3-MeO-PCMo

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3-MeO-PCMo
Legal status
Legal status
Identifiers
  • 4-[1-(3-methoxyphenyl)cyclohexyl]morpholine
CAS Number
PubChem CID
ChemSpider
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC17H25NO2
Molar mass275.392 g·mol−1
3D model (JSmol)
  • COC1=CC(C2(N3CCOCC3)CCCCC2)=CC=C1
  • InChI=1S/C17H25NO2/c1-19-16-7-5-6-15(14-16)17(8-3-2-4-9-17)18-10-12-20-13-11-18/h5-7,14H,2-4,8-13H2,1H3
  • Key:BOGOEDFWPOXWQE-UHFFFAOYSA-N

3-MeO-PCMo is a dissociative anesthetic drug which is similar in structure to phencyclidine[1][2] and been sold online as a designer drug.[3][4] The inhibitory effect of 3-MeO-PCMo on the reduction in the density of the drebrin clusters by NMDAR stimulation with glutamate acid is lower than that of PCP or 3-MeO-PCP, with IC50 values of 26.67 μM (3-MeO-PCMo), 2.02 μM (PCP) and 1.51 μM (3-MeO-PCP).[5]

See also

References

  1. ^ Ahmadi, Abbas; Khalili, Mohsen; Hajikhani, Ramin; Naserbakht, Moslem (April 2011). "New morpholine analogues of phencyclidine: Chemical synthesis and pain perception in rats". Pharmacology Biochemistry and Behavior. 98 (2): 227–233. doi:10.1016/j.pbb.2010.12.019. ISSN 0091-3057. PMID 21215770.
  2. ^ Abiero, Arvie; Botanas, Chrislean Jun; Custodio, Raly James; Sayson, Leandro Val; Kim, Mikyung; Lee, Hyun Jun; Kim, Hee Jin; Lee, Kun Won; Jeong, Youngdo; Seo, Joung-Wook; Ryu, In Soo; Lee, Yong Sup; Cheong, Jae Hoon (December 2019). "4-MeO-PCP and 3-MeO-PCMo, new dissociative drugs, produce rewarding and reinforcing effects through activation of mesolimbic dopamine pathway and alteration of accumbal CREB, deltaFosB, and BDNF levels". Psychopharmacology. doi:10.1007/s00213-019-05412-y. ISSN 1432-2072. PMID 31828394.
  3. ^ Colestock, Tristan; Wallach, Jason; Mansi, Matt; Filemban, Nadine; Morris, Hamilton; Elliott, Simon P.; Westphal, Folker; Brandt, Simon D.; Adejare, Adeboye (February 2018). "Syntheses, analytical and pharmacological characterizations of the 'legal high' 4-[1-(3-methoxyphenyl)cyclohexyl]morpholine (3-MeO-PCMo) and analogues". Drug Testing and Analysis. 10 (2): 272–283. doi:10.1002/dta.2213. ISSN 1942-7611. PMID 28513099.
  4. ^ "3-MeO-PCMo". New Synthetic Drugs Database. Archived from the original on 2016-07-03. Retrieved 2016-02-09.
  5. ^ Mitsuoka, Toshinari; Hanamura, Kenji; Koganezawa, Noriko; Kikura-Hanajiri, Ruri; Sekino, Yuko; Shirao, Tomoaki (September–October 2019). "Assessment of NMDA receptor inhibition of phencyclidine analogues using a high-throughput drebrin immunocytochemical assay". Journal of Pharmacological and Toxicological Methods. 99: 106583. doi:10.1016/j.vascn.2019.106583. ISSN 1056-8719. PMID 31082488.