CAS 186452-09-5
:(S)-3-(Pyridine-3-yl)propyl-1-(3,3-dimethyl-2-oxo-pentanoyl)pyrrolidine-2-carboxylate
Description:
(S)-3-(Pyridine-3-yl)propyl-1-(3,3-dimethyl-2-oxo-pentanoyl)pyrrolidine-2-carboxylate, with CAS number 186452-09-5, is a chemical compound characterized by its complex structure, which includes a pyrrolidine ring, a pyridine moiety, and a carboxylate functional group. This compound is typically classified as a pyrrolidine derivative and may exhibit properties such as solubility in organic solvents, depending on the specific substituents and their interactions. The presence of the pyridine ring suggests potential for coordination with metal ions or involvement in hydrogen bonding, while the carboxylate group can participate in various chemical reactions, including esterification and acid-base reactions. Its stereochemistry, indicated by the (S) configuration, may influence its biological activity and interactions with other molecules. Such compounds are often of interest in medicinal chemistry for their potential therapeutic applications, particularly in the development of pharmaceuticals targeting specific biological pathways. Further studies would be necessary to elucidate its full range of properties and potential uses.
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Found 4 products.
GPI-1046
CAS:<p>GPI-1046: immunophilin ligand, no antibiotic effect, reduces ethanol intake by boosting GLT1 in PFC and NAc-core.</p>Formula:C20H28N2O4Purity:99.69%Color and Shape:SolidMolecular weight:360.45(S)-3-(Pyridine-3-yl)propyl 1-(3,3-dimethyl-2-oxopentanoyl)pyrrolidine-2-carboxylate
CAS:Formula:C20H28N2O4Purity:99%Color and Shape:LiquidMolecular weight:360.44731-(3,3-Dimethyl-1,2-dioxopentyl)-L-proline 3-(3-pyridinyl)propyl Ester
CAS:Controlled Product<p>Applications GPI 1046 shows some effect on neuron survival and regeneration in studies.<br>References Harper, S. et al.: Neurosci., 88, 257 (1998);<br></p>Formula:C20H28N2O4Color and Shape:NeatMolecular weight:360.45



