ethyl 5-amino-3-O-methyl-5-deoxy-1,2-O-isopropylidene-β-L-idoheptofuranuronate | 540491-51-8

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: ethyl 5-amino-3-O-methyl-5-deoxy-1,2-O-isopropylidene-β-L-idoheptofuranuronate
• 英文别名: ethyl [5-amino-3-O-methyl-5,6-dideoxy-1,2-O-isopropylidene]-β-L-ido-heptofuranuronate；ethyl (3S)-3-[(3aR,5R,6S,6aR)-6-methoxy-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]-3-aminopropanoate
• CAS: 540491-51-8
• 化学式: C₁₃H₂₃NO₆
• 分子量: 289.329
• InChiKey: JDNRSDVCBSYGHV-KICMGLQKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.4
• 重原子数：
  20
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.92
• 拓扑面积：
  89.2
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  ethyl 5-amino-3-O-methyl-5-deoxy-1,2-O-isopropylidene-β-L-idoheptofuranuronate 在 sodium tetrahydroborate 作用下， 以 甲醇 、 氯仿 为溶剂， 生成 ethyl 5-(6'-amino-6'-deoxy-1',2';3',4'-di-O-isopropylidene-α-D-galactopyranos-6'-yl)-3-O-methyl-5,6-dideoxy-1,2-O-isopropylidene-β-L-ido-heptafuranuronate
  参考文献：
  名称：

  Reductive Amination of Glycosyl Aldoses: Synthesis ofN‐Glycosylated β‐Glycosyl Amino Alcohols and their Enzyme Inhibitory Effect

  摘要：

  Reductive amination of glycosyl aldehydes (la-c, 2) with glycosyl amino esters (3a-c, 4) in the presence of sodium borohydride gave diglycosylated amino esters (5-15) in good yield. N-Glycosyl-glycosylated amino esters were reduced to the respective diglycosyl amino alcohols (16-26) with LiAlH4 in good yield. All the synthesized compounds were studied for their inhibitory effect, if any, against hepatic glucose-6-phosphatase, glycogen phosphorylase, and intestinal brush border membrane alpha-glucosidase; among these compounds 7, 21, and 25 have shown marked inhibition on these enzymes, respectively.

  DOI：

  10.1081/car-200046779
• 作为产物：
  描述：

  ethyl [3-O-methyl-5,6-dideoxy-1,2-O-isopropylidene-α-D-gluco]-heptofuran-5-en-uronate 在 氨 作用下， 以 乙醇 为溶剂， 以20%的产率得到
  参考文献：
  名称：

  D-葡萄糖多种糖基化脲的合成及抗结核作用评价

  摘要：

  通过将胺1,4-共轭加成到糖基化烯酯上，然后将所得糖基β-氨基酯与二异氰酸酯反应，以良好至优异的产率合成了N,N-二取代的糖基化脲。所开发的糖基分子通过广泛的标准光谱分析（包括 NMR（1 H、13 C 和 DEPT）、IR、MS 和元素分析）得到了很好的表征，并筛选了其抗结核分枝杆菌( M. Tb. )的生物活性。 ，其中一些表现出有效的抗结核活性。这些分子的设计考虑了参与分枝杆菌细胞壁聚合物生物合成的众所周知的酶抑制剂，并且可以作为先导分子进一步探索，以成功开发潜在的抗结核候选药物。

  DOI：

  10.1155/2024/8709672

文献信息

• Asymmetric organocatalysis with glycosyl-β-amino acids: direct asymmetric aldol reaction of acetone with aldehydes
  作者：Namrata Dwivedi、Surendra S. Bisht、Rama P. Tripathi

  DOI：10.1016/j.carres.2006.08.007

  日期：2006.11

  Direct asymmetric aldol reaction of acetone with aromatic aldehydes was achieved in good yields and high enantioselectivity using 5-amino-5-deoxy-beta-L-ido-(alpha-D-gluco)-heptofuranuronic acids as a new class of organocatalysts.

  使用5-氨基-5-脱氧-β-L-氨基-（α-D-葡萄糖）-呋喃呋喃糖醛酸作为一类新型的有机催化剂，可实现丙酮与芳族醛的直接不对称醛醇缩合反应，并具有良好的收率和高对映选择性。
• Synthesis of glycosylated β-amino acids as new class of antitubercular agents
  作者：R.P. Tripathi、R. Tripathi、V.K. Tiwari、Laxmi Bala、S Sinha、A. Srivastava、R. Srivastava、B.S. Srivastava

  DOI：10.1016/s0223-5234(02)01398-3

  日期：2002.9

  A series of glycosylated P-amino acids was prepared and evaluated against Mycohacterium tuberculosis, M. avium, M. fortuitum and M. smegmatis. The compounds were designed to mimic the enzyme D-alanine racemase and glycosyl transferase involved in the biosynthesis of essential cell wall peptidoglycan and arabinogalactan. Though most of the compounds exhibited little activity, however, one showed significant activity against all the strains in cell culture and activity was confirmed by BACTEC method. (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved.