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	<dc:title xml:lang="en-US">Structural characterization, biological evaluation and DNA interaction of some potential drugs based on bifunctional aldehyde functionality</dc:title>
	<dc:creator>Naz, Mehwish</dc:creator>
	<dc:creator>Akhter, Zareen</dc:creator>
	<dc:creator>Zaka, Ayesha</dc:creator>
	<dc:creator>Mirza, Bushra</dc:creator>
	<dc:creator>McKee, Vickie</dc:creator>
	<dc:creator>Ullah, Ehsan</dc:creator>
	<dc:creator>Bolte, Michael</dc:creator>
	<dc:subject xml:lang="en-US">Hyperchromism</dc:subject>
	<dc:subject xml:lang="en-US">DNA damaging assay</dc:subject>
	<dc:subject xml:lang="en-US">Bifunctional aldehyde</dc:subject>
	<dc:subject xml:lang="en-US">Chemotherapeutic agent</dc:subject>
	<dc:subject xml:lang="en-US">Pharmacological activities</dc:subject>
	<dc:subject xml:lang="en-US">Bifunctional aldehyde-DNA interaction</dc:subject>
	<dc:description xml:lang="en-US">Recent work aimed at evaluating the possibility of enhancing biological activities by synthetically modifying bifunctional aldehyde structures. In this article, two series of bifunctional aldehydes were synthesized, structurally characterized (M-1A, M-1C and M-2A) using single crystal X-ray diffraction analysis. Several pharmacological properties like cytotoxic, antifungal, antibacterial, antioxidant and antitumor activities were also evaluated. In addition, bifunctional aldehyde-DNA interaction assay was examined by UV-Vis spectroscopy which revealed the DNA damaging behaviour of these aldehydes. The results of UV-Vis spectroscopy were supported by DNA damaging assay. The overall results reveal that bifunctional aldehyde moiety could be used as potential drug candidates.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2017-09-30</dc:date>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/1576</dc:identifier>
	<dc:identifier>10.5155/eurjchem.8.3.195-202.1576</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 8 No. 3 (2017): September 2017; 195-202</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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