AboulMagd, A., Eid, N., Khorany, A., Elgendy, O., abdelrahman, H. (2020). Synthesis, Antimicrobial and Molecular Modeling Studies of Some Benzophenone-based Thiazole and 4-Thiazolidinone Derivatives. test, 63(11), 4355-4367. doi: 10.21608/ejchem.2020.25721.2503
Asmaa AboulMagd; Nahed Eid; Ahmed Khorany; Osama Elgendy; hamdy abdelrahman. "Synthesis, Antimicrobial and Molecular Modeling Studies of Some Benzophenone-based Thiazole and 4-Thiazolidinone Derivatives". test, 63, 11, 2020, 4355-4367. doi: 10.21608/ejchem.2020.25721.2503
AboulMagd, A., Eid, N., Khorany, A., Elgendy, O., abdelrahman, H. (2020). 'Synthesis, Antimicrobial and Molecular Modeling Studies of Some Benzophenone-based Thiazole and 4-Thiazolidinone Derivatives', test, 63(11), pp. 4355-4367. doi: 10.21608/ejchem.2020.25721.2503
AboulMagd, A., Eid, N., Khorany, A., Elgendy, O., abdelrahman, H. Synthesis, Antimicrobial and Molecular Modeling Studies of Some Benzophenone-based Thiazole and 4-Thiazolidinone Derivatives. test, 2020; 63(11): 4355-4367. doi: 10.21608/ejchem.2020.25721.2503

Synthesis, Antimicrobial and Molecular Modeling Studies of Some Benzophenone-based Thiazole and 4-Thiazolidinone Derivatives

Egyptian Journal of Chemistry
Article 17, Volume 63, Issue 11, November 2020, Pages 4355-4367    PDF (1.46 M)
Document Type: Original Article
DOI: 10.21608/ejchem.2020.25721.2503
Authors
Asmaa AboulMagd* 1; Nahed Eid2; Ahmed Khorany3; Osama Elgendy4; hamdy abdelrahman5
1Department of pharmaceutical chemistry, faculty of pharmacy, Nahda University
2Pharmaceutical Chemistry, Faculty of Pharmacy, Cairo University
3Microbiology and Immunology Department, Faculty of Pharmacy, Nahda University
4Microbiology and Immunology department, Faculty of Pharmacy, Beni Suef University
5Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Nahda University, Beni-suef, Egypt
Abstract
New series of thiazolyl hydrazones were designed and synthesized via the reaction of benzophenone thiosemicarbazone 2 with chloroacetic acid, (un)substituted phenacylbromide and ethyl-2-chloroacetoacetate to yield compounds 3, 5a-d & 6 respectively. Furthermore, reaction of the thiazolidin-4-one 3 with aromatic aldehydes afforded compounds 4a-g. Characterization data, along with in vitro antimicrobial activity for all compounds are herein reported. All the synthesized compounds were screened against Methicillin- Resistant Staphylococcus aureus (MRSA), E. coli, K. pneumonia, P. aeruginosa, A baumannii, C. albicans and C. neoformans var.grubii. Compounds 2 and 4e showed the highest bacterial growth inhibition with 28.6% and 28.7% against MRSA, respectively. Moreover, the trisubstituted thiazole derivative 6 was the most active compound against Gram-negative bacteria A. baumannii with 59% growth inhibition. Furthermore, compounds 4e & 6 showed 22.5% and 17.3% decrease in peptidoglycan density, respectively. Molecular docking into bacterial MurB enzyme active site was used to determine their binding modein which they showed good interactions with Gln229, Arg225 and Ser82 amino acid residues.
Keywords
Thiazoles; 4- thiazolidinone; antimicrobial activity; molecular modelling
Statistics
Article View: 676
PDF Download: 571