Nom du produit: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
Formule moléculaire:C16H21BrF2N2O3Si
Pureté:95%
Numéro de catalogue:CM1076165
Poids moléculaire:435.34

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Détails du produit

N° CAS:2940940-46-3
Formule moléculaire:C16H21BrF2N2O3Si
Point de fusion:-
Code SMILES:C[Si](C)(C)CCOCN1C(=O)CCN(C1=O)C1=C(F)C=C(Br)C=C1F
Densité:
Numéro de catalogue:CM1076165
Poids moléculaire:435.34
Point d'ébullition:
N° Mdl:
Stockage:

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.