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2,4-dichloro-N-((naphthalen-6-yl)methyl)benzamide | 1229445-51-5

中文名称
——
中文别名
——
英文名称
2,4-dichloro-N-((naphthalen-6-yl)methyl)benzamide
英文别名
2,4-dichloro-N-(naphthalen-2-ylmethyl)benzamide
2,4-dichloro-N-((naphthalen-6-yl)methyl)benzamide化学式
CAS
1229445-51-5
化学式
C18H13Cl2NO
mdl
——
分子量
330.213
InChiKey
RARIAPRMVKAZSX-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    5.2
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为产物:
    参考文献:
    名称:
    Small Molecule Modifiers of MicroRNA miR-122 Function for the Treatment of Hepatitis C Virus Infection and Hepatocellular Carcinoma
    摘要:
    MicroRNAs are a recently discovered new class of important endogenous regulators of gene function. Aberrant regulation of microRNAs has been linked to various human diseases, most importantly cancer. Small molecule intervention of microRNA misregulation has the potential to provide new therapeutic approaches to such diseases. Here, we report the first small molecule inhibitors and activators of the liver-specific microRNA miR-122. This microRNA is the most abundant microRNA in the liver and is involved in hepatocellular carcinoma development and hepatitis C virus (HCV) infection. Our small molecule inhibitors reduce viral replication in liver cells and represent a new approach to the treatment of HCV infections. Moreover, small molecule activation of miR-122 in liver cancer cells selectively induced apoptosis through caspase activation, thus having implications in cancer chemotherapy. In addition to providing a new approach for the development of therapeutics, small molecule modifiers of miR-122 function are unique tools for exploring miR-122 biogenesis.
    DOI:
    10.1021/ja910275u
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文献信息

  • [EN] SMALL MOLECULE MODIFIERS OF MICRORNA MIR-122<br/>[FR] MODIFICATEURS À PETITE MOLÉCULE DE MICROARN MIR-122
    申请人:UNIV NORTH CAROLINA STATE
    公开号:WO2011091209A1
    公开(公告)日:2011-07-28
    MicroRNAs are a class of endogenous regulators of gene function. Aberrant regulation of microRNAs has been linked to various human diseases, most importantly cancer. Small molecule intervention of microRNA misregulation has the potential to provide new therapeutic approaches to such diseases. microRNA miR-122 is the most abundant microRNA in the liver and is involved in hepatocellular carcinoma development and hepatitis C virus (HCV) infection. Small molecule inhibitors and activators of the microRNA miR-122 are described, and methods for their identification are reported. These small molecule inhibitors reduce viral replication in liver cells and thus represent a new approach to the treatment of HCV infections. Moreover, small molecule activation of miR-122 in liver cancer cells selectively induced apoptosis through caspase activation, and thus has implications in cancer chemotherapy.
    微小RNA是一类内源性基因功能调节因子。微小RNA的异常调节与各种人类疾病有关,尤其是癌症。对微小RNA的小分子干预可能为这些疾病提供新的治疗途径。微小RNA miR-122是肝脏中最丰富的微小RNA,参与了肝细胞癌和丙型肝炎病毒(HCV)感染的发展。描述了微小RNA miR-122的小分子抑制剂和激活剂,并报告了其鉴定方法。这些小分子抑制剂可以减少肝细胞中的病毒复制,因此代表了治疗HCV感染的新方法。此外,在肝癌细胞中通过小分子激活miR-122可选择性诱导凋亡,通过激活半胱氨酸蛋白酶而在癌症化疗中具有重要意义。
  • SMALL MOLECULE MODIFIERS OF MICRORNA MIR-122
    申请人:Deiters Alexander
    公开号:US20130005759A1
    公开(公告)日:2013-01-03
    MicroRNAs are a class of endogenous regulators of gene function. Aberrant regulation of microRNAs has been linked to various human diseases, most importantly cancer. Small molecule intervention of microRNA misregulation has the potential to provide new therapeutic approaches to such diseases. microRNA miR-122 is the most abundant microRNA in the liver and is involved in hepatocellular carcinoma development and hepatitis C virus (HCV) infection. Small molecule inhibitors and activators of the microRNA miR-122 are described, and methods for their identification are reported. These small molecule inhibitors reduce viral replication in liver cells and thus represent a new approach to the treatment of HCV infections. Moreover, small molecule activation of miR-122 in liver cancer cells selectively induced apoptosis through caspase activation, and thus has implications in cancer chemotherapy.
    MicroRNAs是一类内源性基因调控因子。微小RNA的异常调控已与各种人类疾病,尤其是癌症相关联。小分子干预微小RNA的错调可能为这些疾病提供新的治疗方法。微小RNA miR-122是肝脏中最丰富的微小RNA,参与肝细胞癌的发展和丙型肝炎病毒(HCV)感染。描述了微小RNA miR-122的小分子抑制剂和激活剂,并报道了其鉴定方法。这些小分子抑制剂能够减少肝细胞中的病毒复制,因此代表了治疗HCV感染的新方法。此外,小分子激活miR-122在肝癌细胞中选择性地通过caspase激活诱导凋亡,因此在癌症化疗中具有重要意义。
  • HCV Combination Therapy
    申请人:Hodges Michael
    公开号:US20140127159A1
    公开(公告)日:2014-05-08
    The present invention relates to the treatment of hepatitis C (HCV) infection by the combination treatment with a miR-122 inhibitor and a HCV NS3/4A protease inhibitor.
  • Small Molecule Modifiers of MicroRNA miR-122 Function for the Treatment of Hepatitis C Virus Infection and Hepatocellular Carcinoma
    作者:Douglas D. Young、Colleen M. Connelly、Christoph Grohmann、Alexander Deiters
    DOI:10.1021/ja910275u
    日期:2010.6.16
    MicroRNAs are a recently discovered new class of important endogenous regulators of gene function. Aberrant regulation of microRNAs has been linked to various human diseases, most importantly cancer. Small molecule intervention of microRNA misregulation has the potential to provide new therapeutic approaches to such diseases. Here, we report the first small molecule inhibitors and activators of the liver-specific microRNA miR-122. This microRNA is the most abundant microRNA in the liver and is involved in hepatocellular carcinoma development and hepatitis C virus (HCV) infection. Our small molecule inhibitors reduce viral replication in liver cells and represent a new approach to the treatment of HCV infections. Moreover, small molecule activation of miR-122 in liver cancer cells selectively induced apoptosis through caspase activation, thus having implications in cancer chemotherapy. In addition to providing a new approach for the development of therapeutics, small molecule modifiers of miR-122 function are unique tools for exploring miR-122 biogenesis.
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