MEM

MEM

MEM

Psychoactive Research chemicals are new synthetic substances that are structurally similar to the original drug, while being functional analogs. Research on the effects of, and treatment for, abuse of these drugs is limited due to the fact that they’re fairly new and have avoided mainstream notice. Research chemicals do not have a lot of human consumption data, and thus harm-reduction and special care should be taken if choosing to ingest them.

Psychedelics are drugs which cause profound changes in a one’s perceptions of reality, otherwise known as hallucinations. While under the influence of hallucinogens, users might see images, hear sounds or feel sensations. These chemicals offer some of the most intense psychological experiences and care should be taken when ingesting them.

Experimental drugs have extremely limited human consumption data. There is not enough reliable information about this substance. This is most likely because the substance is is not very old. Information on these substances is limite and incomplete. Please be cautioned. Always practice harm reduction.

Disclaimer: Psychedelic drugs offer some of the most power and intense psychological experiences. Additionally these substances are illegal in many places. We understand that even though these substances are illegal, their use occurs frequently. We do not condone breaking of the law. By providing accurate information about these substances, we encourage the user to make responsible decisions and practice harm reduction.

Read the full disclaimer here.

Practice Harm Reduction. Proceed with Caution.

Description

MEM

Also known as:

  • (8β)-N-[(1S)-1-(hydroxymethyl)propyl]-6-methyl-9,10-didehydroergoline-8-carboxamide
  • (8β)-N-[(2S)-1-Hydroxy-2-butanyl]-6-methyl-9,10-didehydroergolin-8-carboxamid[German][ACD/IUPAC Name]
  • (8β)-N-[(2S)-1-Hydroxy-2-butanyl]-6-methyl-9,10-didehydroergoline-8-carboxamide[ACD/IUPAC Name]
  • (8β)-N-[(2S)-1-Hydroxy-2-butanyl]-6-méthyl-9,10-didéhydroergoline-8-carboxamide[French][ACD/IUPAC Name]
  • (8β)-N-[(2S)-1-Hydroxybutan-2-yl]-6-methyl-9,10-didehydroergoline-8-carboxamide
  • [8b(S)]-9,10-Didehydro-N-[1-(hydroxymethyl)propyl]-6-methylergoline-8-carboxamide
  • D-Lysergic Acid (+)-Butanolamide-(2)
  • D-Lysergic acid-(+)-butanolamide-(2)
  • Ergoline-8-carboxamide, 9,10-didehydro-N-[(1S)-1-(hydroxymethyl)propyl]-6-methyl-, (8β)-[ACD/Index Name]
  • Methylergobasine
  • méthylergométrine[French][INN]
  • methylergometrinum[Latin][INN]
  • metilergometrina[Spanish][INN]
  • N-[a-(Hydroxymethyl)propyl]-D-Iysergamide
  • W53L6FE61V
  • метилэргометрин[Russian][INN]
  • ميثيلإيرغوميترين[Arabic][INN]
  • 甲麦角新碱[Chinese][INN]
  • (4R,7R)-N-[(2S)-1-hydroxybutan-2-yl]-6-methyl-6,11-diazatetracyclo[7.6.1.02,7.012,16]hexadeca-1(16),2,9,12,14-pentaene-4-carboxamide
  • (6aR,9R)-N-[(2S)-1-hydroxybutan-2-yl]-7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide
  • 9,10-Didehydro-N-(1-(hydroxymethyl)propyl)-6-methylergoline-8-carboxamide
  • 9,10-Didehydro-N-(α-(hydroxymethyl)propyl)-6-methyl-ergoline-8-β-carboxamide
  • 9,10-Didehydro-N-[1-(hydroxymethyl)-propyl]-D-lysergamide
  • 9,10-Didehydro-N-[1-(hydroxymethyl)-propyl]-D-lysergamide; D-lysergic acid 1-butanolamide; Methergine; Methylergobasin; Methylergometrin; M??thylergom??trine; Methylergometrine; Methylergometrinum; Methylergonovine; Metilergometrina
  • 9,10-Didehydro-N-[1-(hydroxymethyl)-propyl]-D-lysergamide; D-lysergic acid 1-butanolamide; Methergine; Methylergobasin; Methylergometrin; Méthylergométrine; Methylergometrine; Methylergometrinum; Methylergonovine; Metilergometrina
  • Basofortina[Trade name]
  • Basofortina (Trade name)
