2-(1H-Indol-3-yl)-2-oxo-N-phenylacetamide

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Reagent Code: #192844
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CAS Number 73031-16-0

science Other reagents with same CAS 73031-16-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.28 g/mol
Formula C₁₆H₁₂N₂O₂
inventory_2 Storage & Handling
Density 1.359±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily in pharmaceutical research as a structural analog of tryptophan and indole derivatives, this compound serves as a key intermediate in the synthesis of bioactive molecules. It shows potential in the development of kinase inhibitors and anti-inflammatory agents due to its ability to interact with cellular signaling pathways. Its amide and indole functionalities make it suitable for modifying peptide-like structures to enhance metabolic stability and receptor binding affinity. Additionally, it has been explored in the design of antitumor and antimicrobial compounds, where the scaffold contributes to improved selectivity and potency. Ongoing studies focus on optimizing its derivatives for use in neuropharmacology, particularly targeting serotonin-related receptors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,260.00
inventory 250mg
10-20 days ฿25,920.00

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2-(1H-Indol-3-yl)-2-oxo-N-phenylacetamide
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Used primarily in pharmaceutical research as a structural analog of tryptophan and indole derivatives, this compound serves as a key intermediate in the synthesis of bioactive molecules. It shows potential in the development of kinase inhibitors and anti-inflammatory agents due to its ability to interact with cellular signaling pathways. Its amide and indole functionalities make it suitable for modifying peptide-like structures to enhance metabolic stability and receptor binding affinity. Additionally, it has been explored in the design of antitumor and antimicrobial compounds, where the scaffold contributes to improved selectivity and potency. Ongoing studies focus on optimizing its derivatives for use in neuropharmacology, particularly targeting serotonin-related receptors.
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