N-(4-amino-2-methylphenyl)benzamide, also known by its CAS number 104478-99-1, is an organic compound characterized by the presence of both an amine and an amide functional group. This compound features a benzene ring substituted with an amino group at the para position and a methyl group at the ortho position relative to the amino group. The amide functionality is derived from the attachment of a benzoyl group to the nitrogen of the amino group. This structure contributes to its potential biological activity, making it of interest in pharmaceutical research. The compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its properties, such as melting point, boiling point, and reactivity, can vary based on the specific conditions and purity of the sample. Additionally, the presence of both polar and non-polar regions in its molecular structure may influence its interactions with other molecules, making it relevant in various chemical and biological applications.

N-(4-amino-2-methylphenyl)benzamide

104478-99-1: benzamide, N-(4-amino-2-methylphenyl)-, N-(4-Amino-2-methylphenyl)benzamide

N-(4-Amino-2-methylphenyl)benzamide (NAPB) is a molecule inhibitor that is designed to inhibit the activity of multiple targets. It inhibits the activity of the enzymes COX and LOX, which are proinflammatory enzymes that are involved in the production of prostaglandins and leukotrienes, respectively. NAPB also has been shown to be an effective antidepressant in animal models. This drug binds to a pharmacophore that exhibits high affinity for both COX and LOX, inhibiting their enzymatic activity by binding at nanomolar concentrations. These properties make NAPB a multitargeted agent with the potential for use against inflammation and depression.

CAS 104478-99-1: N-(4-amino-2-methylphenyl)benzamide

N-(4-Amino-2-methylphenyl)benzamide

Ref: 3D-FA117199