(E)-3-methylhept-2-en-1-amine | 808132-27-6

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: (E)-3-methylhept-2-en-1-amine
• CAS: 808132-27-6
• 化学式: C₈H₁₇N
• 分子量: 127.23
• InChiKey: GHKQNVIWHCJNFP-SOFGYWHQSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  9
• 可旋转键数：
  4
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.75
• 拓扑面积：
  26
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (E)-3-methylhept-2-en-1-amine 在 盐酸 、 三乙胺 作用下， 以 甲醇 、 丙酮 、 xylene 为溶剂， 反应 7.08h， 生成 6-Ethyl-4-hydroxy-2-oxo-2H-pyran-3-carboxylic acid ((E)-3-methyl-hept-2-enyl)-amide
  参考文献：
  名称：

  Myxopyronin B analogs as inhibitors of RNA polymerase, synthesis and biological evaluation

  摘要：

  A series of myxopyronin B analogs has been prepared via a convergent synthetic route and were tested for in vitro inhibitory activity against DNA-dependent RNA polymerase and antibacterial activity against E. coli and S. aureus. The parent lead compound proved to be very sensitive to even small changes. Only the achiral desmethyl myxopyronin B (1a) provided enhanced potency. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.08.045
• 作为产物：
  描述：

  (E)-3-methylhept-2-en-1-ol 在 三苯基膦 、 甲胺 、 偶氮二甲酸二乙酯 作用下， 以 四氢呋喃 、 乙醇 为溶剂， 反应 13.0h， 生成 (E)-3-methylhept-2-en-1-amine
  参考文献：
  名称：

  Myxopyronin B analogs as inhibitors of RNA polymerase, synthesis and biological evaluation

  摘要：

  A series of myxopyronin B analogs has been prepared via a convergent synthetic route and were tested for in vitro inhibitory activity against DNA-dependent RNA polymerase and antibacterial activity against E. coli and S. aureus. The parent lead compound proved to be very sensitive to even small changes. Only the achiral desmethyl myxopyronin B (1a) provided enhanced potency. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2004.08.045

文献信息

• Antifungal Agent Containing Pyridine Derivative
  申请人：Nakamoto Kazutaka

  公开号：US20090062348A1

  公开（公告）日：2009-03-05

  The present invention provides an antifungal agent that has superior antifungal action and is also superior in terms of physical properties, safety and metabolic stability. The present invention discloses a compound represented by the formula (I): (wherein X represents an oxygen atom, a sulfur atom or —NH—, R 1 represents a hydrogen atom, a halogen atom, a cyano group, an amino group or a substituent, and R 2 and R 3 independently represent a hydrogen atom, a halogen atom, a hydroxyl group or a substituent, except for a case in which R 2 and R 3 are both hydrogen atoms), and an antifungal agent containing the above compound.

  本发明提供了一种具有优越的抗真菌作用，同时在物理性质、安全性和代谢稳定性方面也具有优越性的抗真菌剂。本发明公开了一种由式(I)表示的化合物：（其中X表示氧原子、硫原子或-NH-，R1表示氢原子、卤素原子、氰基、氨基或取代基，R2和R3独立地表示氢原子、卤素原子、羟基或取代基，但在R2和R3均为氢原子的情况下除外），以及含有上述化合物的抗真菌剂。
• ANTIFUNGAL AGENT CONTAINING PYRIDINE DERIVATIVE
  申请人：Eisai R&D Management Co., Ltd.

  公开号：EP1864980A1

  公开（公告）日：2007-12-12

  The present invention provides an antifungal agent that has superior antifungal action and is also superior in terms of physical properties, safety and metabolic stability. The present invention discloses a compound represented by the formula (I): (wherein X represents an oxygen atom, a sulfur atom or -NH-, R1 represents a hydrogen atom, a halogen atom, a cyano group, an amino group or a substituent, and R2 and R3 independently represent a hydrogen atom, a halogen atom, a hydroxyl group or a substituent, except for a case in which R2 and R3 are both hydrogen atoms), and an antifungal agent containing the above compound.

  本发明提供了一种抗真菌剂，它具有卓越的抗真菌作用，在物理性质、安全性和代谢稳定性方面也更胜一筹。本发明公开了一种由式（I）表示的化合物： (其中 X 代表氧原子、硫原子或-NH-，R1 代表氢原子、卤素原子、氰基、氨基或取代基，R2 和 R3 独立地代表氢原子、卤素原子、羟基或取代基，但 R2 和 R3 均为氢原子的情况除外），以及含有上述化合物的抗真菌剂。
• US7829585B2
  申请人：——

  公开号：US7829585B2

  公开（公告）日：2010-11-09
• Myxopyronin B analogs as inhibitors of RNA polymerase, synthesis and biological evaluation
  作者：Thomas Doundoulakis、Alan X. Xiang、Ricardo Lira、Konstantinos A. Agrios、Stephen E. Webber、Wes Sisson、Robert M. Aust、Amit M. Shah、Richard E. Showalter、James R. Appleman、Klaus B. Simonsen

  DOI：10.1016/j.bmcl.2004.08.045

  日期：2004.11

  A series of myxopyronin B analogs has been prepared via a convergent synthetic route and were tested for in vitro inhibitory activity against DNA-dependent RNA polymerase and antibacterial activity against E. coli and S. aureus. The parent lead compound proved to be very sensitive to even small changes. Only the achiral desmethyl myxopyronin B (1a) provided enhanced potency. (C) 2004 Elsevier Ltd. All rights reserved.