| Literature DB >> 33518669 |
Tatsuyuki Kanamori1, Yuki Okada1, Hiroki Segawa1, Tadashi Yamamuro1, Kenji Kuwayama1, Kenji Tsujikawa1, Yuko Togawa Iwata1.
Abstract
The agonistic activity of fluorinated and nonfluorinated fentanyl analogs on µ-opioid receptor was investigated using a cell-based assay system. Based on the activity, fentanyl analogs were ranked as follows: fentanyl > isobutyrylfentanyl ≈ butyrylfentanyl ≈ methoxyacetylfentanyl > acetylfentanyl. However, among the fentanyl analogs fluorinated on the N-phenyl ring, 2-fluoro analogs and 3-fluoro analogs showed the strongest and weakest activities, respectively. These results suggest that the 2-fluorinated isomers of fentanyl analogs are more likely to cause poisoning.Entities:
Keywords: agonistic activity; cell-based assay; fluoro-fentanyl analog; opioid receptor
Year: 2021 PMID: 33518669 DOI: 10.1248/bpb.b20-00780
Source DB: PubMed Journal: Biol Pharm Bull ISSN: 0918-6158 Impact factor: 2.233