H-β-(2-Quinolyl)-D-Ala-OH, with the CAS number 170421-67-7, is a synthetic peptide that features a quinoline moiety, which contributes to its unique chemical properties. This compound is characterized by its structural components, including a D-alanine residue and a quinoline ring, which may influence its biological activity and interaction with various receptors or enzymes. The presence of the D-amino acid suggests potential applications in the development of peptide-based therapeutics, as D-amino acids can enhance stability against enzymatic degradation. Additionally, the quinoline structure may impart specific pharmacological properties, such as antimicrobial or antitumor activity. The compound is typically studied in the context of medicinal chemistry and drug design, where its interactions at the molecular level can be explored for potential therapeutic applications. Overall, H-β-(2-Quinolyl)-D-Ala-OH represents a class of compounds that bridge organic chemistry and pharmacology, highlighting the importance of structural modifications in the development of bioactive molecules.

H-.beta.-(2-Quinolyl)-D-Ala-OH

170421-67-7: H-β-(2-Quinolyl)-D-Ala-OH, with the CAS number 170421-67-7, is a synthetic peptide that features a quinoline moiety, which contributes to its unique chemical properties. This compound is characterized by its structural components, including a D-alanine residue and a quinoline ring, which may influence its biological activity and interaction with various receptors or enzymes. The presence of the D-amino acid suggests potential applications in the development of peptide-based therapeutics, as D-amino acids can enhance stability against enzymatic degradation. Additionally, the quinoline structure may impart specific pharmacological properties, such as antimicrobial or antitumor activity. The compound is typically studied in the context of medicinal chemistry and drug design, where its interactions at the molecular level can be explored for potential therapeutic applications. Overall, H-β-(2-Quinolyl)-D-Ala-OH represents a class of compounds that bridge organic chemistry and pharmacology, highlighting the importance of structural modifications in the development of bioactive molecules.

CAS 170421-67-7

H-.beta.-(2-Quinolyl)-D-Ala-OH

(R)-2-Amino-3-(quinolin-2-yl)propanoic acid

Ref: IN-DA0078RL

(R)-2-Amino-3-(quinolin-2-yl)propanoic acid

Ref: 10-F323775