UDP-ALPHA-D-GALACTOSE DISODIUM SALT - ≥95% , CAS No.137868-52-1

CAS: 137868-52-1 Cat. No.: U303352 Molecular Weight: 610.27 Beilstein Registry Number: 5374254 EC Number: 634-373-1 PubChem CID: 11365506

GRADE & PURITY ≥95%

Synonyms

UDP-a-D-Galactose disodium salt | UDP-?-D-Galactose (sodium salt) | Uridine 5'-diphospho-a-D-galactose disodium salt | disodium;[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] [(2R,3R,4S,5R,6R)-3,4,5-trihydrox

Storage

Protected from light,Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Overview

A donor substrate for galactosyltransferases used in the biosynthesis of galactose-containing oligosaccharides. Decreased red blood cell levels of UDP-Gal are found in patients with maple syrup urine disease or phenylketonuria.

Specifications

Synonyms

UDP-a-D-Galactose disodium salt | UDP-?-D-Galactose (sodium salt) | Uridine 5'-diphospho-a-D-galactose disodium salt | disodium;[[(2R, 3S, 4R, 5R)-5-(2, 4-dioxopyrimidin-1-yl)-3, 4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] [(2R, 3R, 4S, 5R, 6R)-3, 4, 5-trihydrox

Specifications & Purity

≥95%

Storage

Protected from light, Store at -20°C, Argon charged

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Action Type

AGONIST

Purity

≥95%

Names and Identifiers

• Pubchem Sid: 488197434
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488197434
• Canonical Smiles: C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)([O-])OP(=O)([O-])OC3C(C(C(C(O3)CO)O)O)O)O)O.[Na+].[Na+]
• IUPAC Name: disodium;[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl] [(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate
• InChIKey: PKJQEQVCYGYYMM-QKYKBPIOSA-L
• INCHI: 1S/C15H24N2O17P2.2Na/c18-3-5-8(20)10(22)12(24)14(32-5)33-36(28,29)34-35(26,27)30-4-6-9(21)11(23)13(31-6)17-2-1-7(19)16-15(17)25;;/h1-2,5-6,8-14,18,20-24H,3-4H2,(H,26,27)(H,28,29)(H,16,19,25);;/q;2*+1/p-2/t5-,6-,8+,9-,10+,11-,12-,13-,14-;;/m1../s1
• Isomeric SMILES: C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)([O-])OP(=O)([O-])O[C@@H]3[C@@H]([C@H]([C@H]([C@H](O3)CO)O)O)O)O)O.[Na+].[Na+]
• WGK Germany: 3
• Alternate CAS: 2956-16-3
• PubChem CID: 11365506
• Molecular Weight: 610.27
• Beilstein: 5374254

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Nucleosides, nucleotides, and analogues
    • Class Pyrimidine nucleotides
      • Subclass Pyrimidine nucleotide sugars

• Kingdom: Organic compounds
• Superclass: Nucleosides, nucleotides, and analogues
• Class: Pyrimidine nucleotides
• Subclass: Pyrimidine nucleotide sugars
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyrimidine nucleotide sugars
• Alternative Parents: Pyrimidine ribonucleoside diphosphates Pentose phosphates Glycosylamines Monosaccharide phosphates Organic pyrophosphates Pyrimidones Alkyl phosphates Oxanes Hydropyrimidines Oxolanes Vinylogous amides Heteroaromatic compounds Ureas Lactams Secondary alcohols Polyols Oxacyclic compounds Azacyclic compounds Primary alcohols Hydrocarbon derivatives Organic oxides Organic sodium salts Organonitrogen compounds Organic cations
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Pyrimidine nucleotide sugar - Pyrimidine ribonucleoside diphosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Organic pyrophosphate - Pyrimidone - Hydropyrimidine - Monosaccharide - Organic phosphoric acid derivative - Oxane - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Vinylogous amide - Heteroaromatic compound - Oxolane - Lactam - Urea - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Organic alkali metal salt - Polyol - Azacycle - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic salt - Primary alcohol - Organic sodium salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Organic cation - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as pyrimidine nucleotide sugars. These are pyrimidine nucleotides bound to a saccharide derivative through the terminal phosphate group.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Sensitivity: Heat & Light & Moisture sensitive
• Molecular Weight: 610.270 g/mol
• Hydrogen Bond Donor Count: 7
• Hydrogen Bond Acceptor Count: 17
• Rotatable Bond Count: 9
• Exact Mass: 610.019 Da
• Monoisotopic Mass: 610.019 Da
• Topological Polar Surface Area: 297.000 Ų
• Heavy Atom Count: 38
• Formal Charge: 0
• Complexity: 948.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 9
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 3

XLogP3

References

1. Cao Shiyang, Wang Tong, Ren Yifan, Wu Gengshan, Zhang Yuan, Tan Yafang, Zhou Yazhou, Chen Hongyan, Zhang Yu, Song Yajun, Yang Ruifu, Du Zongmin.  (2024)  A protein O-GlcNAc glycosyltransferase regulates the antioxidative response in Yersinia pestis.  Nature Communications,  15  (1): (1-16).  [PMID:39152136] [10.1038/s41467-024-50959-w]

2. Yuqi Gao, Min Lu, Jitong Wei, Dengyu Zheng, Hongliang Duan, Mingxu Wang, Zhao Ke, Zhongyi Wu, Qing X. Li, Zhongbao Zhang.  (2026)  Cloning, Expression, and Activity and Structure Characterization of an O-Glycosyltransferase, ZmUGT76B1 from Maize (Zea mays L.).  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:41524108] [10.1021/acs.jafc.5c09514]