17479-04-8

Basic information

• Product Name: UDP-glucosamine
• Synonyms: UDP-glucosamine
• CAS NO: 17479-04-8
• Molecular Formula: C₁₅H₂₅N₃O₁₆P₂
• Molecular Weight: 565.317022
• Mol File: 17479-04-8.mol
• Article Data: 13

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.93g/cm³
• Refractive Index: 1.671
• CAS DataBase Reference: UDP-glucosamine(CAS DataBase Reference)
• NIST Chemistry Reference: UDP-glucosamine(17479-04-8)
• EPA Substance Registry System: UDP-glucosamine(17479-04-8)

Safety Data

• Hazardous Substances Data: 17479-04-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H25N3O16P2/c16-8-11(23)9(21)5(3-19)32-14(8)33-36(28,29)34-35(26,27)30-4-6-10(22)12(24)13(31-6)18-2-1-7(20)17-15(18)25/h1-2,5-6,8-14,19,21-24H,3-4,16H2,(H,26,27)(H,28,29)(H,17,20,25)/t5-,6-,8-,9-,10-,11-,12-,13-,14-/m1/s1

Upstream product

• 2152-75-2 2-amino-2-deoxy-D-glucopyranose-1-(dihydrogen phosphate) 
• 63-39-8 UTP 
• 537039-66-0 uridine 5'-diphospho-2-azido-2-deoxy-α-D-glucopyranoside 
• 171032-74-9 1,3,4,6-tetra-O-acetyl-2-azido-2-deoxy-D-glucopyranose 
• 90-76-6 2-deoxy-2-amino glucose 
• 35946-68-0 O³,O⁴,O⁶-triacetyl-2-amino-O¹-diphenoxyphosphoryl-2-deoxy-α-D-glucopyranose; hydrochloride 
• 212137-48-9 Phosphoric acid mono-[(2R,3R,4R,5S,6R)-4,5-dihydroxy-6-hydroxymethyl-3-(2,2,2-trifluoro-acetylamino)-tetrahydro-pyran-2-yl] ester 
• 28719-30-4 3,4,6-Tri-O-acetyl-2-trifluoracetamino-2-desoxy-D-glucose 
• 137766-83-7 2-deoxy-2-trifluoroacetamido-1,3,4,6-tetra-O-acetyl-α,β-D-glucopyranoside 
• 219564-51-9 3,4,6-tri-O-acetyl-2-deoxy-2-trifluoroacetylamino-α-D-glucopyranosyl dibenzyl phosphate 
• 212137-46-7 2-deoxy-2-[(trifluoroacetyl)amino]-D-glucopyranose-3,4,6-triacetate-1-(dihydrogen phosphate) 
• 212137-44-5 3,4,6-tri-O-acetyl-2-deoxy-2-trifluoroacetamido-α-D-glucopyranose 
• 212137-54-7 uridine 5'-diphospho-2-deoxy-2-trifluoroacetamido-α-D-glucopyranoside 
• 90-76-6 glucosamine 

Downstream Products

• 1338332-56-1 uridine 5'-diphospho-2-phenylacetamido-2-deoxy-α-D-glucopyranoside 
• 733810-59-8 C₆₄H₅₆Cl₂N₈O₂₂ 
• 528-04-1 uridine 5'-diphospho-N-acetylglucosamine 

Relevant articles and documents

Exploring the broad nucleotide triphosphate and sugar-1-phosphate specificity of thymidylyltransferase Cps23FL from: Streptococcus pneumonia serotype 23F

Glucose-1-phosphate thymidylyltransferase (Cps23FL) from Streptococcus pneumonia serotype 23F is the initial enzyme that catalyses the thymidylyl transfer reaction in prokaryotic deoxythymidine diphosphate-l-rhamnose (dTDP-Rha) biosynthetic pathway. In this study, the broad substrate specificity of Cps23FL towards six glucose-1-phosphates and nine nucleoside triphosphates as substrates was systematically explored, eventually providing access to nineteen sugar nucleotide analogs.

Compositions and methods for the transfer of a hexosamine to a modified nucleotide in a nucleic acid

Nucleic acids comprising β-glucosaminyloxy-5-methylcytosine; compositions, kits and methods of producing the nucleic acids using a glycosyltransferase; and methods of using the nucleic acids are described.

CHEMOENZYMATIC SYNTHESIS OF HEPARIN AND HEPARAN SULFATE ANALOGS

The present invention provides a one-pot multi-enzyme method for preparing UDP-sugars from simple sugar starting materials. The invention also provides a one-pot multi-enzyme method for preparing oligosaccharides from simple sugar starting materials.