871345-34-5

Upstream product

• 26153-38-8 3,5-dihydroxybenzaldehyde 
• 871345-33-4 5-formyl-1,3-phenylene bis(trifluoromethanesulfonate) 
• 937018-55-8 trifluoro-methanesulfonic acid 3-ethynyl-5-formyl-phenyl ester 

Downstream Products

• 1219077-42-5 C₁₇H₁₄O₃ 
• 1219077-47-0 C₂₀H₁₈O₄S₂ 
• 1219077-61-8 C₂₁H₂₀O₄S₂ 
• 1256478-24-6 C₄₅H₄₉N₅O₆S₄ 
• 1256478-23-5 C₄₁H₄₁N₅O₆S₄ 
• 1256478-22-4 C₄₀H₃₉N₅O₆S₄ 
• 1256478-21-3 C₄₇H₅₅N₅O₇S₄ 
• 1256478-20-2 C₄₃H₄₇N₅O₇S₄ 
• 1256478-19-9 C₄₂H₄₅N₅O₇S₄ 
• 1256478-18-8 C₄₁H₄₃N₅O₇S₄ 
• 1256478-13-3 (E)-S-3-((3-ethynyl-5-((2-(9-mercaptononanoyl)hydrazono)methyl)phenoxy)methyl)benzylethanethioate 
• 1256478-12-2 (E)-S-3-((3-ethynyl-5-((2-(5-mercaptopentanoyl)hydrazono)methyl)phenoxy)methyl)benzylethanethioate 
• 1256478-11-1 (E)-S-3-((3-ethynyl-5-((2-(4-mercaptobutanoyl)hydrazono)methyl)phenoxy)methyl)benzylethanethioate 
• 1256478-10-0 (E)-S-3-((3-ethynyl-5-((2-(3-mercaptopropanoyl)hydrazono)methyl)phenoxy)methyl)benzylethanethioate 

Relevant academic research and scientific papers

Simultaneous dual protein labeling using a triorthogonal reagent

Construction of heterofunctional proteins is a rapidly emerging area of biotherapeutics. Combining a protein with other moieties, such as a targeting element, a toxic protein or small molecule, and a fluorophore or polyethylene glycol (PEG) group, can imp

TRIORTHOGONAL REAGENTS FOR DUAL PROTEIN CONJUGATION

The present invention relates to triorthogonal reagents useful for site-specifically modifying a protein with two orthogonal groups that can be subsequently functionalized in a single one-pot procedure. This approach relies on the selective tagging of pro

Selective and orally bioavailable phenylglycine tissue factor/factor VIIa inhibitors

We describe the structure-based design and synthesis of highly potent, orally bioavailable tissue factor/factor VIIa inhibitors which interfere with the coagulation cascade by selective inhibition of the extrinsic pathway.