In Vitro Evaluation and Bioinformatics Analysis of Schiff Bases Bearing Pyrazole Scaffold as Bioactive Agents: Antioxidant, Anti-Diabetic, Anti-Alzheimer, and Anti-Arthritic

被引:23
作者
Alkahtani, Hamad M. [1 ]
Almehizia, Abdulrahman A. [1 ]
Al-Omar, Mohamed A. [1 ]
Obaidullah, Ahmad J. [1 ]
Zen, Amer A. [2 ]
Hassan, Ashraf S. [3 ]
Aboulthana, Wael M. [4 ]
机构
[1] King Saud Univ, Coll Pharm, Dept Pharmaceut Chem, POB 2457, Riyadh 11451, Saudi Arabia
[2] Nottingham Trent Univ, Chem & Forens Dept, Clifton Campus, Nottingham NG11 8NS, England
[3] Natl Res Ctr, Organometall & Organometalloid Chem Dept, Cairo 12622, Egypt
[4] Natl Res Ctr, Biotechnol Res Inst, Biochem Dept, Cairo 12622, Egypt
来源
MOLECULES | 2023年 / 28卷 / 20期
关键词
Schiff bases; pyrazole scaffold; bioinformatics analysis; anti-arthritic therapeutic; molecular lipophilicity potential; molecular polar surface area; ANTIBACTERIAL;
D O I
10.3390/molecules28207125
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In continuation of our research programs for the discovery, production, and development of the pharmacological activities of molecules for various disease treatments, Schiff bases and pyrazole scaffold have a broad spectrum of activities in biological applications. In this context, this manuscript aims to evaluate and study Schiff base-pyrazole molecules as a new class of antioxidant (total antioxidant capacity, iron-reducing power, scavenging activity against DPPH, and ABTS radicals), anti-diabetic (alpha-amylase% inhibition), anti-Alzheimer's (acetylcholinesterase% inhibition), and anti-arthritic (protein denaturation% and proteinase enzyme% inhibitions) therapeutics. Therefore, the Schiff bases bearing pyrazole scaffold (22a, b and 23a, b) were designed and synthesized for evaluation of their antioxidant, anti-diabetic, anti-Alzheimer's, and anti-arthritic properties. The results for compound 22b demonstrated significant antioxidant, anti-diabetic (alpha-amylase% inhibition), and anti-Alzheimer's (ACE%) activities, while compound 23a demonstrated significant anti-arthritic activity. Prediction of in silico bioinformatics analysis (physicochemical properties, bioavailability radar, drug-likeness, and medicinal chemistry) of the target derivatives (22a, b and 23a, b) was performed. The molecular lipophilicity potential (MLP) of the derivatives 22a, b and 23a, b was measured to determine which parts of the surface are hydrophobic and which are hydrophilic. In addition, the molecular polar surface area (PSA) was measured to determine the polar surface area and the non-polar surface area of the derivatives 22a, b and 23a, b. This study could be useful to help pharmaceutical researchers discover a new series of potent agents that may act as an antioxidant, anti-diabetic, anti-Alzheimer, and anti-arthritic.
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页数:14
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共 48 条
  • [31] Multi-target Polypharmacology of 4-aminoquinoline Compounds against Malaria, Tuberculosis and Cancer
    Nandi, Sisir
    Chauhan, Bhumika
    Tarannum, Heena
    Khede, Mayank Kumar
    [J]. CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2023, 23 (05) : 403 - 414
  • [32] LSD1 inhibitors for cancer treatment: Focus on multi-target agents and compounds in clinical trials
    Noce, Beatrice
    Di Bello, Elisabetta
    Fioravanti, Rossella
    Mai, Antonello
    [J]. FRONTIERS IN PHARMACOLOGY, 2023, 14
  • [33] A review on potential anti-diabetic mechanisms of chitosan and its derivatives
    Priyanka, D. N.
    Prashanth, K. V. Harish
    Tharanathan, R. N.
    [J]. CARBOHYDRATE POLYMER TECHNOLOGIES AND APPLICATIONS, 2022, 3
  • [34] 4-(5-Amino-pyrazol-1-yl)benzenesulfonamide derivatives as novel multi-target anti-inflammatory agents endowed with inhibitory activity against COX-2, 5-LOX and carbonic anhydrase: Design, synthesis, and biological assessments
    Ragab, Mahmoud A.
    Eldehna, Wagdy M.
    Nocentini, Alessio
    Bonardi, Alessandro
    Okda, Hazem E.
    Elgendy, Bahaa
    Ibrahim, Tarek S.
    Abd-Alhaseeb, Mohammad M.
    Gratteri, Paola
    Supuran, Claudiu T.
    Al-Karmalawy, Ahmed A.
    Elagawany, Mohamed
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2023, 250
  • [35] Recent developments in the synthesis of hybrid heterocycles, a promising approach to develop multi-target antibacterial agents
    Sadek, Kamal Usef
    Mekheimer, Ramadan Ahmed
    Abd-Elmonem, Mohamed
    Abo-Elsoud, Fatma A.
    Hayallah, Alaa M.
    Mostafa, Sara M.
    Abdellattif, Magda H.
    Abourehab, Mohammed A. S.
    Farghaly, Thoraya A.
    Elkamhawy, Ahmed
    [J]. JOURNAL OF MOLECULAR STRUCTURE, 2023, 1286
  • [36] Free Radicals and Oxidative Stress: Signaling Mechanisms, Redox Basis for Human Diseases, and Cell Cycle Regulation
    Sadiq, Idris Zubairu
    [J]. CURRENT MOLECULAR MEDICINE, 2023, 23 (01) : 13 - 35
  • [37] New 1,2,3-Triazole Scaffold Schiff Bases as Potential Anti-COVID-19: Design, Synthesis, DFT-Molecular Docking, and Cytotoxicity Aspects
    Said, Musa A.
    Khan, Daoud J. O.
    Al-Blewi, Fawzia F.
    Al-Kaff, Nadia S.
    Ali, Adeeb A.
    Rezki, Nadjet
    Aouad, Mohamed Reda
    Hagar, Mohamed
    [J]. VACCINES, 2021, 9 (09)
  • [38] Design, synthesis, and antibacterial evaluation of new Schiff's base derivatives bearing nitroimidazole and pyrazole nuclei as potent E-coli FabH inhibitors
    Sangani, Chetan B.
    Makwana, Jigar A.
    Duan, Yong-Tao
    Tarpada, Umesh P.
    Patel, Yogesh S.
    Patel, Ketan B.
    Dave, Vivek N.
    Zhu, Hai-Liang
    [J]. RESEARCH ON CHEMICAL INTERMEDIATES, 2015, 41 (12) : 10137 - 10149
  • [39] Newly synthesized lanthanides complexes of ferrocene-based Schiff base with high biological activities and improved molecular docking data
    Sayed, Fatma N.
    Mohamed, Gehad G.
    [J]. JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2022, 977
  • [40] Antiproliferative properties and structural analysis of newly synthesized Schiff bases bearing pyrazole derivatives and molecular docking studies
    Sener, Nesrin
    ozkinali, Sevil
    Altunoglu, Yasemin Celik
    Yerlikaya, Serife
    Gokce, Halil
    Zurnaci, Merve
    Gur, Mahmut
    Baloglu, Mehmet Cengiz
    Sener, Izzet
    [J]. JOURNAL OF MOLECULAR STRUCTURE, 2021, 1241