The solution stability of this product has not been determined. As indicated in the 'DESCRIPTION' section under 'Preparation Note', solutions should be freshly prepared. However, one publication tested the stability of 4.2 mM solutions of MPP+ over 28 days in the dark at 37 °C. Aliquots of the solution were taken and then stored at -80 °C for analysis by HPLC. During this period, no degradation of MPP+ was observed (Yazdani, U., et al., Rat model of Parkinson's disease: Chronic central delivery of 1-methyl-4-phenylpyridinium (MPP+). Exp. Neurol., 200, 172-183 (2006)).
Przejdź do
D048
MPP+ iodide
≥98% (HPLC), ERα antagonist, powder
Synonim(y):
1-Methyl-4-phenylpyridinium iodide
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| Gabaryty przesyłki | SKU | Dostępność | Cena netto |
|---|---|---|---|
| 100 mg | Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności | 728,00 zł | |
| 1 g | Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności | 3120,00 zł |
Informacje o tej pozycji
Wzór empiryczny (zapis Hilla):
C12H12IN
Numer CAS:
Masa cząsteczkowa:
297.13
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77
MDL number:
728,00 zł
Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności
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Pozwól nam pomócNazwa produktu
MPP+ iodide, ≥98% (HPLC), powder
Quality Level
assay
≥98% (HPLC)
form
powder
storage condition
desiccated
color
white to beige
solubility
H2O: 10 mg/mL, clear
SMILES string
[I-].C[n+]1ccc(cc1)-c2ccccc2
InChI
1S/C12H12N.HI/c1-13-9-7-12(8-10-13)11-5-3-2-4-6-11;/h2-10H,1H3;1H/q+1;/p-1
InChI key
RFDFRDXIIKROAI-UHFFFAOYSA-M
Powiązane kategorie
1 of 1
Ta pozycja | |||
|---|---|---|---|
| form powder | form powder | form powder | form powder |
| assay ≥98% (HPLC) | assay ≥97% (titration) | assay ≥98% (HPLC) | assay ≥97% (HPLC) |
| Quality Level 100 | Quality Level 100 | Quality Level - | Quality Level 100 |
| solubility H2O: 10 mg/mL, clear | solubility H2O: >50 mg/mL, clear, yellow to brown | solubility DMSO: 2 mg/mL, clear | solubility DMSO: soluble ≥20 mg/mL |
| storage condition desiccated | storage condition - | storage condition - | storage condition desiccated |
| color white to beige | color off-white to brown | color white to light brown | color white |
General description
1-Methyl-4-phenylpyridinium (MPP+) acts as a selective ERα antagonist.[1]induces neurotoxicity by inhibiting mitochondrial redox functions in the striatal synaptosomes. It is a potential neurotoxin and induces Parkinson′s disease in animal models. It mediates apoptosis by the generation of reactive oxygen species in cerebellar granule neurons and neuroblastoma cells. MPP+ modulates the distribution of dopamine. It elicits neurotoxicity by activating neuronal nitric oxide synthase (nNOS), resulting in excess nitric oxide.[2]
Application
MPP+ iodide has been used:
- to induce oxidative stress in zebrafish embryos[3]
- for the inhibition of glutamate uptake in mitochondria of astrocytes
- in testing cell viability using MTT (3 (4,5-dimethylthiazol)-2-yl-2,5-diphenyltetrazolium bromide) in microglia (BV2) cells
Biochem/physiol Actions
Active metabolite of dopaminergic neurotoxin MPTP
MPP+ iodide is an active metabolite of dopaminergic neurotoxin MPTP.
Preparation Note
Solutions should be freshly prepared.
Disclaimer
Photosensitive.
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Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Klasa składowania
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
1-Methyl-4-phenylpyridinium (MPP+)-induced apoptosis and mitochondrial oxidant generation: role of transferrin-receptor-dependent iron and hydrogen peroxide
Kalivendi SV, et al.
The Biochemical Journal, 371(1), 151-164 (2003)
Lack of PINK1 alters glia innate immune responses and enhances inflammation-induced, nitric oxide-mediated neuron death
Sun L, et al.
Scientific Reports, 8(1), 383-383 (2018)
The MPTP story
Langston, J William
Journal of Parkinson's Disease, 7(s1), S11-S19 (2017)
Bart de Nijs et al.
Nature communications, 8(1), 994-994 (2017-10-24)
Nanoparticles attached just above a flat metallic surface can trap optical fields in the nanoscale gap. This enables local spectroscopy of a few molecules within each coupled plasmonic hotspot, with near thousand-fold enhancement of the incident fields. As a result
1-Methyl-4-phenylpyridinium (MPP+) decreases mitochondrial oxidation-reduction (REDOX) activity and membrane potential (DeltaPsim) in rat striatum
Nakai M, et al.
Experimental Neurology, 179(1), 103-110 (2003)
Numer pozycji handlu globalnego
| SKU | NUMER GTIN |
|---|---|
| D048-1G | 04061833557716 |
| D048-100MG | 04061833557709 |
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