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TCO-PEG3-TCO
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Catalog No. T18770Cas No. 2243569-22-2
TCO-PEG3-TCO is a PEG-based linker commonly used in PROTAC development to connect two essential ligands within a single molecule. By facilitating the formation of bifunctional degraders, TCO-PEG3-TCO linker supports targeted protein degradation through the ubiquitin–proteasome system, enabling precise modulation of intracellular protein levels.
TCO-PEG3-TCO
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Purity: 98%
Catalog No. T18770Cas No. 2243569-22-2
TCO-PEG3-TCO is a PEG-based linker commonly used in PROTAC development to connect two essential ligands within a single molecule. By facilitating the formation of bifunctional degraders, TCO-PEG3-TCO linker supports targeted protein degradation through the ubiquitin–proteasome system, enabling precise modulation of intracellular protein levels.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $48 | - | In Stock | |
| 5 mg | $113 | - | In Stock | |
| 10 mg | $166 | - | In Stock | |
| 25 mg | $278 | - | In Stock | |
| 50 mg | $455 | - | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:98%
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Product Introduction
Bioactivity
Chemical Properties
| Description | TCO-PEG3-TCO is a PEG-based linker commonly used in PROTAC development to connect two essential ligands within a single molecule. By facilitating the formation of bifunctional degraders, TCO-PEG3-TCO linker supports targeted protein degradation through the ubiquitin–proteasome system, enabling precise modulation of intracellular protein levels. |
| In vitro | PROTACs consist of two distinct ligands connected by a linker: one ligand targets an E3 ubiquitin ligase, while the other targets the desired protein. They utilize the intracellular ubiquitin-proteasome system to selectively degrade target proteins [PROteolysis TArgeting Chimeras (PROTACs)]. |
| Molecular Weight | 496.65 |
| Formula | C26H44N2O7 |
| Cas No. | 2243569-22-2 |
| Smiles | O=C(OC1CCC=CCCC1)NCCOCCOCCOCCNC(=O)OC2CCC=CCCC2 |
| Relative Density. | 1.11 g/cm3 (Predicted) |
| Color | Yellow |
| Appearance | Oil |
Storage & Solubility Information
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
Calculator
In Vivo Formulation Calculator (Clear solution)
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:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (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.
(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 DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
Dose Conversion
You can also refer to dose conversion for different animals. More Dose Conversion
Tech Support
Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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