Syntheses, Crystal Structures and Biological Activity of the 1D Chain Benzyltin Complexes Based on 2-Oxo-Propionic Acid Benzoyl Hydrazone
Two new 1D Chain benzyltin complexes {[C 6 H 4 (O)C=N–N=C(Me)COO](CH 3 OH)(C 6 H 5 CH 2 ) 2 Sn} n ( 1 ), {[C 6 H 4 (O)C–NH–N=C(Me)COO](C 6 H 5 CH 2 ) 3 Sn} n ( 2 ) were synthesized by the reactions of 2-oxo-propionic acid benzoyl hydrazone with dibenzyltin dichloride or tribenzyltin chloride, respec...
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Published in | Journal of inorganic and organometallic polymers and materials Vol. 27; no. 1; pp. 342 - 352 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
2017
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Two new 1D Chain benzyltin complexes {[C
6
H
4
(O)C=N–N=C(Me)COO](CH
3
OH)(C
6
H
5
CH
2
)
2
Sn}
n
(
1
), {[C
6
H
4
(O)C–NH–N=C(Me)COO](C
6
H
5
CH
2
)
3
Sn}
n
(
2
) were synthesized by the reactions of 2-oxo-propionic acid benzoyl hydrazone with dibenzyltin dichloride or tribenzyltin chloride, respectively. The two complexes were characterized by FT-IR,
1
H,
13
C and
119
Sn NMR spectra, elemental analysis, X-ray single crystal diffraction and TGA. In vitro antitumor activities of both complexes were evaluated by the 3-(4,5-dimethylthiazoly-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay against three human cancer cell lines (NCI-H460, HepG2, MCF7) and human cell line (HL7702). The
1
exhibited strong antitumor activity than
2
, then it was expected after further chemical optimization of candidate compounds as anti-cancer drugs. The interaction between complexes and calf thymus DNA were studied by EB fluorescent probe, the interaction of
1
and
2
with calf thymus DNA were intercalation and electrostatic attraction. |
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ISSN: | 1574-1443 1574-1451 |
DOI: | 10.1007/s10904-016-0477-5 |