Structural Elucidation, In vitro and In silico Biological Evaluations of New Fluorinated Chalcone Derivatives for Potential Antioxidant Activity

被引:1
|
作者
Rajasagaran, Rineswary [1 ]
Arshad, Ahmad Saifuddin Mohamad [2 ]
Azizi, Juzaili [2 ]
Nizar, Siti Nabilla Aliya Mohd [1 ]
Arshad, Suhana [1 ]
机构
[1] Univ Sains Malaysia, Sch Phys, Xray Crystallog Unit, Gelugor 11800, Penang, Malaysia
[2] Univ Sains Malaysia, Ctr Drug Res, Gelugor 11800, Penang, Malaysia
关键词
Claisen Schmidt; single crystal diffraction; antioxidant; DPPH; molecular docking; ADMET; MOLECULAR DOCKING; ACETYLCHOLINESTERASE; INHIBITION; UPDATE; AGENTS;
D O I
10.2174/1570178620666230616112831
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The newly synthesized fluorinated chalcone derivatives are observed to possess antioxidant potential. Two new fluorinated chalcone compounds were effectively synthesized using the Claisen-Schmidt condensation reaction and were recrystallized using the slow evaporation method. The single crystal structure of the compounds was determined and refined through the X-ray single crystal diffraction method. All compounds were subjected to computational structural characterization and Hirshfeld surface analysis. The compounds were then further characterized through the Ultraviolet-visible (UV-Vis) spectroscopic study. The chalcone derivatives were further analysed with biological experimentation and simulation such as in vitro antioxidant (DPPH) assay, molecular docking and in silico ADMET study. The crystal packing revealed that the molecules in the compounds were linked together through the intermolecular C-H<middle dot><middle dot><middle dot>O and C-H<middle dot><middle dot><middle dot>pi interactions. Hirshfeld surface analysis validated the presence of intermolecular interactions in crystal packing. The UV-Vis spectroscopic study revealed that the absorption wavelength of the compounds that range from 421.79 to 428.98 nm was within the visible region with the energy gap value of 2.58 to 2.62 eV. The DPPH assay disclosed weak antioxidant activity of both compounds (-31 to 20%, 10000 mu g/mL) compared to the standard ascorbic acid (94.5%, 50 mu g/mL). The binding energy of the docked complex inside the target protein, 2CAG was within the range of -7.3 to -7.5 kcal/mol. In the silico model, SwissADME predicted that the two compounds have overall good drug-like properties. Different substituents, more planar configuration and high intramolecular interactions in the crystal packing played their role in increasing the antioxidant activities, binding energy and drug likeliness of the synthesized compounds.
引用
收藏
页码:1136 / 1150
页数:15
相关论文
共 50 条
  • [1] Synthesis, In Silico, and In Vitro Evaluation of the Potential Antioxidant Activity of New Quinazoline Derivatives
    Al-Khuzaie, Mohammed G. A.
    Hama, Lawand Hama karim kaka
    Al-Majidi, Suaad M. H.
    [J]. RUSSIAN JOURNAL OF BIOORGANIC CHEMISTRY, 2024, 50 (04) : 1476 - 1490
  • [2] Synthesis and in vitro biological activity of chalcone derivatives as potential antiparasitic agents
    Setshedi, Koketso J.
    Beteck, Richard M.
    Ilbeigi, Kayhan
    Mabille, Dorien
    Caljon, Guy
    Legoabe, Lesetja J.
    [J]. MEDICINAL CHEMISTRY RESEARCH, 2024, 33 (06) : 977 - 988
  • [3] Antileishmanial Thioureas: Synthesis, Biological Activity and in Silico Evaluations of New Promising Derivatives
    Viana, Gil Mendes
    Soares, Deivid Costa
    Santana, Marcos Vinicius
    do Amaral, Lilian Henriques
    Meireles, Paloma Wetler
    Nunes, Raquel Pinto
    Rodrigues Pereira da Silva, Luiz Claudio
    de Sequeira Aguiar, Lucia Cruz
    Rodrigues, Carlos Rangel
    de Sousa, Valeria Pereira
    Castro, Helena Carla
    Abreu, Paula Alvarez
    Sathler, Plinio Cunha
    Saraiva, Elvira Maria
    Cabral, Lucio Mendes
    [J]. CHEMICAL & PHARMACEUTICAL BULLETIN, 2017, 65 (10) : 911 - 919
  • [4] New chalcone derivatives as potential antimicrobial and antioxidant agent
    Emelda N. Okolo
    David I. Ugwu
    Benjamin E. Ezema
    Joseph C. Ndefo
    Florence U. Eze
    Chidimma G. Ezema
    James A. Ezugwu
    Oguejiofo T. Ujam
    [J]. Scientific Reports, 11
  • [5] New chalcone derivatives as potential antimicrobial and antioxidant agent
    Okolo, Emelda N.
    Ugwu, David, I
    Ezema, Benjamin E.
    Ndefo, Joseph C.
    Eze, Florence U.
    Ezema, Chidimma G.
    Ezugwu, James A.
    Ujam, Oguejiofo T.
    [J]. SCIENTIFIC REPORTS, 2021, 11 (01)
  • [6] In vitro biological activities of new heterocyclic chalcone derivatives
    Raj, Chenna Govindaraju Darshan
    Sarojini, Balladaka Kunchanna
    Hegde, Subramanya
    Sreenivasa, Swamy
    Ravikumar, Yalega Siddappa
    Bhanuprakash, Veerakyathappa
    Revanaiah, Yogisharadhya
    Ragavendra, Ramappa
    [J]. MEDICINAL CHEMISTRY RESEARCH, 2013, 22 (05) : 2079 - 2087
  • [7] In vitro biological activities of new heterocyclic chalcone derivatives
    Chenna Govindaraju Darshan Raj
    Balladaka Kunchanna Sarojini
    Subramanya Hegde
    Swamy Sreenivasa
    Yalega Siddappa Ravikumar
    Veerakyathappa Bhanuprakash
    Yogisharadhya Revanaiah
    Ramappa Ragavendra
    [J]. Medicinal Chemistry Research, 2013, 22 : 2079 - 2087
  • [8] Synthesis, characterization and in vitro, in vivo, in silico biological evaluations of substituted benzimidazole derivatives
    Raka, Sabreena Chowdhury
    Rahman, Arifur
    Hussain, Fahad
    Rahman, S. M. Abdur
    [J]. SAUDI JOURNAL OF BIOLOGICAL SCIENCES, 2022, 29 (01) : 239 - 250
  • [9] Chalcone Derivatives as Potential Inhibitors of P-Glycoprotein and NorA: An In Silico and In Vitro Study
    Minh-Tri Le
    Dieu-Thuong Thi Trinh
    Trieu-Du Ngo
    Viet-Khoa Tran-Nguyen
    Dac-Nhan Nguyen
    Tung Hoang
    Hoang-Minh Nguyen
    Tran-Giang-Son Do
    Tan Thanh Mai
    Thanh-Dao Tran
    Khac-Minh Thai
    [J]. BIOMED RESEARCH INTERNATIONAL, 2022, 2022
  • [10] Synthesis, Structural Elucidation, In Silico and In Vitro Studies of New Class of Methylenedioxyphenyl-Based Amide Derivatives as Potential Myeloperoxidase Inhibitors for Cardiovascular Protection
    Rajan, Reshma
    Karthikeyan, Sambantham
    Desikan, Rajagopal
    [J]. ACS OMEGA, 2024, 9 (07): : 7850 - 7868