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(3S)Lenalidomide-piperazine-C-piperidine

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Catalog No. T201749Cas No. 2520107-24-6

(3S)Lenalidomide-piperazine-C-piperidine is an E3 ubiquitin ligase ligand-linker conjugate (E3 Ligase Ligand-Linker Conjugates). This compound can be utilized in the synthesis of PROTAC ER Degrader-11.

(3S)Lenalidomide-piperazine-C-piperidine

(3S)Lenalidomide-piperazine-C-piperidine

😃Good
Catalog No. T201749Cas No. 2520107-24-6
(3S)Lenalidomide-piperazine-C-piperidine is an E3 ubiquitin ligase ligand-linker conjugate (E3 Ligase Ligand-Linker Conjugates). This compound can be utilized in the synthesis of PROTAC ER Degrader-11.
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Product Introduction

Bioactivity
Description
(3S)Lenalidomide-piperazine-C-piperidine is an E3 ubiquitin ligase ligand-linker conjugate (E3 Ligase Ligand-Linker Conjugates). This compound can be utilized in the synthesis of PROTAC ER Degrader-11.
Chemical Properties
Molecular Weight425.52
FormulaC23H31N5O3
Cas No.2520107-24-6
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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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
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