| Weight | 155.2 g/mol |
|---|---|
| Formula | C11H9N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
3-PHENYLPYRIDINE (1008-88-4)
Score:
#1235 in Neuroscience
,
#5294 in Biology
,
#6960 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)
- 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)
- Theoretical Studies on Photophysical Properties and Mechanism of Phosphorescence in [facIr(2phenylpyridine)3] (Journal of The Chinese Chemical Society, 2006)
- Increasing the Ordering Temperatures in Oxalate-Based 3D Chiral Magnets: the Series [Ir(ppy)2(bpy)][MIIMIII(ox)3]0.5H2O (MIIMIII = MnCr, FeCr, CoCr, NiCr, ZnCr, MnFe, FeFe); bpy = 2,2-Bipyridine; ppy = 2-Phenylpyridine; ox = Oxalate Dianion) (Inorganic Chemistry, 2006)
- Characterization of the binding of N-methyl-4-phenylpyridine, the toxic metabolite of the parkinsonian neurotoxin N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, to neuromelanin (Journal of Neurochemistry, 1987)
- Synthesis and anti-tumor activity of 2-amino-3-cyano-6-(1H-indol-3-yl)-4-phenylpyridine derivatives in vitro (European Journal of Medicinal Chemistry, 2011)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C2=CN=CC=C2
-
InChIKeyHJKGBRPNSJADMB-UHFFFAOYSA-N
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3-PHENYLPYRIDINE
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