![4-Thiazolidinecarboxylic acid,2-[[[(2R)-amino(4-hydroxyphenyl)acetyl]amino]methyl]-5,5-dimethyl-,(…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F14451-4-thiazolidinecarboxylic-acid-2-2r-amino-4-hydroxyphenyl-acetyl-amino-methyl-55-dimethyl-2r-4s.webp&w=3840&q=75)
CAS 178738-48-2
:4-Thiazolidinecarboxylic acid,2-[[[(2R)-amino(4-hydroxyphenyl)acetyl]amino]methyl]-5,5-dimethyl-,(2R,4S)-
Description:
4-Thiazolidinecarboxylic acid, 2-[[[(2R)-amino(4-hydroxyphenyl)acetyl]amino]methyl]-5,5-dimethyl-, (2R,4S)-, is a complex organic compound characterized by its thiazolidine ring structure, which incorporates a carboxylic acid functional group. This compound features a chiral center, indicated by its (2R,4S) configuration, which contributes to its stereochemical properties. The presence of an amino group and a hydroxyphenyl moiety suggests potential biological activity, possibly related to its role in amino acid metabolism or as a precursor in pharmaceutical synthesis. The dimethyl substitution on the thiazolidine ring enhances its steric properties, potentially influencing its reactivity and interaction with biological targets. Additionally, the compound's solubility and stability can be affected by the functional groups present, making it of interest in medicinal chemistry and drug design. Overall, this compound exemplifies the intricate relationship between molecular structure and biological function, warranting further investigation into its applications in therapeutic contexts.
Formula:C15H21N3O4S
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Found 3 products.
(2RS,4S)-2-[[[(2R)-2-Amino-2-(4-hydroxyphenyl)acetyl]amino]methyl]-5,5-dimethylthiazolidine-4-carboxylic Acid (Penilloic Acids of Amoxicillin)
CAS:Controlled ProductFormula:C15H21N3O4SColor and Shape:NeatMolecular weight:339.41Amoxicillin trihydrate impurity E
CAS:<p>Amoxicillin trihydrate impurity E is a β-lactam antibiotic that belongs to the class of penicillins. It is used in the treatment of bacterial infections caused by a wide range of bacteria, such as Staphylococcus aureus, Escherichia coli, and Proteus mirabilis. Amoxicillin trihydrate impurity E has been shown to be effective against many strains of bacteria that are resistant to other antibiotics, including methicillin-resistant Staphylococcus aureus (MRSA). Amoxicillin trihydrate impurity E inhibits bacterial growth by binding to the peptidoglycan layer that surrounds the bacterial cell wall and prevents it from growing or reproducing. The drug also interferes with protein synthesis in the ribosomes located on the cytoplasmic membrane. This results in reduced levels of beta-lactamase, which is an enzyme that breaks down ampicillin and related</p>Formula:C15H21N3O4SPurity:Min. 95%Molecular weight:339.41 g/mol
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