GUVACINE HYDROCHLORIDE

GUVACINE HYDROCHLORIDE Basic information
Product Name:GUVACINE HYDROCHLORIDE
Synonyms:GUVACINE HYDROCHLORIDE >96% \ GABA UPTAK;1,2,5,6-Tetrahydro-;1,2,5,6-Tetrahydro-3-pyridinecarboxylic Acid Hydrochloride;3-Pyridinecarboxylic acid, 1,2,5,6-tetrahydro-, hydrochloride;Guvacine hydrochloride >=97% (NMR), solid;GUVACINE HYDROCHLORIDE;Norareca alkaloid hydrochloride
CAS:6027-91-4
MF:C6H10ClNO2
MW:163.6021
EINECS:
Product Categories:GABA and Glycine Receptor ModulatorsNeurotransmitters;GABAergics;Ion Channels;Ligand-Gated Ion Channels;Others;Amines;Heterocycles;Intermediates & Fine Chemicals;Nicotine Derivatives;Pharmaceuticals
Mol File:6027-91-4.mol
GUVACINE HYDROCHLORIDE Structure
GUVACINE HYDROCHLORIDE Chemical Properties
Melting point 316 °C (decomp)
storage temp. Inert atmosphere,Room Temperature
solubility H2O: soluble
form solid
color white
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HazardClass IRRITANT
MSDS Information
GUVACINE HYDROCHLORIDE Usage And Synthesis
Chemical PropertiesBeige Solid
UsesGuvacine Hydrochloride is a GABA uptake inhibitor (hGABA T-1, rGABA T-2, hGABA T-3 and hBGT-1) (1,2,3). Gamma-Aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the mammalian brain (4). Guvacine Hydrochloride may be useful for treating neuropsychiatric disorders.
UsesGuvacine Hydrochloride is a GABA uptake inhibitor and it is used for the treatment of neurodegenerative diseases.
Biological ActivityGuvacine hydrochloride is an alkaloid from the nut of Areca catechu, acts as an inhibitor of GABA transporter, and dispalys modest selectivity for cloned GABA transporters with IC50s of 14 μM (human GAT-1), 39 μM (rat GAT-1), 58 μM (rat GAT-2), 119 μM (human GAT-3), 378 μM (rat GAT-3), and 1870 μM (human BGT-3).
in vitroGuvacine hydrochloride is a potent inhibitor of GABA transporter, dispalys modest selectivity for cloned GABA transporters with IC50s of 14 μM (human GAT-1), 39 μM (rat GAT-1), 58 μM (rat GAT-2), 119 μM (human GAT-3), 378 μM (rat GAT-3), and 1870 μM (human BGT-3). Guvacine has low affinity at hBGT-1 (IC50 >1 mM). Guvacine hydrochloride is a potent inhibitor of GABA uptake, but does not inhibit sodium-independent GABA binding, and is weak or inactive as a GABA receptor agonist. Guvacine inhibits the uptake GABA and β-alanine with IC50s of 23 ± 2 μM, 66 ± 11 μM in the Cat spinal cord, and 8 ± 1 μM, 123 ± 28 μM in the rat cerebral cortex, respectively.
GUVACINE HYDROCHLORIDE Preparation Products And Raw materials
GUVACINE HYDROCHLORIDE

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