(S)-3-((S)-5-oxopyrrolidine-2-carbonyl)thiazolidine-4-carboxylic acid
95%
- Product Code: 86462
CAS:
162148-16-5
| Molecular Weight: | 244.27 g./mol | Molecular Formula: | C₉H₁₂N₂O₄S |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 663.0±55.0 °C(Predicted) | |
| Density: | 1.526±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both thiazolidine and pyrrolidone rings, makes it a valuable scaffold for developing drugs targeting various diseases, particularly those involving inflammation and central nervous system disorders. The compound’s chiral centers contribute to its potential use in designing enantioselective drugs, enhancing specificity and reducing side effects. Additionally, it has been explored in the development of protease inhibitors, which are crucial in treating conditions like viral infections and certain cancers. Its application extends to peptide mimetics, where it helps mimic natural peptide structures, improving stability and bioavailability of therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,450.00 |
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| 0.250 | 10-20 days | ฿16,200.00 |
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| 1.000 | 10-20 days | ฿32,400.00 |
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(S)-3-((S)-5-oxopyrrolidine-2-carbonyl)thiazolidine-4-carboxylic acid
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both thiazolidine and pyrrolidone rings, makes it a valuable scaffold for developing drugs targeting various diseases, particularly those involving inflammation and central nervous system disorders. The compound’s chiral centers contribute to its potential use in designing enantioselective drugs, enhancing specificity and reducing side effects. Additionally, it has been explored in the development of protease inhibitors, which are crucial in treating conditions like viral infections and certain cancers. Its application extends to peptide mimetics, where it helps mimic natural peptide structures, improving stability and bioavailability of therapeutic agents.
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