(S)-2-Amino-3-(quinolin-4-yl)propanoic acid dihydrochloride

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Reagent Code: #38278
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CAS Number 2563594-83-0

science Other reagents with same CAS 2563594-83-0

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Weight 289.1578 g/mol
Formula C₁₂H₁₄Cl₂N₂O₂
inventory_2 Storage & Handling
Storage room temperature

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This compound is primarily utilized in biochemical research, particularly in the study of enzyme activity and receptor interactions. It serves as a chiral building block in the synthesis of complex molecules, often employed in the development of pharmaceuticals targeting neurological disorders. Its quinoline moiety makes it valuable in designing compounds with potential antimalarial and anticancer properties. Additionally, it is used in peptide synthesis to introduce specific structural features that enhance binding affinity or stability. Researchers also explore its role in modulating biological pathways, making it a versatile tool in medicinal chemistry and drug discovery.

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inventory 100mg
10-20 days ฿23,350.00

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(S)-2-Amino-3-(quinolin-4-yl)propanoic acid dihydrochloride
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This compound is primarily utilized in biochemical research, particularly in the study of enzyme activity and receptor interactions. It serves as a chiral building block in the synthesis of complex molecules, often employed in the development of pharmaceuticals targeting neurological disorders. Its quinoline moiety makes it valuable in designing compounds with potential antimalarial and anticancer properties. Additionally, it is used in peptide synthesis to introduce specific structural features that enh

This compound is primarily utilized in biochemical research, particularly in the study of enzyme activity and receptor interactions. It serves as a chiral building block in the synthesis of complex molecules, often employed in the development of pharmaceuticals targeting neurological disorders. Its quinoline moiety makes it valuable in designing compounds with potential antimalarial and anticancer properties. Additionally, it is used in peptide synthesis to introduce specific structural features that enhance binding affinity or stability. Researchers also explore its role in modulating biological pathways, making it a versatile tool in medicinal chemistry and drug discovery.

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