Alkyne–azide cycloaddition analogues of dehydrozingerone as potential anti-prostate cancer inhibitors via the PI3K/Akt/NF-kB pathway
Year: 2017
Type: article
Abstract: Alkyne–azide cycloaddition derivatives of DHZ ( 1 ) were synthesized and screened for cytotoxic potential in which the derivatives, 3 , 6 , 7 , 8 , 9 and 15 displayed most potent with IC 50 value ranging from 1.8–3.0 μM.
Source: MedChemComm
DOI: 10.1039/c7md00267j
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: green
Award: G7166087668
OpenAlex ID: W2765246760
