Produktname:1-(4-bromo-2,6-difluoro-phenyl)-3-(2-trimethylsilylethoxymethyl)hexahydropyrimidine-2,4-dione
IUPAC Name:1-(4-bromo-2,6-difluorophenyl)-3-{[2-(trimethylsilyl)ethoxy]methyl}-1,3-diazinane-2,4-dione
- CAS:2940940-46-3
- Molekulare Formel:C16H21BrF2N2O3Si
- Reinheit:95%
- Katalognummer:CM1076165
- Molekulargewicht:435.34
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Produkt-Details
- CAS-Nr.:2940940-46-3
- Molekulare Formel:C16H21BrF2N2O3Si
- Schmelzpunkt:-
- SMILES-Code:C[Si](C)(C)CCOCN1C(=O)CCN(C1=O)C1=C(F)C=C(Br)C=C1F
- Dichte:
- Katalognummer:CM1076165
- Molekulargewicht:435.34
- Siedepunkt:
- Mdl-Nr.:
- Lagerung:
Category Infos
- PROTAC-E3 Ligase Ligands
- Bifunctional degrader molecules, also called proteolysis-targeting chimeras (PROTACs), are a new modality of chemical tools and potential therapeutics to understand and treat human disease. A required PROTAC component is a ligand binding to an E3 ubiquitin ligase, which is then joined to another ligand binding to a protein to be degraded via the ubiquitin–proteasome system. The advent of nonpeptidic small-molecule E3 ligase ligands revolutionized the field and ushered in the design of drug-like PROTACs with potent and selective degradation activity.
- PROTAC-E3 Ligase Ligands | PROTACs | Bifunctional Degrader Molecules
- Proteolysis-Targeting Chimeras | PROTAC-E3 Ligase Ligands | PROTACs | Bifunctional Degrader Molecules
- PROTAC (Proteolysis-Targeting Chimeras) is a promising approach in drug discovery that involves the use of small molecules to target specific proteins for degradation by the cellular machinery.