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MLD-41

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
MLD-41
Clinical data
Other namesMLD-41;N1-Methyl-Lysergic Acid Diethylamide; 1-Methyl-LSD; 1-Methyl-N,N-Diethyllysergamide; Methyl-LSD
Routes of
administration
Oral[1][2]
Drug classSerotonergic psychedelic;Hallucinogen
Identifiers
  • (8β)-N,N-Diethyl-1,6-dimethyl-9,10-didehydroergoline-8-carboxamide
CAS Number
PubChemCID
ChemSpider
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC21H27N3O
Molar mass337.467 g·mol−1
3D model (JSmol)
  • O=C(N(CC)CC)[C@@H]3/C=C2/c4cccc1c4c(cn1C)C[C@H]2N(C3)C
  • InChI=1S/C21H27N3O/c1-5-24(6-2)21(25)15-10-17-16-8-7-9-18-20(16)14(12-22(18)3)11-19(17)23(4)13-15/h7-10,12,15,19H,5-6,11,13H2,1-4H3/t15-,19-/m1/s1 checkY
  • Key:VQZYKSWQIQANKB-DNVCBOLYSA-N checkY
  (verify)

MLD-41, also known as1-methyl-LSD, is apsychedelic drug of thelysergamide family related tolysergic acid diethylamide (LSD).[1][2] It has about 33% of thepsychoactivepotency of LSD.[1][2] It has been studied with regard tocross-tolerance with LSD.[3] Extensivemetabolism of other 1-methylated lysergamides to theirsecondary aminederivatives, for instancemethysergide (1-methylmethylergometrine) conversion intomethylergometrine, has been observed.[4][5]

Interactions

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See also:Psychedelic drug § Interactions, andTrip killer § Serotonergic psychedelic antidotes

See also

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References

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  1. ^abcJacob P, Shulgin AT (1994)."Structure-activity relationships of the classic hallucinogens and their analogs"(PDF).NIDA Res Monogr.146:74–91.PMID 8742795. Archived fromthe original(PDF) on August 5, 2023.
  2. ^abcHoffer A (1965). "D-Lysergic acid diethylamide (LSD): A review of its present status".Clin Pharmacol Ther.6:183–255.doi:10.1002/cpt196562183.PMID 14288188.
  3. ^Abramson HA, Rolo A, Sklarofsky B, Stache J (January 1960). "Production of cross-tolerance to psychosis-producing doses of lysergic acid diethylamide and psilocybin".The Journal of Psychology.49 (1):151–154.doi:10.1080/00223980.1960.9916396.
  4. ^Majrashi M, Ramesh S, Deruiter J, Mulabagal V, Pondugula S, Clark R, Dhanasekaran M (2017). "Multipotent and Poly-therapeutic Fungal Alkaloids of Claviceps purpurea". In Agrawal DC, Tsay HS, Shyur LF, Wu YC, Wang SY (eds.).Medicinal Plants and Fungi: Recent Advances in Research and Development. Medicinal and Aromatic Plants of the World. Vol. 4. pp. 229–252.doi:10.1007/978-981-10-5978-0_8.ISBN 978-981-10-5977-3.ISSN 2352-6831.Metabolites of methysergide also exhibit pharmacological activity. Methylergometrine (one of methysergide's metabolites) is responsible for methysergide's therapeutic effects regarding migraine treatment (Müller-Schweinitzer and Tapparelli 1986). [...] The systemic availability of methysergide after oral administration is only 13%, due to a high degree of first-pass metabolism by N-1 demethylation to methylergometrine. After oral administration, the plasma concentrations of the metabolite are considerably higher than those of the parent drug, and the area under the plasma concentration curve (AUC) for methylergometrine is more than ten times greater than for methysergide.
  5. ^Müller-Schweinitzer E, Tapparelli C (March 1986). "Methylergometrine, an active metabolite of methysergide".Cephalalgia: An International Journal of Headache.6 (1):35–41.doi:10.1046/j.1468-2982.1986.0601035.x.PMID 3698092.S2CID 5778173.

External links

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