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A new framework for novel analogues of pazopanib as potent and selective human carbonic anhydrase inhibitors: Design, repurposing rational, synthesis, crystallographic, in vivo and in vitro biological assessments.
Hefny SM, El-Moselhy TF, El-Din N, Ammara A, Angeli A, Ferraroni M, El-Dessouki AM, Shaldam MA, Yahya G, Al-Karmalawy AA, Supuran CT, Tawfik HO. Hefny SM, et al. Among authors: al karmalawy aa. Eur J Med Chem. 2024 May 24;274:116527. doi: 10.1016/j.ejmech.2024.116527. Online ahead of print. Eur J Med Chem. 2024. PMID: 38810335
Rationale design of novel substituted 1,3,5-triazine candidates as dual IDH1(R132H)/ IDH2(R140Q) inhibitors with high selectivity against acute myeloid leukemia: In vitro and in vivo preclinical investigations.
Tawfik HO, Mousa MHA, Zaky MY, El-Dessouki AM, Sharaky M, Abdullah O, El-Hamamsy MH, Al-Karmalawy AA. Tawfik HO, et al. Among authors: al karmalawy aa. Bioorg Chem. 2024 May 21;149:107483. doi: 10.1016/j.bioorg.2024.107483. Online ahead of print. Bioorg Chem. 2024. PMID: 38805913
Rational design, synthesis, biological evaluation, and molecular modeling of novel naphthamide derivatives possessing potent, reversible, and competitive inhibitory mode of action over human monoamine oxidase.
Elkamhawy A, Oh JM, Kim M, El-Halaby LO, Abdellattif MH, Al-Karmalawy AA, Kim H, Lee K. Elkamhawy A, et al. Among authors: al karmalawy aa. Mol Divers. 2024 May 10. doi: 10.1007/s11030-024-10841-9. Online ahead of print. Mol Divers. 2024. PMID: 38727994
Coenzyme Q10 mitigates cadmium cardiotoxicity by downregulating NF-κB/NLRP3 inflammasome axis and attenuating oxidative stress in mice.
Antar SA, Abdo W, Helal AI, Abduh MS, Hakami ZH, Germoush MO, Alsulimani A, Al-Noshokaty TM, El-Dessouki AM, ElMahdy MK, Elgebaly HA, Al-Karmalawy AA, Mahmoud AM. Antar SA, et al. Among authors: al karmalawy aa. Life Sci. 2024 Jul 1;348:122688. doi: 10.1016/j.lfs.2024.122688. Epub 2024 May 4. Life Sci. 2024. PMID: 38710284
122 results