2-(4-((2-Chlorobenzyl)oxy)-3-ethoxyphenyl)thiazolidine-4-carboxylic acid
98%
- Product Code: 129503
CAS:
1033696-31-9
| Molecular Weight: | 393.88 g./mol | Molecular Formula: | C₁₉H₂₀ClNO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD05240973 | |
| Melting Point: | Boiling Point: | 592.4±50.0 °C(Predicted) | |
| Density: | 1.322±0.06 g/cm3(Predicted) | Storage Condition: | -20°C, Sealed, Dry |
Product Description:
Used in pharmaceutical research as a key intermediate in the synthesis of peroxisome proliferator-activated receptor (PPAR) modulators, particularly for developing antidiabetic agents. Its structure supports binding to nuclear receptors involved in glucose and lipid metabolism. Commonly employed in the development of thiazolidinedione-based drugs, where it contributes to improving insulin sensitivity in type 2 diabetes. Also explored for anti-inflammatory and antineoplastic properties due to its ability to influence cell differentiation and apoptosis. Suitable for use in structure-activity relationship (SAR) studies aimed at optimizing metabolic stability and receptor selectivity.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 10mg | 10-20 days | ฿10,990.00 |
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| 25mg | 10-20 days | ฿21,990.00 |
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| 50mg | 10-20 days | ฿35,190.00 |
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-
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2-(4-((2-Chlorobenzyl)oxy)-3-ethoxyphenyl)thiazolidine-4-carboxylic acid
Used in pharmaceutical research as a key intermediate in the synthesis of peroxisome proliferator-activated receptor (PPAR) modulators, particularly for developing antidiabetic agents. Its structure supports binding to nuclear receptors involved in glucose and lipid metabolism. Commonly employed in the development of thiazolidinedione-based drugs, where it contributes to improving insulin sensitivity in type 2 diabetes. Also explored for anti-inflammatory and antineoplastic properties due to its ability to influence cell differentiation and apoptosis. Suitable for use in structure-activity relationship (SAR) studies aimed at optimizing metabolic stability and receptor selectivity.
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