Year: 2025
Type: article
Abstract: Four Juglone-based Pd(0) complexes with varied ligands were synthesized and characterized. They showed strong cytotoxicity and cancer selectivity. The most promising complex inhibited the PIN1 oncoprotein, as confirmed by Western Blot.
Source: Dalton Transactions
DOI: 10.1039/d5dt01792k
Language: English
Subfield: Oncology
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Award: G8152518880
OpenAlex ID: W4417152802
