The synthesis of new planar derivatives characterized by the presence of a pyridothiopyranopyrazole or pyridothiopyranopyrimidine nucleus, carrying a substituted aryl group, is reported. The novel 1,4-dihydropyrido[2’,3’:5,6]thiopyrano[4,3-c]pyrazole derivatives were obtained by condensation of 2,3-dihydro-3-hydroxymethylenethiopyrano[2,3-b]pyridin-4(4H)-ones with appropriate hydrazines. The preparation of 2-substituted pyrido[3’,2’:5,6]thiopyrano[4,3-d]pyrimidines was accomplished from the intermediate 2,3-dihydro-3-dimethylaminomethylenethiopyrano[2,3-b]pyridin-4(4H)ones by reaction with the opportune binucleophile amidines. The antiproliferative activity of some new products was tested by an in vitro assay on human tumour cell lines (HL-60 and HeLa), but none of them showed any significant effect in the tests performed. Accordingly, linear flow dichroism measurements indicated their inability to form a molecular complex with DNA

Synthesis of Novel 1,4-Dihydropyrido[3',2':5,6]thiopyrano[4,3-c]pyrazoles and 5H-Pyrido[3',2':5,6]thiopyrano[4,3-d]pyrimidines as Potential Antiproliferative Agents

DALLA VIA, LISA;MARCIANI MAGNO, SEBASTIANO
2003

Abstract

The synthesis of new planar derivatives characterized by the presence of a pyridothiopyranopyrazole or pyridothiopyranopyrimidine nucleus, carrying a substituted aryl group, is reported. The novel 1,4-dihydropyrido[2’,3’:5,6]thiopyrano[4,3-c]pyrazole derivatives were obtained by condensation of 2,3-dihydro-3-hydroxymethylenethiopyrano[2,3-b]pyridin-4(4H)-ones with appropriate hydrazines. The preparation of 2-substituted pyrido[3’,2’:5,6]thiopyrano[4,3-d]pyrimidines was accomplished from the intermediate 2,3-dihydro-3-dimethylaminomethylenethiopyrano[2,3-b]pyridin-4(4H)ones by reaction with the opportune binucleophile amidines. The antiproliferative activity of some new products was tested by an in vitro assay on human tumour cell lines (HL-60 and HeLa), but none of them showed any significant effect in the tests performed. Accordingly, linear flow dichroism measurements indicated their inability to form a molecular complex with DNA
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/2461412
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 16
  • ???jsp.display-item.citation.isi??? 14
social impact