Chemistry:Butyrylnorfentanyl
From HandWiki
Short description: Synthetic opioid analgesic metabolite
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| Formula | C15H22N2O |
| Molar mass | 246.354 g·mol−1 |
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Butyrnorfentanyl or butyrylnorfentanyl is an inactive synthetic opioid analgesic drug precursor. It is an analog of fentanyl.[1][2][3][4][5][6][7][8][9][10]
See also
- 3-Methylbutyrfentanyl
- 4-Fluorobutyrfentanyl
- 4-Fluorofentanyl
- α-Methylfentanyl
- Acetylfentanyl
- Benzylfentanyl
- Furanylfentanyl
- Homofentanyl
- List of fentanyl analogues
References
- ↑ Strayer, Kraig E. (2018). "LC-MS/MS-based method for the multiplex detection of 24 fentanyl analogues and metabolites in whole blood at sub ng mL–1 concentrations.". ACS Omega 3 (1): 514–523. doi:10.1021/acsomega.7b01536. PMID 29399650.
- ↑ Mannocchi, Giulio (2020). "Development and validation of fast UHPLC-MS/MS screening method for 87 NPS and 32 other drugs of abuse in hair and nails: application to real cases.". Analytical and Bioanalytical Chemistry 412 (21): 5125–5145. doi:10.1007/s00216-020-02462-6. PMID 32062830.
- ↑ Freni, Francesca (2020). "Determination of fentanyl and 19 derivatives in hair: application to an Italian population.". Journal of Pharmaceutical and Biomedical Analysis 189: 113476. doi:10.1016/j.jpba.2020.113476. PMID 32693203.
- ↑ Lanzarotta, Adam (2020). "Identification of opioids and related substances using handheld Raman spectrometers.". Journal of Forensic Sciences 65 (2): 421–427. doi:10.1111/1556-4029.14217. PMID 31643087.
- ↑ Larabi, Islam Amine (2020). "Development and validation of liquid chromatography-tandem mass spectrometry targeted screening of 16 fentanyl analogs and U-47700 in hair: Application to 137 authentic samples". Drug Testing and Analysis 12 (9): 1298–1308. doi:10.1002/dta.2868. PMID 32476263.
- ↑ Strayer, Kraig Edward (2018). A LC-MS/MS-Based Method for the Multiplex Detection of 24 Fentanyl Analogs and Metabolites in Whole Blood at Sub ng mL-1 Concentrations..
- ↑ Vaiano, Fabio (2021). "Development of a new LC-MS/MS screening method for detection of 120 NPS and 43 drugs in blood.". Separations 8 (11): 221. doi:10.3390/separations8110221.
- ↑ Kern, Sara. "Rapid-field-deployable DART-MS screening technique for 87 opioids and drugs of abuse, including fentanyl and fentanyl analogs.". Journal of Regulatory Science 10 (2).
- ↑ Garneau, Béatrice (2021). "A comprehensive analytical process, from NPS threat identification to systematic screening: method validation and one-year prevalence study.". Forensic Science International 318: 110595. doi:10.1016/j.forsciint.2020.110595. PMID 33279767.
- ↑ Carelli, Claudia (2022). "Old and New Synthetic and Semi-synthetic Opioids Analysis in Hair: A Review.". Talanta Open 100108.
Further reading
- "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. June 2008. doi:10.1007/s11419-007-0039-1.
- "Fentanyl receptor assay. II. Utilization of a radioreceptor assay for the analysis of fentanyl analogs in urine". J Anal Toxicol 16 (1): 36–41. 1992. doi:10.1093/jat/16.1.36. PMID 1322477.
- "Evaluation of new compounds for opioid activity: 1987 annual report". NIDA Res. Monogr. 81: 543–90. 1988. PMID 3136388.
- "Dependence studies of new compounds in the rhesus monkey, rat, and mouse, 1987". NIDA Res. Monogr. 81: 485–542. 1988. PMID 3136386.
- "Carbon-13 nuclear magnetic resonance spectra of fentanyl analogs". Journal of Heterocyclic Chemistry 26 (3): 677–686. 2009. doi:10.1002/jhet.5570260329.
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