3,4-MDO-U-47700

3,4-MDO-U-47700 is an opioid analgesic which has been sold as a designer drug, first appearing in 2017 after U-47700 itself was banned in various jurisdictions. It is less potent than U-47700 but is still a full agonist at the mu opioid receptor, with slightly higher potency than morphine.[1][2][3] It is illegal in Virginia.[4]

3,4-MDO-U-47700
Identifiers
  • N-[(1R,2R)-2-(dimethylamino)cyclohexyl]-N-methyl-1,3-benzodioxole-5-carboxamide
CAS Number
PubChem CID
UNII
Chemical and physical data
FormulaC17H24N2O3
Molar mass304.390 g·mol−1
3D model (JSmol)
  • CN(C)[C@@H]1CCCC[C@H]1N(C)C(=O)C2=CC3=C(C=C2)OCO3
  • InChI=1S/C17H24N2O3/c1-18(2)13-6-4-5-7-14(13)19(3)17(20)12-8-9-15-16(10-12)22-11-21-15/h8-10,13-14H,4-7,11H2,1-3H3/t13-,14-/m1/s1
  • Key:UUAVKYBZWVMWSM-ZIAGYGMSSA-N


See also

References
  1. "3,4-metylendioxi-U-47700" (PDF). Åklagarmyndigheten. Sweden. 2019.
  2. Popławska M, Bednarek E, Naumczuk B, Kozerski L, Błażewicz A (January 2021). "Identification and structure characterization of five synthetic opioids: 3, 4-methylenedioxy-U-47700, o-methyl-acetylfentanyl, 2-thiophenefentanyl, benzoylfentanyl and benzoylbenzylfentanyl". Forensic Toxicology. 39: 45–58. doi:10.1007/s11419-020-00539-6. S2CID 219935247.
  3. 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.
  4. "54.1-3446". Code of Virginia. Commonwealth of Virginia.


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