Synthesis, single crystal (XRD), Hirshfeld surface analysis, computational study (DFT) and molecular docking studies of (E)-4-((2-hydroxy-3,5-diio dobenzylidene)amino)-N-(pyrimidine)-2-yl) benzenesulfonamide

被引:66
作者
Elangovan, N. [1 ]
Sowrirajan, S. [2 ]
机构
[1] Bharathidasan Univ, Arignar Anna Govt Arts Coll, Dept Chem, Tiruchirappalli 621211, Tamil Nadu, India
[2] King Fahd Univ Petr & Minerals, Dept Chem, Dhahran 31261, Saudi Arabia
关键词
Synthesis; Single crystal; DFT; Drug-likeness; Molecular docking; Sulfadiazine; ELECTRON LOCALIZATION FUNCTION; NONLINEAR-OPTICAL PROPERTIES; PLACENTA GROWTH-FACTOR; SULFONAMIDE DERIVATIVES; BASIS SETS; DENSITY; AFFINITY; ABSORPTION; DISCOVERY; HARDNESS;
D O I
10.1016/j.heliyon.2021.e07724
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Schiff base (E)-4-((2-hydroxy-3,5-diiodobenzylidene)amino)-N-(pyrimidine)-2-yl) benzene sulfonamide (DIDA) compound was synthesis with condensation of 3,5-diiodosalicylaldehyde and sulfadiazine. The compound characterized with FTIR, X-ray crystallography and electronic spectra. The titled compound associated with experimental and theoretical method, DFT used for the theoretical method. The IR was calculated from DFT mode with B3LYP/GENSEP basic set. The electronic spectra computed from TD-DFT method with CAM-B3LYP functional, with IEFPCM solvation model and DMSO used as the solvent. Wave function based properties like localized orbital locator, electron localization function and non-covalent interactions have been studied extensively. The ADMET properties of the compound DIDA indicated that the compound has excellent drug likeness properties and PASS studies showed that it has anti-infective properties, which is confirmed by a docking score of -7.4 kcal/mol.
引用
收藏
页数:13
相关论文
共 67 条
[1]   Insights towards sulfonamide drug specificity in α-carbonic anhydrases [J].
Aggarwal, Mayank ;
Kondeti, Bhargav ;
McKenna, Robert .
BIOORGANIC & MEDICINAL CHEMISTRY, 2013, 21 (06) :1526-1533
[2]   Synthesis and characterization of curcumin-sulfonamide hybrids: Biological evaluation and molecular docking studies [J].
Banuppriya, Govindharasu ;
Sribalan, Rajendran ;
Padmini, Vediappen .
JOURNAL OF MOLECULAR STRUCTURE, 2018, 1155 :90-100
[3]   Quantum computational, spectroscopic investigations on 6-aminobenzimidazole by DFT/TD-DFT with different solvents and molecular docking studies [J].
Basha, Shaik Jaheer ;
Chamundeeswari, S. P. Vijaya ;
Muthu, S. ;
Raajaraman, B. R. .
JOURNAL OF MOLECULAR LIQUIDS, 2019, 296
[4]   Jaguar: A high-performance quantum chemistry software program with strengths in life and materials sciences [J].
Bochevarov, Art D. ;
Harder, Edward ;
Hughes, Thomas F. ;
Greenwood, Jeremy R. ;
Braden, Dale A. ;
Philipp, Dean M. ;
Rinaldo, David ;
Halls, Mathew D. ;
Zhang, Jing ;
Friesner, Richard A. .
INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, 2013, 113 (18) :2110-2142
[5]   Revealing strong interactions with the reduced density gradient: a benchmark for covalent, ionic and charge-shift bonds` [J].
Boto, Roberto A. ;
Piquemal, Jean-Philip ;
Contreras-Garcia, Julia .
THEORETICAL CHEMISTRY ACCOUNTS, 2017, 136 (12)
[6]   Some new biologically active metal-based sulfonamide [J].
Chohan, Zahid H. ;
Shad, Hazoor A. ;
Youssoufi, Moulay H. ;
Ben Hadda, Taibi .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2010, 45 (07) :2893-2901
[7]   Quantum Chemical Studies of Light Harvesting [J].
Curutchet, Carles ;
Mennucci, Benedetta .
CHEMICAL REVIEWS, 2017, 117 (02) :294-343
[8]   Antibiotic resistance is ancient [J].
D'Costa, Vanessa M. ;
King, Christine E. ;
Kalan, Lindsay ;
Morar, Mariya ;
Sung, Wilson W. L. ;
Schwarz, Carsten ;
Froese, Duane ;
Zazula, Grant ;
Calmels, Fabrice ;
Debruyne, Regis ;
Golding, G. Brian ;
Poinar, Hendrik N. ;
Wright, Gerard D. .
NATURE, 2011, 477 (7365) :457-461
[9]   The discovery of placenta growth factor and its biological activity [J].
De Falco, Sandro .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2012, 44 (01) :1-9
[10]   Calculation of negative electron affinity and aqueous anion hardness using Kohn-Sham HOMO and LUMO energies [J].
De Proft, Frank ;
Sablon, Nick ;
Tozer, David J. ;
Geerlings, Paul .
FARADAY DISCUSSIONS, 2007, 135 :151-159