913625-15-7

Upstream product

• 95485-08-8 α-methyl γ-tert-butyl N--L-glutamate 
• 79640-68-9 α-methyl γ-tert-butyl N-(4-amino-4-deoxy-N¹⁰-methylpteroyl)-L-glutamate 
• 52853-40-4 6-bromomethyl-2,4-diaminopteridine hydrobromide 
• 6234-01-1 L-glutamic acid 5-tert-butyl 1-methyl ester hydrochloride 
• 10541-83-0 N-methyl-p-aminobenzoic acid 
• 5514-98-7 6-aminohexanoic acid tert-butyl ester 
• 66147-29-3 (S)-2-{4-[(2,4-Diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-pentanedioic acid 1-methyl ester 

Downstream Products

• 913625-17-9 2-{4-[(2,4-diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-4-(5-{2-[3,4,5-triacetoxy-6-(4,5,6-triacetoxy-2-acetoxymethyl-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-2-ylmethylsulfanyl]-ethylcarbamoyl}-pentylcarbamoyl)-butyric acid methyl ester 
• 913625-18-0 C₅₃H₇₁FN₁₀O₂₀S 
• 913625-16-8 6-((S)-4-{4-[(2,4-Diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-4-methoxycarbonyl-butyrylamino)-hexanoic acid 

Relevant academic research and scientific papers

Optimized design and synthesis of chemical dimerizer substrates for detection of glycosynthase activity via chemical complementation

Glycosynthases catalyze the formation of a glycosidic bond between a glycosyl fluoride donor substrate and a glycosyl acceptor substrate with high yield, thus providing a valuable approach for the synthesis of carbohydrates and glycoconjugates. Chemical c