Journal
JOURNAL OF MOLECULAR STRUCTURE
Volume 1127, Issue -, Pages 345-354Publisher
ELSEVIER
DOI: 10.1016/j.molstruc.2016.07.082
Keywords
Mercaptodiaminopyrimidine Schiff base; Single crystal XRD; Molecular docking; DNA and beta-CD binding; DFT
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Funding
- UGC-Hyderabad [4995/14]
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Novel Schiff bases derived from the treatment of mercapto-diamino pyrimidine with two different aldehydes are characterized using elemental analysis, single crystal X-ray diffraction and H-1 NMR spectroscopy. The pharmacological action of the synthesized compounds viz., antimicrobial, anticancer and antitubercular activities is studied. The Schiff bases show a very good activity against various test pathogens. DNA and beta-CD binding interactions of the compounds are studied using UV-Visible absorption and fluorescence spectral measurements. The binding constants of the compounds towards beta-CD are in the order of 10(3) to 10(4). Molecular docking is done using MOE program on the 3D structure of the enzymes, viz., human thymidylate synthase complexed with dump and raltitrex, candida albicans N-myristoyltransferasepeptidic inhibitor, catalytic domain of protein kinase pKnb from mycobacterium tuberculosis in complex with mitoxantrone, pare, topoisomerase atpase inhibitor, E. calf and lactobacillus casdihydrofolatereductase. The MIC/IC50 values of the Schiff bases are compared with the glide scores from the molecular docking studies. The number of hydrogen bonding interactions between the Schiff bases and amino acid residues are also reported. (C) 2016 Elsevier B.V. All rights reserved.
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