16370-58-4Relevant articles and documents
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Dreyfus et al.
, p. 7027 (1977)
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Lignopurines: A new family of hybrids between cyclolignans and purines. Synthesis and biological evaluation
ángeles Castro,Miguel Del Corral, José M.,García, Pablo A.,Victoria Rojo,Bento, Ana C.,Mollinedo, Faustino,Francesch, Andrés M.,San Feliciano, Arturo
supporting information, p. 377 - 389 (2013/02/23)
A new family of hybrids between cyclolignans related to podophyllic aldehyde, a non-lactonic cyclolignan, and purines were prepared and evaluated against several human tumour cell lines. Both fragments, cyclolignan and purine, were linked through aliphatic and aromatic chains. The influence on the cytotoxicity of the purine substitution and the nature of the linker is analyzed. The new family was slightly less cytotoxic than the parent podophyllic aldehyde, although the selectivity is maintained or even improved and among the linkers used, the presence of an aromatic ring gave the most potent and selective derivatives within the new series tested. Cell cycle and confocal studies demonstrate that these derivatives interfere with the tubulin polymerization and arrest cells at the G2/M phase, in the same way than the parent compounds podophyllotoxin and podophyllic aldehyde do.
Process for preparing N6,9-disubstituted adenine
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, (2008/06/13)
A process for preparing N6, 9-disubstituted adenines which comprises reacting a metal salt of N6 -substituted adenine with a benzyl halide compound, preferably in the presence of a phase transfer catalyst. According to the process, the N6,9-disubstuted adenines can be obtained in high yields and good selectivity.
