Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Moustafa K. Soltan"'
Autor:
Mohamed Abd Elrahman, Noha Salah Katamesh, Marwa M. Soliman, Moustafa K. Soltan, Hani Mohammed Hafez, Sona Soliman Barghash
Publikováno v:
F1000Research, Vol 12 (2023)
Background: Tigecycline (TGC) is a recently developed antibiotic to battle resistant bacteria. The procedures outlined in the literature for analyzing TGC involve chemical solvents that could be hazardous. Therefore, this study aimed to create a sust
Externí odkaz:
https://doaj.org/article/f2518b3d0b4a47fc9cd35e4e135f5850
Publikováno v:
Molecules, Vol 28, Iss 18, p 6663 (2023)
Herein, we report the preparation of lipase immobilised on single-walled carbon nanotubes (SWCNTs) as an enantioselector for capillary monolithic columns and their application in the chiral separation of racemic pharmaceuticals. The columns were prep
Externí odkaz:
https://doaj.org/article/ad61b45bdea2402ea34fbd43e4a6babc
Publikováno v:
Molecules, Vol 28, Iss 4, p 1925 (2023)
New antioxidant agents are urgently required to combat oxidative stress, which is linked to the emergence of serious diseases. In an effort to discover potent antioxidant agents, a novel series of 2-thiouracil-5-sulfonamides (4–9) were designed and
Externí odkaz:
https://doaj.org/article/bf95a9407d03493ab3dd5dc9b64ce779
A simple, sensitive, selective, accurate and precise method was developed and fully validated for determination of oxcarbazepine (OXC) in presence of their preservatives and determination of oxcarbazepine (OXC) in human plasma. A reversed phase liqui
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce1070b9203522fedb8e96df23582a7b
https://doi.org/10.21203/rs.3.rs-2680188/v1
https://doi.org/10.21203/rs.3.rs-2680188/v1
Publikováno v:
Molecules, Vol 26, Iss 7, p 1838 (2021)
Scaffolds hybridization is a well-known drug design strategy for antitumor agents. Herein, series of novel indolyl-pyrimidine hybrids were synthesized and evaluated in vitro and in vivo for their antitumor activity. The in vitro antiproliferative act
Externí odkaz:
https://doaj.org/article/a269a84d41f745559e1c6b347e964601
Autor:
Mоhsеn M. Zаrеh, Mоnir Z. Sааd, Wаfаа S. Hаssаn, Mоstаfа Е. Еlhеnnаwу, Moustafa K. Soltan, Mаhmоud M. Sеbаiу
Publikováno v:
Pharmaceuticals, Vol 13, Iss 2, p 32 (2020)
А grаdiеnt HPLC mеthоd was dеvеlоpеd аnd vаlidаtеd fоr rаpid simultаnеоus sеpаrаtiоn аnd dеtеrminаtiоn оf the following eight drugs оf sаrtаn аnd stаtin clаssеs in thеir purе аnd dоsаgе fоrms within 15 minute
Externí odkaz:
https://doaj.org/article/97e0b89b0446425eaf1ce6ddb3696ef1
Autor:
Dina S. El-Shaprawy, Khaled Elgendy, Mohamed A. F. Elmosallamy, Moustafa K. Soltan, Alaa S. Amin
Publikováno v:
Reviews in Analytical Chemistry, Vol 40, Iss 1, Pp 127-135 (2021)
Two new potentiometric sensors were created for the quantification of bisoprolol fumarate and alverine citrate in bulk pharmaceutical dosage forms and human serum. Bisoprolol and alverine sensors were manufactured by combining potassium tetrakis (p-c
Autor:
Hani Mohammed Hafez, Sona Soliman Barghash, Marwa M. Soliman, Moustafa K. Soltan, Mohamed Abd Elrahman, Noha Salah Katamesh
Publikováno v:
F1000Research. 12:341
Background: Tigecycline (TGC) is a recently developed antibiotic to battle resistant bacteria. The procedures outlined in the literature for analyzing TGC involve chemical solvents that could be hazardous. Therefore, this study aimed to create a sust
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 34, Iss 1, Pp 1110-1120 (2019)
Journal of Enzyme Inhibition and Medicinal Chemistry
Journal of Enzyme Inhibition and Medicinal Chemistry
New anticancer agents are highly needed to overcome cancer cell resistance. A novel series of pyrimidine pyrazoline-anthracene derivatives (PPADs) (4a-t) were designed and synthesised. The anti-liver cancer activity of all compounds was screened in v
Publikováno v:
Molecules
Volume 26
Issue 7
Molecules, Vol 26, Iss 1838, p 1838 (2021)
Volume 26
Issue 7
Molecules, Vol 26, Iss 1838, p 1838 (2021)
Scaffolds hybridization is a well-known drug design strategy for antitumor agents. Herein, series of novel indolyl-pyrimidine hybrids were synthesized and evaluated in vitro and in vivo for their antitumor activity. The in vitro antiproliferative act