Weight | 125.175 g/mol |
---|---|
Formula | C6H11N3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
3-Methylhistamine (644-42-8)
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- METABOLISM OF METHYLHISTAMINE FORMED THROUGH A NEW PATHWAY: DECARBOXYLATION OF L-3-METHYLHISTIDINE (Journal of Pharmacology and Experimental Therapeutics, 1973)
- Identification of 1,4-methylhistamine, 1,3-diaminopropane and 2,4-diaminobutyric acid in bovine brain. (Journal of Neurochemistry, 1967)
- Rapid and highly sensitive high-performance liquid chromatographic method for the determination of histamine and 3-methylhistamine in biological samples using fluorescamine as the derivatizing agent (Journal of Chromatography B: Biomedical Sciences and Applications, 1993)
- Comparison of the use of the MNDO and MINDO/3 methods with ab initio methods to study tautomerism in histamine, 2- and 4-methylhistamine (Journal of Computational Chemistry, 1987)
- An alternative route for biosynthesis of methylhistamine: In vitro and in vivo formation through decarboxylation ofl-3-methylhistidine (Cellular and Molecular Life Sciences, 1972)
- A rapid determination of histamine and 3-methylhistamine in human plasma by high performance liquid chromatography (Toxicological & Environmental Chemistry, 2008)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN1C=NC=C1CCN
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InChIKeyCPAGZVLINCPJEH-UHFFFAOYSA-N
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