Agmatine sulfate

Agmatine sulfate Basic information
General Uses
Product Name:Agmatine sulfate
Synonyms:N-(4-AMINOBUTYL)GUANIDINE SULFATE;N-(4-Aminobutyl)guanidine sulfate salt;1-AMINO-4-GUANIDINOBUTANE SULFATE;1-AMINO-4-GUANIDINOBUTANE SULFATE SALT;1-AMINO-4-GUANIDOBUTANE SULFATE;4-GUANIDINOBUTANE SULFATE;4-GUANIDINO-BUTYLAMINE SULFATE;4-GUANIDINO-BUTYLAMINE SULFATE SALT
CAS:2482-00-0
MF:C5H16N4O4S
MW:228.27
EINECS:219-617-3
Product Categories:inhibitor;Imidazoline binding site;Active Pharmaceutical Ingredients;2482-00-0
Mol File:2482-00-0.mol
Agmatine sulfate Structure
Agmatine sulfate Chemical Properties
Melting point 234-238 °C(lit.)
RTECS ME8413000
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility H2O: 50 mg/mL
form powder
color white to off-white
Water Solubility Soluble in water, nearly insoluble in alcohol
Merck 14,188
BRN 3918807
InChIInChI=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)
InChIKeyPTAYFGHRDOMJGC-UHFFFAOYSA-N
SMILESC(CCCN)NC(N)=N.S(O)(O)(=O)=O
CAS DataBase Reference2482-00-0(CAS DataBase Reference)
Safety Information
Safety Statements 22-24/25
WGK Germany 3
10
HS Code 29252900
MSDS Information
ProviderLanguage
Agmatine sulfate English
SigmaAldrich English
Agmatine sulfate Usage And Synthesis
General UsesNeuroprotective, CNS studies, Autism and depression research
Description: Agmatine Sulfate is a polyamine derived from L-arginine decarboxylation and is a known putative endogenous neurotransmitter at imidazoline receptors. Agmatine sulfate displaces clonidine at α2-adrenergic and at imidazoline receptors and was recently shown to exert some neuroprotective effects. It blocks NMDA-receptor associated cation channels. Acts as a competitive inhibitor of nitric oxide synthase (NOS). It functions as neurotransmitter since it is stored in synaptic vesicles and is related from axon terminals by depolarization(1). Protects autistic behavior in rats and reverses depressive like behavior in mice.
DescriptionAgmatine sulfate is the sulfate of the Agmatine. Agmatine is an aninoguanidine that is naturally derived from the arginine. It can exert modulatory effect on many molecular targets such as neurotransmitter systems, opioid analgesia, ion channels, and nitric oxide (NO) synthesis and polyamine metabolism. It has been also found that it can reverse the pain induced from inflammation, neuropathy, and spinal cord injury. Those effects make it a potential candidate for multiple pharmacological applications in the future.
Chemical PropertiesWhite to off-white powder
UsesAgmatine Sulfate is a a polyamine derived from L-arginine (A769500) decarboxylation and is a known putative endogenous neurotransmitter at imidazoline receptors. Agmatine sulfate displaces clonidine a t α2-adrenergic and at imidazoline receptors and was recently shown to exert some neuroprotective effects.
UsesAgmatine is an intermediate in the biosynthesis of the polyamines putrescine and spermine. Agmatine binds with high affinity to α2-adrenergic receptors and imidazoline binding sites and produces blockade of the NMDA-receptor associated cation channels. Agmatine is a competitive inhibitor of nitric oxide synthase activity owing to mimicry of the natural NOS substrate arginine.
Biological ActivityArginine metabolite that is synthesized within bovine brain and exhibits clonidine-displacing substance (CDS) activity. Putative endogenous ligand for the imidazoline binding site.
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.
Purification MethodsCrystallise the salt from aqueous MeOH. The free base has m 101.5-103o, the gold chloride hydrochloride crystallises from H2O with m 223o(dec), and the picrate has m 236-238o. [Odo J Chem Soc Jpn 67 132 1946, Beilstein 4 I 420, 4 II 703, 4 III 575, 4 IV 1291.]
ReferencesFairbanks, C. A., et al. "Agmatine reverses pain induced by inflammation, neuropathy, and spinal cord injury." Proceedings of the National Academy of Sciences of the United States of America97.19(2000):10584.
Kolesnikov, Yuri, S. Jain, and G. W. Pasternak. "Modulation of opioid analgesia by agmatine." European Journal of Pharmacology296.1(1996):17-22.
Su, R. B., J. Li, and B. Y. Qin. "A biphasic opioid function modulator: agmatine. "Acta Pharmacologica Sinica24.7(2003):631.
Galea, Elena, et al. "Inhibition of mammalian nitric oxide synthases by agmatine, an endogenous polyamine formed by decarboxylation of arginine." Biochemical Journal 316 ( Pt 1).1(1996):247.
https://en.wikipedia.org/wiki/Agmatine



Agmatine sulfate Preparation Products And Raw materials
Neomycin sulfate Heparitin, sulfate Zinc sulphate Salbutamol sulfate Sodium sulfate D-Glucosamine sulfate DOBUTAMINE SODIUM SULFATE FERROUS SULFATE Amikacin Disulfate Copper(II) sulfate Ferrous sulfate monohydrate Guanidine-2-cation Atropine sulfate Colistin sulfate SULFATE STANDARD Magnesium sulfate Agmatine Sulfate Salt

Email:[email protected] [email protected]
Copyright © 2024 Mywellwork.com All rights reserved.