A7127

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A7127

Sigma

 

Agmatine sulfate salt

≥97%, powder

Synonym:1-Amino-4-guanidinobutane sulfate salt, 4-Guanidinobutylamine sulfate salt, N-(4-Aminobutyl)guanidine sulfate salt
CAS Number:2482-00-0
Linear Formula:H2N(CH2)4NHC(=NH)NH2·H2SO4
Molecular Weight:228.27
Beilstein Registry Number:3918807
EC Number:219-617-3
MDL number:MFCD00013109
PubChem Substance ID:24277749

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Description

Biochem/physiol ActionsPutative endogenous neurotransmitter at imidazoline receptors; displaces clonidine at α2-adrenergic and at imidazoline receptors; blocks NMDA-activated ion channels in hippocampal neurons.

Properties

assay≥97%
formpowder
color white to off-white
mp234-238 °C(lit.)
solubilityH2O: 50 mg/mL
 ethanol:  insoluble
Gene Informationhuman ... ADRA2A(150), ADRA2B(151), ADRA2C(152), GRIN1(2902), GRIN2A(2903), GRIN2B(2904), GRIN2C(2905), GRIN2D(2906), GRINA(2907)

Safety

Personal Protective EquipmentEyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Safety Statements22-24/25
WGK Germany3

References

referenceReis, D.J., and Regunathan, S., Is agmatine a novel neurotransmitter in brain? Trends Pharmacol. Sci. 21, 187-193, (2000) Abstract
 Yang, Y.C., and Reis, D.J., Agmatine selectively blocks the N-methyl-D-aspartate subclass of glutamate receptor channels in rat hippocampal neurons. J. Pharmacol. Exp. Ther. 288, 544-549, (1999) Abstract
 Li, et al., Agmatine: An endogenous clonidine-displacing substance in the brain. Science 263, 966, (1994) Abstract
MerckMerck 13,188
BeilsteinBeil. 4,IV,1291
 FT-IR 2 (1), 1392:C / FT-IR 1 (1), 821:B / FT-NMR 1 (1), 1330:A / IR-Spectra (2), 430:H / IR-Spectra (3), 487:C / NMR-Reference 2 (1), 680:C / RegBook 1 (1), 965:J / Sigma FT-IR 1 (2), 249:C / Structure Index 1, 150:C:4