[feed] Atom [feed] RSS 1.0 [feed] RSS 2.0

Sivakrishna, B. and Islam, S. and Santra, M.K. and Pal, S. (2019) Synthesis and cytotoxic evaluation of apioarabino furanosyl pyrimidines. Drug Development Research .

Full text not available from this repository. (Request a copy)


In view of the potent anticancer activity of the d‐arabino‐configured cytosine nucleoside (ara‐C), apioarabinofuranosyl pyrimidine nucleosides were designed and synthesized from d‐ribose as starting material. The synthetic strategy signifies that tosylation followed by in situ cyclization, one‐pot controlled oxidative cleavage and acetylation by Pb(OAc)4, stereoselective nucleobase condensation, inversion of hydroxyl group and uracil group converted to cytosine as the key steps. Synthesized apioarabinofuranosyl pyrimidine nucleosides were tested using breast, colon, and ovarian cancer cell lines. However, only compound 19a, 19b, and 22b have a moderate growth‐suppressive effect against the luminal A breast cancer cell line MCF7.

Item Type: Article
Depositing User: Mr. Rameshwar Nema
Date Deposited: 24 Feb 2020 09:30
Last Modified: 24 Feb 2020 09:30
URI: http://nccs.sciencecentral.in/id/eprint/766

Actions (login required)

View Item View Item