European Journal of Chemistry 2014, 5(4), 628-634 | doi: https://doi.org/10.5155/eurjchem.5.4.628-634.1120 | Get rights and content

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Synthesis and biological evaluation of new quinazolinone derivatives


Firyal Weli Asker (1) , Salma Abdul Rudha Abbas (2,*) , Redha Ibrahim Al-Bayati (3) , Hanaa Abd Al-Tamemi (4)

(1) Department of Chemistry, College of Science, Al-Mustansiriya University, 10052, Baghdad, Iraq
(2) Department of Chemistry, College of Science, Al-Mustansiriya University, 10052, Baghdad, Iraq
(3) Department of Chemistry, College of Science, Al-Mustansiriya University, 10052, Baghdad, Iraq
(4) Department of Chemistry, College of Science, Al-Mustansiriya University, 10052, Baghdad, Iraq
(*) Corresponding Author

Received: 12 Jul 2014 | Revised: 01 Aug 2014 | Accepted: 15 Aug 2014 | Published: 31 Dec 2014 | Issue Date: December 2014

Abstract


New N-substituted-2-methyl quinazolin-4(3H)-ones derivatives comprising 1,3,4-thiadiazole, Schiff bases and 2-azetidinone moieties are reported. The structures of the newly prepared compounds were confirmed by FT-IR and 1H NMR spectra. The compounds were also evaluated for their antimicrobial, antioxidant and study of inhibition on some enzymes activities. The results suggest that the compounds possess broad spectrum of in-vitro antimicrobial activity. Antioxidant results obtained into the present study indicate that compound 5 show moderate better scavenging activity. Compound 5 demonstrated inhibitory effects on GOT, GPT, GGT and ALP activities, and these effects increase with increasing the concentration of the compound.


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Editor-in-Chief
European Journal of Chemistry

Keywords


Schiff bases; Azetidinone; Quinazolinone; Enzymes activities; Antioxidant activity; Antimicrobial activity

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DOI: 10.5155/eurjchem.5.4.628-634.1120

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Funding information


Department of Chemistry, College of Science, Al-Mustansiriyah University, Baghdad, Iraq

Citations

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[1]. Leqaa A Mohammed, Olfat A Nief, Firyal W Askar, Abdulwahhab H Majeed
Synthesis, Characterization and Antimicrobial Activities of Silver Nanoparticles coated [1,3] Thiazin-4-One derivatives
Journal of Physics: Conference Series  1294(5), 052028, 2019
DOI: 10.1088/1742-6596/1294/5/052028
/


[2]. Nawal Daamy Resen, Asia Hameed Abed, Albayati Zeyad sefauldeen, Askar Firyal Weli, Thoraia M. Alkhaisy
Metal Complexes of acetohydrazide Derivative: Characterization, and Antimicrobial Activity Study
Journal of Physics: Conference Series  1664(1), 012087, 2020
DOI: 10.1088/1742-6596/1664/1/012087
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[3]. Xinyang Lv, Lan Yang, Zhijiang Fan, Xiaoping Bao
Synthesis and antimicrobial activities of novel quinazolin-4(3 H )-one derivatives containing a 1,2,4-triazolo[3,4- b ][1,3,4]thiadiazole moiety
Journal of Saudi Chemical Society  22(1), 101, 2018
DOI: 10.1016/j.jscs.2017.07.008
/


[4]. Bo-Ren Yan, Xin-Yang Lv, Huan Du, Man-Ni Gao, Jian Huang, Xiao-Ping Bao
Synthesis and biological activities of novel quinazolinone derivatives containing a 1,2,4-triazolylthioether moiety
Chemical Papers  70(7), , 2016
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[5]. Jing Li, Martin Berger, Wojciech Zawodny, Marwan Simaan, Nuno Maulide
A Chemoselective α-Oxytriflation Enables the Direct Asymmetric Arylation of Amides
Chem  5(7), 1883, 2019
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How to cite


Asker, F.; Abbas, S.; Al-Bayati, R.; Al-Tamemi, H. Eur. J. Chem. 2014, 5(4), 628-634. doi:10.5155/eurjchem.5.4.628-634.1120
Asker, F.; Abbas, S.; Al-Bayati, R.; Al-Tamemi, H. Synthesis and biological evaluation of new quinazolinone derivatives. Eur. J. Chem. 2014, 5(4), 628-634. doi:10.5155/eurjchem.5.4.628-634.1120
Asker, F., Abbas, S., Al-Bayati, R., & Al-Tamemi, H. (2014). Synthesis and biological evaluation of new quinazolinone derivatives. European Journal of Chemistry, 5(4), 628-634. doi:10.5155/eurjchem.5.4.628-634.1120
Asker, Firyal, Salma Abdul Rudha Abbas, Redha Ibrahim Al-Bayati, & Hanaa Abd Al-Tamemi. "Synthesis and biological evaluation of new quinazolinone derivatives." European Journal of Chemistry [Online], 5.4 (2014): 628-634. Web. 28 Sep. 2023
Asker, Firyal, Abbas, Salma, Al-Bayati, Redha, AND Al-Tamemi, Hanaa. "Synthesis and biological evaluation of new quinazolinone derivatives" European Journal of Chemistry [Online], Volume 5 Number 4 (31 December 2014)

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DOI Link: https://doi.org/10.5155/eurjchem.5.4.628-634.1120


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