4-(4-(benzyloxy)phenyl)-3,6-dihydro-2H-pyran

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: 4-(4-(benzyloxy)phenyl)-3,6-dihydro-2H-pyran
• 英文别名: 4-[4-(Benzyloxy)phenyl]-3,6-dihydro-2H-pyran；4-(4-phenylmethoxyphenyl)-3,6-dihydro-2H-pyran
• 化学式: C₁₈H₁₈O₂
• 分子量: 266.34
• InChiKey: ARDJHPVBXVNOHU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  20
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  18.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4-(4-(benzyloxy)phenyl)-3,6-dihydro-2H-pyran 在 palladium 10% on activated carbon 氢气 作用下， 以 乙醇 为溶剂， 反应 72.0h， 以90%的产率得到4-(四氢-2H-吡喃-4-基)苯酚
  参考文献：
  名称：

  Novel Compounds 002

  摘要：

  式I的化合物，或其药用可接受的盐： 其中R1、R2和Y如规范中定义的那样，以及包括这些化合物的盐和药物组合物已经准备好。它们在治疗中很有用，特别是在疼痛管理中。

  公开号：

  US20090062251A1
• 作为产物：
  描述：

  4-苄氧基溴苯 在 盐酸 、 magnesium 作用下， 以 甲醇 为溶剂， 生成 4-(4-(benzyloxy)phenyl)-3,6-dihydro-2H-pyran
  参考文献：
  名称：

  (2R)-2-Methylchromane-2-carboxylic acids: Discovery of selective PPARα agonists as hypolipidemic agents

  摘要：

  A SAR study was conducted on chromane-2-carboxylic acid toward selective PPAR alpha agonisim. As a result, highly potent, and selective PPAR alpha agonists were discovered. The optimized compound 43 exhibited robust lowering of total cholesterol levels in hamster and dog animal models. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.05.028

文献信息

• SUBSTITUTED METHYL PYRAZOLOPYRIMIDINONE AND METHYL IMIDAZOPYRAZINONE COMPOUNDS AS PDE1 INHIBITORS
  申请人：Dart NeuroScience, LLC

  公开号：US20190177327A1

  公开（公告）日：2019-06-13

  A chemical entity of Formula (I) or Formula (II): wherein R a , R b , R e , and R f have any of the values described herein, and compositions comprising such chemical entities; methods of making them; and their use in a wide range of methods, including metabolic and reaction kinetic studies; detection and imaging techniques; radioactive treatments; modulating and treating disorders mediated by PDE1 activity or dopaminergic signaling; treating neurological disorders, CNS disorders, dementia, neurodegenerative diseases, and trauma-dependent losses of function; treating stroke, including cognitive and motor deficits during stroke rehabilitation; facilitating neuroprotection and neurorecovery; enhancing the efficiency of cognitive and motor training, including animal skill training protocols; and treating peripheral disorders, including cardiovascular, renal, hematological, gastroenterological, liver, cancer, fertility, and metabolic disorders.

  化学实体的化学式（I）或化学式（II）：其中Ra、Rb、Re和Rf可以具有本文中描述的任何值，以及包含这种化学实体的组合物；制备它们的方法；以及它们在各种方法中的使用，包括代谢和反应动力学研究；检测和成像技术；放射性治疗；调节和治疗由PDE1活性或多巴胺信号传导介导的疾病；治疗神经系统疾病、中枢神经系统疾病、痴呆、神经退行性疾病以及依赖创伤的功能丧失；治疗中风，包括中风康复期间的认知和运动功能障碍；促进神经保护和神经恢复；增强认知和运动训练的效率，包括动物技能训练方案；以及治疗外周疾病，包括心血管、肾脏、血液、胃肠、肝脏、癌症、生育和代谢紊乱。
• Cannabinoid Receptor Ligands
  申请人：Beha Sara

  公开号：US20110160180A1

  公开（公告）日：2011-06-30

  Compounds of Formulae (I), or pharmaceutically acceptable salts thereof: wherein R 1 , R 2 and Y are as defined in the specification as well as salts and pharmaceutical compositions including the compounds are prepared. They are useful in therapy, in particular in the management of pain.

  化学式（I）的化合物，或其药学上可接受的盐：其中R1，R2和Y的定义如规范中所述，以及包括这些化合物的盐和药物组合物已经制备。它们在治疗中有用，特别是在疼痛管理中。
• [EN] COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH STING ACTIVITY<br/>[FR] COMPOSÉS ET COMPOSITIONS POUR TRAITER DES ÉTATS PATHOLOGIQUES ASSOCIÉS À L'ACTIVITÉ DE STING
  申请人：IFM DUE INC

  公开号：WO2023018781A1

  公开（公告）日：2023-02-16

  This disclosure features chemical entities (e.g., a compound or a pharmaceutically acceptable salt, and/or hydrate, and/or cocrystal, and/or drug combination of the compound) that inhibit (e.g., antagonize) Stimulator of Interferon Genes (STING). Said chemical entities are useful, e.g., for treating a condition, disease or disorder in which increased (e.g., excessive) STING activation (e.g., STING signaling) contributes to the pathology and/or symptoms and/or progression of the condition, disease or disorder (e.g., cancer) in a subject (e.g., a human). This disclosure also features compositions containing the same as well as methods of using and making the same.

  本公开涉及化学实体（例如，化合物或药学上可接受的盐，水合物，共晶体或化合物的药物组合物），其抑制（例如，拮抗）干扰素基因刺激剂（STING）。所述化学实体是有用的，例如用于治疗在其中增加（例如，过度）STING激活（例如，STING信号传导）对主体（例如，人类）的病理学和/或症状和/或疾病或疾病的进展有贡献的情况，疾病或疾病（例如，癌症）。本公开还涉及包含相同的组合物以及使用和制备相同的方法。
• CANNABINOID RECEPTOR LIGANDS
  申请人：AstraZeneca AB

  公开号：EP2190838A1

  公开（公告）日：2010-06-02
• [EN] CANNABINOID RECEPTOR LIGANDS<br/>[FR] LIGANDS DES RÉCEPTEURS CANNABINOÏDES
  申请人：ASTRAZENECA AB

  公开号：WO2009024819A1

  公开（公告）日：2009-02-26

  Compounds of Formulae (I), or pharmaceutically acceptable salts thereof: wherein R1, R2 and Y are as defined in the specification as well as salts and pharmaceutical compositions including the compounds are prepared. They are useful in therapy, in particular in the management of pain.