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For: Fayed EA, Ammar YA, Saleh MA, Bayoumi AH, Belal A, Mehany AB, Ragab A. Design, synthesis, antiproliferative evaluation, and molecular docking study of new quinoxaline derivatives as apoptotic inducers and EGFR inhibitors. Journal of Molecular Structure 2021;1236:130317. [DOI: 10.1016/j.molstruc.2021.130317] [Cited by in Crossref: 22] [Cited by in F6Publishing: 26] [Article Influence: 22.0] [Reference Citation Analysis]
Number Citing Articles
1 Abdelgalil MM, Ammar YA, Elhag Ali GA, Ali AK, Ragab A. A novel of quinoxaline derivatives tagged with pyrrolidinyl scaffold as a new class of antimicrobial agents: Design, synthesis, antimicrobial activity, and molecular docking simulation. Journal of Molecular Structure 2023;1274:134443. [DOI: 10.1016/j.molstruc.2022.134443] [Reference Citation Analysis]
2 Saleh MA, Elmaaty AA, El Saeed HS, Saleh MM, Salah M, Ezz Eldin RR. Structure based design and synthesis of 3-(7-nitro-3-oxo-3,4-dihydroquinoxalin-2-yl)propanehydrazide derivatives as novel bacterial DNA-gyrase inhibitors: In-vitro, In-vivo, In-silico and SAR studies. Bioorganic Chemistry 2022;129:106186. [DOI: 10.1016/j.bioorg.2022.106186] [Reference Citation Analysis]
3 Fayed EA, Ebrahim MA, Fathy U, Saeed HSE, Khalaf WS. Evaluation of quinoxaline derivatives as potential ergosterol biosynthesis inhibitors: design, synthesis, ADMET, molecular docking studies, and antifungal activities. Journal of Molecular Structure 2022;1267:133578. [DOI: 10.1016/j.molstruc.2022.133578] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Ammar YA, Micky JA, Aboul‐magd DS, Abd El‐hafez SMA, Hessein SA, Ali AM, Ragab A. Development and radiosterilization of new hydrazono‐quinoline hybrids as DNA gyrase and topoisomerase IV inhibitors: Antimicrobial and hemolytic activities against uropathogenic isolates with molecular docking study. Chem Biol Drug Des 2022. [DOI: 10.1111/cbdd.14154] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
5 Fayed EA, Mohsen M, El-gilil SMA, Aboul-magd DS, Ragab A. Novel cyclohepta[b]thiophene derivative incorporating pyrimidine, pyridine, and chromene moiety as potential antimicrobial agents targeting DNA gyrase. Journal of Molecular Structure 2022;1262:133028. [DOI: 10.1016/j.molstruc.2022.133028] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
6 Fayed EA, Al-arab EME, Saleh AS, Bayoumi AH, Ammar YA. Design, synthesis, in silico studies, in vivo and in vitro assessment of pyridones and thiazolidinones as anti-inflammatory, antipyretic and ulcerogenic hits. Journal of Molecular Structure 2022;1260:132839. [DOI: 10.1016/j.molstruc.2022.132839] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
7 Ragab A, Abusaif MS, Aboul-Magd DS, Wassel MMS, Elhagali GAM, Ammar YA. A new exploration toward adamantane derivatives as potential anti-MDR agents: Design, synthesis, antimicrobial, and radiosterilization activity as potential topoisomerase IV and DNA gyrase inhibitors. Drug Dev Res 2022. [PMID: 35716118 DOI: 10.1002/ddr.21960] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
8 Kamble O, Chatterjee R, Dandela R, Shinde S. Ultrasonic energy for construction of bioactive heterocycles. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.132893] [Reference Citation Analysis]
9 Saadon KE, Taha NMH, Mahmoud NA, Elhagali GAM, Ragab A. Synthesis, characterization, and in vitro antibacterial activity of some new pyridinone and pyrazole derivatives with some in silico ADME and molecular modeling study. J IRAN CHEM SOC. [DOI: 10.1007/s13738-022-02575-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
10 Ragab A, Ammar YA, Ezzat A, Mahmoud AM, Mohamed MBI, El-Tabl AS, Farag RS. Synthesis, characterization, thermal properties, antimicrobial evaluation, ADMET study, and molecular docking simulation of new mono Cu (II) and Zn (II) complexes with 2-oxoindole derivatives. Comput Biol Med 2022;145:105473. [PMID: 35395516 DOI: 10.1016/j.compbiomed.2022.105473] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
11 Eldeeb M, Sanad EF, Ragab A, Ammar YA, Mahmoud K, Ali MM, Hamdy NM. Anticancer Effects with Molecular Docking Confirmation of Newly Synthesized Isatin Sulfonamide Molecular Hybrid Derivatives against Hepatic Cancer Cell Lines. Biomedicines 2022;10:722. [DOI: 10.3390/biomedicines10030722] [Cited by in Crossref: 6] [Cited by in F6Publishing: 8] [Article Influence: 6.0] [Reference Citation Analysis]
12 Desouky SE, Abu-elghait M, Fayed EA, Selim S, Yousuf B, Igarashi Y, Abdel-wahab BA, Mohammed Alsuhaibani A, Sonomoto K, Nakayama J. Secondary Metabolites of Actinomycetales as Potent Quorum Sensing Inhibitors Targeting Gram-Positive Pathogens: In Vitro and In Silico Study. Metabolites 2022;12:246. [DOI: 10.3390/metabo12030246] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
