(18S,25S,35S)-35-[(S)-hydroxy(phenyl)methyl]-28-(methoxymethyl)-21-methyl-18-[2-(methylamino)-2-oxoethyl]-16,23,30,33-tetraoxo-25-propan-2-yl-3,13,20,27,37-pentathia-7,17,24,31,34,39,40,41,42,43-decazaheptacyclo[34.2.1.12,5.112,15.119,22.126,29.06,11]tritetraconta-1(38),2(43),4,6(11),7,9,12(42),14,19(41),21,26(40),28,36(39)-tridecaene-8-carboxamide | 1277183-93-3

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 大环内酰胺类
• 英文名称: (18S,25S,35S)-35-[(S)-hydroxy(phenyl)methyl]-28-(methoxymethyl)-21-methyl-18-[2-(methylamino)-2-oxoethyl]-16,23,30,33-tetraoxo-25-propan-2-yl-3,13,20,27,37-pentathia-7,17,24,31,34,39,40,41,42,43-decazaheptacyclo[34.2.1.12,5.112,15.119,22.126,29.06,11]tritetraconta-1(38),2(43),4,6(11),7,9,12(42),14,19(41),21,26(40),28,36(39)-tridecaene-8-carboxamide
• CAS: 1277183-93-3
• 化学式: C₄₅H₄₄N₁₂O₈S₅
• 分子量: 1041.25
• InChiKey: VWEJBPFFISOPOP-HFOPRICVSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  70
• 可旋转键数：
  8
• 环数：
  8.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  437
• 氢给体数：
  7
• 氢受体数：
  19

反应信息

• 作为产物：
  描述：

  在 sodium azide 、 caesium carbonate 、 三氟乙酸 作用下， 以 二氯甲烷 、 水 、 丙酮 、 乙腈 为溶剂， 反应 89.33h， 生成 (18S,25S,35S)-35-[(S)-hydroxy(phenyl)methyl]-28-(methoxymethyl)-21-methyl-18-[2-(methylamino)-2-oxoethyl]-16,23,30,33-tetraoxo-25-propan-2-yl-3,13,20,27,37-pentathia-7,17,24,31,34,39,40,41,42,43-decazaheptacyclo[34.2.1.12,5.112,15.119,22.126,29.06,11]tritetraconta-1(38),2(43),4,6(11),7,9,12(42),14,19(41),21,26(40),28,36(39)-tridecaene-8-carboxamide
  参考文献：
  名称：

  4-Aminothiazolyl Analogues of GE2270 A: Antibacterial Lead Finding

  摘要：

  4-Aminothiazolyl analogues of the antibacterial natural product GE2270 A (1) were designed, synthesized, and evaluated for Gram positive bacteria growth inhibition. The aminothiazole-based chemical template was evaluated for chemical stability, and its decomposition revealed a novel, structurally simplified, des-thiazole analogue of 1. Subsequent stabilization of the 4-aminothiazolyl functional motif was achieved and initial structure activity relationships defined.

  DOI：

  10.1021/jm101602q

文献信息

• 4-Aminothiazolyl Analogues of GE2270 A: Antibacterial Lead Finding
  作者：Matthew J. LaMarche、Jennifer A. Leeds、JoAnne Dzink-Fox、Karl Gunderson、Philipp Krastel、Klaus Memmert、Michael A. Patane、Elin M. Rann、Esther Schmitt、Stacey Tiamfook、Bing Wang

  DOI：10.1021/jm101602q

  日期：2011.4.14

  4-Aminothiazolyl analogues of the antibacterial natural product GE2270 A (1) were designed, synthesized, and evaluated for Gram positive bacteria growth inhibition. The aminothiazole-based chemical template was evaluated for chemical stability, and its decomposition revealed a novel, structurally simplified, des-thiazole analogue of 1. Subsequent stabilization of the 4-aminothiazolyl functional motif was achieved and initial structure activity relationships defined.