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Thalidomide-O-amido-PEG-C2-NH2 hydrochloride

Thalidomide-O-amido-PEG-C2-NH2 hydrochloride
Thalidomide-O-amido-PEG-C2-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate, incorporating a Thalidomide-based cereblon ligand and a linker. This compound is used in the synthesis of PROTACs.
Catalog No. T18818Cas No. 2204226-02-6
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Purity:95%
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Thalidomide-O-amido-PEG-C2-NH2 hydrochloride

Catalog No. T18818Cas No. 2204226-02-6

Thalidomide-O-amido-PEG-C2-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate, incorporating a Thalidomide-based cereblon ligand and a linker. This compound is used in the synthesis of PROTACs.
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Pack SizePriceAvailabilityQuantity
5 mg$29In Stock
10 mg$44In Stock
25 mg$73In Stock
50 mg$107In Stock
1 mL x 10 mM (in DMSO)$38In Stock
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Product Introduction

Bioactivity
Description
Thalidomide-O-amido-PEG-C2-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate, incorporating a Thalidomide-based cereblon ligand and a linker. This compound is used in the synthesis of PROTACs.
In vitro
PROTACs consist of two ligands joined by a linker: one ligand targets an E3 ubiquitin ligase, and the other targets the protein of interest. They leverage the intracellular ubiquitin-proteasome system to selectively degrade these target proteins [1].
Chemical Properties
Molecular Weight454.862
FormulaC19H23ClN4O7
Cas No.2204226-02-6
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: 100 mg/mL (219.85 mM), Sonication is recommended.
DMSO: 125 mg/mL (274.81 mM), Sonication is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM2.1985 mL10.9923 mL21.9847 mL109.9234 mL
5 mM0.4397 mL2.1985 mL4.3969 mL21.9847 mL
10 mM0.2198 mL1.0992 mL2.1985 mL10.9923 mL
20 mM0.1099 mL0.5496 mL1.0992 mL5.4962 mL
50 mM0.0440 mL0.2198 mL0.4397 mL2.1985 mL
100 mM0.0220 mL0.1099 mL0.2198 mL1.0992 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
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
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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