(1R)-3-(3,4-dimethoxyphenyl)-1-(3-(2-((6-((2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)oxy)hexyl)amino)-2-oxoethoxy)phenyl)propyl (2S)-1-((S)-2-(3,4,5-trimethoxyphenyl)butanoyl)piperidine-2-carboxylate 2055023-35-1 Orthogonal Hydroxyl Functionalization of cGAMP

Name: (1R)-3-(3,4-dimethoxyphenyl)-1-(3-(2-((6-((2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)oxy)hexyl)amino)-2-oxoethoxy)phenyl)propyl (2S)-1-((S)-2-(3,4,5-trimethoxyphenyl)butanoyl)piperidine-2-carboxylate 2055023-35-1 Orthogonal Hydroxyl Functionalization of cGAMP
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Description

Orthogonal Hydroxyl Functionalization of cGAMP Confers Metabolic Stability and Enables Antibody Conjugation

201703929 Keywords: Biotinylation Reagent

via site-selective modification

11326-11337 DOI: 10

Site-Selective Functionalization of Methionine Residues via Photoredox Catalysis J

(1R)-3-(3,4-dimethoxyphenyl)-1-(3-(2-((6-((2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)oxy)hexyl)amino)-2-oxoethoxy)phenyl)propyl (2S)-1-((S)-2-(3,4,5-trimethoxyphenyl)butanoyl)piperidine-2-carboxylate 2055023-35-1 Orthogonal Hydroxyl Functionalization of cGAMP

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