Organo-Metalloid Compounds
Medchemexpress LLC M-PEG5-Br | 854601-80-2 | 98.0% | C11H23BrO5 | 5 G
m-PEG5-Br is a PEG-based PROTAC linker. It is for research use only and not for sale to patients. This linker can be used in the synthesis of PROTACs, which consist of two different ligands connected by a linker; one ligand is for an E3 ubiquitin ligase and the other is for the target protein. PROTACs utilize the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- Used in the synthesis of PROTACs
- Utilizes the intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
- For research use only
Medchemexpress LLC m-PEG5-Br | 854601-80-2 | 98.0% | C11H23BrO5 | 500 MG
m-PEG5-Br is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. These molecules contain two different ligands connected by a linker, where one ligand is for an E3 ubiquitin ligase and the other targets a specific protein.
- Exploits the intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
Medchemexpress LLC M-PEG5-Br | 854601-80-2 | 98.0% | C11H23BrO5 | 10 G
m-PEG5-Br is a PEG-based PROTAC linker utilized in the synthesis of PROTACs. PROTACs consist of two distinct ligands connected by a linker, with one ligand targeting an E3 ubiquitin ligase and the other targeting the protein of interest. These compounds function by exploiting the intracellular ubiquitin-proteasome system to facilitate the selective degradation of target proteins.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Facilitates selective degradation of target proteins
Medchemexpress LLC Br-PEG3-MS | 2702323-73-5 | >95.0% | 291.16 | 50 MG
Br-PEG3-MS is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
Medchemexpress LLC m-PEG5-Br | 854601-80-2 | 98.0% | C11H23BrO5 | 25 G
m-PEG5-Br is a PEG-based PROTAC linker used in the synthesis of PROTACs. PROTACs are designed to selectively degrade target proteins by utilizing the intracellular ubiquitin-proteasome system. They achieve this by connecting two ligands: one for an E3 ubiquitin ligase and another for the target protein.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Exploits the ubiquitin-proteasome system
- Selectively degrades target proteins
Sigma Aldrich Polyamide/Imide
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Sigma Aldrich 4-(4-Fluorobenzyl)piperidine hydrochloride
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Sigma Aldrich 2-(Trifluoromethyl)cyclohexanone
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Sigma Aldrich 3-bromo-2-fluorobenzaldehyde
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Sigma Aldrich Pomalidomide-Peg3-Nh2 Hydrochloride
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Sigma Aldrich 5-(Chloromethyl)-1,3-thiazole hydrochloride
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Sigma Aldrich Bis[(Pinacolato)Boryl]Methane
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Sigma Aldrich 2-[(Methoxycarbonyl)amino]acetic acid
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Sigma Aldrich Diisopropyl malonate
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Sigma Aldrich 6-Chloro-3-nitro-2-pyridinecarbonitrile
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