Synthesis, Characterization and Biological Evaluation of Novel Thiourea Derivatives
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[1] Yusuf Sıcak,et al. SYNTHESIS, PREDICTIONS OF DRUG-LIKENESS AND PHARMACOKINETIC PROPERTIES OF SOME CHIRAL THIOUREAS AS POTENT ENZYME INHIBITION AGENTS , 2022, TURKISH JOURNAL OF CHEMISTRY.
[2] Murat Yiğit,et al. Selenourea and thiourea derivatives of chiral and achiral enetetramines: Synthesis, characterization and enzyme inhibitory properties. , 2021, Bioorganic chemistry.
[3] M. Romero,et al. Synthesis, bioevaluation and docking studies of new imidamide derivatives as nitric oxide synthase inhibitors. , 2021, Bioorganic & medicinal chemistry.
[4] J. Wietrzyk,et al. Synthesis and antiproliferative screening of novel doubly modified colchicines containing urea, thiourea and guanidine moieties. , 2021, Bioorganic & medicinal chemistry letters.
[5] Yusuf Sıcak,et al. Bioactivities and phenolic constituents relationship of Muğla thyme and pine honey of Turkey with the chemometric approach , 2021, Journal of Food Measurement and Characterization.
[6] Yusuf Sıcak,et al. Design and antiproliferative and antioxidant activities of furan-based thiosemicarbazides and 1,2,4-triazoles: their structure-activity relationship and SwissADME predictions , 2021, Medicinal Chemistry Research.
[7] Visweswara Rao Pasupuleti,et al. Synthesis, antioxidant activity and bioinformatics studies of L-3-hydroxytyrosine templated N-alkyl/aryl substituted urea/thioureas. , 2021, Bioorganic chemistry.
[8] M. Choudhary,et al. Synthesis, crystal structure and Hirshfeld Surface analysis of benzamide derivatives of thiourea as potent inhibitors of α-glucosidase in-vitro. , 2020, Bioorganic chemistry.
[9] Shovan Mondal,et al. Synthesis of sulfonamide and their synthetic and therapeutic applications: Recent advances , 2020 .
[10] S. Karakuş,et al. Synthesis, anticancer evaluation and in silico ADMET studies on urea/thiourea derivatives from gabapentin , 2020 .
[11] M. Tilby,et al. Primary Sulfonamide Synthesis Using the Sulfinylamine Reagent N-Sulfinyl-O-(tert-butyl)hydroxylamine, t-BuONSO , 2020, Organic letters.
[12] F. Tok,et al. Design, Synthesis and Biological Screening of Novel 1,5-Diphenyl-3-(4-(trifluoromethyl)phenyl)-2-pyrazoline Derivatives. , 2020, Acta Chimica Slovenica.
[13] Wei Wei,et al. Synthesis and evaluation of new thiourea derivatives as antitumor and antiangiogenic agents , 2020 .
[14] A. Dwivedi,et al. Synthesis, antidiabetic, antioxidant and anti-inflammatory activities of novel hydroxytriazenes based on sulpha drugs , 2020, Heliyon.
[15] M. Głuch-Lutwin,et al. Synthesis, Anticonvulsant and Antinociceptive Activity of New Hybrid Compounds: Derivatives of 3-(3-Methylthiophen-2-yl)-pyrrolidine-2,5-dione , 2020, International journal of molecular sciences.
[16] G. Elgemeie,et al. Sulfa drug analogs: new classes of N-sulfonyl aminated azines and their biological and preclinical importance in medicinal chemistry (2000–2018) , 2019, Medicinal Chemistry Research.
[17] Muhammad Imran Malik,et al. Synthesis, antimicrobial, antioxidant, cytotoxic, antiurease and molecular docking studies of N-(3-trifluoromethyl)benzoyl-N'-aryl thiourea derivatives. , 2019, Bioorganic chemistry.
[18] W. Frey,et al. Thioureas and their cyclized derivatives: Synthesis, conformational analysis and antimicrobial evaluation , 2019, Journal of Molecular Structure.
[19] T. Xuan,et al. Antioxidant, α-Amylase and α-Glucosidase Inhibitory Activities and Potential Constituents of Canarium tramdenum Bark , 2019, Molecules.
[20] S. Karakuş,et al. Synthesis, anticancer activity and ADMET studies of N-(5-methyl-1,3,4-thiadiazol-2-yl)-4-[(3-substituted)ureido/thioureido] benzenesulfonamide derivatives , 2018 .
[21] Omprakash Tanwar,et al. Synthesis and biological evaluation of some new pyrazoline substituted benzenesulfonylurea/thiourea derivatives as anti-hyperglycaemic agents and aldose reductase inhibitors. , 2014, European journal of medicinal chemistry.
[22] R. Apak,et al. Novel total antioxidant capacity index for dietary polyphenols and vitamins C and E, using their cupric ion reducing capability in the presence of neocuproine: CUPRAC method. , 2004, Journal of agricultural and food chemistry.
[23] Jong-Sang Kim,et al. Inhibition of Alpha-glucosidase and Amylase by Luteolin, a Flavonoid , 2000, Bioscience, biotechnology, and biochemistry.
[24] K. Courtney,et al. A new and rapid colorimetric determination of acetylcholinesterase activity. , 1961, Biochemical pharmacology.
[25] M. S. Blois,et al. Antioxidant Determinations by the Use of a Stable Free Radical , 1958, Nature.