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Thalidomide-O-amido-C6-NH2 hydrochloride

Catalog No. T18816Cas No. 2376990-31-5

Thalidomide-O-amido-C6-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate, integrating a Thalidomide-based cereblon ligand with a linker, suitable for PROTAC synthesis.

Thalidomide-O-amido-C6-NH2 hydrochloride

Thalidomide-O-amido-C6-NH2 hydrochloride

Purity: 97.33%
Catalog No. T18816Cas No. 2376990-31-5
Thalidomide-O-amido-C6-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate, integrating a Thalidomide-based cereblon ligand with a linker, suitable for PROTAC synthesis.
Pack SizePriceAvailabilityQuantity
1 mg$54In Stock
5 mg$127In Stock
10 mg$188In Stock
25 mg$317In Stock
50 mg$472In Stock
100 mg$678In Stock
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Purity:97.33%
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Product Introduction

Bioactivity
Description
Thalidomide-O-amido-C6-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate, integrating a Thalidomide-based cereblon ligand with a linker, suitable for PROTAC synthesis.
In vitro
PROTACs comprise two distinct ligands linked together: one binds to an E3 ubiquitin ligase, while the other targets a specific protein. They harness the intracellular ubiquitin-proteasome system to selectively degrade target proteins[1].
Chemical Properties
Molecular Weight466.915
FormulaC21H27ClN4O6
Cas No.2376990-31-5
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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