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Details

Stereochemistry ABSOLUTE
Molecular Formula C5H7NO4.Mg.BrH
Molecular Weight 250.33
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MAGNESIUM GLUTAMATE HYDROBROMIDE

SMILES

[Mg++].Br.N[C@@H](CCC([O-])=O)C([O-])=O

InChI

InChIKey=IMSNBENJLMCAJL-QTNFYWBSSA-L
InChI=1S/C5H9NO4.BrH.Mg/c6-3(5(9)10)1-2-4(7)8;;/h3H,1-2,6H2,(H,7,8)(H,9,10);1H;/q;;+2/p-2/t3-;;/m0../s1

HIDE SMILES / InChI

Molecular Formula BrH
Molecular Weight 80.912
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C5H7NO4
Molecular Weight 145.1134
Charge -2
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula Mg
Molecular Weight 24.305
Charge 2
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Magnesium glutamate hydrobromide (Psychoverlan) is a known sedative and muscle relaxant. In a long-term study 19 young females were treated with Psychoverlan capsules or syrup for an average of 11.4 months. Intolerance phenomena and side-effects were not seen. It was even decided to increase the standard dose. None of the patients developed brominism or bromine intoxication. The general state of health of 13 of the 19 subjects was improved by the harmonizing effect of the drug on psychic and vegetative functions. Tiredness and somnolence were not observed.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
PSYCHOVERLAN

Approved Use

Nervous system disorders
PubMed

PubMed

TitleDatePubMed
Synthesis and biological evaluation of (-)-6-O-desmethylcryptopleurine and analogs.
2015-01-15
No enhancing effects of calcium/magnesium salts of L-glutamate and L-ascorbate on tumor development in a rat medium-term multiorgan carcinogenesis bioassay.
1993-05
[Long-term treatment with psychoverlan in children and adolescents with behavior disorders].
1978-08-24
[The management of nervous disturbances with psychoverlan].
1974-05
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Rats were given diet containing 5% monocalcium di-L-glutamate tetrahydrate (Ca-glutamate), 2.5% monomagnesium di-L-glutamate tetrahydrate (Mg-glutamate), 5% L-glutamic acid, 5% monocalcium di-L-ascorbate dihydrate (Ca-ascorbate), 2.5% monomagnesium di-L-ascorbate dihydrate (Mg-ascorbate), or 5% L-ascorbic acid for 16 wk.
Unknown
Route of Administration: Oral
60 g (0.160 mol) magnesium-L-glutamate-tetrahydrate in a spherical flask were suhmerged in the rotary evaporator under a vacuum of 50 mbar in an oil bath that had been preheated to 190C. The separation of water and the formation of the magnesium-L-pyroglutamate began after 2 minutes and ended after 45 minutes, a solid being involved at each stage of the reaction.
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:10:07 GMT 2025
Edited
by admin
on Mon Mar 31 22:10:07 GMT 2025
Record UNII
5Q5ZYJ43UH
Record Status Validated (UNII)
Record Version
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Name Type Language
MAGNESIUM GLUTAMATE HYDROBROMIDE
WHO-DD  
Systematic Name English
L-GLUTAMIC ACID, MAGNESIUM SALT (1:1), HYDROBROMIDE
Preferred Name English
Magnesium glutamate hydrobromide [WHO-DD]
Common Name English
Code System Code Type Description
EVMPD
SUB14426MIG
Created by admin on Mon Mar 31 22:10:07 GMT 2025 , Edited by admin on Mon Mar 31 22:10:07 GMT 2025
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SMS_ID
100000076803
Created by admin on Mon Mar 31 22:10:07 GMT 2025 , Edited by admin on Mon Mar 31 22:10:07 GMT 2025
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PUBCHEM
171266
Created by admin on Mon Mar 31 22:10:07 GMT 2025 , Edited by admin on Mon Mar 31 22:10:07 GMT 2025
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FDA UNII
5Q5ZYJ43UH
Created by admin on Mon Mar 31 22:10:07 GMT 2025 , Edited by admin on Mon Mar 31 22:10:07 GMT 2025
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CAS
53459-38-4
Created by admin on Mon Mar 31 22:10:07 GMT 2025 , Edited by admin on Mon Mar 31 22:10:07 GMT 2025
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EPA CompTox
DTXSID10201622
Created by admin on Mon Mar 31 22:10:07 GMT 2025 , Edited by admin on Mon Mar 31 22:10:07 GMT 2025
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ECHA (EC/EINECS)
258-566-1
Created by admin on Mon Mar 31 22:10:07 GMT 2025 , Edited by admin on Mon Mar 31 22:10:07 GMT 2025
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