13 Fayed EA, Gohar NA, Farrag AM, Ammar YA. Upregulation of BAX and caspase-3, as well as downregulation of Bcl-2 during treatment with indeno[1,2-b]quinoxalin derivatives, mediated apoptosis in human cancer cells. Arch Pharm (Weinheim) 2022;:e2100454. [PMID: 35174895 DOI: 10.1002/ardp.202100454] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Ali Mohamed H, Ammar YA, A M Elhagali G, A Eyada H, S Aboul-Magd D, Ragab A. In Vitro Antimicrobial Evaluation, Single-Point Resistance Study, and Radiosterilization of Novel Pyrazole Incorporating Thiazol-4-one/Thiophene Derivatives as Dual DNA Gyrase and DHFR Inhibitors against MDR Pathogens. ACS Omega 2022;7:4970-90. [PMID: 35187315 DOI: 10.1021/acsomega.1c05801] [Cited by in Crossref: 8] [Cited by in F6Publishing: 11] [Article Influence: 8.0] [Reference Citation Analysis]
15 Jiang X, Wu K, Bai R, Zhang P, Zhang Y. Functionalized quinoxalinones as privileged structures with broad-ranging pharmacological activities. Eur J Med Chem 2022;229:114085. [PMID: 34998058 DOI: 10.1016/j.ejmech.2021.114085] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 10.0] [Reference Citation Analysis]
16 Anahmadi H, Fathi M, El hajri F, Benzekri Z, Sibous S, Idrissi BCE, El youbi MS, Souizi A, Boukhris S. Synthesis, characterization and application of α-Ca3 (PO4)2 as a heterogeneous catalyst for the synthesis of 2.3-diphenylquinoxaline derivatives and knoevenagel condensation under green conditions. Journal of Molecular Structure 2022;1248:131449. [DOI: 10.1016/j.molstruc.2021.131449] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
17 Ragab A, Elsisi DM, Abu Ali OA, Abusaif MS, Askar AA, Farag AA, Ammar YA. Design, synthesis of new novel quinoxalin-2(1H)-one derivatives incorporating hydrazone, hydrazine, and pyrazole moieties as antimicrobial potential with in-silico ADME and molecular docking simulation. Arabian Journal of Chemistry 2022;15:103497. [DOI: 10.1016/j.arabjc.2021.103497] [Cited by in Crossref: 14] [Cited by in F6Publishing: 16] [Article Influence: 14.0] [Reference Citation Analysis]
18 Alzahrani AY, Ammar YA, Abu-Elghait M, Salem MA, Assiri MA, Ali TE, Ragab A. Development of novel indolin-2-one derivative incorporating thiazole moiety as DHFR and quorum sensing inhibitors: Synthesis, antimicrobial, and antibiofilm activities with molecular modelling study. Bioorg Chem 2021;119:105571. [PMID: 34959177 DOI: 10.1016/j.bioorg.2021.105571] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 12.0] [Reference Citation Analysis]
19 Rizk HF, El-borai MA, Ragab A, Ibrahim SA, Sadek ME. A Novel of Azo-Thiazole Moiety Alternative for Benzidine-Based Pigments: Design, Synthesis, Characterization, Biological Evaluation, and Molecular Docking Study. Polycyclic Aromatic Compounds. [DOI: 10.1080/10406638.2021.2015402] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
20 Alzahrani AY, Ammar YA, Salem MA, Abu-Elghait M, Ragab A. Design, synthesis, molecular modeling, and antimicrobial potential of novel 3-[(1H-pyrazol-3-yl)imino]indolin-2-one derivatives as DNA gyrase inhibitors. Arch Pharm (Weinheim) 2021;:e2100266. [PMID: 34747519 DOI: 10.1002/ardp.202100266] [Cited by in Crossref: 11] [Cited by in F6Publishing: 15] [Article Influence: 11.0] [Reference Citation Analysis]
21 Ibrahim SA, Fayed EA, Rizk HF, Desouky SE, Ragab A. Hydrazonoyl bromide precursors as DHFR inhibitors for the synthesis of bis-thiazolyl pyrazole derivatives; antimicrobial activities, antibiofilm, and drug combination studies against MRSA. Bioorg Chem 2021;116:105339. [PMID: 34530234 DOI: 10.1016/j.bioorg.2021.105339] [Cited by in Crossref: 21] [Cited by in F6Publishing: 25] [Article Influence: 21.0] [Reference Citation Analysis]
22 Fayed EA, Ragab A, Ezz Eldin RR, Bayoumi AH, Ammar YA. In vivo screening and toxicity studies of indolinone incorporated thiosemicarbazone, thiazole and piperidinosulfonyl moieties as anticonvulsant agents. Bioorg Chem 2021;116:105300. [PMID: 34525393 DOI: 10.1016/j.bioorg.2021.105300] [Cited by in Crossref: 15] [Cited by in F6Publishing: 19] [Article Influence: 15.0] [Reference Citation Analysis]
23 Ibrahim SA, Rizk HF, Aboul-magd DS, Ragab A. Design, synthesis of new magenta dyestuffs based on thiazole azomethine disperse reactive dyes with antibacterial potential on both dyes and gamma-irradiated dyed fabric. Dyes and Pigments 2021;193:109504. [DOI: 10.1016/j.dyepig.2021.109504] [Cited by in Crossref: 19] [Cited by in F6Publishing: 15] [Article Influence: 19.0] [Reference Citation Analysis]