  • Basofortina; Bledstop; Demergin; Ergogin; Ergomed; Ergomin; Ergotyl; Expogin; Glomethyl; Ingagen-M; Mem; Mergot; Mergotrex; Metenarin; Metermin; Méthergin; Methergin; Metherinal; Metherspan; Methovin; Methylergobrevin; Methylergometrin; Metilat; Metiler; Metilergometrina; Metrine; Metrol; Metvell; Myomergin; Myometril; Neo-ergo; Partan M; Pospargin; Satergin; Usamema; Utergin; Uterine; Uterjin; Uterowin; Utesel
  • Biomol-NT_000154
  • Bledstop
  • Bledstop (Trade name)
  • BPBio1_000442
  • BPBio1_000581
  • BSPBio_000527
  • BSPBio_002023
  • Demergin
  • Demergin (Trade name)
  • D-lysergic acid 1-butanolamide
  • D-Lysergic acid-dl-hydroxybutylamide-2
  • EINECS 204-027-0
  • Ergogin
  • Ergogin (Trade name)
  • Ergoline-8-carboxamide, 9,10-didehydro-N-(1-(hydroxymethyl)propyl)-6-methyl-, (8β(S))-
  • Ergoline-8-β-carboxamide, 9,10-didehydro-N-((S)-1-(hydroxymethyl)propyl)-6-methyl-
  • Ergomed
  • Ergomed (Trade name)
  • Ergometrine, methyl-
  • Ergomin
  • Ergomin (Trade name)
  • Ergotyl
  • Ergotyl (Trade name)
  • Expogin
  • Expogin (Trade name)
  • Glomethyl
  • Glomethyl (Trade name)
  • IDI1_000357
  • Ingagen-M
  • Ingagen-M (Trade name)
  • Lopac0_000794
  • Lysergamide, N-((S)-1-(hydroxymethyl)propyl)-
  • Lysergic acid butanolamide
  • M??thergin
  • M??thylergom??trine
  • MEM
  • Mem (Trade name)
  • Mergot
  • Mergot (Trade name)
  • Mergotrex
  • Mergotrex (Trade name)
  • Metenarin[Trade name]
  • Metenarin (Trade name)
  • Metermin
  • Metermin (Trade name)
  • Methergen
  • Methergin[Trade name]
  • Méthergin
  • Methergin (Trade name)
  • Méthergin (Trade name)
  • Methergine Methylergonovine
  • Methergine®
  • Methergine®|methylergobasin
  • Metherinal
  • Metherinal (Trade name)
  • Metherspan
  • Metherspan (Trade name)
  • Methovin
  • Methovin (Trade name)
  • Methylergobasin
  • Methylergobrevin[Trade name]
  • Methylergobrevin (Trade name)
  • Methylergometrin
  • Methylergometrin (Trade name)
  • Méthylergométrine
  • Methylergometrine maleate[JP15]
  • Methylergometrinum
  • Methylergometrinum [INN-Latin]
  • Methylergonovin
  • Metilat
  • Metilat (Trade name)
  • Metiler
  • Metiler (Trade name)
  • Metilergometrina
  • Metilergometrina (Trade name)
  • Metilergometrina [DCIT]
  • Metilergometrinio[Spanish][INN]
  • Metilergometrinio [INN-Spanish]
  • Metrine
  • Metrine (Trade name)
  • Metrol
  • Metrol (Trade name)
  • Metvell
  • Metvell (Trade name)
  • Myomergin
  • Myomergin (Trade name)
  • Myometril
  • Myometril (Trade name)
  • N-(α-(Hydroxymethyl)propyl)-D-lysergamide
  • NCGC00024646-03
  • Neo-ergo
  • Neo-ergo (Trade name)
  • Partan M
  • Partan M (Trade name)
  • Partergin
  • Pospargin
  • Pospargin (Trade name)
  • Prestwick3_000374
  • Satergin
  • Satergin (Trade name)
  • Spectrum5_001879
  • UNII:W53L6FE61V
  • UNII-W53L6FE61V
  • Usamema
  • Usamema (Trade name)
  • Utergin
  • Utergin (Trade name)
  • Uterine
  • Uterine (Trade name)
  • Uterjin
  • Uterjin (Trade name)
  • Uterowin
  • Uterowin (Trade name)
  • Utesel

A rare stimulant, psychedelic and amphetamine discovered by Alexander Shulgin. Related to the DOx class of drugs, little is known about this obscure compound’s pharmacology, however it is likely to be potent and have a long duration.

Summary

History

Chemistry

MEM

MEM

Common NameMethylergometrine
Systematic nameMethylergometrine
FormulaC_{20}H_{25}N_{3}O_{2}
SMILESCC[[email protected]@H](CO)NC(=O)[[email protected]]1CN([[email protected]@H]2Cc3c[nH]c4c3c(ccc4)C2=C1)C
Std. InChiInChI=1S/C20H25N3O2/c1-3-14(11-24)22-20(25)13-7-16-15-5-4-6-17-19(15)12(9-21-17)8-18(16)23(2)10-13/h4-7,9,13-14,18,21,24H,3,8,10-11H2,1-2H3,(H,22,25)/t13-,14+,18-/m1/s1
Std. InChiKeyUNBRKDKAWYKMIV-QWQRMKEZSA-N
Avg. Mass339.4314 Da
Molecular Weight339.4314
Monoisotopic Mass339.194672 Da
Nominal Mass339
ChemSpider ID7933

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Dosing Guide

Oral
Threshold15mg
Low15-25mg
Common25-35mg
Strong35-45mg+.

