2-([1,1'-biphenyl]-4-yl)-N-(1,4-dioxo-1,4-dihydronaphthalen-2-yl)acetamide | 1421609-42-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-([1,1'-biphenyl]-4-yl)-N-(1,4-dioxo-1,4-dihydronaphthalen-2-yl)acetamide
• 英文别名: N-(1,4-dioxonaphthalen-2-yl)-2-(4-phenylphenyl)acetamide
• CAS: 1421609-42-8
• 化学式: C₂₄H₁₇NO₃
• 分子量: 367.404
• InChiKey: GSUVBQWPSFWEQF-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：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.04
• 拓扑面积：
  63.2
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  1,4-萘醌 在 sodium azide 、 sodium hydride 、 溶剂黄146 作用下， 以 四氢呋喃 、 水 为溶剂， 反应 6.0h， 生成 2-([1,1'-biphenyl]-4-yl)-N-(1,4-dioxo-1,4-dihydronaphthalen-2-yl)acetamide
  参考文献：
  名称：

  Structure–Activity Relationship Study of Vitamin K Derivatives Yields Highly Potent Neuroprotective Agents

  摘要：

  Historically known for its role in blood coagulation and bone formation, vitamin K (VK) has begun to emerge as an important nutrient for brain function. While VK involvement in the brain has not been fully explored, it is well-known that oxidative stress plays a critical role in neuro-degenerative diseases. It was recently reported that VK protects neurons and oligodendrocytes from oxidative injury and rescues Drosophila from mitochondrial defects associated with Parkinson's disease. In this study, we take a chemical approach to define the optimal and minimum pharmacophore responsible for the neuroprotective effects of VK. In doing so, we have developed a series of potent VK analogues with favorable drug characteristics that provide full protection at nanomolar concentrations in a well-defined model of neuronal oxidative stress. Additionally, we have characterized key cellular responses and biomarkers consistent with the compounds' ability to rescue cells from oxidative stress induced cell death.

  DOI：

  10.1021/jm301485d

文献信息

• [EN] COMPOSITIONS AND METHODS FOR TREATING NEUROLOGICAL DISEASES OR INJURY<br/>[FR] COMPOSITIONS ET MÉTHODES DE TRAITEMENT DE MALADIES OU DE LÉSIONS NEUROLOGIQUES
  申请人：MUSC FOUND FOR RES DEV

  公开号：WO2014074976A1

  公开（公告）日：2014-05-15

  Provided are compounds for the treatment of neurological diseases or injuries, including neurodegenerative diseases, stroke, trauma, epilepsy, acute and chronic kidney injuries, diabetes mellitus, and/or seizures. In some embodiments, derivatives of vitamin K are provided.

  提供了用于治疗神经系统疾病或损伤的化合物，包括神经退行性疾病、中风、创伤、癫痫、急性和慢性肾脏损伤、糖尿病和/或癫痫。在某些实施例中，提供了维生素K的衍生物。
• COMPOSITIONS AND METHODS FOR TREATING NEUROLOGICAL DISEASES OR INJURY
  申请人：MUSC FOUNDATION FOR RESEARCH DEVELOPMENT

  公开号：US20150320702A1

  公开（公告）日：2015-11-12

  Provided are compounds for the treatment of neurological diseases or injuries, including neurodegenerative diseases, stroke, trauma, epilepsy, acute and chronic kidney injuries, diabetes mellitus, and/or seizures. In some embodiments, derivatives of vitamin K are provided.

  提供了用于治疗神经系统疾病或损伤的化合物，包括神经退行性疾病、中风、创伤、癫痫、急性和慢性肾脏损伤、糖尿病和/或癫痫。在某些实施例中，提供了维生素K的衍生物。
• Compositions and methods for treating neurological diseases or injury
  申请人：MUSC FOUNDATION FOR RESEARCH DEVELOPMENT

  公开号：US10391070B2

  公开（公告）日：2019-08-27

  Provided are compounds for the treatment of neurological diseases or injuries, including neurodegenerative diseases, stroke, trauma, epilepsy, acute and chronic kidney injuries, diabetes mellitus, and/or seizures. In some embodiments, derivatives of vitamin K are provided.

  所提供的化合物用于治疗神经系统疾病或损伤，包括神经退行性疾病、中风、创伤、癫痫、急性和慢性肾损伤、糖尿病和/或癫痫发作。 在某些实施方案中，提供了维生素 K 的衍生物。
• US9861596B2
  申请人：——

  公开号：US9861596B2

  公开（公告）日：2018-01-09
• Structure–Activity Relationship Study of Vitamin K Derivatives Yields Highly Potent Neuroprotective Agents
  作者：Benjamin J. Josey、Elizabeth S. Inks、Xuejun Wen、C. James Chou

  DOI：10.1021/jm301485d

  日期：2013.2.14

  Historically known for its role in blood coagulation and bone formation, vitamin K (VK) has begun to emerge as an important nutrient for brain function. While VK involvement in the brain has not been fully explored, it is well-known that oxidative stress plays a critical role in neuro-degenerative diseases. It was recently reported that VK protects neurons and oligodendrocytes from oxidative injury and rescues Drosophila from mitochondrial defects associated with Parkinson's disease. In this study, we take a chemical approach to define the optimal and minimum pharmacophore responsible for the neuroprotective effects of VK. In doing so, we have developed a series of potent VK analogues with favorable drug characteristics that provide full protection at nanomolar concentrations in a well-defined model of neuronal oxidative stress. Additionally, we have characterized key cellular responses and biomarkers consistent with the compounds' ability to rescue cells from oxidative stress induced cell death.