Three new acrylic acid derivatives from Achillea mellifolium as potential thymidine phosphorylase inhibitor: molecular docking and MD simulation studies. Issue 18 (12th December 2021)

• Record Type: Journal Article
• Authors: Naz, Sadia; Farooq, Umar; Ma, Hongwu; Sarwar, Rizwana; Riaz, Nadia
• Is Part Of: Journal of biomolecular structure & dynamics. Volume 39:Issue 18(2021)
• Page Start: 7138
• Page End: 7149
• Publication Date: 2021-12-12
• Subjects: Acrylic acid -- spectroscopic analysis -- TP inhibition -- Achillea mellifolium -- molecular docking -- molecular dynamics simulations; Biomolecules -- Periodicals; Molecular structure -- Periodicals; Molecular Biology -- Periodicals; Biomechanics -- Periodicals; 572
• DOI: 10.1080/07391102.2020.1808071
• Languages: English
• ISSNs: 0739-1102

Abstract

Abstract: Discovery of potent inhibitors of thymidine phosphorylase (TP) can offer appropriate approach in cancer treatment owing to it's over expression in various human tumors compared to normal healthy tissues. Thymidine phosphorylase alongside 2-deoxy-D-ribose are reported as promoters of unwanted angiogenesis in cancerous cells. In this study, three new acrylic acid derivatives (1–3 ) have been isolated from ethyl acetate fraction of Achillea mellifolium . The characterization of these compounds (1–3 ) was done using UV, IR, 1 D and 2 D-NMR spectroscopy ( 1 H-NMR, 13 C-NMR, HMBC, NOESY) and mass spectrometry. The structure of these acrylic acid derivatives were ethyl (E)-3-((1S, 5R)-5-methoxy-2, 6, 6-trimethyl-4-oxocyclohex-2-en-1-yl)acrylate (1), methyl (E)-3-((1S, 5R)-5-methoxy-2, 6, 6-trimethyl-4-oxocyclohex-2-en-1-yl)acrylate (2) and (4S, 6R)-6-methoxy-3, 5, 5-trimethyl-4-((E)-3-oxobut-1-en-1-yl)cyclohex-2-en-1-one (3) . Thymidine phosphorylase (TP) inhibition studies showed compound 3 as most active inhibitor of TP with IC50 value 57.81 ± 3.41 while compound 1 and 2 showed IC50 value as 158.9 ± 0.97 and 89.92 ± 0.37, respectively. In addition, molecular docking studies of compound (1–3 ) were performed to shed light on their binding interaction patterns for binding into active pocket of TP. Similarly, all compounds (1–3 ) were evaluated for their anti-oxidant potential showing anti-oxidant activities with IC50 value ranging from 49.73 ± 0.41 to 79.81 ± 0.39. Later, these compound-protein (1–3 ) complexes were further subjected to MD simulations studies (50 ns) involving root mean square deviation, root mean square fluctuation, and secondary structure analysis to explore their binding mode stability inside active pocket. Communicated by Ramaswamy H. Sarma