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1.
Anticancer Agents Med Chem ; 6(2): 75-109, 2006 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-16529534

RESUMEN

The use of polyhedral boron hydrides for cancer treatment is traditionally connected with boron neutron capture therapy. More recently, polyhedral borate anions were proposed as carriers of radionuclide label for targeted radionuclide therapy and diagnostics of cancer. Some metal derivatives of carboranes were found to demonstrate significant antitumor activity themselves. This review is designed to highlight the recent work concerning various fields of potential application of polyhedral boron compounds in anticancer diagnostics and therapy.


Asunto(s)
Antineoplásicos/uso terapéutico , Compuestos de Boro/uso terapéutico , Neoplasias/diagnóstico , Neoplasias/tratamiento farmacológico , Animales , Boranos/farmacocinética , Boranos/uso terapéutico , Terapia por Captura de Neutrón de Boro/métodos , Línea Celular Tumoral , Humanos , Neoplasias/radioterapia
2.
Met Based Drugs ; 4(2): 75-80, 1997.
Artículo en Inglés | MEDLINE | ID: mdl-18475772

RESUMEN

X-ray diffraction studies reveal the structure of {[(2-C(6)H(5)-1,2-C(2)B(10)H(10)-1-COO)Bu(2)Sn](2)O}(2), 1, to conform to the common motif found for {[(R'COO)R(2)Sn](2)O}(2) compounds. The dimer features a central Bu(2)Sn(2)O(2) unit (two-fold symmetry) with the two Bu(2)Sn groups being linked via bridging oxygen atoms, each of which also carries an exocyclic Bu(2)Sn moiety. The two pairs of exo- and endo-cyclic tin atoms are each linked via an almost symmetrically bridging carboxylate ligand and the two remaining ligands coordinate an exocyclic tin atom only, in the monodentate mode. The in vitro anti-tumour activity of 1, determined against a variety of cell lines, is compared with those of the corresponding 2-methylcarboranylacetate, derivative 2, and with clinically used compounds.

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