2-(2,3-epoxy-2-phenylpropyl)-2-ethylindan-1,3-dione

• 分子结构分类: 有机化合物 - 苯类化合物 - 茚满类
• 英文名称: 2-(2,3-epoxy-2-phenylpropyl)-2-ethylindan-1,3-dione
• 英文别名: 2-ethyl-2-[(2-phenyloxiran-2-yl)methyl]indene-1,3-dione
• 化学式: C₂₀H₁₈O₃
• 分子量: 306.361
• InChiKey: NUCUUSTZOIILDL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  23
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  46.7
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-(2,3-epoxy-2-phenylpropyl)-2-ethylindan-1,3-dione 、 吡啶溴化氢盐 以 N-甲基乙酰胺 、 氯仿 为溶剂， 生成 2-(3 bromo-2-hydroxy-2-phenylpropyl)-2-ethylindan-1,3-dione
  参考文献：
  名称：

  Indan-1,3-dione derivative and herbicidal composition containing the

  摘要：

  本发明提供了吲哚酮衍生物，包括以下式子（I）所代表的衍生物：##STR1## 其中，R1代表氢原子或低碳基；R2代表由以下式子所代表的基：##STR2## 其中，E代表取代的苯基或取代的吡啶基；Y代表羟基；Z代表卤素原子，取代的烷基磺酰氧基或取代的苯基磺酰氧基，或Y和Z结合代表--O--；A代表取代的1,3-丁二烯基或取代的1,3-氮杂丁二烯基；以及一种含有该化合物作为活性成分的除草剂组合物。式子（I）的化合物对禾本科杂草、莎草科杂草等表现出高除草活性，但对作物的植物毒性明显降低。

  公开号：

  US05076830A1

文献信息

• Treatment of viral infections by modulation of host cell metabolic pathways
  申请人：Munger Josh

  公开号：US20090239830A1

  公开（公告）日：2009-09-24

  Alterations of certain metabolite concentrations and fluxes that occur in response to viral infection are described. Host cell enzymes in the involved metabolic pathways are selected as targets for intervention; i.e., to restore metabolic flux to disadvantage viral replication, or to further derange metabolic flux resulting in “suicide” of viral-infected cells (but not uninfected cells) in order to limit viral propagation. While any of the enzymes in the relevant metabolic pathway can be selected, pivotal enzymes at key control points in these metabolic pathways are preferred as candidate antiviral drug targets. Inhibitors of these enzymes are used to reverse, or redirect, the effects of the viral infection. Drug candidates are tested for antiviral activity using screening assays in vitro and host cells, as well as in animal models. Animal models are then used to test efficacy of candidate compounds in preventing and treating viral infections. The antiviral activity of enzyme inhibitors is demonstrated.

  描述了在病毒感染时发生的某些代谢物浓度和通量的改变。选择涉及代谢途径的宿主细胞酶作为干预靶点；即恢复代谢通量以不利于病毒复制，或进一步扰乱代谢通量导致病毒感染细胞的“自杀”（但不包括未感染的细胞），以限制病毒传播。虽然可以选择相关代谢途径中的任何酶，但是在这些代谢途径中关键控制点的关键酶更适合作为候选抗病毒药物靶点。使用这些酶的抑制剂来逆转或重定向病毒感染的影响。使用体外筛选分析和宿主细胞以及动物模型测试药物候选物的抗病毒活性。然后使用动物模型测试候选化合物在预防和治疗病毒感染方面的功效。证明了酶抑制剂的抗病毒活性。
• TREATMENT OF VIRAL INFECTIONS BY MODULATION OF HOST CELL METABOLIC PATHWAYS
  申请人：MUNGER Josh

