Thalidomide-O-amido-C3-NH2

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Reagent Code: #63068
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CAS Number 2022182-58-5

science Other reagents with same CAS 2022182-58-5

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Weight 502.4 g/mol
Formula C₂₀H₂₁F₃N₄O₃
inventory_2 Storage & Handling
Storage -20°C, airtight, dry

description Product Description

Used primarily in the field of medicinal chemistry and drug development, Thalidomide-O-amido-C3-NH2 serves as a key intermediate in the synthesis of more complex pharmaceutical compounds derived from thalidomide analogs. Its structure, featuring an O-amido-C3-NH2 modification, allows for further chemical modifications that can enhance binding affinity and selectivity towards specific biological targets, such as those involved in immunomodulation. This compound is particularly valuable in the design of prodrugs, where it can be tailored to improve pharmacokinetic properties, such as absorption and distribution. Additionally, it plays a role in the development of targeted therapies for conditions like cancer and inflammatory diseases, where precise drug delivery is crucial. Researchers also explore its potential in creating novel immunomodulatory agents, leveraging the thalidomide scaffold's ability to influence immune responses.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿17,280.00

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Thalidomide-O-amido-C3-NH2
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Used primarily in the field of medicinal chemistry and drug development, Thalidomide-O-amido-C3-NH2 serves as a key intermediate in the synthesis of more complex pharmaceutical compounds derived from thalidomide analogs. Its structure, featuring an O-amido-C3-NH2 modification, allows for further chemical modifications that can enhance binding affinity and selectivity towards specific biological targets, such as those involved in immunomodulation. This compound is particularly valuable in the design of pr

Used primarily in the field of medicinal chemistry and drug development, Thalidomide-O-amido-C3-NH2 serves as a key intermediate in the synthesis of more complex pharmaceutical compounds derived from thalidomide analogs. Its structure, featuring an O-amido-C3-NH2 modification, allows for further chemical modifications that can enhance binding affinity and selectivity towards specific biological targets, such as those involved in immunomodulation. This compound is particularly valuable in the design of prodrugs, where it can be tailored to improve pharmacokinetic properties, such as absorption and distribution. Additionally, it plays a role in the development of targeted therapies for conditions like cancer and inflammatory diseases, where precise drug delivery is crucial. Researchers also explore its potential in creating novel immunomodulatory agents, leveraging the thalidomide scaffold's ability to influence immune responses.

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