101443
Agmatine sulfate salt
Enzymatic decarboxylation product of arginine., 97%
Synonym(s):
1-Amino-4-guanidinobutane sulfate salt, 4-Guanidinobutylamine sulfate salt, N-(4-Aminobutyl)guanidine sulfate salt
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About This Item
Linear Formula:
H2N(CH2)4NHC(=NH)NH2·H2SO4
CAS Number:
Molecular Weight:
228.27
EC Number:
219-617-3
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
3918807
MDL number:
InChI key
PTAYFGHRDOMJGC-UHFFFAOYSA-N
InChI
1S/C5H14N4.H2O4S/c6-3-1-2-4-9-5(7)8;1-5(2,3)4/h1-4,6H2,(H4,7,8,9);(H2,1,2,3,4)
SMILES string
OS(O)(=O)=O.NCCCCNC(N)=N
assay
97%
mp
234-238 °C (lit.)
Biochem/physiol Actions
Putative endogenous neurotransmitter at imidazoline receptors; displaces clonidine at α2-adrenergic and at imidazoline receptors; blocks NMDA-activated ion channels in hippocampal neurons.
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Well-balanced and timed metabolism is essential for making a high-quality egg. However, the metabolic framework that supports oocyte development remains poorly understood. Here, we obtained the temporal metabolome profiles of mouse oocytes during in vivo maturation by isolating large number of
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Journal of chromatography. A, 1366, 110-119 (2014-09-30)
Histamine and agmatine amino acid derivatives were immobilized into monolithic disks, in order to combine the specificity and selectivity of the ligand with the high mass transfer and binding capacity offered by monolithic supports, to purify potential plasmid DNA biopharmaceuticals.
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