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For: Litim B, Djahoudi A, Meliani S, Boukhari A. Synthesis and potential antimicrobial activity of novel α-aminophosphonates derivatives bearing substituted quinoline or quinolone and thiazole moieties. Med Chem Res 2021;:1-15. [PMID: 34744408 DOI: 10.1007/s00044-021-02815-5] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Gao J, Hou H, Gao F. Current scenario of quinolone hybrids with potential antibacterial activity against ESKAPE pathogens. Eur J Med Chem 2023;247:115026. [PMID: 36577217 DOI: 10.1016/j.ejmech.2022.115026] [Reference Citation Analysis]
2 Vashistha A, Kumar S, Kirar S, Sharma N, Das B, Banerjee UC, Pawar SV, Kumar R, Yadav AK. Synthesis, biological evaluation and in silico studies of 2-aminoquinolines and 1-aminoisoquinolines as antimicrobial agents. Comput Biol Chem 2023;102:107807. [PMID: 36587565 DOI: 10.1016/j.compbiolchem.2022.107807] [Reference Citation Analysis]
3 Barqi MM, Abdellah IM, Eletmany MR, Ali NM, Elhenawy AA, Abd El Latif FM. Synthesis, Characterization, Bioactivity Screening and Computational Studies of Diphenyl−malonohydrazides and Pyridines Derivatives. ChemistrySelect 2023;8. [DOI: 10.1002/slct.202203913] [Reference Citation Analysis]
4 Al-warhi T, Abualnaja M, Abu Ali OA, Alyamani NM, Elsaid FG, Shati AA, Albogami S, Fayad E, Abu Almaaty AH, Mohamed KO, Alamoudi WM, Zaki I. Design, Synthesis and Cytotoxicity Screening of New Thiazole Derivatives as Potential Anticancer Agents through VEGFR-2 Inhibition. Symmetry 2022;14:1814. [DOI: 10.3390/sym14091814] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
5 Tople MS, Patel NB, Patel PP, Purohit AC, Ahmad I, Patel H. An in silico-in vitro antimalarial and antimicrobial investigation of newer 7- Chloroquinoline based Schiff-bases. Journal of Molecular Structure 2022. [DOI: 10.1016/j.molstruc.2022.134016] [Reference Citation Analysis]
6 Gandhi B, Greeshma K, Ruvulapalli DP, Kaki SS. Design, synthesis, and antimicrobial evaluation of novel 10-Undecenoic acid-based lipidic triazoles. Med Chem Res. [DOI: 10.1007/s00044-022-02940-9] [Reference Citation Analysis]
7 Silva J, Esmeraldo Rocha J, da Cunha Xavier J, Sampaio de Freitas T, Douglas Melo Coutinho H, Nogueira Bandeira P, Rodrigues de Oliveira M, Nunes da Rocha M, Machado Marinho E, de Kassio Vieira Monteiro N, Ribeiro LR, Róseo Paula Pessoa Bezerra de Menezes R, Machado Marinho M, Magno Rodrigues Teixeira A, Silva dos Santos H, Silva Marinho E. Antibacterial and antibiotic modifying activity of chalcone (2E)-1-(4′-aminophenyl)-3-(4-methoxyphenyl)-prop-2-en-1-one in strains of Staphylococcus aureus carrying NorA and MepA efflux pumps: In vitro and in silico approaches. Microbial Pathogenesis 2022. [DOI: 10.1016/j.micpath.2022.105664] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Fall SAK, Hajib S, Aouine Y, Ouarsal R, Alami A, El Omari M, Assani A, Saadi M, El Ammari L. X-ray Structure Determination of Naphthalen-2-yl 1-(Benzamido(diethoxyphosphoryl)methyl)-1H-1,2,3-triazole-4-carboxylate. Molbank 2022;2022:M1360. [DOI: 10.3390/m1360] [Reference Citation Analysis]
9 Guo H, Liu Y, Wen C, Wan J. Electrochemical enaminone C–H thiolation/C–N amination cascade for thiazole synthesis and its diastereoselective dearomatization. Green Chem . [DOI: 10.1039/d2gc01644c] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]