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Merck

389374

Sigma-Aldrich

D-葡萄糖-13C6

≥99 atom % 13C, ≥99% (CP)

别名:

标记葡萄糖, D-葡萄糖-ul-13C, 葡萄糖-13C6

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About This Item

经验公式(希尔记法):
13C6H12O6
分子量:
186.11
MDL號碼:
分類程式碼代碼:
12142200
PubChem物質ID:
NACRES:
NA.12

同位素純度

≥99 atom % 13C

化驗

≥99% (CP)

形狀

powder

光學活性

[α]25/D +52.0°, c = 2 in H2O (trace NH4OH)

技術

bio NMR: suitable
protein expression: suitable
protein purification: suitable

mp

150-152 °C (lit.)

質量偏移

M+6

SMILES 字串

O[13CH2][13C@H]1O[13C@H](O)[13C@H](O)[13C@@H](O)[13C@@H]1O

InChI

1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6?/m1/s1/i1+1,2+1,3+1,4+1,5+1,6+1

InChI 密鑰

WQZGKKKJIJFFOK-NYKRWLDMSA-N

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應用

D-葡萄糖-13C6 已被用作:
  • 作为 从头合成 脂肪酸(FA)的示踪剂分析了稳定同位素示踪剂在重组蛋白生产中的作用
  • 作为示踪介质中分析稳定同位素示踪剂的组分
  • 用于重组蛋白生产的基本培养基中
  • 用于悬浮细胞

生化/生理作用

D-葡萄糖-13C6 充当示踪剂,有助于评估体内葡萄糖动力学。

包裝

该产品具有大量储备,可按需包装。 有关定价、供货和包装的信息,请联系稳定同位素客户服务部

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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Zoran Dinev et al.
Carbohydrate research, 341(10), 1743-1747 (2006-04-11)
A simple gram-scale synthesis of uridine diphospho(13C6)glucose is presented from D-(13C6)glucose. The critical step uses a 1H-tetrazole-catalyzed coupling of 2,3,4,6-tetra-O-acetyl-alpha-D-glucopyranosyl-1-phosphate and UMP-morpholidate. The uridine diphospho(13C6)glucose was used in the structural identification of (1-->3)-beta-D-glucan from Lolium multiflorum.
Metabolic profiling reveals a coordinated response of isolated lamb's (Valerianella locusta, L.) lettuce cells to sugar starvation and low oxygen stress
Victor BMM, et al.
Postharvest biology and technology, 126, 23-33 (2017)
RSK Regulates PFK-2 Activity to Promote Metabolic Rewiring in Melanoma
Houles T, et al.
Cancer Research, canres-ca2215 (2018)
Y Oda et al.
Biochemistry, 33(17), 5275-5284 (1994-05-03)
All of the individual carboxyl groups (the side-chain carboxyl groups of Asp and Glu, and the C-terminal alpha-carboxyl group) in Escherichia coli ribonuclease HI, which is an enzyme that cleaves the RNA strand of a RNA/DNA hybrid, were pH-titrated, and
Frank Malz et al.
Carbohydrate research, 342(1), 65-70 (2006-12-06)
Double Quantum (DQ) NMR, which utilizes the magnetic dipole interaction between the (13)C atoms, was used for the complete assignment of the (13)C NMR resonances to the corresponding carbon ring positions for the monoclinic and triclinic allomorphs of methyl 4'-O-methyl-beta-D-cellobioside-(13)C(12)(1-(13)C(12))

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