Synthesis, Characterization and In Vitro Antitumour Activity of Di-n-Butyl, Tri-n-Butyl and Triphenyltin 3,6-Dioxaheptanoates and 3,6,9-Trioxadecanoates |
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Authors: | Kemmer M Gielen M Biesemans M de Vos D Willem R |
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Affiliation: | Université Libre de Bruxelles Service de Chimie Organique Av. F. D. Roosevelt, 50 Bruxelles B-1050 Belgium. |
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Abstract: | A series of di- and triorganotin 3,6-dioxaheptanoates and 3,6,9-trioxadecanoates were synthesized and
characterized by 1H, 13 and 117Sn NMR, electrospray mass and 119mSn Mössbauer spectroscopy, as well as
elemental analysis. Their in vitro antitumour activity against seven tumoural cell lines of human origin, two
breast cancers (MCF-7, EVSA-T), a colon carcinoma (WiDr), an ovarian cancer (IGROV), a melanoma (M 19
MEL), a renal cancer (A 498) and a non small cell lung cancer (H 226), is reported. They are characterized by
similar inhibition doses ID50 as the analogous di- and triorganotin derivatives of 4-carboxybenzo-15-crown-5
and -18-crown-6 and in some cases by much lower ID50 values than clinically used reference compounds such
as doxorubicine and methotrexate. |
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