1-methyl-4-phenylpyridinium

MPP+
Names

IUPAC name 1-Methyl-4-phenylpyridin-1-ium
Other names Cyperquat; 1-Methyl-4-phenylpyridinium; N-Methyl-4-phenylpyridine
Identifiers
CAS Number	39794-99-5^N
3D model (Jmol)	Interactive image
ChEBI	CHEBI:641^Y
ChemSpider	36101^Y
EC Number	248-939-7
IUPHAR/BPS	4568
MeSH	1-Methyl-4-phenylpyridinium
PubChem CID	39484
InChI InChI=1S/C12H12N/c1-13-9-7-12(8-10-13)11-5-3-2-4-6-11/h2-10H,1H3/q+1^Y Key: FMGYKKMPNATWHP-UHFFFAOYSA-N^Y
SMILES C[n+]1ccc(cc1)c2ccccc2
Properties
Chemical formula	C₁₂H₁₂N⁺
Molar mass	170.25 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N (what is ^YN ?)
Infobox references

MPP+ (1-methyl-4-phenylpyridinium) is a positively charged molecule with chemical formula C₁₂H₁₂N⁺. It is toxic and acts by interfering with oxidative phosphorylation in by inhibiting complex I, leading to the depletion of ATP and cell death. Mitochondria in cells treated with MPP+ also display a phenotype indicative of apoptosis: small, round, and fewer in number. It also inhibits the synthesis of catecholamines, reduces levels of dopamine and cardiac norepinephrine, and inactivates tyrosine hydroxylase.

The neurotoxin MPTP is converted in the brain into MPP+ by the enzyme MAO-B, causing parkinsonism in primates by killing certain dopamine-producing neurons in the substantia nigra. MPP+-induced neurodegeneration is specific to dopamine neurons and can be prevented by drug treatment or by limiting the function of the dopamine transporter.

The chloride salt of MPP+ has been used as a herbicide under the trade name cyperquat and is structurally similar to the herbicide paraquat.

In a rat model of Parkinson's disease, nobiletin, a flavonoid found in citrus, can rescue dopaminergic neurons from degeneration caused by treatment with MPP+.

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Wikipedia