LSM-775

Chemical compound
  • DE: NpSG (Industrial and scientific use only)
  • UK: Under Psychoactive Substances Act
  • Illegal in France[1]
Pharmacokinetic dataMetabolismhepaticExcretionrenalIdentifiers
  • (8β)-6-Methyl-8-(morpholin-4-ylcarbonyl)-9,10-didehydroergoline
CAS Number
  • 4314-63-0 checkY
PubChem CID
  • 199507
ChemSpider
  • 172695 checkY
UNII
  • 168Y0PXM7S
CompTox Dashboard (EPA)
  • DTXSID50195718 Edit this at Wikidata
Chemical and physical dataFormulaC20H23N3O2Molar mass337.423 g·mol−13D model (JSmol)
  • Interactive image
  • O=C(N1CCOCC1)[C@@H]5C=C4c2cccc3c2c(c[nH]3)C[C@H]4N(C)C5
InChI
  • InChI=1S/C20H23N3O2/c1-22-12-14(20(24)23-5-7-25-8-6-23)9-16-15-3-2-4-17-19(15)13(11-21-17)10-18(16)22/h2-4,9,11,14,18,21H,5-8,10,12H2,1H3/t14-,18-/m1/s1 checkY
  • Key:OTQWCDNEJVKXKG-RDTXWAMCSA-N checkY
  (verify)

N-Morpholinyllysergamide (LSM-775) is a derivative of ergine.[2] It is less potent than LSD but is reported to have some LSD-like effects at doses ranging from 75 to 700 micrograms and a shorter duration. There are fewer signs of cardiovascular stimulation and peripheral toxicity with LSM-775 compared to LSD.[3][dubious – discuss]

See also

References

  1. ^ "Arrêté du 20 mai 2021 modifiant l'arrêté du 22 février 1990 fixant la liste des substances classées comme stupéfiants" [Order of May 20, 2021 amending the order of February 22, 1990 setting the list of substances classified as narcotics]. www.legifrance.gouv.fr (in French). 20 May 2021.
  2. ^ Gogerty JH, Dille JM (July 1957). "Pharmacology of d-lysergic acid morpholide (LSM)". The Journal of Pharmacology and Experimental Therapeutics. 120 (3): 340–8. PMID 13476356.
  3. ^ Shulgin A, Shulgin A. "TiHKAL #26, LSD-25". Erowid.


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