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Merck
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文件

U6751

Sigma-Aldrich

尿苷 5′-二磷酸葡萄糖醛酸 三钠盐

98-100%

同義詞:

UDP-GlcA, UDPGA, Uridine[5′]diphospho[1]-α-D-glucopyranosuronic acid 三钠盐, 尿苷-二磷酸-葡萄糖醛酸 三钠盐

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About This Item

經驗公式（希爾表示法）:
C15H19N2Na3O18P2
CAS號碼:
63700-19-6
分子量：:
646.23
MDL號碼:
MFCD03452710
分類程式碼代碼:
41106305
PubChem物質ID:
24900659
NACRES:
NA.51

生物源

bovine liver
rabbit muscle
yeast

化驗

98-100%

形狀

powder

儲存溫度

−20°C

SMILES 字串

[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 密鑰

XXXUNWUNTOMVIG-QWGSIYABSA-K

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相關類別

應用

尿苷5′-二磷酸-葡糖醛酸三钠盐已用于优化孵育检测和葡糖醛酸检测。

生化／生理作用

尿苷5′-二磷酸-葡糖醛酸（UDP-GlcA）是一种羧酸形成的糖核苷酸。它可稳参与到多种细胞成分的生物合成中。UDP-GlcA是一种糖基转移酶的糖基供体，用于数种细胞成分的生物合成，如糖胺聚糖、某些N-和O-连接的聚糖、糖鞘脂和果胶。

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)

分析證明 (COA)

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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
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Glycosyltransferases

Glycosyltransferases were initially considered to be specific for a single glycosyl donor and acceptor, which led to the one enzyme-one linkage concept. Subsequent observations have refuted the theory of absolute enzymatic specificity by describing the transfer of analogs of some nucleoside mono- or diphosphate sugar donors.

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