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2-(2-((7-(TERT-BUTOXY)-7-OXOHEPTYL)OXY)&
Кат. №: 909998-100MG
Производитель: Sigma-Aldrich
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2-(2-((7-(TERT-BUTOXY)-7-OXOHEPTYL)OXY)&
Main image
Кат. №: 909998-100MG
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Main image
Печать
2-(2-((7-(TERT-BUTOXY)-7-OXOHEPTYL)OXY)&
Кат. №: 909998-100MG
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Description Application This heterobifunctional, PEGylated crosslinker 2-(2-((7-(tert-butoxy)-7-oxoheptyl)oxy)ethoxy)acetic acid features a carboxyl group at one end and a t-butyl protected carboxylic acid at the other and exhibits both hydrophobic and hydrophilic moieties for use in biological applications. The linker can be used for bioconjugation or as a building block for synthesis of small molecules, conjugates of small molecules and/or biomolecules, or other tool compounds for chemical biology and medicinal chemistry that require ligation. Examples of applications include its synthetic incorporation into antibody-drug conjugates or proteolysis-targeting chimeras (PROTAC® molecules) for targeted protein degradation where the linker region is referred to as 2-2-6. Other Notes Modular PROTAC Design for the Degradation of Oncogenic BCR-ABL Technology Spotlight: Degrader Building Blocks for Targeted Protein Degradation Legal Information PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license
Related Categories
Bifunctional Linkers, Chemical Biology, Chemical Synthesis, Linkers and Crosslinkers assay
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.
Description Application This heterobifunctional, PEGylated crosslinker 2-(2-((7-(tert-butoxy)-7-oxoheptyl)oxy)ethoxy)acetic acid features a carboxyl group at one end and a t-butyl protected carboxylic acid at the other and exhibits both hydrophobic and hydrophilic moieties for use in biological applications. The linker can be used for bioconjugation or as a building block for synthesis of small molecules, conjugates of small molecules and/or biomolecules, or other tool compounds for chemical biology and medicinal chemistry that require ligation. Examples of applications include its synthetic incorporation into antibody-drug conjugates or proteolysis-targeting chimeras (PROTAC® molecules) for targeted protein degradation where the linker region is referred to as 2-2-6. Other Notes Modular PROTAC Design for the Degradation of Oncogenic BCR-ABL Technology Spotlight: Degrader Building Blocks for Targeted Protein Degradation Legal Information PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license
Related Categories
Bifunctional Linkers, Chemical Biology, Chemical Synthesis, Linkers and Crosslinkers assay
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.