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3,5-dichlorophenylsulfonylacetonitrile | 797036-07-8

中文名称
——
中文别名
——
英文名称
3,5-dichlorophenylsulfonylacetonitrile
英文别名
2-(3,5-Dichlorophenyl)sulfonylacetonitrile
3,5-dichlorophenylsulfonylacetonitrile化学式
CAS
797036-07-8
化学式
C8H5Cl2NO2S
mdl
——
分子量
250.105
InChiKey
DQPBCNHYVMPJCQ-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):
    2.2
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    66.3
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Synthesis and biological evaluation of triazolothienopyrimidine derivatives as novel HIV-1 replication inhibitors
    摘要:
    We identified a novel class of triazolothienopyrimidine (TTPM) compounds as potent HIV-1 replication inhibitors during a high-throughput screening campaign that evaluated more than 200,000 compounds using a cell-based full replication assay. Herein, we report the optimization of the antiviral activity in a cell-based assay system leading to the discovery of aryl-substituted TTPM derivatives (38, 44, and 45), which exhibited significant inhibition of HIV-1 replication with acceptable safety margins. These novel and potent TTPMs could serve as leads for further development. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.10.134
  • 作为产物:
    描述:
    3,5-二氯苯磺酰氯氯乙腈碳酸氢钠 、 sodium sulfite 作用下, 以 为溶剂, 反应 0.83h, 生成 3,5-dichlorophenylsulfonylacetonitrile
    参考文献:
    名称:
    Synthesis and biological evaluation of triazolothienopyrimidine derivatives as novel HIV-1 replication inhibitors
    摘要:
    We identified a novel class of triazolothienopyrimidine (TTPM) compounds as potent HIV-1 replication inhibitors during a high-throughput screening campaign that evaluated more than 200,000 compounds using a cell-based full replication assay. Herein, we report the optimization of the antiviral activity in a cell-based assay system leading to the discovery of aryl-substituted TTPM derivatives (38, 44, and 45), which exhibited significant inhibition of HIV-1 replication with acceptable safety margins. These novel and potent TTPMs could serve as leads for further development. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.10.134
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文献信息

  • Chemical uncouplers for the treatment of obesity
    申请人:——
    公开号:US20040138301A1
    公开(公告)日:2004-07-15
    This invention relates to chemical uncouplers with a broader safety window making the use of them in treating obesity and, consequently, in the treatment of obesity related diseases and conditions such as atherosclerosis, hypertension, diabetes, especially type 2 diabetes (NIDDM (non-insulin dependent diabetes mellitus)), impaired glucose tolerance, dyslipidemia, coronary heart disease, gallbladder disease, osteoarthritis and various types of cancer such as endometrial, breast, prostate and colon cancers and the risk for premature death as well as other conditions, such as diseases and disorders, which conditions are improved by an increase in mitochondrial respiration, more attractive.
    这项发明涉及一种化学偶联剂,它具有更宽的安全窗口,使其在治疗肥胖症以及因此引发的相关疾病和状况,如动脉硬化、高血压、糖尿病(尤其是2型糖尿病(非胰岛素依赖型糖尿病))、葡萄糖耐量受损、血脂异常、冠心病、胆结石病、骨关节炎以及子宫内膜、乳房、前列腺和结肠等各种癌症以及过早死亡的风险等方面更具吸引力。此外,还包括其他通过增加线粒体呼吸得到改善的条件、疾病和紊乱。
  • COMPOSITION, SYNTHESIS, AND USE OF NEW ARYLSULFONYL ISONITRILES
    申请人:DUQUESNE UNIVERSITY OF THE HOLY GHOST
    公开号:US20150239833A1
    公开(公告)日:2015-08-27
    This invention relates to novel isonitriles, including arylsulfonyl isonitriles, and methods for their synthesis. The isonitriles include a conjugated ring system. The structure is designed with the flexibility to have multiple substitution patterns. The isonitriles may be used in applications including, but not limited to, pharmaceutical compositions.
    这项发明涉及新型异腈,包括芳基磺酰异腈,以及它们的合成方法。异腈包括一个共轭环系统。该结构设计具有多种取代模式的灵活性。异腈可用于包括但不限于药物组合物在内的应用中。
  • Pyridopyrimidine derivatives as 5-HT6 antagonists
    申请人:——
    公开号:US20040019064A1
    公开(公告)日:2004-01-29
    Novel pyridopyrimidine derivatives which have a binding affinity for the human 5-HT 6 receptor and, therefore, are useful in treating disorders responsive to antagonism of the 5-HT 6 receptor such as psychosis, schizophrenia, manic depression, depression, neurological disorder, memory disorder, Parkinson's disease, amyotrophic lateral sclerosis, Alzheimer's disease and Huntington's chorea.
    新型吡啶嘧啶生物具有与人类5-HT6受体结合亲和力,因此可用于治疗对5-HT6受体拮抗作用敏感的疾病,如精神病、精神分裂症、躁郁症、抑郁症、神经障碍、记忆障碍、帕森病、肌萎缩侧索硬化、阿尔茨海默病和亨廷顿舞蹈症。
  • [EN] NOVEL COMPOUNDS FOR TREATMENT OF OBESITY<br/>[FR] NOUVEAUX COMPOSES POUR LE TRAITEMENT DE L'OBESITE
    申请人:NOVO NORDISK AS
    公开号:WO2004101505A1
    公开(公告)日:2004-11-25
    Hydroxyl styrene sulfonyl derivatives of formula (I), in which the variables are as defined in the claims, are provided which are useful in the treatment of obesity.
    提供了式(I)的羟基苯乙烯磺酰衍生物,其中变量如权利要求所定义的那样,这些衍生物在肥胖症的治疗中是有用的。
  • Novel compounds for treatment of obesity
    申请人:Tagmose Moller Tina
    公开号:US20060128662A1
    公开(公告)日:2006-06-15
    Novel hydroxyl styrene sulfonyl derivatives of Formula (I) are provided which are useful in the treatment of obesity.
    提供了化学式(I)的新型羟基苯乙烯磺酰衍生物,可用于肥胖症的治疗。
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