From Wikipedia, the free encyclopedia
Opioid analgesic designer drug
3,4-MDO-U-47700
N-[(1R,2R)-2-(dimethylamino)cyclohexyl]-N-methyl-1,3-benzodioxole-5-carboxamide
CAS Number
PubChem
CID
UNII
Formula C 17 H 24 N 2 O 3
Molar mass 304.390 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
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
μ-opioid receptor , with slightly higher potency than
morphine .
[1]
[2]
[3] It is illegal in Virginia.
[4]
See also
References
^
"3,4-metylendioxi-U-47700" (PDF) . Åklagarmyndigheten . Sweden. 2019.
^ 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 .
^ 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 .
^
"54.1-3446" . Code of Virginia . Commonwealth of Virginia.