Investigation of Novel Imidazole Analogues with Terminal Sulphonamides as Potential V600E-BRAF Inhibitors Through Computational Approaches-Reference-Cited by-同舟云学术

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Investigation of Novel Imidazole Analogues with Terminal Sulphonamides as Potential V600E-BRAF Inhibitors Through Computational Approaches

Published:2023-05-04 Issue:6 Volume:6 Page:3027-3038
ISSN:2522-5758
Container-title:Chemistry Africa
language:en
Short-container-title:Chemistry Africa

Author:

Umar Abdullahi Bello,Uzairu Adamu,Ibrahim Muhammad Tukur,Usman Abdulfatai,Habib Aliyu,Usman Bishir

Publisher

Springer Science and Business Media LLC

Subject

Physical and Theoretical Chemistry,Environmental Chemistry,Chemistry (miscellaneous),Catalysis

Link

https://link.springer.com/content/pdf/10.1007/s42250-023-00687-3.pdf

Reference46 articles.

1. Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A (2018) Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. Cancer J Clin 68(6):394–424

2. Hassan AH, Lee K-T, Lee YS (2020) Flavone-based arylamides as potential anticancer: design, synthesis and in vitro cell-based/cell-free evaluations. Eur J Med Chem 187:111965

3. Umar AB, Uzairu A, Shallangwa GA, Uba S (2020) Molecular Docking Strategy to Design Novel V600E-BRAF kinase inhibitors with prediction of their drug-likeness and Pharmacokinetics ADMET Properties. Chemistry Africa, pp 1–17

4. Ammar UM, Abdel-Maksoud MS, Oh C-H (2018) Recent advances of RAF (rapidly accelerated fibrosarcoma) inhibitors as anti-cancer agents. Eur J Med Chem 158:144–166

5. Amin KM, El-Badry OM, Rahman DEA, Ammar UM, Abdalla MM (2016) Design, synthesis, anticancer evaluation and molecular docking of new V600EBRAF inhibitors derived from pyridopyrazinone. Eur J Chem 7(1):19–29

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