Pomalidomide-5'-C2-OH piperidine The azide group (N3) reacts

The azide group (N3) reacts with terminal alkynes to produce a stable triazole

Compared to tetramethylrhodamine maleimides and iodoacetamides

NCCOCCOCCOCCOCCNC(=O)COC1=C2C(=O)N(C3CCC(=O)NC3=O)C(=O)C2=CC=C1 Purity (HPLC) >= 95% Shipping Conditions Room temperature Storage Conditions Refrigerated Shelf Life 12 months after the date of delivery Regulatory Statement For Research Use Only

85 SMILES: CC1(C)\C(=C/C=C/C2=[N+](CCCCCC(=O)NCCCN=[N]#N)C3=CC=CC=C3C2(C)C)N(CCCS([O-])(=O)=O)C2=CC=CC=C12 Purity (HPLC): ≥ 95% Shipping Conditions: room temperature Storage Conditions: Refrigerated Regulatory Statement: For Research Use Only

Also a fluorescent transglutaminase substrate to label proteins by transaminidation

Pomalidomide-5'-C2-OH piperidine The azide group (N3) reactsDegrader building block for targeted protein degradation. Contains an E3 ligase ligand with a linker and a function group, which can be conjugated to target protein ligands through straightforward chemical reactions. Product Name Pomalidomide 5' C2 OH Synonyms CAS Number n a Related CAS Molecular Formula C15H15N3O5 Molecular Weight 317. 301 SMILES OCCNC1=CC=C2C(=O)N(C3CCC(=O)NC3=O)C(=O)C2=C1 Purity (HPLC) >= 95% Shipping Conditions Room temperature