In vitro anticancer potentiality and molecular modelling study of novel amino acid derivatives based on N1,N3-bis-(1-hydrazinyl-1-oxopropan-2-yl) isophthalamide

A series of N1,N3-bis (1-oxopropan-2-yl) isophthalamide-based derivatives 4-16 were prepared and their structures were confirmed by different spectral tools. The cytotoxic potentiality of novel compounds 4-16 was assessed by the MTT assay method on colon, lung and breast tumour cell lines. Compound...

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Main Authors: Asmaa F. Kassem (Author), Gaber O. Moustafa (Author), Eman S. Nossier (Author), Hemat S. Khalaf (Author), Marwa M. Mounier (Author), Suliman A. Al-Yousef (Author), Sabry Y. Mahmoud (Author)
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Published: Taylor & Francis Group, 2019-01-01T00:00:00Z.
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100 1 0 |a Asmaa F. Kassem  |e author 
700 1 0 |a Gaber O. Moustafa  |e author 
700 1 0 |a Eman S. Nossier  |e author 
700 1 0 |a Hemat S. Khalaf  |e author 
700 1 0 |a Marwa M. Mounier  |e author 
700 1 0 |a Suliman A. Al-Yousef  |e author 
700 1 0 |a Sabry Y. Mahmoud  |e author 
245 0 0 |a In vitro anticancer potentiality and molecular modelling study of novel amino acid derivatives based on N1,N3-bis-(1-hydrazinyl-1-oxopropan-2-yl) isophthalamide 
260 |b Taylor & Francis Group,   |c 2019-01-01T00:00:00Z. 
500 |a 1475-6366 
500 |a 1475-6374 
500 |a 10.1080/14756366.2019.1613390 
520 |a A series of N1,N3-bis (1-oxopropan-2-yl) isophthalamide-based derivatives 4-16 were prepared and their structures were confirmed by different spectral tools. The cytotoxic potentiality of novel compounds 4-16 was assessed by the MTT assay method on colon, lung and breast tumour cell lines. Compound 5 gave the most significant specificity anticancer activity with safety response on normal cell lines. In vitro enzyme assay and several apoptotic parameters were examined to elucidate the mode of action of compound 5. Molecular docking studies also were simulated to put insight and give better understanding to its structural features. 
546 |a EN 
690 |a isophthalamide 
690 |a amino acids 
690 |a peptides 
690 |a anticancer activity 
690 |a molecular docking 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 34, Iss 1, Pp 1247-1258 (2019) 
787 0 |n http://dx.doi.org/10.1080/14756366.2019.1613390 
787 0 |n https://doaj.org/toc/1475-6366 
787 0 |n https://doaj.org/toc/1475-6374 
856 4 1 |u https://doaj.org/article/ae3a3224d3d242d68f95da0ad4e3d80d  |z Connect to this object online.