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Pomalidomide-PEG3-C2-NH2 hydrochloride

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Catalog No. T40105Cas No. 2446474-09-3
Alias Pomalidomide-PEG3-C2-NH2 hydrochloride, E3ligaseLigand-LinkerConjugates30hydrochloride, Cereblon Ligand-Linker Conjugates 5 hydrochloride

Pomalidomide-PEG3-C2-NH2 hydrochloride, also known as Cereblon Ligand-Linker Conjugate 5, is a chemically synthesized E3 ligase ligand-linker conjugate. This compound incorporates a cereblon ligand based on Pomalidomide and a linker commonly employed in PROTAC technology.

Pomalidomide-PEG3-C2-NH2 hydrochloride
Other Forms of Pomalidomide-PEG3-C2-NH2 hydrochloride:

Pomalidomide-PEG3-C2-NH2 hydrochloride

😃Good
Catalog No. T40105Alias Pomalidomide-PEG3-C2-NH2 hydrochloride, E3ligaseLigand-LinkerConjugates30hydrochloride, Cereblon Ligand-Linker Conjugates 5 hydrochlorideCas No. 2446474-09-3
Pomalidomide-PEG3-C2-NH2 hydrochloride, also known as Cereblon Ligand-Linker Conjugate 5, is a chemically synthesized E3 ligase ligand-linker conjugate. This compound incorporates a cereblon ligand based on Pomalidomide and a linker commonly employed in PROTAC technology.
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25 mg$52335 days
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Product Introduction

Bioactivity
Description
Pomalidomide-PEG3-C2-NH2 hydrochloride, also known as Cereblon Ligand-Linker Conjugate 5, is a chemically synthesized E3 ligase ligand-linker conjugate. This compound incorporates a cereblon ligand based on Pomalidomide and a linker commonly employed in PROTAC technology.
In vitro
PROTACs consist of two ligands linked together: one binds to an E3 ubiquitin ligase, and the other targets the protein. They utilize the intracellular ubiquitin-proteasome system to selectively degrade target proteins [2].
AliasPomalidomide-PEG3-C2-NH2 hydrochloride, E3ligaseLigand-LinkerConjugates30hydrochloride, Cereblon Ligand-Linker Conjugates 5 hydrochloride
Chemical Properties
Molecular Weight484.93
FormulaC21H29ClN4O7
Cas No.2446474-09-3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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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.
1 Enter information below:
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2 Enter the in vivo formulation:
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Keywords

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