3-formyl-2-pyrrolidino-5,6-dichloro-1-(β-D-ribofuranosyl)indole

• 分子结构分类: 有机化合物 - 核苷、核苷酸和类似物 - 吲哚核糖核苷和核糖核苷酸
• 英文名称: 3-formyl-2-pyrrolidino-5,6-dichloro-1-(β-D-ribofuranosyl)indole
• 英文别名: 5,6-dichloro-2-pyrrolidino-3-formyl-1-(β-D-ribofuranosyl)indole；5,6-dichloro-1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2-pyrrolidin-1-ylindole-3-carbaldehyde
• 化学式: C₁₈H₂₀Cl₂N₂O₅
• 分子量: 415.273
• InChiKey: BNLPBZFPQXXENP-YFHUEUNASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  27
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  95.2
• 氢给体数：
  3
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  3-formyl-2,5,6-trichloro-1-(2,3-O-isopropylidene-β-D-ribofuranosyl)indole 在 三氟乙酸 作用下， 以 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 16.03h， 生成 3-formyl-2-pyrrolidino-5,6-dichloro-1-(β-D-ribofuranosyl)indole
  参考文献：
  名称：

  Synthesis and Antiviral Activity of Some 2-Substituted 3-Formyl-and 3-Cyano-5,6-Dichloroindole Nucleosides

  摘要：

  A series of dichlorinated indole nucleosides has been synthesized and tested for activity against human cytomegalovirus (HCMV) and herpes simplex virus type-1 (HSV-1) and for cytotoxicity. The isopropylidene-protected analogs of the previously reported 3-formyl-2,5,6-trichloro-1-(beta-D-ribofuranosyl)indole (FTCRI) and 3-cyano-2,5,6-trichloro-1-(beta-D-ribofuranosyl)indole (CTCRI) were modified by nucleophilic displacement of the 2-chloro substituent using secondary amines. Deprotection of the intermediates provided 2-substituted analogs of FTCRI and CTCRI in good yield. There was a significant difference in reactivity between the isopropylidene-protected and the fully deprotected FTCRI and CTCRI with respect to nucleophilic displacement of the 2-chloro substituent using dialkylamines. This difference in reactivity was not observed with monoalkylamines or with alkoxides, and the corresponding 2-alkylamino- and 2-methoxy substituted analogs were synthesized from FTCRI and CTCRI directly. None of the synthesized analogs demonstrated potent antiviral activity without some corresponding cytotoxicity.

  DOI：

  10.1080/15257770500265836

文献信息

• [EN] INDOLE ANTIVIRAL COMPOSITIONS AND METHODS<br/>[FR] COMPOSITIONS ANTIVIRALES A BASE D'INDOLE ET PROCEDES CORRESPONDANTS
  申请人：UNIV MICHIGAN

  公开号：WO2005034943A1

  公开（公告）日：2005-04-21

  The present invention provides novel chemical compounds and methods for their use. In particular, the present invention provides indole derivatives (e.g. as shown in Formula (I)) and related compounds and methods of using indole derivatives and related compounds as therapeutic agents to treat a number of conditions, including those associated with viral infection and cardiovascular diseases.

  本发明提供了新颖的化合物和它们的使用方法。具体来说，本发明提供了吲哚衍生物（例如如公式（I）所示）和相关化合物，以及使用吲哚衍生物和相关化合物作为治疗剂治疗多种疾病的方法，包括与病毒感染和心血管疾病相关的疾病。
• Indole antiviral compositions and methods
  申请人：Townsend B. Leroy

  公开号：US20050143329A1

  公开（公告）日：2005-06-30

  The present invention provides novel chemical compounds, and methods for their use. In particular, the present invention provides indole derivatives (e.g. as shown in Formula (I)) and related compounds and methods of using indole derivatives and related compounds as therapeutic agents to treat a number of conditions, including those associated with viral infection and cardiovascular diseases.

  本发明提供了新的化合物和其使用方法。特别地，本发明提供吲哚衍生物（例如如式（I）所示）和相关化合物以及使用吲哚衍生物和相关化合物作为治疗剂治疗多种疾病的方法，包括与病毒感染和心血管疾病有关的疾病。
• Indole Antiviral Compositions And Methods
  申请人：Townsend Leroy B.

  公开号：US20090281052A1

  公开（公告）日：2009-11-12

  The present invention provides novel chemical compounds, and methods for their use. In particular, the present invention provides indole derivatives (e.g. as shown in Formula (I)) and related compounds and methods of using indole derivatives and related compounds as therapeutic agents to treat a number of conditions, including those associated with viral infection and cardiovascular diseases.

  本发明提供了新型化合物及其使用方法。具体来说，本发明提供吲哚衍生物（例如如式（I）所示）和相关化合物，以及使用吲哚衍生物和相关化合物作为治疗剂治疗多种疾病的方法，包括与病毒感染和心血管疾病相关的疾病。
• US7419963B2
  申请人：——

  公开号：US7419963B2

  公开（公告）日：2008-09-02
• US7625871B2
  申请人：——

  公开号：US7625871B2

  公开（公告）日：2009-12-01