Furanylnorfentanyl is an inactive synthetic opioid analgesic drug precursor. It is an analog of fentanyl.[1][2][3][4][5]
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| Formula | C16H18F0N2O2 |
| Molar mass | 270.332 g·mol−1 |
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See also
editReferences
edit- ^ Goggin, Melissa M. (2017). "Identification of unique metabolites of the designer opioid furanyl fentanyl". Journal of Analytical Toxicology. 41 (5): 367–375. doi:10.1093/jat/bkx022. PMID 28369517.
- ^ Palmquist, Kaitlyn B. (2020). "Quantification of furanylfentanyl and its metabolites in human and rat plasma using LC–MS-MS". Journal of Analytical Toxicology. 44 (6): 589–595. doi:10.1093/jat/bkaa013. PMID 32064536.
- ^ Larabi, Islam Amine (2020). "Hair testing for 3-fluorofentanyl, furanylfentanyl, methoxyacetylfentanyl, carfentanil, acetylfentanyl and fentanyl by LC–MS/MS after unintentional overdose". Forensic Toxicology. 38 (1): 277-286. doi:10.1007/s11419-019-00502-0. S2CID 207916035.
- ^ Daniulaityte, Raminta (2019). "Street fentanyl use: Experiences, preferences, and concordance between self-reports and urine toxicology". International Journal of Drug Policy. 71: 3–9. doi:10.1016/j.drugpo.2019.05.020. PMC 6868314. PMID 31146200. S2CID 171094309.
- ^ Shoemaker, Alyssa K. (2020). Cholinesterase Based System for Fentanyl Detection (MS thesis). State University of New York at Albany.
Further reading
edit- Higashikawa Y, Suzuki S (June 2008). "Studies on 1-(2-phenethyl)-4-(N-propionylanilino)piperidine (fentanyl) and its related compounds. VI. Structure-analgesic activity relationship for fentanyl, methyl-substituted fentanyls and other analogues". Forensic Toxicology. 26 (1): 1–5. doi:10.1007/s11419-007-0039-1. S2CID 22092512.
- Alburges ME, Hanson GR, Gibb JW, Sakashita CO, Rollins DE (1992). "Fentanyl receptor assay. II. Utilization of a radioreceptor assay for the analysis of fentanyl analogs in urine". J Anal Toxicol. 16 (1): 36–41. doi:10.1093/jat/16.1.36. PMID 1322477.
- Woods J, Medzihradsky F, Smith C, Winger G, Gmerek D (1988). "Evaluation of new compounds for opioid activity: 1987 annual report". NIDA Res. Monogr. 81: 543–90. PMID 3136388.
- Aceto M, Bowman E, Harris L, May E (1988). "Dependence studies of new compounds in the rhesus monkey, rat, and mouse, 1987". NIDA Res. Monogr. 81: 485–542. PMID 3136386.
- Brine GA, Boldt KG, Huang PT, Sawyer DK, Carroll FI (2009). "Carbon-13 nuclear magnetic resonance spectra of fentanyl analogs". Journal of Heterocyclic Chemistry. 26 (3): 677–686. doi:10.1002/jhet.5570260329.