CAS 480439-73-4
:L-Aspartic acid,3-[[3-[[4-(trifluoromethyl)benzoyl]amino]phenyl]methoxy]-, (3S)-
Description:
L-Aspartic acid, 3-[[3-[[4-(trifluoromethyl)benzoyl]amino]phenyl]methoxy]-, (3S)-, identified by CAS number 480439-73-4, is a synthetic compound that features a complex structure incorporating both amino acid and aromatic functionalities. As a derivative of L-aspartic acid, it retains the characteristic carboxylic acid and amino groups, which contribute to its solubility in polar solvents and its potential biological activity. The presence of a trifluoromethyl group enhances its lipophilicity and may influence its interaction with biological targets. The methoxy and benzoyl substituents suggest potential applications in medicinal chemistry, possibly as a pharmaceutical agent or a biochemical probe. This compound's stereochemistry, indicated by the (3S) designation, is crucial for its biological activity, as the spatial arrangement of atoms can significantly affect how it interacts with enzymes or receptors. Overall, this compound exemplifies the intricate relationship between molecular structure and function in the realm of organic and medicinal chemistry.
Formula:C19H17F3N2O6
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Found 2 products.
(3S)-3-[(3-{[4-(Trifluoromethyl)Benzoyl]Amino}Benzyl)Oxy]-L-Aspartic Acid
CAS:<p>The 3S-3-[(3-{[4-(Trifluoromethyl)Benzoyl]Amino}Benzyl)Oxy]-L-Aspartic Acid is a synthetic amino acid that binds to the α subunit of the glutamate receptor. This binding leads to increased neuronal activity, increased levels of ATP and glutamate, and an increase in locomotor activity. The 3S-3-[(3-{[4-(Trifluoromethyl)Benzoyl]Amino}Benzyl)Oxy]-L-Aspartic Acid has been shown to be cytotoxic in vivo, as well as inhibiting mitochondrial function and causing neuronal death in vitro.</p>Formula:C19H17F3N2O6Purity:Min. 95%Molecular weight:426.34 g/molTFB-TBOA
CAS:<p>glial glutamate transporter EAAT1 and EAAT2 inhibitor</p>Formula:C19H17F3N2O6Purity:98%Color and Shape:SolidMolecular weight:426.34

