3-Aminopyridine-2-carboxamide, with the CAS number 50608-99-6, is an organic compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. This compound features an amino group (-NH2) and a carboxamide group (-C(=O)NH2) attached to the pyridine ring, specifically at the 3 and 2 positions, respectively. It is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols due to the presence of the amino and carboxamide functional groups, which can engage in hydrogen bonding. The compound is of interest in various fields, including medicinal chemistry, due to its potential biological activities, such as acting as a building block for pharmaceuticals or as a ligand in coordination chemistry. Its reactivity can be influenced by the functional groups present, allowing for further chemical modifications. Safety data should be consulted for handling and storage, as with any chemical substance.

3-Aminopyridine-2-carboxamide

50608-99-6: 2-Pyridinecarboxamide, 3-Amino-, 3-Aminopyridine-2-carboxylic acid amide, 50608-99-6,  3-Aminopyridine-2-carboxamide

3-Amino-pyridine-2-carboxylic acid amide

3-Aminopyridine-2-carboxylic acid amide is a metabotropic glutamate receptor (mGluR) agonist with high affinity for the mGluR5 receptor subtype. It has been shown to act as an allosteric modulator of the mGluR1 and mGluR2 receptors. 3-Aminopyridine-2-carboxylic acid amide has also been shown to inhibit chemokine production by myceliophthora, an agent that causes mycosis in humans. This compound has also been shown to have inhibitory potency against drug targets such as serotonin transporter and dopamine transporter.

CAS 50608-99-6: 3-Aminopyridine-2-carboxamide

3-Aminopyridine-2-carboxamide

Ref: 10-F048148

3-Amino-pyridine-2-carboxylic acid amide

Ref: 54-OR315090

3-Aminopyridine-2-carboxylic acid amide

Ref: 3D-FA56520

3-AMINO-PYRIDINE-2-CARBOXYLIC ACID AMIDE

Ref: IN-DA00D81S