Duration

MEM Duration Data
OnsetWithin minutes
Duration8-16 hours
After-effects1-12 hours

Interactions and Synergies

There are no existing interaction or synergy data for this drug.

General Information

Experiences
Oral
Vaporization
Come up
Dosage
EffectsEuphoria, empathy, insight, brightened colour, Closed/Open eye visuals, enhanced tactile sensation, mental/physical stimulation, decreased appetite, pupil dilation, restlessness, change in perception, ego softening, sweating/chills, muscle tension, confusion, insomnia.
After Effects
Avoid
Warning
Risks
Test Kits
Marguis Test Result
Tolerance
Detection
Half-life
Advice
Note
Note 2:
Note 3:

Effects

Pharmacological Effects

Subjective Effects

Physical Effects

Psychological Effects

Visual Effects

Auditory Effects

Sensory Effects

Transpersonal Effects

Legal Status


References

    Resources

    1. Alfa Chemistry 113-42-8
    2. American Custom Chemicals Corp API0006820
    3. Aurora Fine Chemicals K18.030.485
    4. BGS International BG04337234
    5. BindingDB 50330860
    6. ChEBI CHEBI:92607
    7. ChemBank DivK1c_000357
    8. ChemBank KBio1_000357
    9. ChemBank KBio2_000743
    10. ChemBank KBio2_003311
    11. ChemBank KBio2_005879
    12. ChemBank KBio3_001523
    13. ChemBank KBioSS_000743
    14. ChemBank NINDS_000357
    15. ChemBank SPBio_000546
    16. ChemBank Spectrum_000263
    17. ChemBank Spectrum2_000613
    18. ChemBank Spectrum3_000502
    19. ChEMBL CHEMBL1201356
    20. ChemIDplus 000113428
    21. ChemIDplus 057432618
    22. Chemspace CSC020617820
    23. Collaborative Drug Discovery 436
    24. CSDeposition Service DB00353
    25. DiscoveryGate 5281072
    26. DiscoveryGate 8226
    27. DrugBank DB00353
    28. DSigDB d1_436
    29. DSigDB d3_1172
    30. DSigDB d3_1173
    31. DSigDB d4ctd_6315
    32. DSigDB d4ttd_9260
    33. eMolecules 1933812
    34. EPA DSSTox DTXCID303283
    35. FDA UNII - NLM UNII: W53L6FE61V
    36. FDA UNII - NLM W53L6FE61V
    37. Guide to PHARMACOLOGY 150
    38. Human Metabolome Database HMDB0014497
    39. Human Metabolome Database HMDB14497
    40. iChemical EBD268378
    41. Jean-Claude Bradley Open Melting Point Dataset 16879
    42. KEGG D00680
    43. KEGG D08207
    44. Laboratory Chemical Safety Summary 8226
    45. LeadScope LS-64363
    46. Mcule MCULE-5032066915
    47. PubChem 8226
    48. Royal Society of Chemistry 10.1039/C6NP00110F
    49. RSC Learn Chemistry Wiki Methylergometrine
    50. Serum Metabolome Database HMDB0014497
    51. Springer Nature Ergot Alkaloids
    52. Springer Nature Methylergometrine
    53. Springer Nature Methylergometrine
    54. Springer Nature Methylergometrine/ergotamine/methysergide
    55. Springer Nature Methylergometrine/oxytocin
    56. Springer Nature Methylergometrine/ritodrine
    57. Springer Nature Nifedipine and molsidomine suppress coronary artery spasm equally
    58. Springer Nature Oral methylergometrine after caesarean section reduces endometritis
    59. Springer Nature Oral misoprostol compared with conventional oxytocics
    60. Springer Nature Oxytocin
    61. Springer Nature Relief for headache sufferers
    62. The Merck Index Online cs000000012372
    63. Thieme Chemistry KD-13-0106
    64. Thomson Pharma 00056774
    65. Toxin, Toxin-Target Database T3D3686
    66. Urine Metabolome Database HMDB0014497
    67. VulcanChem VC184565
    68. Wikidata Q424477
    69. Wikipedia Methylergometrine
    70. xPharm 8940
    71. ZINC ZINC03831067

    Sources

    Information made possible with:

    1. PsychonautWiki is a community-driven online encyclopedia that aims to document the field of psychonautics in a comprehensive, scientifically-grounded manner.
    2. Erowid is a non-profit educational & harm-reduction resource with 60 thousand pages of online information about psychoactive drugs
    3. PubChem National Center for Bio Informatics
    4. Chemspider is a free chemical structure database providing fast access to over 34 million structures, properties and associated information.
    5. Wikipedia

    Additional APIs were used to construct this information. Thanks for ChemSpider, NCBI, PubChem etc.

    Data is constantly updated so please check back later to see if there is any more available information on this substance.