
CAS 1012886-75-7
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8 Produkte.
Paroxetine Related Compound E (4-(4-Fluorophenyl)-1-methyl-1,2,3,6-tetrahydropyridine hydrochloride)
CAS:Compounds containing an unfused pyridine ring in the structure, nesoiFormel:C12H14FN·HClFarbe und Form:White PowderMolekulargewicht:191.111034-(4-Fluorophenyl)-1-methyl-1,2,3,6-tetrahydropyridine hydrochloride (Paroxetine Hydrochloride Impurity)
CAS:4-(4-Fluorophenyl)-1-methyl-1,2,3,6-tetrahydropyridine hydrochloride (Paroxetine Hydrochloride Impurity)Reinheit:98%Paroxetine EP Impurity G HCl (Paroxetine USP Related Compound E)
CAS:Formel:C12H14FN·HClFarbe und Form:Off-White SolidMolekulargewicht:191.25 36.46Paroxetine EP Impurity G (Paroxetine USP Related Compound E) as Hydrochloride
CAS:Kontrolliertes ProduktFormel:C12H14FN·ClHFarbe und Form:NeatMolekulargewicht:227.714-(4-Fluorophenyl)-1-methyl-1,2,3,6-tetrahydropyridine Hydrochloride
CAS:Kontrolliertes Produkt<p>Impurity Paroxetine EP Impurity G<br>Applications 4-(4-Fluorophenyl)-1-methyl-1,2,3,6-tetrahydropyridine Hydrochloride (Paroxetine EP Impurity G) is the active metabolite of 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) (M325910), N-Methyl-4-phenylpyridinium (MPP+), selectively destroys the dopaminergic neurons and induces the symptoms of Parkinson's disease.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Gerlach, M., et al.: Eur. J. Pharmacol., 208, 273 (1991), Tipton, K., et al.: J. Neurochem., 61, 1191 (1993), Wimalasena, D., et al.: J. Biol. Chem., 279, 15298 (2004),<br></p>Formel:C12H14FN·ClHFarbe und Form:Light YellowMolekulargewicht:227.714-(4-Fluorophenyl)-1,2,3,6-tetrahydro-1-methylpyridine hydrochloride (1:1)
CAS:<p>4-(4-Fluorophenyl)-1,2,3,6-tetrahydro-1-methylpyridine hydrochloride (1:1) is a neuroleptic drug that has analgesic and antihistaminic effects. It is an alkylthio compound that inhibits serotonin release from the pre-synaptic neuron. 4-(4-Fluorophenyl)-1,2,3,6-tetrahydro-1-methylpyridine hydrochloride (1:1) also blocks the uptake of dopamine by nerve cells in the brain and prevents its conversion to norepinephrine. This medicine acts as an antagonist for both alpha and beta receptors because it binds to the benzene ring of these neurotransmitters. The alpha receptor antagonist properties of this drug are due to its ability to prevent norepinephrine from binding with alpha receptors on muscle cells. The beta receptor antagonist properties are due to its ability</p>Formel:C12H14FN•HClReinheit:Min. 95%Farbe und Form:PowderMolekulargewicht:227.71 g/molUSP Paroxetine Related Compound E Mixture
CAS:Kontrolliertes Produkt<p>Applications USP Paroxetine Related Compound E Mixture is a reference standard composed of Paroxetine Hydrochloride (P205750) spiked with 4-(4-Fluorophenyl)-1,2,3,6-tetrahydro-1-methyl-pyridine Hydrochloride (F595220). Paroxetine Hydrochloride (P205750) is a selective serotonin reuptake inhibitor. Used as an antidepressant. 4-(4-Fluorophenyl)-1,2,3,6-tetrahydro-1-methyl-pyridine Hydrochloride (F595220) is the active metabolite of 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) (M325910), N-Methyl-4-phenylpyridinium (MPP+), selectively destroys the dopaminergic neurons and induces the symptoms of Parkinson's disease.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Lassen, J.B.: Eur. J. Pharmacol., 47, 351 (1978), Lund, J., et al.: Acta Pharmacol. Toxicol., 51, 351, (1982); Gerlach, M., et al.: Eur. J. Pharmacol., 208, 273 (1991), Tipton, K., et al.: J. Neurochem., 61, 1191 (1993), Wimalasena, D., et al.: J. Biol. Chem., 279, 15298 (2004),<br></p>Formel:C19H20FNO3·C12H14FN·HClFarbe und Form:NeatMolekulargewicht:557.07







