(S)-3-Amino-3-(3-pyridyl)-propionic acid, also known as (S)-3-amino-3-(3-pyridyl)propanoic acid, is an amino acid derivative characterized by its chiral center, which imparts specific stereochemical properties. This compound features a pyridine ring, contributing to its aromatic characteristics and potential biological activity. The presence of the amino group (-NH2) and the carboxylic acid group (-COOH) makes it a zwitterionic molecule, allowing it to participate in various biochemical interactions. It is soluble in water due to its polar functional groups, which enhances its reactivity in biological systems. This compound is of interest in pharmaceutical research, particularly for its potential role as a neurotransmitter or in modulating neurotransmitter systems. Its specific stereochemistry may influence its interaction with biological receptors, making it a subject of study in medicinal chemistry. Overall, (S)-3-Amino-3-(3-pyridyl)-propionic acid is a significant compound in the context of drug development and neurobiology.

(S)-3-Amino-3-(3-pyridyl)-propionic acid

129043-04-5: (3S)-3-amino-3-(pyridin-3-yl)propanoic acid

(S)-3-Amino-3-(3-pyridyl)propionic acid is a β-amino acid that is the racemic mixture of (R)- and (S)-enantiomers. It is an ester and tertiary amine that can be used as a reagent in organic synthesis. The compound has been shown to be hydrolyzed by lipases, such as from Burkholderia cepacia, and diisopropyl ether. It also undergoes enantioselective hydrolysis by the enzyme β-aminoacylase to form (R)-3-pyridylalanine and methyl ethyl ether.

CAS 129043-04-5: (S)-3-Amino-3-(3-pyridyl)-propionic acid

(S)-3-Amino-3-(3-pyridyl)propionic acid

Ref: 3D-FA50071

(S)-3-Amino-3-(pyridin-3-yl)propanoic acid

Ref: IN-DA0080JR

(S)-3-Amino-3-(pyridin-3-yl)propanoic acid

Ref: 10-F319415