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For: Hachim ME, Oubella A, Byadi S, Fawzi M, Laamari Y, Bahsis L, Aboulmouhajir A, Morjani H, Podlipnik Č, Auhmani A, Ait Itto MY. Newly synthesized (R)-carvone-derived 1,2,3-triazoles: structural, mechanistic, cytotoxic and molecular docking studies. Journal of Biomolecular Structure and Dynamics. [DOI: 10.1080/07391102.2021.1894984] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 7.5] [Reference Citation Analysis]
Number Citing Articles
1 Bimoussa A, Fawzi M, Oubella A, Ejaz SA, Sajjad Bilal M, Labd Taha M, Auhmani A, Morjani H, Robert A, Riahi A, Ait Itto MY. Hybrids of thiazolidinone with 1,2,3-triazole derivatives: design, synthesis, biological evaluation, in silico studies, molecular docking, molecular dynamics simulations, and ADMET profiling. J Biomol Struct Dyn 2023;:1-13. [PMID: 36617941 DOI: 10.1080/07391102.2022.2164357] [Reference Citation Analysis]
2 Oubella A, Bimoussa A, Byadi S, Fawzi M, Laamari Y, Auhmani A, Morjani H, Robert A, Riahi A, Ait Itto MY. Design, synthesis, in vitro anticancer activity, and molecular docking studies of new (R)-carvone-pyrazole-1,2,3-triazoles. Journal of Molecular Structure 2022;1265:133383. [DOI: 10.1016/j.molstruc.2022.133383] [Reference Citation Analysis]
3 Bimoussa A, Oubella A, Bamou FZ, Khdar ZA, Fawzi M, Laamari Y, Ait Itto MY, Morjani H, Auhmani A. New 1,3,4-thiadiazoles derivatives: synthesis, antiproliferative activity, molecular docking and molecular dynamics. Future Medicinal Chemistry. [DOI: 10.4155/fmc-2022-0016] [Reference Citation Analysis]
4 Bimoussa A, Oubella A, Bjij I, Fawzi M, Laamari Y, Ait Itto MY, Auhmani A, Morjani H, Cherqaoui D, Auhmani A. Design, Synthesis, Biological and Computational Assessment of New Thiazolidin‐4‐one Derivatives as Potential Anticancer Agents Through the Apoptosis Pathway. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202200165] [Reference Citation Analysis]
5 Fawzi M, Oubella A, Bimoussa A, Bamou FZ, Khdar ZA, Auhmani A, Riahi A, Robert A, Morjani H, Itto MYA. Design, synthesis, evaluation of new 3-acetylisoxazolines and their hybrid analogous as anticancer agents: In vitro and in silico analysis. Computational Biology and Chemistry 2022;98:107666. [DOI: 10.1016/j.compbiolchem.2022.107666] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
6 Oubella A, Laamari Y, Hachim ME, Byadi S, Auhmani A, Morjani H, Riahi A, Podlipnik C, Rohand T, Van Meervelt L, Ait Itto MY. New gem‑dichlorocyclopropane-pyrazole hybrids with monoterpenic skeleton: Synthesis, crystal structure, cytotoxic evaluation, molecular dynamics and theoretical study. Journal of Molecular Structure 2022;1256:132573. [DOI: 10.1016/j.molstruc.2022.132573] [Reference Citation Analysis]
7 Elqars E, Oubella A, Byadi S, Hachim ME, auhmani A, Guennoun M, Essadki A, Riahi A, Robert A, Itto MYA, Nbigui T. Synthesis, spectroscopic characterization, and prevention of carbon steel corrosion in hydrochloric acid of a new bis-isoxazoline-carvone. Journal of Molecular Structure 2022;1256:132526. [DOI: 10.1016/j.molstruc.2022.132526] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
