| Weight | 121.139 g/mol |
|---|---|
| Formula | C7H7NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
3-ACETYLPYRIDINE (350-03-8)
Score:
#905 in Neuroscience
,
#1832 in Biochemistry
,
#3975 in Biology
,
#5006 in Chemistry
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- Effects of 3-acetylpyridine on the central nervous system of the rat, as demonstrated by silver methods (Brain Research, 1974)
- Effects of the nicotinamide-sensitive teratogen 3-acetylpyridine on chick limb cells in culture (Experimental Cell Research, 1970)
- 2-Acetylpyridine thiosemicarbazones. 5. 1-[1-(2-Pyridyl)ethyl]-3-thiosemicarbazides as potential antimalarial agents. (Journal of Medicinal Chemistry, 1983)
- CHEMISTRY AND PROPERTIES OF THE 3-ACETYLPYRIDINE ANALOGUE OF DIPHOSPHOPYRIDINE NUCLEOTIDE (Journal of Biological Chemistry, 1956)
- 3-Acetylpyridine: a tool to inhibit the tremor and the increase of cGMP content in cerebellar cortex elicited by harmaline (Brain Research, 1975)
- Central neurotoxic effects of intraperitoneally administered 3-acetylpyridine, harmaline and niacinamide in Sprague-Dawley and Long-Evans rats: A critical review of central 3-acetylpyridine neurotoxicity (Brain Research Reviews, 1985)
-
Predict GHS Hazards for Any Chemical in silico.
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SMILESCC(=O)C1=CN=CC=C1
-
InChIKeyWEGYGNROSJDEIW-UHFFFAOYSA-N
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1-pyridin-3-ylacetone
(6302-03-0)
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1-(3-pyridinyl)acetone hydrochloride
(69966-56-9)
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3-pyridineacetic acid
(6419-36-9, 501-81-5)
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3-Pyridylacetic acid hydrochloride
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(41038-69-1)
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(71532-24-6)
1 alternate name
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(3724-16-1)
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(104-90-5)
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(7521-41-7)
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(39931-77-6)
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MFCD11841278
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(499-81-0)
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3-ACETYLPYRIDINE
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