L-Aspartic acid, N-[2-(1H-indol-3-yl)acetyl]-

97%

Reagent Code: #201636
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CAS Number 2456-73-7

science Other reagents with same CAS 2456-73-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 290.2714 g/mol
Formula C₁₄H₁₄N₂O₅
badge Registry Numbers
MDL Number MFCD00079391
thermostat Physical Properties
Boiling Point 641.7±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.478±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used in pharmaceutical research as a precursor or intermediate in the synthesis of bioactive compounds. Shows potential in studies related to neuroprotective agents and anti-inflammatory drugs due to its structural similarity to indole derivatives, which are known to interact with central nervous system receptors. Also investigated for its role in modulating cell signaling pathways involved in apoptosis and immune response. Employed in peptide-based drug design where the indoleacetyl group enhances membrane permeability and target specificity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,860.00
inventory 1g
10-20 days ฿26,500.00
inventory 250mg
10-20 days ฿11,960.00

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L-Aspartic acid, N-[2-(1H-indol-3-yl)acetyl]-
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Used in pharmaceutical research as a precursor or intermediate in the synthesis of bioactive compounds. Shows potential in studies related to neuroprotective agents and anti-inflammatory drugs due to its structural similarity to indole derivatives, which are known to interact with central nervous system receptors. Also investigated for its role in modulating cell signaling pathways involved in apoptosis and immune response. Employed in peptide-based drug design where the indoleacetyl group enhances membr

Used in pharmaceutical research as a precursor or intermediate in the synthesis of bioactive compounds. Shows potential in studies related to neuroprotective agents and anti-inflammatory drugs due to its structural similarity to indole derivatives, which are known to interact with central nervous system receptors. Also investigated for its role in modulating cell signaling pathways involved in apoptosis and immune response. Employed in peptide-based drug design where the indoleacetyl group enhances membrane permeability and target specificity.

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