Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nagwa M. Fawzy"'
Autor:
Heba M. Abo-Salem, Sahar S. M. El Souda, Heba I. Shafey, Khairy M. A. Zoheir, Khadiga M. Ahmed, Kh. Mahmoud, Karima F. Mahrous, Nagwa M. Fawzy
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-24 (2024)
Abstract In consideration of the chromones' therapeutic potential and anticancer activity, a new series of chromanone derivatives have been synthesized through a straightforward reaction between 6-formyl-7-hydroxy-5-methoxy-2-methylchromone (2) and v
Externí odkaz:
https://doaj.org/article/27809bcf930940b8a8a8b071cc3f25dd
Publikováno v:
Molecules, Vol 23, Iss 6, p 1398 (2018)
Curcumin, a widely utilized flavor and coloring agent in food, has been shown to demonstrate powerful antioxidant, antitumor promoting and anti-inflammatory properties in vitro and in vivo. In the present work, synthesis of new heterocyclic derivativ
Externí odkaz:
https://doaj.org/article/5275eba5cf1b4db682f9f4f179f59aa2
Publikováno v:
Russian Journal of Bioorganic Chemistry. 46:1117-1127
Novel pyrrole derivatives were synthesized by one-pot four components condensation reaction of khellin and/or visnagin carbaldehyde; amine derivatives; curcumin and nitro methane. In another approach with lack of curcumin molecular structure, new pyr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::62cf1c69dc4207540de5193a50c2df2f
https://doi.org/10.1134/s1068162020060072
https://doi.org/10.1134/s1068162020060072
Publikováno v:
Journal of Heterocyclic Chemistry. 57:2748-2761
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24511d6d78ea532d05e059ed50b15c0f
https://doi.org/10.1002/jhet.3984
https://doi.org/10.1002/jhet.3984
Autor:
Enas M. Awad, Joanna Wietrzyk, Hanaa M. F. Roaiah, Magdalena Milczarek, Abdel-mohsen M. Soliman, Nagwa M Fawzy
Publikováno v:
Egyptian Pharmaceutical Journal. 17:85
Background and objectives Indoles derivatives are natural products, which are well known for their anticancer activity due to its ability to induce cell death for many cancer cell lines. The aim of this study is to synthesize some new heterocyclic co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6fc094eda454866784cc8d914336732
https://doi.org/10.4103/epj.epj_45_17
https://doi.org/10.4103/epj.epj_45_17
Publikováno v:
Biotechnology(Faisalabad). 7:43-50
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b8307f5da54fe36e3c88800256b4a70
https://doi.org/10.3923/biotech.2008.43.50
https://doi.org/10.3923/biotech.2008.43.50