CAS 104501-33-9

Glycine, N-2-propynyl-, hydrochloride

Description:

Glycine, N-2-propynyl-, hydrochloride is a chemical compound characterized by its structure, which includes a glycine backbone modified with a propynyl group. As a hydrochloride salt, it is typically encountered in a crystalline form and is soluble in water, which enhances its utility in various applications. This compound is primarily of interest in the fields of biochemistry and pharmaceuticals, where it may serve as an intermediate in the synthesis of more complex molecules or as a potential therapeutic agent. The presence of the propynyl group can impart unique properties, potentially influencing its biological activity and interaction with other molecules. Glycine itself is the simplest amino acid, and modifications to its structure can affect its reactivity and functionality. Safety data sheets should be consulted for handling and storage guidelines, as with any chemical substance, to ensure proper safety measures are taken. Overall, Glycine, N-2-propynyl-, hydrochloride represents a specialized compound with potential applications in research and development.

Formula: C₅H₇NO₂ClH

H-Prg-OH hydrochloride

CAS: 104501-33-9

H-Prg-OH hydrochloride

Purity: 98%

Molecular weight: 149.58g/mol

Ref: 54-OR1059858

2-[(prop-2-yn-1-yl)amino]acetic acid hydrochloride

CAS: 104501-33-9

Formula: C₅H₈ClNO₂

Purity: 95.0%

Molecular weight: 149.57

Ref: 10-F515392

2-[(Prop-2-yn-1-yl)amino]acetic acid hydrochloride

CAS: 104501-33-9

2-[(Prop-2-yn-1-yl)amino]acetic acid hydrochloride (PAH) is a molecule that is being studied for its potential as a broad-spectrum antimicrobial. PAH has been shown to inhibit the growth of bacteria, fungi, and viruses by binding to the ATP channel on the mitochondrial membrane. This binding inhibits ATP synthesis and prevents cell division. PAH also has antimicrobial activity against Gram negative bacteria through a mechanism that is not yet known. PAH has been shown to decrease muscle cell proliferation in rats by inhibiting protein synthesis and increasing apoptosis. PAH is synthesized from propionic acid and acetamide via asymmetric hydrogenation, which can be accomplished using an organocatalyst such as palladium on carbon or nickel on carbon.

Formula: C₅H₈ClNO₂

Purity: Min. 95%

Molecular weight: 149.57 g/mol

Ref: 3D-EEA50133