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For: Novais JS, Moreira CS, Silva ACJA, Loureiro RS, Sá Figueiredo AM, Ferreira VF, Castro HC, da Rocha DR. Antibacterial naphthoquinone derivatives targeting resistant strain Gram-negative bacteria in biofilms. Microb Pathog 2018;118:105-14. [PMID: 29550501 DOI: 10.1016/j.micpath.2018.03.024] [Cited by in Crossref: 19] [Cited by in F6Publishing: 15] [Article Influence: 4.8] [Reference Citation Analysis]
Number Citing Articles
1 Yıldız M. Design, synthesis, characterization, and antimicrobial activity of novel piperazine substituted 1,4-benzoquinones. Journal of Molecular Structure 2020;1203:127422. [DOI: 10.1016/j.molstruc.2019.127422] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
2 Mataracı-kara E, Bayrak N, Yıldırım H, Yıldız M, Ataman M, Ozbek-celik B, Tuyun AF. Plastoquinone analogs: a potential antimicrobial lead structure intensely suppressing Staphylococcus epidermidis and Candida albicans growth. Med Chem Res 2021;30:1728-37. [DOI: 10.1007/s00044-021-02772-z] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Di Marco NI, Páez PL, Lucero-estrada CSM, Pungitore CR. Naphthoquinones inhibit formation and viability of Yersinia enterocolitica biofilm. World J Microbiol Biotechnol 2021;37. [DOI: 10.1007/s11274-020-02971-7] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
4 Yıldız M, Bayrak N, Yıldırım H, Mataracı-Kara E, Shilkar D, Jayaprakash V, Fatih Tuyun A. Exploration of brominated Plastoquinone analogs: Discovery and structure-activity relationships of small antimicrobial lead molecules. Bioorg Chem 2021;116:105316. [PMID: 34509796 DOI: 10.1016/j.bioorg.2021.105316] [Reference Citation Analysis]
5 Ogawa T, Nakamoto M, Tanaka Y, Sato K, Okazawa A, Kanaya S, Ohta D. Exploration and characterization of chemical stimulators to maximize the wax ester production by Euglena gracilis. J Biosci Bioeng 2021:S1389-1723(21)00332-7. [PMID: 34952786 DOI: 10.1016/j.jbiosc.2021.12.005] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Figueredo FG, Ramos ITL, Paz JA, Silva TMS, Camara CA, Oliveira-Tintino CDM, Relison Tintino S, de Farias PAM, Coutinho HDM, Fonteles MMF. In silico evaluation of the antibacterial and modulatory activity of lapachol and nor-lapachol derivates. Microb Pathog 2020;144:104181. [PMID: 32277994 DOI: 10.1016/j.micpath.2020.104181] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
7 Novais JS, Rosandiski AC, de Carvalho CM, de Saules Silva LS, Dos S Velasco de Souza LC, Santana MV, Martins NRC, Castro HC, Ferreira VF, Gonzaga DTG, de Resende GO, de C da Silva F. Efficient Synthesis and Antibacterial Profile of Bis(2-hydroxynaphthalene- 1,4-dione). Curr Top Med Chem 2020;20:121-31. [PMID: 31820692 DOI: 10.2174/1568026619666191210160342] [Cited by in Crossref: 4] [Article Influence: 1.3] [Reference Citation Analysis]
8 Wellington KW, Kolesnikova NI, Nyoka NBP, McGaw LJ. Investigation of the antimicrobial and anticancer activity of aminonaphthoquinones. Drug Dev Res 2019;80:138-46. [PMID: 30284739 DOI: 10.1002/ddr.21477] [Cited by in Crossref: 11] [Cited by in F6Publishing: 6] [Article Influence: 2.8] [Reference Citation Analysis]
9 Lara LS, Lechuga GC, Moreira CDS, Santos TB, Ferreira VF, da Rocha DR, Pereira MCS. Optimization of 1,4-Naphthoquinone Hit Compound: A Computational, Phenotypic, and In Vivo Screening against Trypanosoma cruzi. Molecules 2021;26:E423. [PMID: 33467422 DOI: 10.3390/molecules26020423] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Li J, Feng S, Liu X, Jia X, Qiao F, Guo J, Deng S. Effects of Traditional Chinese Medicine and its Active Ingredients on Drug-Resistant Bacteria. Front Pharmacol 2022;13:837907. [PMID: 35721131 DOI: 10.3389/fphar.2022.837907] [Reference Citation Analysis]
