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Evaluation of novel pyrazol-4-yl pyridine derivatives possessing arylsulfonamide tethers as c-Jun N-terminal kinase (JNK) inhibitors in leukemia cells.
Mersal KI, Abdel-Maksoud MS, Ali EMH, Ammar UM, Zaraei SO, Haque MM, Das T, Hassan NF, Kim EE, Lee JS, Park H, Lee KH, El-Gamal MI, Kim HK, Ibrahim TM, Oh CH. Mersal KI, et al. Among authors: kim ee, kim hk. Eur J Med Chem. 2023 Dec 5;261:115779. doi: 10.1016/j.ejmech.2023.115779. Epub 2023 Sep 15. Eur J Med Chem. 2023. PMID: 37776574
Design, synthesis, biological evaluation, and docking studies of novel (imidazol-5-yl)pyrimidine-based derivatives as dual BRAFV600E/p38α inhibitors.
Ali EMH, El-Telbany RFA, Abdel-Maksoud MS, Ammar UM, Mersal KI, Zaraei SO, El-Gamal MI, Choi SI, Lee KT, Kim HK, Lee KH, Oh CH. Ali EMH, et al. Among authors: kim hk. Eur J Med Chem. 2021 Apr 5;215:113277. doi: 10.1016/j.ejmech.2021.113277. Epub 2021 Feb 7. Eur J Med Chem. 2021. PMID: 33601311 Free article.
Structural optimization of 4-(imidazol-5-yl)pyridine derivatives affords broad-spectrum anticancer agents with selective B-RAFV600E/p38α kinase inhibitory activity: Synthesis, in vitro assays and in silico study.
Ali EMH, Mersal KI, Ammar UM, Zaraei SO, Abdel-Maksoud MS, El-Gamal MI, Haque MM, Das T, Kim EE, Lee JS, Lee KH, Kim HK, Oh CH. Ali EMH, et al. Among authors: kim ee, kim hk. Eur J Pharm Sci. 2022 Apr 1;171:106115. doi: 10.1016/j.ejps.2022.106115. Epub 2022 Jan 4. Eur J Pharm Sci. 2022. PMID: 34995782 Free article.
5,801 results