Efficient one-pot synthesis of trans-Pt( ii )(salicylaldimine)(4-picoline)Cl complexes: effective agents for enhanced expression of p53 tumor suppressor genes
A series of trans -Pt( ii )(salicylaldimine)(4-picoline)Cl complexes were synthesized in 78–87% yield using a one-pot procedure from commercially available precursors. The structures of these complexes were characterized by 1 H, 19 F and 13 C NMR spectroscopy, HRMS (ESI) as well as single crystal X-...
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Published in | Dalton transactions : an international journal of inorganic chemistry Vol. 44; no. 21; pp. 9872 - 9880 |
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Main Authors | , , , , , , , |
Format | Journal Article Web Resource |
Language | English |
Published |
England
Royal Society of Chemistry (RSC)
07.06.2015
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Subjects | |
Online Access | Get full text |
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Summary: | A series of
trans
-Pt(
ii
)(salicylaldimine)(4-picoline)Cl complexes were synthesized in 78–87% yield using a one-pot procedure from commercially available precursors. The structures of these complexes were characterized by
1
H,
19
F and
13
C NMR spectroscopy, HRMS (ESI) as well as single crystal X-ray analysis. Bioactivity investigations including bio-assay, time- and dose-dependent, cell cycle progression study, caspase 3 and 9 apoptosis marker assay and DNA interaction using pBR322 plasmid DNA by gel electrophoresis were performed. The results indicated that the complexes showed promising
in vitro
cytotoxicity in MCF-7 and A549 cancer cell lines. Moreover these complexes enhanced the expression of p53 tumor suppressor gene family members such as p63 and p73. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 scopus-id:2-s2.0-84930221833 |
ISSN: | 1477-9226 1477-9234 1477-9234 |
DOI: | 10.1039/C5DT01098E |