108320-87-2

108320-87-2 structure

Name: UDP-Alpha-d-n-acetylgalactosamine, disodium salt
Chemical Name: disodium,[(3R,4R,5R,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] [[(2R,3S,4R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] phosphate
CAS Number: 108320-87-2
Molecular Formula: C₁₇H₂₅N₃Na₂O₁₇P₂
Molecular Weight: 651.31700
Catalog: Biochemical Carbohydrate Monosaccharide
Create Date: 2019-01-01 12:00:02
Modify Date: 2026-07-16 18:28:21
UDP-GalNAc (UDP-N-acetyl-D-galactosamine) disodium is a sugar nucleotide and a substrate of EpsC115. EpsC115 is an exopolymeric substances (EPS) N-terminal deletion mutant with the residue 1-115 deletion. UDP-GalNAc UDP-GalNAc is the donor substrate of many N-acetylgalactosaminyltransferases, enzymes which transfer GalNAc from the nucleotide sugar to a saccharide or peptide acceptor[1].

Name	disodium,[(3R,4R,5R,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] [[(2R,3S,4R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] phosphate
Synonyms	UDP-α-D-N-Acetylgalactosamine, Disodium Salt - - Calbiochem uridine 5-diphospho-N-acetylgalactosamine disod Uridine[5']diphospho(2-acetamino-2-deoxy-α-D-galactopyranose) disodium salt URIDINE[5']DIPHOSPHO(2-ACETAMINO-2-DEOXY-ALPHA-D-GALACTOPYRANOSE) DISODIUM SALT UDP-N-acetylgalactosamine Uridine 5'-diphospho-N-acetylgalactosamine disodium salt >= Uridine 5'-diphospho-N-acetylgalactosamine sodium salt URIDINE-DIPHOSPHATE-N-ACETYLGALACTOSAMINE DISODIUM SALT UDP-N-acetyl-D-Galactosamine (sodium salt) UDP-GalNAc disodium Uridine 5 inverted exclamation marka-diphospho-N-acetylgalactosamine disodium salt Uridine 5'-diphospho-N-acetylgalactosamine disodium 2-Acetamido-2-deoxy-a-D-galactopyranosyl uridine diphosphate disodium salt Uridine 5′-diphospho-N-acetylgalactosamine URIDINE-5'-DIPHOSPHO-N-ACETYL-GALACTOS-& UDP-ALPHA-D-N-ACETYLGALACTOSAMINE, DISODIUM SALT Uridine 5'-diphospho-N-acetylgalactosamine disodium salt UDP-N-acetyl-D-galactosamine disodium salt UDP-α-N-acetyl-D-galactosamine ammonium salt URIDINE 5'-DIPHOSPHO-N-ACETYLGALACTOSAMINE DISODIUM SALT URIDINE 5'-DIPHOSPHO-N-ACETYLGALACTOSAM INE DISODIU UDP-GALNAC, 2NA MFCD00077894 UDP-a-D-N-Acetylgalactosamine,Disodium Salt Uridine-5'-diphospho-N-acetylgalactosamine disodium salt Uridine 5'-(trihydrogen diphosphate) P'-[2-(acetylamino)-2-deoxy-alpha-D-galactopyranosyl] ester disodium salt UDP-Galc.2 UDP-GalNAc, UDP-N-acetylgalactosamine, Uridine[5μ]diphospho(2-acetamino-2-deoxy-α-D-galactopyranose) disodium salt Uridine 5'-diphospho-D-N-acetylgalactosamine disodium salt Uridine 5′-diphospho-N-acetylgalactosamine disodium salt Uridine 5'-diphospho-N-acetylgalactosaMine sodiuM salt UDP-α-D-N-Acetylgalactosamine, Disodium Salt

Description	UDP-GalNAc (UDP-N-acetyl-D-galactosamine) disodium is a sugar nucleotide and a substrate of EpsC115. EpsC115 is an exopolymeric substances (EPS) N-terminal deletion mutant with the residue 1-115 deletion. UDP-GalNAc UDP-GalNAc is the donor substrate of many N-acetylgalactosaminyltransferases, enzymes which transfer GalNAc from the nucleotide sugar to a saccharide or peptide acceptor[1].
Related Catalog	Research Areas >> Metabolic Disease
References	[1]. Kaundinya CR, et al. In vitro characterization of N-terminal truncated EpsC from Bacillus subtilis 168, a UDP-N-acetylglucosamine 4,6-dehydratase. Arch Biochem Biophys. 2018 Nov 1;657:78-88. [2]. Hang HC, et al. Probing glycosyltransferase activities with the Staudinger ligation. J Am Chem Soc. 2004 Jan 14;126(1):6-7.

Molecular Formula	C₁₇H₂₅N₃Na₂O₁₇P₂
Molecular Weight	651.31700
Exact Mass	651.04500
PSA	331.14000
Storage condition	−20°C
Water Solubility	H2O: 50 mg/mL, clear, colorless

Personal Protective Equipment	dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes	Xi: Irritant;
Risk Phrases	36/37/38
Safety Phrases	26-36
RIDADR	NONH for all modes of transport
WGK Germany	3

50711-33-6

108320-87-2

Literature: Journal of Organic Chemistry, , vol. 77, # 3 p. 1449 - 1456

76375-60-5

108320-87-2

Literature: Journal of Organic Chemistry, , vol. 77, # 3 p. 1449 - 1456

14464-29-0

137848-39-6

108320-87-2

Literature: Journal of Organic Chemistry, , vol. 57, # 1 p. 152 - 157

Precursor 3
76375-60-5 14464-29-0 137848-39-6
DownStream 0

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