4-Methyl-5-aminoindole is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features a methyl group at the 4-position and an amino group at the 5-position of the indole ring, contributing to its unique chemical properties. It is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amino group. The compound is of interest in various fields, including medicinal chemistry, due to its potential biological activities. It may participate in various chemical reactions, such as electrophilic substitutions, owing to the electron-rich nature of the indole ring. Additionally, 4-Methyl-5-aminoindole can serve as a building block for the synthesis of more complex molecules. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken. Overall, its structural features and reactivity make it a compound of interest in both research and industrial applications.

4-Methyl-5-aminoindole

196205-06-8: 1H-Indol-5-amine,4-methyl-(9CI), 4-methyl-1H-indol-5-amine

4-Methyl-5-aminoindole is a solubilizing agent that belongs to the group of pyridine derivatives. It is soluble in water and other polar solvents. 4-Methyl-5-aminoindole has been shown to be an isoform selective inhibitor of the enzyme tyrosine hydroxylase, which catalyzes the conversion of tyrosine to dopamine. This drug also inhibits monoamine oxidase (MAO) and reversibly inhibits phenylethanolamine N-methyltransferase (PNMT). The potency of 4-Methyl-5-aminoindole as an inhibitor of tyrosine hydroxylase is 10 times higher than that of propranolol.
4 Methyl 5 amino indole can be used for the treatment of Parkinson's disease, attention deficit hyperactivity disorder, depression, and narcolepsy.

CAS 196205-06-8: 4-Methyl-5-aminoindole

4-Methyl-5-aminoindole

Ref: 10-F208983

4-Methyl-5-aminoindole

Ref: 3D-FM152572

4-Methyl-1H-indol-5-amine

Ref: IN-DA007R5D