Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Rehab H. Abd El-Aleam"'
Autor:
Lamya Azmy, Ibraheem B. M. Ibraheem, Sulaiman A. Alsalamah, Mohammed Ibrahim Alghonaim, Ahmed Zayed, Rehab H. Abd El-Aleam, Soad A. Mohamad, Usama Ramadan Abdelmohsen, Khaled N. M. Elsayed
Publikováno v:
Biology, Vol 13, Iss 8, p 581 (2024)
Liposomes and niosomes can be considered excellent drug delivery systems due to their ability to load all compounds, whether hydrophobic or hydrophilic. In addition, they can reduce the toxicity of the loaded drug without reducing its effectiveness.
Externí odkaz:
https://doaj.org/article/dd28fe33acea445dab52343637841362
Autor:
Raya Soltane, Ahlam Alasiri, Mostafa N. Taha, Rehab H. Abd El-Aleam, Kawthar Saad Alghamdi, Mosad A. Ghareeb, Doaa El-Ghareeb Keshek, Susana M. Cardoso, Ahmed M. Sayed
Publikováno v:
Biomolecules, Vol 13, Iss 11, p 1573 (2023)
In the present study, norlobaridone (NBD) was isolated from Parmotrema and then evaluated as a new potent quorum sensing (QS) inhibitor against Pseudomonas aeruginosa biofilm development. This phenolic natural product was found to reduce P. aeruginos
Externí odkaz:
https://doaj.org/article/ffe204971c54463a8446f1d27e4cb68a
Autor:
Rehab H. Abd El-Aleam, Ahmed M. Sayed, Mostafa N. Taha, Riham F. George, Hanan H. Georgey, Hamdy M. Abdel-Rahman
Publikováno v:
Journal of Molecular Structure. 1277:134856
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1156f5e47cdfcddcc603907d8eb8b38e
https://doi.org/10.1016/j.molstruc.2022.134856
https://doi.org/10.1016/j.molstruc.2022.134856
Publikováno v:
RSC advances. 11(58)
Antibiotic resistance is one of the most important challenges of the 21st century. However, the growing understanding of bacterial pathogenesis and cell-to-cell communication has revealed many potential strategies for the discovery of drugs that can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89b199dcad4f9682f6b20d27a09fdefa
https://pubmed.ncbi.nlm.nih.gov/35494393
https://pubmed.ncbi.nlm.nih.gov/35494393
Publikováno v:
Bioorganic chemistry. 94
A series of 1,2,4-triazolo[1,5-a]pyrimidine derivatives was designed, synthesized and screened for their antibacterial and antifungal activities as well as their safety profile. Compounds 2b, 3a, 6b, 8b, 8c, 8h, 9a,b, 10b, 11a,b and 12a,b showed high
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed773b9f55f2eb16da94db84787d8ba9
https://pubmed.ncbi.nlm.nih.gov/31711767
https://pubmed.ncbi.nlm.nih.gov/31711767
Autor:
Rehab H. Abd El‐Aleam, Amr Kamel, Hamdy M. Abdel-Rahman, Ghaneya S. Hassan, Kevin Lee, Mahmoud El-Daly, Gary A. Piazza, Adam B. Keeton, Riham F. George
Publikováno v:
Archiv der Pharmazie. 352:1900002
A series of 1,2,4-triazolo[1,5-a]pyrimidine derivatives was designed, synthesized, and screened for their phosphodiesterase (PDE 4B) inhibitory activity and bronchodilation ability. Compound 7e showed 41.80% PDE 4B inhibition at 10 µM. Eight compoun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c845cbfddc9f42d28697bc487e9123e
https://doi.org/10.1002/ardp.201900002
https://doi.org/10.1002/ardp.201900002