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2-Aminoadamantane-2-carboxylic acid, characterized by its unique geminally functionalized structure, stands out as an achiral, tricycloaliphatic aminocarboxylic acid. This compound is noted for its ability to disrupt the normal transportation processes of amino acids, such as L-leucine and L-methionine, specifically targeting their uptake into Ehrlich ascites tumor cells. This inhibition mechanism is pivotal in the context of biochemical research, as it allows scientists to explore the fundamental aspects of cellular transport mechanisms and amino acid metabolism. The molecule′s distinctive tricyclic framework, combined with its functional groups, offers a robust tool for dissecting the nuances of cell membrane permeability and transport protein interactions. Consequently, 2-Aminoadamantane-2-carboxylic acid serves as a valuable probe in the study of cellular processes, aiding in the elucidation of the intricate dynamics of amino acid transport and its regulation within cellular environments. This exploration contributes significantly to our understanding of cellular nutrition and the metabolic pathways critical to cell growth and maintenance, thereby facilitating advancements in biochemical and molecular biology research fields.
Ordering Information
Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-Aminoadamantane-2-carboxylic acid, 500 mg | sc-306873 | 500 mg | $900.00 |