8 Oubella A, Taia A, Byadi S, Ait Lahcen M, Bimoussa A, Essaber M, Podlipnik C, Morjani H, Ait Itto MY, Aatif A. Chemical profiling, cytotoxic activities through apoptosis induction in human fibrosarcoma and carcinoma cells, and molecular docking of some 1,2,3-triazole-isoxazoline hybrids using the eugenol as a precursors. J Biomol Struct Dyn 2022;:1-13. [PMID: 35174765 DOI: 10.1080/07391102.2022.2037466] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
9 Elqars E, Oubella A, Eddine Hachim M, Byadi S, Auhmani A, Guennoun M, Essadki A, Riahi A, Robert A, Youssef Ait Itto M, Nbigui T. New 3-(2-methoxyphenyl)-isoxazole-carvone: synthesis, spectroscopic characterization, and prevention of carbon steel corrosion in hydrochloric acid. Journal of Molecular Liquids 2022;347:118311. [DOI: 10.1016/j.molliq.2021.118311] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
10 Oubella A, Bimoussa A, N'ait Oussidi A, Fawzi M, Auhmani A, Morjani H, Riahi A, Esseffar M, Parish C, Ait Itto MY. New 1,2,3-Triazoles from (R)-Carvone: Synthesis, DFT Mechanistic Study and In Vitro Cytotoxic Evaluation. Molecules 2022;27:769. [PMID: 35164037 DOI: 10.3390/molecules27030769] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
11 Oubella A, Fawzi M, Bimoussa A, N’ait Ousidi A, Auhmani A, Riahi A, Robert A, El Firdoussi L, Morjani H, Ait Itto MY. Convenient route to benzo[1,2,3]selenadiazole–isoxazole hybrids and evaluation of their in vitro cytotoxicity. Chem Pap . [DOI: 10.1007/s11696-022-02083-6] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
12 Elqars E, Hachim ME, Oubella A, Byadi S, Bahsis L, Auhmani A, Guennoun M, Essadki A, Ait Itto MY, Nbigui T. L'action inhibitrice de la 3-phényl-isoxazoline-carvone sur l'acier au carbone en solution de HCl a été étudiée expérimentalement et théoriquement. Journal of Adhesion Science and Technology. [DOI: 10.1080/01694243.2021.2010973] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
13 Bimoussa A, Oubella A, Laamari Y, Fawzi M, Hachim ME, Ait Itto MY, Morjani H, Ketatni EM, Mentre O, Auhmani A. Hybrid of the 1,2,3‐triazole nucleus and sesquiterpene skeleton as a potential antitumor agent: Hemisynthesis, molecular structure, Hirshfeld surface analysis, density functional theory, and in vitro cytotoxic and apoptotic effects. J Heterocyclic Chem 2021;58:2334-47. [DOI: 10.1002/jhet.4359] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
14 Moussaoui O, Byadi S, Eddine Hachim M, Sghyar R, Bahsis L, Moslova K, Aboulmouhajir A, Rodi YK, Podlipnik Č, Hadrami EME, Chakroune S. Selective synthesis of novel quinolones-amino esters as potential antibacterial and antifungal agents: Experimental, mechanistic study, docking and molecular dynamic simulations. Journal of Molecular Structure 2021;1241:130652. [DOI: 10.1016/j.molstruc.2021.130652] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
15 Alam MM. 1,2,3-Triazole hybrids as anticancer agents: A review. Arch Pharm (Weinheim) 2022;355:e2100158. [PMID: 34559414 DOI: 10.1002/ardp.202100158] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 9.0] [Reference Citation Analysis]
16 Oubella A, El Mansouri AE, Fawzi M, Bimoussa A, Laamari Y, Auhmani A, Morjani H, Robert A, Riahi A, Youssef Ait Itto M. Thiazolidinone-linked1,2,3-triazoles with monoterpenic skeleton as new potential anticancer agents: Design, synthesis and molecular docking studies. Bioorg Chem 2021;115:105184. [PMID: 34333421 DOI: 10.1016/j.bioorg.2021.105184] [Cited by in Crossref: 21] [Cited by in F6Publishing: 23] [Article Influence: 10.5] [Reference Citation Analysis]