2-Amino-3-(2-Oxo-1,2-Dihydroquinolin-4-Yl)Propanoic Acid Dihydrochloride Dihydrate

98%

Reagent Code: #138872
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CAS Number 914769-50-9

science Other reagents with same CAS 914769-50-9

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Weight 341.19 g/mol
Formula C₁₂H₁₈Cl₂N₂O₅
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in biochemical and pharmaceutical research as a key intermediate in the synthesis of quinoline-based compounds with potential therapeutic activity. Shows relevance in studies targeting neurological pathways due to structural similarity to amino acids involved in neurotransmission. Also employed in the development of enzyme inhibitors, particularly for proteases and kinases, owing to its ability to mimic natural substrates. Its zwitterionic nature and hydrogen bonding capacity make it useful in crystallography studies for analyzing protein-ligand interactions. Additionally, it serves as a building block in the design of peptidomimetic drugs aimed at improving metabolic stability and bioavailability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,990.00
inventory 250mg
10-20 days ฿4,970.00
inventory 1g
10-20 days ฿12,170.00

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2-Amino-3-(2-Oxo-1,2-Dihydroquinolin-4-Yl)Propanoic Acid Dihydrochloride Dihydrate
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Used in biochemical and pharmaceutical research as a key intermediate in the synthesis of quinoline-based compounds with potential therapeutic activity. Shows relevance in studies targeting neurological pathways due to structural similarity to amino acids involved in neurotransmission. Also employed in the development of enzyme inhibitors, particularly for proteases and kinases, owing to its ability to mimic natural substrates. Its zwitterionic nature and hydrogen bonding capacity make it useful in cryst

Used in biochemical and pharmaceutical research as a key intermediate in the synthesis of quinoline-based compounds with potential therapeutic activity. Shows relevance in studies targeting neurological pathways due to structural similarity to amino acids involved in neurotransmission. Also employed in the development of enzyme inhibitors, particularly for proteases and kinases, owing to its ability to mimic natural substrates. Its zwitterionic nature and hydrogen bonding capacity make it useful in crystallography studies for analyzing protein-ligand interactions. Additionally, it serves as a building block in the design of peptidomimetic drugs aimed at improving metabolic stability and bioavailability.

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