51368-18-4

Usage

InChI:InChI=1/C12H15N3O6/c13-15-14-6-1-3-7(4-2-6)20-12-11(19)10(18)9(17)8(5-16)21-12/h1-4,8-12,16-19H,5H2/t8-,9+,10+,11-,12-/m1/s1

Upstream product

• 100-02-7 4-nitro-phenol 
• 3767-28-0 4-nitrophenyl-α-D-glucopyranoside 
• 3398-86-5 4-aminophenyl α-D-galactopyranoside 
• 10357-27-4 4-nitrophenyl-α-D-mannopyranoside 
• 83-87-4 D-Mannose pentaacetate 
• 13242-51-8 1-O-p-nitrophenyl-2,3,4,6-tetra-O-acetyl α-D-mannopyranoside 
• 34213-86-0 p-aminophenyl-α-D-mannopyranoside 

Relevant academic research and scientific papers

Photolabeling of dextransucrase from Streptococcus sanguis with p-azidophenyl α-D-glucopyranoside

Dextransucrase from Streptococeus sanguis ATCC 10558 was photolabeled using p-azidophenyl α-D-glucopyranoside with an apparent rate constant of inactivation of 1.40 min-1. The dissociation constant for this compound, which acts as an acceptor m

Post-photoaffinity labeling modification using aldehyde chemistry to produce a fluorescent lectin toward saccharide-biosensors

A new method to construct a fluorescent saccharide biosensor based on a lectin protein is successfully proposed using post-photoaffinity labeling modification coupled to aldehyde chemistry.

Syntheses and properties of photoactivatable sugar derivatives designed to probe the sugar-binding site of melibiose permease

Three new photoreactive sugar analogues bearing an azido, a diazonium salt or a diazirine group as the photophore as well as a tritium atom were developed. Two of these new photoactivatable compounds gave excellent preliminary results, with a high affinity for the melibiose permease of Escherichia coli. (C) 2000 Elsevier Science Ltd. All rights reserved.