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Catalytic Double Cyclization Process for Antitumor Agents against Breast Cancer Cell Lines.


ABSTRACT: The development of efficient synthetic strategies for the discovery of novel antitumor molecules is a major goal in current research. In this context, we report here a catalytic double cyclization process leading to bicyclic heterocycles with significant antitumor activity on different human breast cancer (BC) cell lines. The products, 6,6a-dihydrofuro[3,2-b]furan-2(5H)-ones, were obtained in one step, starting from simple substrates (4-yne-1,3-diols, CO, and O2), under the catalytic action of PdI2 in conjunction with KI. These compounds have significant antiproliferative activity in vitro on human BC cell lines, both hormone receptor positive (MCF-7) and triple negative (triple-negative breast cancer [TNBC]; MDA-MB-231 and MDAMB-468), while exhibiting practically no effects on normal MCF-10A (human mammary epithelial) and 3T3-L1 (murine fibroblasts) cells. Thus, these compounds have the potential to expand the therapeutic options against BC, and in particular, against its most aggressive forms (TNBCs). Moreover, the present synthetic approach may provide an economic benefit for their production.

SUBMITTER: Mancuso R 

PROVIDER: S-EPMC6137400 | biostudies-literature | 2018 May

REPOSITORIES: biostudies-literature

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Catalytic Double Cyclization Process for Antitumor Agents against Breast Cancer Cell Lines.

Mancuso Raffaella R   Ziccarelli Ida I   Chimento Adele A   Marino Nadia N   Della Ca' Nicola N   Sirianni Rosa R   Pezzi Vincenzo V   Gabriele Bartolo B  

iScience 20180503


The development of efficient synthetic strategies for the discovery of novel antitumor molecules is a major goal in current research. In this context, we report here a catalytic double cyclization process leading to bicyclic heterocycles with significant antitumor activity on different human breast cancer (BC) cell lines. The products, 6,6a-dihydrofuro[3,2-b]furan-2(5H)-ones, were obtained in one step, starting from simple substrates (4-yne-1,3-diols, CO, and O<sub>2</sub>), under the catalytic  ...[more]

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