2-((2-carboxyethyl)thio)nicotinic acid

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Reagent Code: #86624
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CAS Number 286472-02-4

science Other reagents with same CAS 286472-02-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.24 g/mol
Formula C₉H₉NO₄S
badge Registry Numbers
MDL Number MFCD02250406
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting inflammatory and metabolic disorders. Its structure, featuring both carboxylic acid and thiol groups, makes it a versatile building block for designing drugs with enhanced binding affinity and specificity. Additionally, it is explored in the development of chelating agents for metal ions, which can be applied in diagnostic imaging or therapeutic agents for metal overload conditions. Its potential in modifying peptides and proteins to improve their stability and efficacy is also under investigation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,510.00
inventory 250mg
10-20 days ฿6,750.00
inventory 1g
10-20 days ฿13,500.00
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2-((2-carboxyethyl)thio)nicotinic acid
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting inflammatory and metabolic disorders. Its structure, featuring both carboxylic acid and thiol groups, makes it a versatile building block for designing drugs with enhanced binding affinity and specificity. Additionally, it is explored in the development of chelating agents for metal ions

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting inflammatory and metabolic disorders. Its structure, featuring both carboxylic acid and thiol groups, makes it a versatile building block for designing drugs with enhanced binding affinity and specificity. Additionally, it is explored in the development of chelating agents for metal ions, which can be applied in diagnostic imaging or therapeutic agents for metal overload conditions. Its potential in modifying peptides and proteins to improve their stability and efficacy is also under investigation.

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