11 Chaves-carballo K, Lamoureux GV, Perez AL, Bella Cruz A, Cechinel Filho V. Novel one-pot synthesis of a library of 2-aryloxy-1,4-naphthoquinone derivatives. Determination of antifungal and antibacterial activity. RSC Adv 2022;12:18507-23. [DOI: 10.1039/d2ra01814d] [Reference Citation Analysis]
12 Sabutski YE, Menchinskaya ES, Shevchenko LS, Chingizova EA, Chingizov AR, Popov RS, Denisenko VA, Mikhailov VV, Aminin DL, Polonik SG. Synthesis and Evaluation of Antimicrobial and Cytotoxic Activity of Oxathiine-Fused Quinone-Thioglucoside Conjugates of Substituted 1,4-Naphthoquinones. Molecules 2020;25:E3577. [PMID: 32781642 DOI: 10.3390/molecules25163577] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
13 Mataracı-Kara E, Bayrak N, Yıldız M, Yıldırım H, TuYuN AF. Active Quinolinequinones against Methicillin-Resistant Staphylococcus spp. Chem Biodivers 2021;:e202100616. [PMID: 34812587 DOI: 10.1002/cbdv.202100616] [Reference Citation Analysis]
14 Kara EM, Bayrak N, Yıldırım H, Yıldız M, Celik BO, Tuyun AF. Chlorinated plastoquinone analogs that inhibit Staphylococcus epidermidis and Candida albicans growth. Folia Microbiol (Praha) 2020;65:785-95. [PMID: 32458315 DOI: 10.1007/s12223-020-00783-8] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
15 Dudek-Wicher R, Paleczny J, Kowalska-Krochmal B, Szymczyk-Ziółkowska P, Pachura N, Szumny A, Brożyna M. Activity of Liquid and Volatile Fractions of Essential Oils against Biofilm Formed by Selected Reference Strains on Polystyrene and Hydroxyapatite Surfaces. Pathogens 2021;10:515. [PMID: 33922823 DOI: 10.3390/pathogens10050515] [Reference Citation Analysis]
16 Song H, Zhang J, Qu J, Liu J, Yin P, Zhang G, Shang D. Lactobacillus rhamnosus GG microcapsules inhibit Escherichia coli biofilm formation in coculture. Biotechnol Lett 2019;41:1007-14. [DOI: 10.1007/s10529-019-02694-2] [Cited by in Crossref: 16] [Cited by in F6Publishing: 13] [Article Influence: 5.3] [Reference Citation Analysis]
17 Patel OPS, Beteck RM, Legoabe LJ. Antimalarial application of quinones: A recent update. Eur J Med Chem 2021;210:113084. [PMID: 33333397 DOI: 10.1016/j.ejmech.2020.113084] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
18 B A, Fernandez A, Laila SP, Nair AS, Vishnu VS. Synthesis, characterization, molecular docking and anticancer studies of fluoroaniline derivatives of hydroxybenzoquinone and hydroxynaphthoquinone. J Biomol Struct Dyn 2020;:1-11. [PMID: 33314966 DOI: 10.1080/07391102.2020.1852116] [Reference Citation Analysis]
19 De Grandis RA, Santos PWDSD, Oliveira KMD, Machado ART, Aissa AF, Batista AA, Antunes LMG, Pavan FR. Novel lawsone-containing ruthenium(II) complexes: Synthesis, characterization and anticancer activity on 2D and 3D spheroid models of prostate cancer cells. Bioorganic Chemistry 2019;85:455-68. [DOI: 10.1016/j.bioorg.2019.02.010] [Cited by in Crossref: 16] [Cited by in F6Publishing: 14] [Article Influence: 5.3] [Reference Citation Analysis]
20 da Silva RE, Ribeiro FOS, de Carvalho AMA, Daboit TC, Marinho-Filho JDB, Matos TS, Pessoa ODL, de Souza de Almeida Leite JR, de Araújo AR, Dos Santos Soares MJ. Antimicrobial and antibiofilm activity of the benzoquinone oncocalyxone A. Microb Pathog 2020;149:104513. [PMID: 32950640 DOI: 10.1016/j.micpath.2020.104513] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
21 Mataracı-Kara E, Bayrak N, Yıldız M, Yıldırım H, Özbek-Çelik B, Tuyun AF. Discovery and structure-activity relationships of the quinolinequinones: Promising antimicrobial agents and mode of action evaluation. Drug Dev Res 2021. [PMID: 34668593 DOI: 10.1002/ddr.21893] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
22 Ravichandiran P, Masłyk M, Sheet S, Janeczko M, Premnath D, Kim AR, Park BH, Han MK, Yoo DJ. Synthesis and Antimicrobial Evaluation of 1,4-Naphthoquinone Derivatives as Potential Antibacterial Agents. ChemistryOpen 2019;8:589-600. [PMID: 31098338 DOI: 10.1002/open.201900077] [Cited by in Crossref: 24] [Cited by in F6Publishing: 17] [Article Influence: 8.0] [Reference Citation Analysis]