Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Ayad M.R. Raauf"'
Publikováno v:
F1000Research, Vol 12 (2024)
Background Conventional chemotherapy results in severe toxic side effects due to affecting normal and cancer cells. The conjugation of chemotherapy with mAb will improve the chemotherapy selectivity towards cancer cells and at the same time will pote
Externí odkaz:
https://doaj.org/article/614a2f1a7f434f8793c12eca906b9f56
Publikováno v:
Al-Mustansiriyah Journal of Pharmaceutical Sciences, Vol 22, Iss 3 (2022)
A variety of new pyrazolines, isoxazolines, and amide derivatives were designed, synthesized, and tested in vitro for their cytotoxic potential against the breast cancer cell line MCF-7. Nabumetone is a prodrug that is used as non-steroidal anti-infl
Externí odkaz:
https://doaj.org/article/4a2ec9c96b5b45f0b84d93a8ecdb078e
Publikováno v:
Al-Mustansiriyah Journal of Pharmaceutical Sciences, Vol 20, Iss 3 (2020)
Lipids are organic fatty or waxy compounds which are used to make nanocarriers that are promising for drug delivery. When lipids associated covalently (lipid-drug conjugate LDC) or non- covalently (drug-lipid complex) to drugs to form Lipid Drug Conj
Externí odkaz:
https://doaj.org/article/e8fd84d119f24d07b0fdf9d57473a73d
Publikováno v:
Al Mustansiriyah Journal of Pharmaceutical Sciences. 22:24-34
A variety of new pyrazolines, isoxazolines, and amide derivatives were designed, synthesized, and tested in vitro for their cytotoxic potential against the breast cancer cell line MCF-7. Nabumetone is a prodrug that is used as non-steroidal anti-infl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9fb086ae26973290ec84c9e050991e50
https://doi.org/10.32947/ajps.v22i3.886
https://doi.org/10.32947/ajps.v22i3.886
Publikováno v:
Al-Mustansiriyah Journal of Pharmaceutical Sciences, Vol 19, Iss 4 (2019)
This work includes Synthesis of new series of sulfa drugs derived from sulfamethoxazole containing substituted Imidazolidine moiety. These compounds expected to have antibacterial activity, due to their Imidazolidine moiety This work includes synthes
Externí odkaz:
https://doaj.org/article/d2826fda7e0443fa81a4fdefdc15e55d
Publikováno v:
Al-Mustansiriyah Journal of Pharmaceutical Sciences, Vol 19, Iss 4 (2019)
New series of Nabumetone containing 5-arylidene-4-thiazolidinones pharmacophore as in compounds 3(a-e) were designed and synthesized by using nabumetone and hydrazinethiocarboamide to synthesize compound (1) (Schiff base), next step compound (1)
Externí odkaz:
https://doaj.org/article/4171f62fdd9a4eb196c17c0d890c9d93
Publikováno v:
Al Mustansiriyah Journal of Pharmaceutical Sciences. 20:1-13
Lipids are organic fatty or waxy compounds which are used to make nanocarriers that are promising for drug delivery. When lipids associated covalently (lipid-drug conjugate LDC) or non- covalently (drug-lipid complex) to drugs to form Lipid Drug Conj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a34bfba6efbf5b5ecc4f31f001cb2c8a
https://doi.org/10.32947/ajps.v20i3.754
https://doi.org/10.32947/ajps.v20i3.754
Publikováno v:
INTERNATIONAL JOURNAL OF PHARMACEUTICAL QUALITY ASSURANCE. 11:141-144
Background: Cancer is considered as one of the major leading causes of death. Tyrosine kinase inhibitors are recognized for their potential antiproliferative effects. Materials and methods: In the previous study, the authors designed, synthesized, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::390df78c6a34b46d8a85d56a7ce842ff
https://doi.org/10.25258/ijpqa.11.1.22
https://doi.org/10.25258/ijpqa.11.1.22
Publikováno v:
Egyptian Journal of Chemistry.
Infectious diseases are caused by pathogens, such as viruses, bacteria, fungi, and parasites. Quinolones work by inhibition of bacterial topoisomerase IV and/or gyrase, a group of oxadiazole derivatives were incorporated into C7 piperazine ring of Ga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f8d0169d4b8e8173dbaf33cc2bed2eb
https://doi.org/10.21608/ejchem.2021.92699.4390
https://doi.org/10.21608/ejchem.2021.92699.4390
Publikováno v:
Egyptian Journal of Chemistry.
A series of new 1-(3-imino-2-oxoindolin-5-yl)-3-phenylurea derivatives were synthesized starting from 5-aminoisatin; as a part of our program to compose multicomponent hybrid templates with potential pharmaceutical recognition and evaluate them as in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5df1ecd3d2f491e48ba728e3dae95a7
https://doi.org/10.21608/ejchem.2021.72747.3607
https://doi.org/10.21608/ejchem.2021.72747.3607