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A propos de cet article
Formule linéaire :
H2N(CH2)4NHC(=NH)NH2·H2SO4
Numéro CAS:
Poids moléculaire :
228.27
NACRES:
NA.32
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
219-617-3
MDL number:
Beilstein/REAXYS Number:
3918807
Assay:
≥97%
Form:
powder
Service technique
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Laissez-nous vous aiderNom du produit
Agmatine sulfate salt, ≥97%, powder
Quality Segment
assay
≥97%
form
powder
color
white to off-white
mp
234-238 °C (lit.)
solubility
H2O: 50 mg/mL, ethanol: insoluble
SMILES string
OS(O)(=O)=O.NCCCCNC(N)=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)
InChI key
PTAYFGHRDOMJGC-UHFFFAOYSA-N
Gene Information
human ... ADRA2A(150), ADRA2B(151), ADRA2C(152), GRIN1(2902), GRIN2A(2903), GRIN2B(2904), GRIN2C(2905), GRIN2D(2906), GRINA(2907)
Application
Agmatine sulfate salt has been used:
- to study its effects on nod-like receptor protein 3 (NLRP3) inflammasome activation and cytokine responses in sub-chronic restraint stress rat models
- as an N-methyl-
D -aspartate (NMDA) receptor blocker to study its therapeutic effects on autistic behaviors in the valproic acid-induced animal model of autism - as a standard to determine the bioactive amines in vegetables by high-performance liquid chromatography (HPLC)
Biochem/physiol Actions
Agmatine is a decarboxylated arginine that is present ubiquitously in all living organisms. It is found in food sources such as plant source food and animal products. It exhibits cryoprotective effects against several body functions such as nephroprotection, neuroprotection, gastroprotection, and cardioprotection. Agmatine also exhibits therapeutic effects against neurotrauma, neuropathic pain, diabetes, neurodegenerative diseases, and psychiatric diseases. It is involved in blocking many ionic channels such as ATP-sensitive K+ channels and voltage-gated Ca2+ channels. Agmatine modulates nitric oxide production and inhibits matrix metalloproteases.
Putative endogenous neurotransmitter at imidazoline receptors; displaces clonidine at α2-adrenergic and at imidazoline receptors; blocks NMDA-activated ion channels in hippocampal neurons.
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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