| Weight | 121.183 g/mol |
|---|---|
| Formula | C8H11N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,3,5-Trimethylpyridine (695-98-7)
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- Effects of diethyl-1, 4-dihydro-2, 4,6-trimethylpyridine-3,5-dicarboxylate on the metabolism of porphyrins and iron. (Journal of Biological Chemistry, 1963)
- Experimental hepatic porphyria caused by feeding 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine. Comparison with sedormid porphyria. (Biochemical Journal, 1962)
- Disturbance in Porphyrin Metabolism Caused by Feeding Diethyl 1, 4-dihydro-2, 4, 6-trimethylpyridine-3, 5-dicarboxylate (Experimental Biology and Medicine, 1959)
- Suicidal destruction of cytochrome P-450 and reduction of ferrochelatase activity by 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine and its analogues in chick embryo liver cells. (Molecular Pharmacology, 1985)
- Drug-induced porphyrin biosynthesisXIX: Potentiation of the porphyrin-inducing effects of SKF 525-A in the chick embryo liver by 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine, an inhibitor of ferrochelatase (Biochemical Pharmacology, 1979)
- Ferrochelatase-inhibitory activity and N-alkylprotoporphyrin formation with analogues of 3,5-diethoxycarbonyl-1,4-dihydro-2,4,6-trimethylpyridine (DDC) containing extended 4-alkyl groups: implications for the active site of ferrochelatase. (Molecular Pharmacology, 1986)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCC1=CC(=C(N=C1)C)C
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InChIKeyGFYHSKONPJXCDE-UHFFFAOYSA-N
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