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文件

U5625

Sigma-Aldrich

尿苷-5′-二磷酸葡糖醛酸 铵盐

98-100%

同義詞:

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

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About This Item

經驗公式（希爾表示法）:
C15H22N2O18P2 · xNH3
CAS號碼:
43195-60-4
分子量：:
580.29 (free acid basis)
分類程式碼代碼:
41106305
PubChem物質ID:
24900657
NACRES:
NA.51

生物源

Saccharomyces cerevisiae
enzyme from bovine liver (catalase)
enzyme from rabbit muscle (LDH)

化驗

98-100%

形狀

powder

儲存溫度

−20°C

SMILES 字串

N.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.H3N/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);1H3/t4-,6-,7+,8+,9-,10-,11+,12-,14-;/m1./s1

InChI 密鑰

WMWKTCPGFOEPBD-YGIWDPDDSA-N

相關類別

一般說明

尿苷 5′-二磷酸葡萄糖醛酸 (UDPGA) 是辅助因子，由 udp-葡萄糖和烟酰胺腺嘌呤二核苷酸 (NAD +) 在细胞内通过 udp-葡萄糖脱氢酶的催化活性合成。许多肝制备液中 UDPGA 的浓度范围为 0.3-0.5 mM。

應用

尿苷 5'-二磷酸葡萄糖醛酸铵盐已用于肝 S9 蛋白中 14 C-睾酮的 UDP-葡糖醛酸基转移酶 (UDGPT) 试验的启动。适用于 UDGPT 含量测定。

生化／生理作用

尿苷 5'-二磷酸葡萄糖醛酸 (UDGPA) 是内质网中胆红素结合的葡萄糖醛酸供体。

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

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, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

分析證明 (COA)

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1. Absorption, distribution, metabolism, transport and elimination properties of omadacycline, an aminomethylcycline antibiotic, were investigated in vitro and in a study in healthy male subjects. 2. Omadacycline was metabolically stable in human liver microsomes and hepatocytes and did not inhibit or induce
Seasonal testosterone UDP-glucuronosyltransferase activity and biliary steroids in Eurasian perch: Response to leachate exposure
Linderoth M, et al.
Ecotoxicology and Environmental Safety, 68(1), 49-56 (2007)
Molly Lin et al.
Xenobiotica; the fate of foreign compounds in biological systems, 48(10), 1021-1027 (2017-08-29)
1. Glucuronidation of amines has been shown to exhibit large species differences, where the activity is typically more pronounced in human than in many preclinical species such as rat, mouse, dog and monkey. The purpose of this work was to
Shupeng Yang et al.
Journal of agricultural and food chemistry, 65(33), 7217-7227 (2017-07-25)
After being incubated with animal and human liver microsomes, metabolites of phase I and II were investigated. A comparison was performed by ultrahigh performance liquid chromatography-quadrupole/time-of-flight coupled to mass spectrometry (UHPLC-Q/TOF). Consequently, a total of four phase I metabolites and
Justine Badée et al.
Drug metabolism and disposition: the biological fate of chemicals, 47(2), 124-134 (2018-11-28)
UDP-glucuronosyltransferase (UGT)-mediated metabolism is possibly the most important conjugation reaction for marketed drugs. However, there are currently no generally accepted standard incubation conditions for UGT microsomal assays, and substantial differences in experimental design and methodology between laboratories hinder cross-study comparison
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