Synthesis of 1,7-bis(carboxyalkylcarbamoyl)-m-carboranes as precursors of possible water-soluble preparations for boron-neutron-capture treatment of cancer

Сергеев, В. А.; Bekasova, N.I.; Baryshnikova, E. A.; Surikova, M. A.; Mishina, N. M.

doi:10.1007/bf01431139

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1998

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“…Other compounds involved variously substituted o - and m -carboranes. These included benzonitriles, bis(carboxyalkylcarbamoyl) derivatives, phosphordiamidate nucleosides, carboranes containing the azulene framework, 589,590 kojic acid, 591 isocyanates, and carborane superclusters of dendrimers , The biochemical/physiological basis by which any of these compounds would selectively target tumor cells is, in most instances, not clearly enunciated, justified, or even addressed.…”

Section: Other Compoundsmentioning

confidence: 99%

“…585 Other compounds involved variously substituted oand m-carboranes. These included benzonitriles, 586 bis(carboxyalkylcarbamoyl) derivatives, 587 phosphordiamidate nucleosides, 588 carboranes containing the azulene framework, 589,590 kojic acid, 591 isocyanates, 592 and carborane superclusters of dendrimers. 593 Others have involved the insertion of nido-7-CB 10 H 12 2nucleus into various structures.…”

Section: Other Compoundsmentioning

confidence: 99%

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