Abstract:
:The photophysical properties of naphthalimide-based fluorophores can be easily tuned by chemical manipulation of the substituents on that privileged scaffold. Replacement of a OMe group at position 6 in 2-(hydroxyl)ethyl-naphthalimide derivatives by diverse amines, including 2-(hydroxyl)ethylamine, trans-(4-acetamido)cyclohexylamine and azetidine increases the solvatochromic (ICT) character, while this replacement in 2-(dimethylamino)ethyl-naphthalimide analogues (PET fluorophores) decrease their solvent polarity sensitivity or even reversed them to solvatochromic fluorophores. These fluorophores resulted macrophage nucleus imaging probes, which bind DNA as intercalants and showed low cytotoxicity in human cancer cells.
journal_name
Eur J Med Chemjournal_title
European journal of medicinal chemistryauthors
Fueyo-González F,Fernández-Gutiérrez M,García-Puentes D,Orte A,González-Vera JA,Herranz Rdoi
10.1016/j.ejmech.2020.112407subject
Has Abstractpub_date
2020-08-15 00:00:00pages
112407eissn
0223-5234issn
1768-3254pii
S0223-5234(20)30378-0journal_volume
200pub_type
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