CAS 100723-71-5
:L-Proline, N-[(4-methylphenyl)sulfonyl]glycyl-
Description:
L-Proline, N-[(4-methylphenyl)sulfonyl]glycyl- is a synthetic compound that belongs to the class of amino acid derivatives. It features a proline backbone, which is a cyclic amino acid known for its role in protein structure and function. The presence of a sulfonyl group attached to a 4-methylphenyl moiety indicates that this compound has potential applications in medicinal chemistry, particularly in the design of bioactive molecules. The sulfonyl group can enhance solubility and stability, while the aromatic ring may contribute to interactions with biological targets. This compound is likely to exhibit characteristics typical of amino acids, such as being polar and capable of forming hydrogen bonds, which can influence its reactivity and interactions in biological systems. Additionally, the specific arrangement of functional groups may impart unique properties, making it of interest for research in drug development or biochemical applications. As with many synthetic compounds, its safety and efficacy would need to be evaluated through appropriate studies.
Formula:C14H18N2O5S
Synonyms:- Tos-Gly-Pro
- Tos-Gly-L-Pro-OH
- TOS-GLY-PRO-OH
- (S)-1-(2-(4-MethylphenylsulfonaMido)acetyl)pyrrolidine-2-carboxylic acid
- L-Proline, N-[(4-methylphenyl)sulfonyl]glycyl-
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Found 4 products.
Tos-Gly-Pro-OH
CAS:<p>Bachem ID: 4000810.</p>Formula:C14H18N2O5SPurity:≥ 99%Color and Shape:White PowderMolecular weight:326.37L-Proline, N-[(4-methylphenyl)sulfonyl]glycyl-
CAS:Formula:C14H18N2O5SPurity:97%Molecular weight:326.3681(2s)-1-[2-(4-methylbenzenesulfonamido)acetyl]pyrrolidine-2-carboxylic acid
CAS:Purity:97%Molecular weight:326.3699951Tos-Gly-Pro-OH
CAS:<p>Tos-Gly-Pro-OH is a fluorescent histone deacetylase (HDAC) inhibitor. It has been validated as a competitive inhibitor of HDACs by using a fluorescence assay to detect the deacetylated form of 7-amino-4-methylcoumarin. Tos-Gly-Pro-OH is used in the treatment of malignant tumors, such as leukemia and lymphoma, by inhibiting HDACs that are responsible for cellular proliferation. In addition, Tos-Gly-Pro-OH may be useful in the treatment of diseases caused by bacterial infection because it inhibits bacterial HDACs that are responsible for protein synthesis and chemotaxis. This drug also inhibits trypsin activity and can be used as an alternative to nonisotopic solvents for peptide synthesis.</p>Formula:C14H18N2O5SPurity:Min. 95%Molecular weight:326.37 g/mol



