γ-D-Glutamylaminomethylsulfonic acid

Modify Date: 2026-07-16 15:26:41

γ-D-Glutamylaminomethylsulfonic acid Structure
γ-D-Glutamylaminomethylsulfonic acid structure
Common Name γ-D-Glutamylaminomethylsulfonic acid
CAS Number 90237-02-8 Molecular Weight 240.23400
Density 1.593g/cm3 Boiling Point N/A
Molecular Formula C6H12N2O6S Melting Point N/A
MSDS USA Flash Point N/A

 Use of γ-D-Glutamylaminomethylsulfonic acid


γ-D-Glutamylaminomethylsulfonic acid is a glutamic acid derivative[1].

 Names

This table lists Chinese names, IUPAC names and various aliases of this chemical substance.

Name gams
Synonym More Synonyms

 γ-D-Glutamylaminomethylsulfonic acid Biological Activity

This table contains bioactivity, target information and biological‑assay experimental data of this compound.

Description γ-D-Glutamylaminomethylsulfonic acid is a glutamic acid derivative[1].
Related Catalog
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

 Chemical & Physical Properties

This table shows physicochemical parameters including melting point, boiling point, density, solubility and optical rotation. Missing data is marked as N/A.

Density 1.593g/cm3
Molecular Formula C6H12N2O6S
Molecular Weight 240.23400
Exact Mass 240.04200
PSA 155.17000
LogP 0.31200
Index of Refraction 1.566

 MSDS

This table provides MSDS information including hazard classification, first‑aid, fire‑fighting, spill handling, operation and storage instructions.

 Safety Information

This table covers safety warnings, protective measures, incompatible substances and disposal guidelines for this compound.

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport

 Articles32

More Articles

This table lists relevant public references with title, journal and publication metadata for this compound.

Effects of some excitatory amino acid antagonists on imipenem-induced seizures in DBA/2 mice.

Brain Res. 671(1) , 131-40, (1995)

The behavioural and convulsant effects of imipenem (Imi), a carbapenem derivative, were studied after intraperitoneal (i.p.) or intracerebroventricular (i.c.v.) administration in DBA/2 mice, a strain ...

Glutamate and vasopressin interact to control scent marking in Syrian hamsters (Mesocricetus auratus).

Brain Res. 731(1-2) , 213-6, (1996)

In Syrian hamsters, vasopressin (AVP) in the medial preoptic-anterior hypothalamus (MPOA-AH) controls a form of scent marking called flank marking. Another neurochemical signal that may interact with ...

Excitatory neurotransmitters in the lateral habenula and pedunculopontine nucleus of rat modulate limbic seizures induced by pilocarpine.

Brain Res. 591(2) , 209-22, (1992)

The involvement of the excitatory neurotransmitter system in the lateral habenula and pedunculopontine nucleus in the initiation and propagation of limbic seizures induced by pilocarpine has been inve...

 γ-D-Glutamylaminomethylsulfonic acidBioassay

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This table contains target information, in‑vitro & in‑vivo assay data for this compound.

Name: 96-well format Chlamydomonas reinhardtii Algae Gravitaxis Assay to measure the differ...
Source: University of Pittsburgh Molecular Library Screening Center
Target: N/A
External Id: MH081217, Chlamydomonas reinhardtii Gravitaxis Assay to Identify Small Molecule Inhibitors of Cilia.
Name: Inhibition of neurosphere proliferation of mouse neural precursor cells by MTT assay
Source: ChEMBL
Target: N/A
External Id: CHEMBL1266185
Name: Screen for inhibitors of RMI FANCM (MM2) intereaction
Source: 11908
Target: N/A
External Id: RMI-FANCM-MM2
Name: Small-molecule inhibitors of ST2 (IL1RL1)
Source: 20881
Target: interleukin-1 receptor-like 1 isoform [homo sapiens]
External Id: ST2_IL33_Inhibitors_Primary_Screening_77700
Name: Cell-based high throughput primary assay to identify activators of GPR151
Source: The Scripps Research Institute Molecular Screening Center
Target: RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id: GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
Name: AlphaScreen-based biochemical high throughput primary assay to identify activators of...
Source: The Scripps Research Institute Molecular Screening Center
Target: N/A
External Id: FBW7_ACT_ALPHA_1536_1X%ACT PRUN
Name: AlphaScreen-based biochemical high throughput primary assay to identify inhibitors of...
Source: The Scripps Research Institute Molecular Screening Center
External Id: MITF_INH_Alpha_1536_1X%INH PRUN
Name: The chemical genetic matrix (CGM) dataset as reported in Wildenhain et al. (2015) Pre...
Source: 11924
Target: N/A
External Id: CGM data for Cell Systems paper Dec 2015
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 Synonyms

This table collects all English aliases, systematic names and CAS‑related synonyms of the compound.

N5-(Sulfomethyl)-D-glutamine
G-D-GLUTAMYLAMINOMETHYLSULFONIC ACID
D-R-GLUTAMYLAMINO METHANESULFONIC
N-(Sulfomethyl)-D-glutamine

 γ-D-Glutamylaminomethylsulfonic acid | FAQ

This section contains frequently‑asked‑questions about this compound, including basic parameters, properties, storage conditions and corresponding answers.

Q: What English synonyms does gams have?
A: English synonyms of gams: N5-(Sulfomethyl)-D-glutamine, G-D-GLUTAMYLAMINOMETHYLSULFONIC ACID, D-R-GLUTAMYLAMINO METHANESULFONIC, N-(Sulfomethyl)-D-glutamine.
Q: What is the molecular formula of gams?
A: Molecular formula of gams is C6H12N2O6S.
Q: What is the LogP of gams?
A: LogP of gams is 0.31200.
Q: What is the polar surface area (PSA) of gams?
A: Polar surface area (PSA) of gams is 155.17000.
Q: What are the uses of gams?
A: Main uses of gams: γ-D-Glutamylaminomethylsulfonic acid is a glutamic acid derivative[1].
Q: What is the CAS number of gams?
A: CAS number of gams is 90237-02-8.
Q: What is the English name of gams?
A: The English name of gams is gams.
Q: What is the molecular weight of gams?
A: Molecular weight of gams is 240.23400.

 γ-D-Glutamylaminomethylsulfonic acidfactory

This table lists manufacturers and suppliers of this compound, including vendor names and product supply reference information.

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