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U6751

Sigma-Aldrich

Uridine 5′-diphosphoglucuronic acid trisodium salt

98-100%

Synonym(s):

UDP-GlcA, UDPGA, Uridine-diphosphate-glucuronic acid trisodium salt, Uridine[5′]diphospho[1]-α-D-glucopyranosuronic acid trisodium salt

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25 MG
CN¥1,175.46
100 MG
CN¥4,688.75
250 MG
CN¥8,802.16
500 MG
CN¥16,233.65
1 G
CN¥26,708.40

CN¥1,175.46

Available to ship onApril 17, 2025Details

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25 MG
CN¥1,175.46
100 MG
CN¥4,688.75
250 MG
CN¥8,802.16
500 MG
CN¥16,233.65
1 G
CN¥26,708.40

About This Item

Empirical Formula (Hill Notation):
C15H19N2Na3O18P2
CAS Number:
63700-19-6
Molecular Weight:
646.23
MDL number:
MFCD03452710
UNSPSC Code:
41106305
PubChem Substance ID:
24900659
NACRES:
NA.51

CN¥1,175.46

Available to ship onApril 17, 2025Details

Request a Bulk Order

biological source

bovine liver
rabbit muscle
yeast

Assay

98-100%

form

powder

storage temp.

−20°C

SMILES string

[Na+].[Na+].[Na+].O[C@@H]1[C@@H](O)[C@H](O[C@@H]([C@H]1O)C([O-])=O)OP([O-])(=O)OP([O-])(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N3C=CC(=O)NC3=O

InChI

1S/C15H22N2O18P2.3Na/c18-5-1-2-17(15(26)16-5)12-9(22)6(19)4(32-12)3-31-36(27,28)35-37(29,30)34-14-10(23)7(20)8(21)11(33-14)13(24)25;;;/h1-2,4,6-12,14,19-23H,3H2,(H,24,25)(H,27,28)(H,29,30)(H,16,18,26);;;/q;3*+1/p-3/t4-,6-,7+,8+,9-,10-,11+,12-,14-;;;/m1.../s1

InChI key

XXXUNWUNTOMVIG-QWGSIYABSA-K

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Show Differences

1 of 4

This Item
U5750U5625U5252
Uridine 5′-diphosphoglucuronic acid trisodium salt 98-100%

U6751

Uridine 5′-diphosphoglucuronic acid trisodium salt

Uridine 5′-diphosphomannose disodium salt ≥95%

U5750

Uridine 5′-diphosphomannose disodium salt

Uridine 5′-diphosphoglucuronic acid ammonium salt 98-100%

U5625

Uridine 5′-diphosphoglucuronic acid ammonium salt

Uridine 5′-diphospho-N-acetylgalactosamine disodium salt ≥97%

U5252

Uridine 5′-diphospho-N-acetylgalactosamine disodium salt

Quality Level

300

Quality Level

200

Quality Level

200

Quality Level

200

form

powder

form

-

form

powder

form

powder

assay

98-100%

assay

≥95%

assay

98-100%

assay

≥97%

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

Application

Uridine 5′-diphosphoglucuronic acid trisodium salt has been used in optimization of incubation assay[1] and glucuronidation assay.[2]

Biochem/physiol Actions

Uridine 5′-diphosphate-glucuronic acid (UDP-GlcA) is a carboxylic acid-formed sugar nucleotide. It participates in the biosynthesis of numerous cell components.[3] UDP-GlcA is a glycosyl donor for glycosyltransferases in the biosynthesis of several cell components like glycosaminoglycans, some N- and O-linked glycans, glycosphingolipids and pectins.[3]

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves
  • Specification Sheet

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    Certificates of Analysis (COA)

    Lot/Batch Number
    0000381162
    0000381163
    0000381164
    0000381160
    0000377450

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    Already Own This Product?

    Find documentation for the products that you have recently purchased in the Document Library.

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    Comparing substrate specificity of two UDP-sugar pyrophosphorylases and efficient one-pot enzymatic synthesis of UDP-GlcA and UDP-GalA
    Guo Y, et al.
    Carbohydrate Research, 411, 1-5 (2015)
    In vitro inhibitory effects of Andrographis paniculata, Gynura procumbens, Ficus deltoidea, and Curcuma xanthorrhiza extracts and constituents on human liver glucuronidation activity
    Husni Z, et al.
    Pharmacognosy magazine, 13( 2), S236-S236 (2017)
    Jan J Lyczakowski et al.
    The New phytologist, 231(5), 1720-1733 (2021-06-05)
    Wood of coniferous trees (softwood), is a globally significant carbon sink and an important source of biomass. Despite that, little is known about the genetic basis of softwood cell wall biosynthesis. Branching of xylan, one of the main hemicelluloses in
    Soy isoflavone metabolism in cats compared with other species: urinary metabolite concentrations and glucuronidation by liver microsomes
    Redmon J M, et al.
    Xenobiotica, 46(5), 406-415 (2016)
    Bao-Li Mi et al.
    Xenobiotica; the fate of foreign compounds in biological systems, 44(8), 716-721 (2014-03-13)
    1. The aurantio-obtusin's glucuronide was detected when aurantio-obtusin was incubated with human liver microsomes (HLMs). Recombinant UGT isoforms screening experiment showed that UGT1A8 was the major isoform contributed to the glucuronidation. 2. The metabolic profiles for aurantio-obtusin in liver microsomes
    View All Related Papers

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