Synthesis of novel Schiff bases and azol-β-lactam derivatives starting from morpholine and thiomorpholine and investigation of their antitubercular, antiurease activity, acethylcolinesterase inhibition effect and antioxidant capacity

被引:37
作者
Cebeci, Yildiz Uygun [1 ]
Bayrak, Hacer [2 ]
Sirin, Yakup [1 ]
机构
[1] Karadeniz Tech Univ, Dept Chem, TR-61080 Trabzon, Turkey
[2] Karadeniz Tech Univ, Dept Chem & Chem Proc Technol, TR-61080 Trabzon, Turkey
关键词
Schiff base; beta-Lactam; Morpholine; Thiomorpholine; Azole; Antitubercular activity; Antiurease activity; Acethylcolinesterase; Antioxidant; BIOLOGICAL EVALUATION; ANTIBACTERIAL; PRODUCTS; DRUG;
D O I
10.1016/j.bioorg.2019.102928
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 this study, new Schiff bases and beta-lactam derivatives containing morpholine and thio morpholine nuclei were synthesized. Antimicrobial, antioxidant, antimicrobial and antioxidant properties of all synthesized compounds were investigated and highly effective products were obtained. In this context, new effective structures were introduced to the literature.
引用
收藏
页数:9
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共 31 条
[1]   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 [J].
Apak, R ;
Güçlu, K ;
Özyürek, M ;
Karademir, SE .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2004, 52 (26) :7970-7981
[2]  
Benzie IFF, 1999, METHOD ENZYMOL, V299, P15
[3]   ANTIOXIDANT DETERMINATIONS BY THE USE OF A STABLE FREE RADICAL [J].
BLOIS, MS .
NATURE, 1958, 181 (4617) :1199-1200
[4]   Design, synthesis, and biological evaluation of 4-alkyliden-beta lactams: New products with promising antibiotic activity against resistant bacteria [J].
Broccolo, F ;
Cainelli, G ;
Caltabiano, G ;
Cocuzza, CEA ;
Fortuna, CG ;
Galletti, P ;
Giacomini, D ;
Musumarra, G ;
Musumeci, R ;
Quintavalla, A .
JOURNAL OF MEDICINAL CHEMISTRY, 2006, 49 (09) :2804-2811
[5]   New β-lactam antibiotics and β-lactamase inhibitors [J].
Bush, Karen ;
Macielag, Mark J. .
EXPERT OPINION ON THERAPEUTIC PATENTS, 2010, 20 (10) :1277-1293
[6]   The antiviral drug ribavirin is a selective inhibitor of S-adenosyl-L-homocysteine hydrolase from Trypanosoma cruzi [J].
Cai, Sumin ;
Li, Qing-Shan ;
Borchardt, Ronald T. ;
Kuczera, Krzysztof ;
Schowen, Richard L. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2007, 15 (23) :7281-7287
[7]   Synthesis and in vitro antimicrobial studies of medicinally important novel N-alkyl and N-sulfonyl derivatives of 1-[bis(4-fluorophenyl)-methyl]piperazine [J].
Chandra, J. N. Narendra Sharath ;
Sadashiva, C. T. ;
Kavitha, C. V. ;
Rangappa, K. S. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2006, 14 (19) :6621-6627
[8]   Synthesis of 1-[3-(4-benzotriazol-1/2-yl-3-fluoro-phenyl)-2-oxo-oxazolidin-5-ylmethyl]-3-substituted-thiourea derivatives as antituberculosis agents [J].
Dixit, PP ;
Patil, VJ ;
Nair, PS ;
Jain, S ;
Sinha, N ;
Arora, SK .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2006, 41 (03) :423-428
[9]   A NEW AND RAPID COLORIMETRIC DETERMINATION OF ACETYLCHOLINESTERASE ACTIVITY [J].
ELLMAN, GL ;
COURTNEY, KD ;
ANDRES, V ;
FEATHERSTONE, RM .
BIOCHEMICAL PHARMACOLOGY, 1961, 7 (02) :88-&
[10]   Separation of 1,4-benzodiazepines by micellar elektrokinetic capillary chromatography [J].
Hancu, Gabriel ;
Gaspar, Attila ;
Gyeresi, Arpad .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 2007, 69 (03) :251-259