From Wikipedia, the free encyclopedia
U-48800
Identifiers
  • 2-(2,4-dichlorophenyl)-N-[(1S,2S)-2-(dimethylamino)cyclohexyl]-N-methylacetamide
CAS Number
PubChem CID
Chemical and physical data
FormulaC17H24Cl2N2O
Molar mass343.29 g·mol−1
3D model ( JSmol)
  • CN(C)[C@H]1CCCC[C@@H]1N(C)C(=O)CC2=C(C=C(C=C2)Cl)Cl
  • InChI=1S/C17H24Cl2N2O/c1-20(2)15-6-4-5-7-16(15)21(3)17(22)10-12-8-9-13(18)11-14(12)19/h8-9,11,15-16H,4-7,10H2,1-3H3/t15-,16-/m0/s1
  • Key:FKUWIGXXBMULOI-HOTGVXAUSA-N

U-48800 is an opioid analgesic which has been sold as a designer drug. Unlike U-47700, it is primarily active as a kappa opioid receptor agonist with only moderate affinity at the mu opioid receptor. Nevertheless, it has still appeared on the recreational drug market, often as a component of combinations with other drugs, and has been linked to numerous drug overdose cases. [1] [2] [3] [4] [5]


See also

References

  1. ^ Gampfer TM, Richter LH, Schäper J, Wagmann L, Meyer MR (October 2019). "Toxicokinetics and analytical toxicology of the abused opioid U-48800 - in vitro metabolism, metabolic stability, isozyme mapping, and plasma protein binding". Drug Testing and Analysis. 11 (10): 1572–1580. doi: 10.1002/dta.2683. PMID  31424163.
  2. ^ Baumann MH, Tocco G, Papsun DM, Mohr AL, Fogarty MF, Krotulski AJ (November 2020). "U-47700 and Its Analogs: Non-Fentanyl Synthetic Opioids Impacting the Recreational Drug Market". Brain Sciences. 10 (11): 895. doi: 10.3390/brainsci10110895. PMC  7700279. PMID  33238449.
  3. ^ Fogarty MF, Mohr AL, Papsun DM, Logan BK (February 2022). "Analysis of the Illicit Opioid U-48800 and Related Compounds by LC-MS-MS and Case Series of Fatalities Involving U-48800". Journal of Analytical Toxicology. 46 (1): 17–24. doi: 10.1093/jat/bkaa180. PMID  33237987.
  4. ^ Otte L, Wilde M, Auwärter V, Grafinger KE (July 2022). "Investigation of the μ- and κ-opioid receptor activation by eight new synthetic opioids using the [35 S]-GTPγS assay: U-47700, isopropyl U-47700, U-49900, U-47931E, N-methyl U-47931E, U-51754, U-48520, and U-48800". Drug Testing and Analysis. 14 (7): 1187–1199. doi: 10.1002/dta.3238. PMID  35142070.
  5. ^ Amend N, Thiermann H, Worek F, Wille T (June 2023). "A pharmacologically pre-contracted smooth muscle bowel model for the study of highly-potent opioid receptor agonists and antagonists". Toxicology Letters. 382: 41–46. doi: 10.1016/j.toxlet.2023.05.010. PMID  37245850.



From Wikipedia, the free encyclopedia
U-48800
Identifiers
  • 2-(2,4-dichlorophenyl)-N-[(1S,2S)-2-(dimethylamino)cyclohexyl]-N-methylacetamide
CAS Number
PubChem CID
Chemical and physical data
FormulaC17H24Cl2N2O
Molar mass343.29 g·mol−1
3D model ( JSmol)
  • CN(C)[C@H]1CCCC[C@@H]1N(C)C(=O)CC2=C(C=C(C=C2)Cl)Cl
  • InChI=1S/C17H24Cl2N2O/c1-20(2)15-6-4-5-7-16(15)21(3)17(22)10-12-8-9-13(18)11-14(12)19/h8-9,11,15-16H,4-7,10H2,1-3H3/t15-,16-/m0/s1
  • Key:FKUWIGXXBMULOI-HOTGVXAUSA-N

U-48800 is an opioid analgesic which has been sold as a designer drug. Unlike U-47700, it is primarily active as a kappa opioid receptor agonist with only moderate affinity at the mu opioid receptor. Nevertheless, it has still appeared on the recreational drug market, often as a component of combinations with other drugs, and has been linked to numerous drug overdose cases. [1] [2] [3] [4] [5]


See also

References

  1. ^ Gampfer TM, Richter LH, Schäper J, Wagmann L, Meyer MR (October 2019). "Toxicokinetics and analytical toxicology of the abused opioid U-48800 - in vitro metabolism, metabolic stability, isozyme mapping, and plasma protein binding". Drug Testing and Analysis. 11 (10): 1572–1580. doi: 10.1002/dta.2683. PMID  31424163.
  2. ^ Baumann MH, Tocco G, Papsun DM, Mohr AL, Fogarty MF, Krotulski AJ (November 2020). "U-47700 and Its Analogs: Non-Fentanyl Synthetic Opioids Impacting the Recreational Drug Market". Brain Sciences. 10 (11): 895. doi: 10.3390/brainsci10110895. PMC  7700279. PMID  33238449.
  3. ^ Fogarty MF, Mohr AL, Papsun DM, Logan BK (February 2022). "Analysis of the Illicit Opioid U-48800 and Related Compounds by LC-MS-MS and Case Series of Fatalities Involving U-48800". Journal of Analytical Toxicology. 46 (1): 17–24. doi: 10.1093/jat/bkaa180. PMID  33237987.
  4. ^ Otte L, Wilde M, Auwärter V, Grafinger KE (July 2022). "Investigation of the μ- and κ-opioid receptor activation by eight new synthetic opioids using the [35 S]-GTPγS assay: U-47700, isopropyl U-47700, U-49900, U-47931E, N-methyl U-47931E, U-51754, U-48520, and U-48800". Drug Testing and Analysis. 14 (7): 1187–1199. doi: 10.1002/dta.3238. PMID  35142070.
  5. ^ Amend N, Thiermann H, Worek F, Wille T (June 2023). "A pharmacologically pre-contracted smooth muscle bowel model for the study of highly-potent opioid receptor agonists and antagonists". Toxicology Letters. 382: 41–46. doi: 10.1016/j.toxlet.2023.05.010. PMID  37245850.




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