الصفحة الرئيسية>>Signaling Pathways>> PROTAC>> E3 Ligase Ligand-Linker Conjugate>>E3 Ligase Ligand-Linker Conjugates 19

E3 Ligase Ligand-Linker Conjugates 19 (Synonyms: Cereblon Ligand-Linker Conjugates 6; E3 Ligase Ligand-Linker Conjugates 19)

رقم الكتالوجGC33129

يمكن استخدام E3 Ligase Ligand-Linker Conjugates 19 (Cereblon Ligand-Linker Conjugates 6) ، وهو اتحاد مركب E3 ligase ligand-linker الذي يشتمل على يجند cereblon القائم على ثاليدوميد ورابط ، في تخليق PROTACs.

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E3 Ligase Ligand-Linker Conjugates 19 التركيب الكيميائي

Cas No.: 1799711-24-2

الحجم السعر المخزون الكميّة
100mg
321٫00
متوفر
500mg
1241٫00
متوفر
1g
2298٫00
متوفر
2g
3218٫00
متوفر

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

E3 Ligase Ligand-Linker Conjugates 19 is a degron-linker. The PROTAC linker is bound lo at least one targeting ligand.

E3 Ligase Ligand-Linker Conjugates 19 is an amine intermediate (Compound 41), which can be used as is a heterobifunctional PROTAC BET degrader. The bromodomain and extra-terminal (BET) family proteins, consisting of BRD2, BRD3, BRD4, and testis-specific BRDT members, are epigenetic "readers" and play a key role in the regulation of gene transcription. BET proteins are considered to be attractive therapeutic targets for cancer and other human diseases. Recently, heterobifunctional small-molecule BET degraders have been designed based upon the proteolysis targeting chimera (PROTAC) concept to induce BET protein degradation[1]. E3 Ligase Ligand-Linker Conjugates 19 is a degron-linker (refer to Compound DL6-TL). Degron-linker-targeting ligand, wherein the linker is covalently bound lo at least one degron and at least one targeting ligand, the degron is a compound capable of binding to an ubiquitin ligase such as an E3 ubiquitin ligase (e g, cereblon), and the targeting ligand is capable of binding to the targeted protein (s)[2].

[1]. Zhou B, et al. Discovery of a Small-Molecule Degrader of Bromodomain and Extra-Terminal (BET) Proteins withPicomolar Cellular Potencies and Capable of Achieving Tumor Regression. J Med Chem. 2017 Mar 24. [2]. James Bradner, et al. Methods to induce targeted protein degradation through bifunctional molecules. WO 2017024317 A2.

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