2-Amino-N-phenylquinoline-3-carboxamide

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Reagent Code: #138206
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CAS Number 121217-60-5

science Other reagents with same CAS 121217-60-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.29 g/mol
Formula C₁₆H₁₃N₃O
badge Registry Numbers
MDL Number MFCD02625574
inventory_2 Storage & Handling
Storage Room temperature, light-proof

description Product Description

Used as a key intermediate in the synthesis of antimalarial drugs, particularly in the development of compounds targeting Plasmodium species. Exhibits strong affinity for heme binding, making it valuable in disrupting the detoxification process in malaria parasites. Also employed in the design of fluorescent probes for biological imaging due to its inherent photoluminescent properties. Shows potential in medicinal chemistry for anticancer research, where it acts as a scaffold for kinase inhibitors. Additionally, utilized in the study of protein-protein interactions as a biochemical tool compound.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,780.00
inventory 250mg
10-20 days ฿7,990.00
inventory 1g
10-20 days ฿23,350.00

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2-Amino-N-phenylquinoline-3-carboxamide
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Used as a key intermediate in the synthesis of antimalarial drugs, particularly in the development of compounds targeting Plasmodium species. Exhibits strong affinity for heme binding, making it valuable in disrupting the detoxification process in malaria parasites. Also employed in the design of fluorescent probes for biological imaging due to its inherent photoluminescent properties. Shows potential in medicinal chemistry for anticancer research, where it acts as a scaffold for kinase inhibitors. Addit

Used as a key intermediate in the synthesis of antimalarial drugs, particularly in the development of compounds targeting Plasmodium species. Exhibits strong affinity for heme binding, making it valuable in disrupting the detoxification process in malaria parasites. Also employed in the design of fluorescent probes for biological imaging due to its inherent photoluminescent properties. Shows potential in medicinal chemistry for anticancer research, where it acts as a scaffold for kinase inhibitors. Additionally, utilized in the study of protein-protein interactions as a biochemical tool compound.

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