  公开号：US20130065850A1

  公开（公告）日：2013-03-14

  Alterations of certain metabolite concentrations and fluxes that occur in response to viral infection are described. Host cell enzymes in the involved metabolic pathways are selected as targets for intervention; i.e., to restore metabolic flux to disadvantage viral replication, or to further derange metabolic flux resulting in “suicide” of viral-infected cells (but not uninfected cells) in order to limit viral propagation. While any of the enzymes in the relevant metabolic pathway can be selected, pivotal enzymes at key control points in these metabolic pathways are preferred as candidate antiviral drug targets. Inhibitors of these enzymes are used to reverse, or redirect, the effects of the viral infection. Drug candidates are tested for antiviral activity using screening assays in vitro and host cells, as well as in animal models. Animal models are then used to test efficacy of candidate compounds in preventing and treating viral infections. The antiviral activity of enzyme inhibitors is demonstrated.

  描述了某些代谢物浓度和通量的改变，这些改变是对病毒感染的反应。选择参与代谢途径的宿主细胞酶作为干预的目标，即恢复代谢通量以削弱病毒复制，或进一步扰乱代谢通量导致病毒感染细胞的“自杀”（但不包括未感染的细胞），以限制病毒传播。虽然可以选择相关代谢途径中的任何酶，但是在这些代谢途径的关键控制点上的关键酶被优先选择作为候选抗病毒药物靶点。使用这些酶的抑制剂来扭转或重定向病毒感染的影响。通过体外和宿主细胞的筛选试验以及动物模型来测试药物候选物的抗病毒活性。然后使用动物模型来测试候选化合物在预防和治疗病毒感染方面的功效。证明了酶抑制剂的抗病毒活性。
• Indan-1,3-dione derivative and herbicidal composition containing the same as active ingredient
  申请人：MITSUBISHI KASEI CORPORATION

  公开号：EP0398258A1

  公开（公告）日：1990-11-22

  The present invention provides an indan-1,3-dione derivative represented by the following formula (I): wherein R¹ represents a hydrogen atom or a lower alkyl group; R² represents a group represented by wherein E represents a (substituted) phenyl group or a (substituted) pyridyl group; Y represents a hydroxyl group; and Z represents a halogen atom, a (substituted) alkylsulfonyloxy group or a (substituted) phenylsulfonyloxy group, or Y and Z are bonded to represent -O-; and A represents a (substituted) 1,3-butadienylene group or a (substituted) 1,3-­azabutadienylene group, and a herbicidal composition containing the same as an active ingredient. The present invention further provides an indan-1,3-dione derivative represented by the following formula (II): wherein R¹ and A represent the same meanings as above and R³ represents a group represented by wherein E represents the same meanings as above; and W¹ and W² each represents hydroxyl group or form a carbon-carbon bond by combining with each other, which is available as a synthetic intermediate for the compound of the formula (I). The compound of the formula (I) shows high herbicidal activity against gramineous weeds, cyperaceous weeds, etc. but shows markedly low phytotoxicity against crops.

  本发明提供了由下式(I)代表的茚-1,3-二酮衍生物： 其中 R¹代表氢原子或低级烷基； R²代表由以下式子表示的基团 其中E代表(取代的)苯基或(取代的)吡啶基；Y代表羟基；和Z代表卤素原子、(取代的)烷基磺酰氧基或(取代的)苯基磺酰氧基，或Y和Z键合代表-O-；和A代表(取代的)1，3-丁二烯基或(取代的)1，3-氮杂丁二烯基、 以及含有相同活性成分的除草组合物。 本发明进一步提供了由下式(II)代表的茚满-1,3-二酮衍生物： 其中 R¹ 和 A 代表与上述相同的含义，R³ 代表由下列式子表示的基团 其中 E 代表与上述相同的含义；W¹和 W² 各自代表羟基或通过相互结合形成碳-碳键，可作为式 (I) 化合物的合成中间体。 式（I）化合物对禾本科杂草、莎草科杂草等具有较高的除草活性，但对农作物的植物毒性明显较低。
• US5076830A
  申请人：——

  公开号：US5076830A

  公开（公告）日：1991-12-31
• US5110342A
  申请人：——

  公开号：US5110342A

  公开（公告）日：1992-05-05