![]() Azido-PEG3-azide structure
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Common Name | Azido-PEG3-azide | ||
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CAS Number | 101187-39-7 | Molecular Weight | 244.25100 | |
Density | 1.1703g/mL | Boiling Point | 163-196°C | |
Molecular Formula | C8H16N6O3 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | N/A | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Use of Azido-PEG3-azideAzido-PEG3-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. |
Name | 1,11-Diazido-3,6,9-trioxaundecane |
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Synonym | More Synonyms |
Description | Azido-PEG3-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. |
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Related Catalog | |
Target |
PEGs |
In Vitro | PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins[1]. |
References |
Density | 1.1703g/mL |
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Boiling Point | 163-196°C |
Molecular Formula | C8H16N6O3 |
Molecular Weight | 244.25100 |
Exact Mass | 244.12800 |
PSA | 127.19000 |
LogP | 0.56232 |
Storage condition | -20°C |
~88% Azido-PEG3-azide CAS#:101187-39-7 |
Literature: WO2006/73314 A1, ; Page/Page column 31 ; |
~92% Azido-PEG3-azide CAS#:101187-39-7 |
Literature: Chemical Communications, , vol. 48, # 45 p. 5650 - 5652 |
~99% Azido-PEG3-azide CAS#:101187-39-7 |
Literature: WO2008/11157 A2, ; Page/Page column 174 ; |
~99% Azido-PEG3-azide CAS#:101187-39-7 |
Literature: Tetrahedron, , vol. 65, # 36 p. 7385 - 7392 |
~15% Azido-PEG3-azide CAS#:101187-39-7 |
Literature: Angewandte Chemie - International Edition, , vol. 51, # 9 p. 2151 - 2154 |
~99% Azido-PEG3-azide CAS#:101187-39-7 |
Literature: Journal of the American Chemical Society, , vol. 127, # 36 p. 12434 - 12435 |
Precursor 5 | |
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DownStream 4 | |
Novel analogs of antitumor agent calixarene 0118: Synthesis, cytotoxicity, click labeling with 2-[(18)F]fluoroethylazide, and in vivo evaluation.
Eur. J. Med. Chem. 89 , 279-95, (2014) Calixarene 0118 is a potent anti-angiogenic agent that effectively inhibited tumor growth in preclinical studies, and is currently being evaluated in a phase I clinical trial. We have designed two clo... |
1-azido-2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethane |