α-D-[2-3H]glucopyranose | 70833-84-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: α-D-[2-3H]glucopyranose
• 英文别名: β-D-[2-3H]mannopyranose；<2-3H>glucose；D-[2-³H]-glucose；D-[2-³H]glucose；D-Glucose-2-t
• CAS: 70833-84-0；70833-86-2
• 化学式: C₆H₁₂O₆
• 分子量: 182.15
• InChiKey: WQZGKKKJIJFFOK-BTDSMANOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -3.22
• 重原子数：
  12.0
• 可旋转键数：
  1.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  110.38
• 氢给体数：
  5.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  α-D-[2-3H]glucopyranose 在 DL-谷氨酰胺 作用下， 生成
  参考文献：
  名称：

  Enzymic Synthesis of NAD+ with the Specific Incorporation of Atomic Labels

  摘要：

  An enzymatic synthesis is described for the production of NAD(+) labeled with a radioactive or stable isotope at any desired position in the AMP or NMN(+) portions of the molecule. In the first step, ten enzyme-catalyzed reactions are coupled for the synthesis of nicotinic acid adenine dinucleotide (NaAD(+)) from glucose, nicotinic acid, and ATP. NAD(+) is formed from NaAD(+) and glutamine in the second step. Oxidized nicotinamide adenine dinucleotide was synthesized with H-3, C-14, or N-15 label specifically incorporated in the ribose or nicotinamide of the NMN(+) portion of NAD(+) as [H(N)1'H-3]NAD(+), [H(N)2'-H-3]NAD(+), [H(N)4'-H-3]NAD(+), [H(N)5'-H-3]NAD(+), [C(N)1'-C-14]NAD(+), [C(N)5'-C-14]NAD(+), [N(N)1-N-15, C(N)1'-C-14]NAD(+), and [N(N)1-N-15, C(N)5'-C-14]NAD(+). Nuclear magnetic resonance spectroscopy of [H(N)2'-H-2]NAD(+) as well as enzymatic degradation were used to verify the position of labels. Appropriately labeled glucose, ribose 5-phosphate, or nicotinic acid were the starting materials and were converted to NAD(+) using enzymes from the pentose pathway and the pathway for NAD(+) de novo synthesis. Yields of purified NAD(+) to 96% were obtained from starting glucose. The labeled NAD(+) is catalytically competent and is chromatographically and spectrophotometrically indistinguishable from authentic NAD(+). By using specifically labeled ATP as a precursor (Parkin, D. W.; Schramm, V. L. Biochemistry 1987, 26, 913-920), the method is readily adaptable for the synthesis of NAD(+) with single or multiple atomic labels at various positions in the AMP portion of the molecule. NAD(+) was synthesized from [8-C-14]ATP to give [C(A)8-C-14]NAD(+) as an example. Together these methods provide a general scheme for the efficient synthesis of NAD(+) of high purity with H-3, C-14, Or Other labels at any nonexchangeable position of the NMN(+) or AMP portions of the NAD(+) molecule.

  DOI：

  10.1021/ja00094a006