| Weight | 155.2 g/mol |
|---|---|
| Formula | C11H9N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
4-PHENYLPYRIDINE (52642-16-7, 939-23-1)
p-phenylpyridine
Score:
#1834 in Physics
,
#4516 in Biology
,
#5718 in Chemistry
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- Parkinsonism-inducing neurotoxin, N-methyl-4-phenyl-1,2,3,6 -tetrahydropyridine: uptake of the metabolite N-methyl-4-phenylpyridine by dopamine neurons explains selective toxicity. (Proceedings of the National Academy of Sciences of the United States of America, 1985)
- Uptake of the neurotoxin 1-methyl-4-phenylpyridine (MPP+) by mitochondria and its relation to the inhibition of the mitochondrial oxidation of NAD+-linked substrates by MPP+ (Biochemical and Biophysical Research Communications, 1986)
- The nature of the lowest excited state in fac-tricarbonylhalobis(4-phenylpyridine)rhenium(I) and fac-tricarbonylhalobis(4,4'-bipyridine)rhenium(I): emissive organometallic complexes in fluid solution (Journal of the American Chemical Society, 1979)
- Stable single-layer light-emitting electrochemical cell using 4,7-diphenyl-1,10-phenanthroline-bis(2-phenylpyridine)iridium(III) hexafluorophosphate. (Journal of the American Chemical Society, 2006)
- 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) and 1-methyl-4-phenylpyridine (MPP+) cause rapid ATP depletion in isolated hepatocytes. (Biochemical and Biophysical Research Communications, 1986)
- Energy-driven uptake of N-methyl-4-phenylpyridine by brain mitochondria mediates the neurotoxicity of MPTP (Life Sciences, 1986)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - p-phenylpyridine
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SMILESC1=CC=C(C=C1)C2=CC=NC=C2
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InChIKeyJVZRCNQLWOELDU-UHFFFAOYSA-N
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(8004-13-5)
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4-PHENYLPYRIDINE
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