Zobrazeno 1 - 10
of 192
pro vyhledávání: '"Emilia Sicilia"'
Publikováno v:
ACS Omega, Vol 5, Iss 48, Pp 31456-31466 (2020)
Externí odkaz:
https://doaj.org/article/dfd34174e09542dc82084c9e16792e94
Publikováno v:
Molecules, Vol 27, Iss 17, p 5635 (2022)
Ruthenium-based complexes represent a new frontier in light-mediated therapeutic strategies against cancer. Here, a density functional-theory-based computational investigation, of the photophysical properties of a conjugate BODIPY-Ru(II) complex, is
Externí odkaz:
https://doaj.org/article/c2c18c1f94a1415da4fbc6d56e126860
Publikováno v:
Molecules, Vol 27, Iss 13, p 4046 (2022)
The photophysical properties of two classes of porphyrins and metalloporphyrins linked to N-heterocyclic carbene (NHC) Au(I) complexes have been investigated by means of density functional theory and its time-dependent extension for their potential a
Externí odkaz:
https://doaj.org/article/bae7a97a6f58495992a900a2a196266d
Autor:
Sherif Ashraf Fahmy, Fortuna Ponte, Giulia Grande, Iten M. Fawzy, Asmaa A. Mandour, Emilia Sicilia, Hassan Mohamed El-Said Azzazy
Publikováno v:
Pharmaceuticals, Vol 15, Iss 2, p 259 (2022)
Para-sulfocalix[n]arenes are promising host molecules that can accommodate various chemotherapeutic drugs. Pt(IV)-based complexes, including satraplatin and asplatin, are promising alternatives that overcome the shortcomings of Pt(II) complexes. In t
Externí odkaz:
https://doaj.org/article/99364f9d44754b26987cac5a84c70a70
Publikováno v:
Applied Sciences, Vol 12, Iss 3, p 1095 (2022)
A computational investigation of the mechanism of dihydrosanguinarine (DHSAN) photoactivation and its conversion into the active drug sanguinarine (SAN) is here reported. The reaction mechanism of DHSAN photoconversion was fully explored by consideri
Externí odkaz:
https://doaj.org/article/7ffd850087474fbe9c04185ffd1e43b5
Publikováno v:
Frontiers in Physics, Vol 6 (2018)
The photophysical properties of some monomeric and dimeric BODIPY systems were investigated at the density functional theory level and herein reported. In particular, the absorption spectra were fully characterized, low energy singlet and triplet exc
Externí odkaz:
https://doaj.org/article/7bba97d78e924aa5b169820971bde24c
Autor:
Sherif Ashraf Fahmy, Fortuna Ponte, Iten M. Fawzy, Emilia Sicilia, Udo Bakowsky, Hassan Mohamed El-Said Azzazy
Publikováno v:
Molecules, Vol 25, Iss 24, p 5926 (2020)
P-sulfonatocalix[n]arenes have demonstrated a great potential for encapsulation of therapeutic drugs via host-guest complexation to improve solubility, stability, and bioavailability of encapsulated drugs. In this work, guest-host complexes of a thir
Externí odkaz:
https://doaj.org/article/92f8d543500d44189840b55842cd578f
Publikováno v:
Molecules, Vol 22, Iss 7, p 1093 (2017)
The effects of Mg, Zn, Cd, and Pd dications on the photophysical properties of the tetraphenylporphyrin ligand have been explored, considering the corresponding complexes and by using the density functional theory and its time-dependent extension. Re
Externí odkaz:
https://doaj.org/article/25529610a9694006b8dfdd0370a5dfc7
Autor:
Alessandra G. Ritacca, Enrico Falcone, Iman Doumi, Bertrand Vileno, Peter Faller, Emilia Sicilia
Publikováno v:
Inorganic Chemistry. 62:3957-3964
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc5649a47931556f725e95a7800b65e0
https://doi.org/10.1021/acs.inorgchem.2c04392
https://doi.org/10.1021/acs.inorgchem.2c04392
Autor:
Xin Yang, Limin Ma, Hongwei Shao, Zikai Zhou, Xia Ling, Mengyu Yao, Guowen Luo, Stefano Scoditti, Emilia Sicilia, Gloria Mazzone, Meng Gao, Ben Zhong Tang
Publikováno v:
Journal of Medicinal Chemistry. 65:15738-15748
Cancer therapies usually suffer from poor targeting ability and serious side effects. Photoactivatable cancer therapy has the significant advantage of a high spatiotemporal resolution, but most photoactivatable prodrugs require decoration with stoich
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d411ee5fea0793d029828e139d4edb25
https://doi.org/10.1021/acs.jmedchem.2c01262
https://doi.org/10.1021/acs.jmedchem.2c01262