C. Frank ShawAnvarhusein A. IsabGiancarlo StoccoFilippa Gattusosubject
Antitumor activityBicyclic moleculeDithioerythritolStereochemistryChemistrychemistry.chemical_elementBiological activityNuclear magnetic resonance spectroscopySulfurBiochemistryCombinatorial chemistryInorganic Chemistrychemistry.chemical_compoundMaterials ChemistryPhysical and Theoretical ChemistryBinding sitePurine metabolismBifunctionalPhosphinedescription
Abstract New complexes of the type R 3 PAuL or (R 3 PAu) 2 (μ-L) where R=ethyl or phenyl and L=6-thioguanine, 2, 6- dithioxanthine, 2, 4-dithiouracil and/or dithioerythritol have been prepared. These complexes have been identified by using elemental analysis, 1 H, 13 C and 31 P NMR spectroscopy. The structures have been proposed based on these spectroscopic studies. Sulfur appears to be the binding site in disubstituted complexes of 2, 4-dithiouracil and 1, 4-dithioerythritol, while the phosphine gold( I ) moieties appear to be S and N bonded in 2, 6-dithioxanthine and 6-thioguanine. The potential use of these complexes as antitumor drugs is discussed.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 1991-08-01 | Journal of Inorganic Biochemistry |