solo para uso en investigación
Cat. No.: S4732
| Dianas relacionadas | Adrenergic Receptor AChR 5-HT Receptor COX Calcium Channel Histamine Receptor GABA Receptor TRP Channel Cholinesterase (ChE) GluR |
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| Otros Dopamine Receptor Inhibidores | Trifluoperazine Trifluoperazine 2HCl Penfluridol Rotundine Domperidone Sulpiride Azaperone Levosulpiride SCH-23390 hydrochloride ONC206 |
| Líneas celulares | Tipo de ensayo | Concentración | Tiempo de incubación | Formulación | Descripción de la actividad | PMID |
|---|---|---|---|---|---|---|
| insect cells | Function assay | 120 mins | Inhibition of human recombinant MAOA expressed in insect cells assessed as oxidation of kynuramine substrate at 50 uM measured after additional enzyme added after 120 mins incubation | 22078410 | ||
| insect cells | Function assay | 90 mins | Inhibition of human recombinant MAOA expressed in insect cells assessed as oxidation of kynuramine substrate at 50 uM measured after additional substrate added after 90 mins incubation | 22078410 | ||
| Haga clic para ver más datos experimentales de líneas celulares | ||||||
| Peso molecular | 209.72 | Fórmula | C12H15N·HCl |
Almacenamiento (Desde la fecha de recepción) | |
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| Nº CAS | 23007-85-4 | Descargar SDF | Almacenamiento de soluciones madre |
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| Sinónimos | N/A | Smiles | CN1CCC(=CC1)C2=CC=CC=C2.Cl | ||
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In vitro |
Water : 41 mg/mL Ethanol : 41 mg/mL
DMSO
: 26 mg/mL
(123.97 mM)
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In vivo |
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Paso 1: Introduzca la información a continuación (Recomendado: Un animal adicional para tener en cuenta la pérdida durante el experimento)
Paso 2: Introduzca la formulación in vivo (Esto es solo la calculadora, no la formulación. Por favor, contáctenos primero si no hay una formulación in vivo en la sección de Solubilidad.)
Resultados del cálculo:
Concentración de trabajo: mg/ml;
Método para preparar el líquido maestro de DMSO: mg fármaco predissuelto en μL DMSO ( Concentración del líquido maestro mg/mL, Por favor, contáctenos primero si la concentración excede la solubilidad del DMSO del lote del fármaco. )
Método para preparar la formulación in vivo: Tomar μL DMSO líquido maestro, luego añadirμL PEG300, mezclar y clarificar, luego añadirμL Tween 80, mezclar y clarificar, luego añadir μL ddH2O, mezclar y clarificar.
Método para preparar la formulación in vivo: Tomar μL DMSO líquido maestro, luego añadir μL Aceite de maíz, mezclar y clarificar.
Nota: 1. Por favor, asegúrese de que el líquido esté claro antes de añadir el siguiente disolvente.
2. Asegúrese de añadir el (los) disolvente(s) en orden. Debe asegurarse de que la solución obtenida, en la adición anterior, sea una solución clara antes de proceder a añadir el siguiente disolvente. Se pueden utilizar métodos físicos como el vórtice, el ultrasonido o el baño de agua caliente para ayudar a la disolución.
| In vitro |
The morphology of N2AB-1 and glioma cells was unaltered when these cells were exposed to all doses of MPTP hydrochloride. And, C6 glioma cell proliferation was also unaffected by this compound treatment. MPTP Promotes Apoptosis and Tau Phosphorylation in Human Neuroblastoma M17 Cells. This compound significantly promotes Tau phosphorylation at Ser262 in human neuroblastoma M17 cells. It caused a dose-dependent increase in the intracellular α-synuclein level in our M17 human neuroblastoma cells. This chemical appears to promote Tau phosphorylation in the brain by activating both PKA and GSK3β.
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| In vivo |
The number of tyrosine hydroxylase-positive neurons was decreased in the substantia nigra pars compacta of MPTP-treated mice. This compound decreased thioredoxin reductase 1 expression and thioredoxin reductase activity in the mouse midbrain, reduced the number of thioredoxin reductase 1-positive cells in the substantia nigra pars compacta of mice. Administration of this toxin can cause neurochemical, behavioral and histopathological alterations in human and nonhuman primates that are similar to those observed in Parkinsonian patients. Compared with primates, rodents are insensitive to MPTP. This chemical can be administered by various routes, such as gavage and stereotactic injection, but the most common and reproducible route is systemic administration, including subcutaneous, intravenous, intraperitoneal and intramuscular injection. It is a lipophilic protoxin that can rapidly cross the blood-brain barrier following systemic injection. Once it enters the brain, MPTP is converted to 1-methyl-4-phenylpyridine by monoamine oxidase B. It has been shown to be toxic to dopaminergic neurons of the nigrostriatal system in humans, monkeys, and mice and to produce long-lasting depletion of DA and its metabolites in the striatum.
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Referencias |
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| Métodos | Biomarcadores | Imágenes | PMID |
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| Western blot | TH / Actin pCaMKIIβ / pCaMKIIα / CaMKIIβ / CaMKIIα / β-Actin TH / p-α-Syn / α-Syn / β-actin / CDK5 / LC3-I / LC3-II / p62 / NLRP3 / ASC / Casp1 p20 / Procasp1 p-ERK1/2 / ERK1/2 / GAPDH GDH2 / GDH1 / GFAP / GAPDH |
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23391753 |
| IHC | tyrosine hydroxylase (TH) tyrosine hydroxylase (TH) SNpc tyrosine hydroxylase (TH) Substantia nigra |
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31427934 |
| Immunofluorescence | tyrosine hydroxylase (TH) / miR-188-3p α-Syn tyrosine hydroxylase (TH) / Tunel tyrosine hydroxylase (TH) / Tunel tyrosine hydroxylase (TH) GFAP |
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33717653 |