2-(2,6-Dioxopiperidin-3-yl)-1-oxoisoindoline-5-carboxylic acid

97%

  • Product Code: 130707
  CAS:    2171780-01-9
Molecular Weight: 288.26 g./mol Molecular Formula: C₁₄H₁₂N₂O₅
EC Number: MDL Number: MFCD31735773
Melting Point: Boiling Point: 667.4±55.0 °C(Predicted)
Density: 1.535±0.06 g/cm3(Predicted) Storage Condition: Room temperature, light-proof, inert gas
Product Description: Used primarily in pharmaceutical research as a key intermediate in the synthesis of immunomodulatory drugs, particularly analogs of thalidomide such as lenalidomide. It plays a critical role in targeted protein degradation therapies, including the development of cereblon E3 ligase modulators. These compounds are investigated for their anticancer, anti-inflammatory, and antiproliferative properties, especially in hematological malignancies like multiple myeloma and myelodysplastic syndromes. Its structure enables selective binding to cereblon, facilitating the degradation of disease-causing proteins. Widely utilized in medicinal chemistry for designing PROTACs (proteolysis-targeting chimeras) and optimizing drug candidates with improved efficacy and safety profiles.
Sizes / Availability / Pricing:
Size Availability Price Quantity
100mg 10-20 days ฿5,050.00
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-
250mg 10-20 days ฿9,590.00
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-
1g 10-20 days ฿28,740.00
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-
2-(2,6-Dioxopiperidin-3-yl)-1-oxoisoindoline-5-carboxylic acid
Used primarily in pharmaceutical research as a key intermediate in the synthesis of immunomodulatory drugs, particularly analogs of thalidomide such as lenalidomide. It plays a critical role in targeted protein degradation therapies, including the development of cereblon E3 ligase modulators. These compounds are investigated for their anticancer, anti-inflammatory, and antiproliferative properties, especially in hematological malignancies like multiple myeloma and myelodysplastic syndromes. Its structure enables selective binding to cereblon, facilitating the degradation of disease-causing proteins. Widely utilized in medicinal chemistry for designing PROTACs (proteolysis-targeting chimeras) and optimizing drug candidates with improved efficacy and safety profiles.
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