2-[1-[(3-Benzyloxyphenyl)methyl]indol-3-yl]acetic acid | 1048345-76-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 2-[1-[(3-Benzyloxyphenyl)methyl]indol-3-yl]acetic acid
• 英文别名: 2-[1-[(3-phenylmethoxyphenyl)methyl]indol-3-yl]acetic acid
• CAS: 1048345-76-1
• 化学式: C₂₄H₂₁NO₃
• 分子量: 371.436
• InChiKey: CZPCAPHBWLRQHN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.5
• 重原子数：
  28
• 可旋转键数：
  7
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  51.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-[1-[(3-Benzyloxyphenyl)methyl]indol-3-yl]acetic acid 在 palladium 10% on activated carbon 、 氢气 作用下， 以 甲醇 、 乙酸乙酯 为溶剂， 反应 4.0h， 以52%的产率得到[1-(3-hydroxybenzyl)-1H-indol-3-yl]acetic acid
  参考文献：
  名称：

  Integrated Strategies for Identifying Leads That Target the NS3 Helicase of the Hepatitis C Virus

  摘要：

  Future treatments for individuals infected by the hepatitis C virus (HCV) will likely involve combinations of compounds that inhibit multiple viral targets. The helicase of HCV is an attractive target with no known drug candidates in clinical trials. Herein we describe an integrated strategy for identifying fragment inhibitors using structural and biophysical techniques. Based on an X-ray structure of apo HCV helicase and in silico and bioinformatic analyses of HCV variants, we identified that one site in particular (labeled 3 + 4) was the most conserved and attractive pocket to target for a drug discovery campaign. Compounds from multiple sources were screened to identify inhibitors or binders to this site, and enzymatic and biophysical assays (NMR and SPR) were used to triage the most promising ligands for 3D structure determination by X-ray crystallography. Medicinal chemistry and biophysical evaluations focused on exploring the most promising lead series. The strategies employed here can have general utility in drug discovery.

  DOI：

  10.1021/jm401432c
• 作为产物：
  描述：

  3-吲哚乙酸 、 3-苄氧基溴苄 在 sodium hydride 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 1.5h， 以99%的产率得到2-[1-[(3-Benzyloxyphenyl)methyl]indol-3-yl]acetic acid
  参考文献：
  名称：

  Integrated Strategies for Identifying Leads That Target the NS3 Helicase of the Hepatitis C Virus

  摘要：

  Future treatments for individuals infected by the hepatitis C virus (HCV) will likely involve combinations of compounds that inhibit multiple viral targets. The helicase of HCV is an attractive target with no known drug candidates in clinical trials. Herein we describe an integrated strategy for identifying fragment inhibitors using structural and biophysical techniques. Based on an X-ray structure of apo HCV helicase and in silico and bioinformatic analyses of HCV variants, we identified that one site in particular (labeled 3 + 4) was the most conserved and attractive pocket to target for a drug discovery campaign. Compounds from multiple sources were screened to identify inhibitors or binders to this site, and enzymatic and biophysical assays (NMR and SPR) were used to triage the most promising ligands for 3D structure determination by X-ray crystallography. Medicinal chemistry and biophysical evaluations focused on exploring the most promising lead series. The strategies employed here can have general utility in drug discovery.

  DOI：

  10.1021/jm401432c

文献信息

• NOVEL INHIBITORS OF HEPATITIS C VIRUS REPLICATION
  申请人：Beigelman Leonid

  公开号：US20090047246A1

  公开（公告）日：2009-02-19

  The embodiments provide compounds of the general Formula I, as well as compositions, including pharmaceutical compositions, comprising a subject compound. The embodiments further provide treatment methods, including methods of treating a hepatitis C virus infection, the methods generally involving administering to an individual in need thereof an effective amount of a subject compound or composition.

  本实施例提供通式I的化合物，以及包括制剂（包括制药制剂）的组合物，其中包括一种主体化合物。本实施例进一步提供治疗方法，包括治疗丙型肝炎病毒感染的方法，该方法通常涉及向需要的个体施用主体化合物或组合物的有效量。
• [EN] NOVEL INHIBITORS HEPATITIS C VIRUS REPLICATION<br/>[FR] NOUVEAUX INHIBITEURS DE RÉPLICATION DU VIRUS DE L'HÉPATITE C
  申请人：INTERMUNE INC

  公开号：WO2008100867A2

  公开（公告）日：2008-08-21

  [EN] The embodiments provide compounds of the general Formula I, as well as compositions, including pharmaceutical compositions, comprising a subject compound. The embodiments further provide treatment methods, including methods of treating a hepatitis C virus infection, the methods generally involving administering to an individual in need thereof an effective amount of a subject compound or composition.
  [FR] L'invention porte sur des composés de la formule générale I, ainsi que sur des compositions, y compris des compositions pharmaceutiques, comprenant un composé de l'invention. L'invention porte en outre sur des procédés de traitement, y compris des procédés de traitement d'une infection par le virus de l'hépatite C, les procédés impliquant généralement l'administration à un individu qui en a besoin d'une quantité efficace d'un composé ou d'une composition de l'invention.
• Integrated Strategies for Identifying Leads That Target the NS3 Helicase of the Hepatitis C Virus
  作者：Steven R. LaPlante、Anil K. Padyana、Asitha Abeywardane、Pierre Bonneau、Mireille Cartier、René Coulombe、Araz Jakalian、Jessi Wildeson-Jones、Xiang Li、Shuang Liang、Ginette McKercher、Peter White、Qiang Zhang、Steven J. Taylor

  DOI：10.1021/jm401432c

  日期：2014.3.13

  Future treatments for individuals infected by the hepatitis C virus (HCV) will likely involve combinations of compounds that inhibit multiple viral targets. The helicase of HCV is an attractive target with no known drug candidates in clinical trials. Herein we describe an integrated strategy for identifying fragment inhibitors using structural and biophysical techniques. Based on an X-ray structure of apo HCV helicase and in silico and bioinformatic analyses of HCV variants, we identified that one site in particular (labeled 3 + 4) was the most conserved and attractive pocket to target for a drug discovery campaign. Compounds from multiple sources were screened to identify inhibitors or binders to this site, and enzymatic and biophysical assays (NMR and SPR) were used to triage the most promising ligands for 3D structure determination by X-ray crystallography. Medicinal chemistry and biophysical evaluations focused on exploring the most promising lead series. The strategies employed here can have general utility in drug discovery.