Green Synthesis and Molecular Docking Study of Some New Thiazoles Using Terephthalohydrazide Chitosan Hydrogel as Ecofriendly Biopolymeric Catalyst

被引:26
作者
Al-Humaidi, Jehan Y. [1 ]
Gomha, Sobhi M. [2 ]
Abd El-Ghany, Nahed A. [3 ]
Farag, Basant [4 ]
Zaki, Magdi E. A. [5 ]
Abolibda, Tariq Z. [2 ]
Mohamed, Nadia A. [3 ,6 ]
机构
[1] Princess Nourah Bint Abdulrahman Univ, Coll Sci, Dept Chem, POB 84428, Riyadh 11671, Saudi Arabia
[2] Islamic Univ Madinah, Fac Sci, Dept Chem, POB 170, Madinah 42351, Saudi Arabia
[3] Cairo Univ, Fac Sci, Dept Chem, Giza 12613, Egypt
[4] Zagazig Univ, Fac Sci, Dept Chem, Zagazig 44519, Egypt
[5] Imam Mohammad Ibn Saud Islamic Univ IMSIU, Fac Sci, Dept Chem, POB 5701, Riyadh 11623, Saudi Arabia
[6] Qassim Univ, Dept Chem, Coll Sci, POB 6644, Buraydah 51452, Saudi Arabia
关键词
thiosemicarbazones; thiazoles; thiadiazoles; hydrazonoyl halides; antimicrobial; molecular docking studies; in silico ADMET; ONE-POT SYNTHESIS; CYTOTOXICITY EVALUATION; ANTIMICROBIAL ACTIVITY; DERIVATIVES; ANTICANCER; EFFICIENT; 1,3-THIAZINES; INHIBITORS; NITRILES; HYBRIDS;
D O I
10.3390/catal13091311
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Terephthalohydrazide chitosan hydrogel (TCs) was prepared and investigated as an ecofriendly biopolymeric catalyst for synthesis of some novel thiazole and thiadiazole derivatives. Thus, TCs was used as a promising ecofriendly basic biocatalyst for preparation of three new series of thiazoles and two thiadiazoles derivatives via reacting 2-(2-oxo-1,2-diphenylethylidene) hydrazine-1-carbothio-amide with various hydrazonoyl chlorides and alpha-haloketones under mild ultrasonic irradiation. Also, their yield% was estimated using chitosan and TCs in a comparative study. The procedure being employed has the advantages of mild reaction conditions, quick reaction durations, and high reaction yields. It also benefits from the catalyst's capacity to be reused several times without significantly losing potency. The chemical structures of the newly prepared compounds were confirmed by IR, MS, and 1H-NMR. Docking analyses of the synthesized compounds' binding modes revealed promising binding scores against the various amino acids of the selected protein (PDB Code-1JIJ). SwissADME's online tool is then used to analyze the physiochemical and pharmacokinetic characteristics of the most significant substances. The majority of novel compounds showed zero violation from Lipinski's rule (Ro5).
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页数:24
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