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Details

Stereochemistry ACHIRAL
Molecular Formula 2C11H17NO3.H2O4S
Molecular Weight 520.594
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MESCALINE HEMISULFATE

SMILES

OS(O)(=O)=O.COC1=CC(CCN)=CC(OC)=C1OC.COC2=CC(CCN)=CC(OC)=C2OC

InChI

InChIKey=FXAXLGPRODRRHB-UHFFFAOYSA-N
InChI=1S/2C11H17NO3.H2O4S/c2*1-13-9-6-8(4-5-12)7-10(14-2)11(9)15-3;1-5(2,3)4/h2*6-7H,4-5,12H2,1-3H3;(H2,1,2,3,4)

HIDE SMILES / InChI

Molecular Formula H2O4S
Molecular Weight 98.078
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C11H17NO3
Molecular Weight 211.2576
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P28223
Gene ID: 3356.0
Gene Symbol: HTR2A
Target Organism: Homo sapiens (Human)
PubMed

PubMed

TitleDatePubMed
1-[(1-methyl-1H-imidazol-2-yl)methyl]-4-phenylpiperidines as mGluR2 positive allosteric modulators for the treatment of psychosis.
2011-03-24
Investigating the mechanisms of hallucinogen-induced visions using 3,4-methylenedioxyamphetamine (MDA): a randomized controlled trial in humans.
2010-12-02
Novel, unifying mechanism for mescaline in the central nervous system: electrochemistry, catechol redox metabolite, receptor, cell signaling and structure activity relationships.
2010-08-19
Development and clinical application of an LC-MS-MS method for mescaline in urine.
2008-04
The analysis and distribution of mescaline in postmortem tissues.
2003-09
Synthesis and 5-HT2A radioligand receptor binding assays of DOMCl and DOMOM, two novel 5-HT2A receptor ligands.
2003-06
Jekyll and Hyde revisited: paradoxes in the appreciation of drug experiences and their effects on creativity.
2002-11-09
Interactions of amphetamine analogs with human liver CYP2D6.
1997-06-01
Chloroquine psychosis: a chemical psychosis?
1981-11
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:50:55 GMT 2025
Edited
by admin
on Mon Mar 31 17:50:55 GMT 2025
Record UNII
OQA17E96XM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MESCALINE HEMISULFATE
Common Name English
MESCALINE, SULFATE (2:1)
Preferred Name English
NSC-127486
Code English
BIS(3,4,5-TRIMETHOXYPHENETHYLAMMONIUM) SULPHATE
Systematic Name English
BENZENEETHANAMINE, 3,4,5-TRIMETHOXY-, SULFATE (2:1)
Systematic Name English
M (PSYCHEDELIC) HEMISULFATE
Common Name English
PHENETHYLAMINE, 3,4,5-TRIMETHOXY-, SULFATE (2:1)
Systematic Name English
3,4,5-trimethoxyphenethylamine hemisulfate
Common Name English
Code System Code Type Description
CAS
1152-76-7
Created by admin on Mon Mar 31 17:50:55 GMT 2025 , Edited by admin on Mon Mar 31 17:50:55 GMT 2025
NON-SPECIFIC STOICHIOMETRY
CAS
642-73-9
Created by admin on Mon Mar 31 17:50:55 GMT 2025 , Edited by admin on Mon Mar 31 17:50:55 GMT 2025
PRIMARY
FDA UNII
OQA17E96XM
Created by admin on Mon Mar 31 17:50:55 GMT 2025 , Edited by admin on Mon Mar 31 17:50:55 GMT 2025
PRIMARY
NSC
127486
Created by admin on Mon Mar 31 17:50:55 GMT 2025 , Edited by admin on Mon Mar 31 17:50:55 GMT 2025
PRIMARY
ECHA (EC/EINECS)
211-389-3
Created by admin on Mon Mar 31 17:50:55 GMT 2025 , Edited by admin on Mon Mar 31 17:50:55 GMT 2025
PRIMARY
PUBCHEM
21115064
Created by admin on Mon Mar 31 17:50:55 GMT 2025 , Edited by admin on Mon Mar 31 17:50:55 GMT 2025
PRIMARY
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ACTIVE MOIETY