Work

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
Language: English
Field: Chemistry
Open Access status: green
OpenAlex ID: W2765246760
FWCI: 1.166
Cites: 31
Cited by: 23
Related to: 10