5-(苄氧基)-2-溴-4-甲氧基苯酚 | 524713-42-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 酚类
• 中文名称: 5-(苄氧基)-2-溴-4-甲氧基苯酚
• 英文名称: 5-benzyloxy-2-bromo-4-methoxyphenol
• 英文别名: 5-(Benzyloxy)-2-bromo-4-methoxyphenol；2-bromo-4-methoxy-5-phenylmethoxyphenol
• CAS: 524713-42-6
• 化学式: C₁₄H₁₃BrO₃
• 分子量: 309.159
• InChiKey: ZKKBDJHAEFPFSX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  18
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  38.7
• 氢给体数：
  1
• 氢受体数：
  3

安全信息

• 海关编码：
  2909500000

反应信息

• 作为反应物：
  描述：

  5-(苄氧基)-2-溴-4-甲氧基苯酚 在 palladium on activated charcoal sodium hydroxide 、 四(三苯基膦)钯 、 正丁基锂 、 氯化亚砜 、 ammonium formate 、 sodium hydride 、 potassium carbonate 作用下， 以 四氢呋喃 、 甲醇 、 乙二醇二甲醚 、 乙醇 、 乙酸乙酯 、 1,2-二氯乙烷 为溶剂， 反应 93.66h， 生成 8-Acetyl-3-hydroxy-2-methoxybenzo[c]chromen-6-one
  参考文献：
  名称：

  Synthesis and Evaluation of a Novel Nonsteroidal-Specific Endothelial Cell Proliferation Inhibitor

  摘要：

  The identification of agents with specific antiproliferative or cytostatic activity against endothelial cells has significant value for the treatment of pathologies associated with angiogenesis, including solid tumors. Here, we describe a novel substituted dibenzo[b,d]pyran-6-one scaffold, exemplified by structures 9a and 10, and report preliminary in vitro activity data indicating that this scaffold is a promising lead for the development of specific inhibitors of endothelial cell proliferation.

  DOI：

  10.1021/jm034007d
• 作为产物：
  描述：

  2-溴-5-羟基-4-甲氧基苯甲醛 在 potassium carbonate 、 间氯过氧苯甲酸 作用下， 以 二氯甲烷 、 乙腈 为溶剂， 反应 34.0h， 生成 5-(苄氧基)-2-溴-4-甲氧基苯酚
  参考文献：
  名称：

  Synthesis and Evaluation of a Novel Nonsteroidal-Specific Endothelial Cell Proliferation Inhibitor

  摘要：

  The identification of agents with specific antiproliferative or cytostatic activity against endothelial cells has significant value for the treatment of pathologies associated with angiogenesis, including solid tumors. Here, we describe a novel substituted dibenzo[b,d]pyran-6-one scaffold, exemplified by structures 9a and 10, and report preliminary in vitro activity data indicating that this scaffold is a promising lead for the development of specific inhibitors of endothelial cell proliferation.

  DOI：

  10.1021/jm034007d

文献信息

• [EN] AZAINDOLE COMPOUNDS AS HISTONE METHYLTRANSFERASE INHIBITORS<br/>[FR] COMPOSÉS D'AZAINDOLE UTILISÉS EN TANT QU'INHIBITEURS D'HISTONE MÉTHYLTRANSFÉRASE
  申请人：GLOBAL BLOOD THERAPEUTICS INC

  公开号：WO2018226998A1

  公开（公告）日：2018-12-13

  The present disclosure provides certain angular tricyclic compounds that are histone methyltransferases G9a and/or GLP inhibitors and are therefore useful for the treatment of diseases treatable by inhibition of G9a and/or GLP such as cancers and hemoglobinopathies (e.g., beta-thalassemia and sickle cell disease). Also provided are pharmaceutical compositions containing such compounds and processes for preparing such compounds.

  本公开提供了一些特定的角三环化合物，它们是组蛋白甲基转移酶G9a和/或GLP抑制剂，因此可用于治疗通过抑制G9a和/或GLP可治疗的疾病，如癌症和血红蛋白病（例如β地中海贫血和镰状细胞病）。还提供了含有这些化合物的药物组合物和制备这些化合物的方法。
• Revision of the Structure and Total Synthesis of Altenuisol
  作者：Gregor Nemecek、Judith Cudaj、Joachim Podlech

  DOI：10.1002/ejoc.201200506

  日期：2012.7

  A total synthesis of the reported structure of altenuisol is described. Comparison of the 1H NMR spectra of the synthesized compound and of the natural product revealed that the originally proposed structure was not correct. Consequently, two constitutional isomers were synthesized. The spectra of one of these compounds – a structure originally proposed as the structure of altertenuol – matched perfectly

  描述了所报道的阿替尼醇结构的全合成。合成化合物和天然产物的 1H NMR 谱的比较表明最初提出的结构不正确。因此，合成了两种结构异构体。其中一种化合物的光谱——一种最初被提议为交替烯醇结构的结构——与天然产物的光谱完美匹配。因此，以间苯二酚和原儿茶醛为起始原料，以 10 步和 23% 的产率实现了阿替尼醇的全合成，其中最长的线性序列由 6 步组成。关键步骤是伴随内酯环形成的 Suzuki 偶联。交替性与交替性是否相同尚不能确定。
• Compositions and methods to treat skin diseases characterized by cellular proliferation and angiogenesis
  申请人：Sherris David

  公开号：US20060257337A1

  公开（公告）日：2006-11-16

  Described herein are compositions and methods for preventing and/or treating skin diseases including, but not limited to, psoriasis and atopic dermatitis as well as providing anti-aging benefits which results in reduced appearance of wrinkles and aged skin, improved skin color, treatment of photodamaged skin, improvement in skin's radiance and clarity and finish, and an overall healthy and youthful appearance of the skin, involving aberrant angiogenesis and hyperplasia employing one or more benzo[c]chromen-6-one derivatives.

  本文描述了一种预防和/或治疗皮肤疾病的组合物和方法，包括但不限于银屑病和特应性皮炎，以及提供抗衰老益处，减少皱纹和老化皮肤的出现，改善皮肤颜色，治疗光损伤皮肤，改善皮肤的光泽和清晰度以及完美度，以及使皮肤呈现整体健康和年轻外观，涉及使用一个或多个苯并[c]色素-6-酮衍生物的异常血管生成和增生。
• COMPOSITIONS AND METHODS TO TREAT DISEASES CHARACTERIZED BY CELLULAR PROLIFERATION AND ANGIOGENESIS
  申请人：Sherris I. David

  公开号：US20070197567A1

  公开（公告）日：2007-08-23

  Described herein are compositions and methods for preventing and/or treating diseases involving aberrant angiogenesis employing one or more benzo[c]chromen-6-one derivatives.

  本文描述了使用一种或多种苯并[c]色酮-6-酮衍生物预防和/或治疗涉及异常血管生成的疾病的组合物和方法。
• COMPOSITIONS AND METHODS TO TREAT SKIN DISEASES CHARACTERIZED BY CELLULAR PROLIFERATION AND ANGIOGENESIS
  申请人：SHERRIS David

  公开号：US20110268679A1

  公开（公告）日：2011-11-03

  Described herein are compositions and methods for preventing and/or treating skin diseases including, but not limited to, psoriasis and atopic dermatitis as well as providing anti-aging benefits which results in reduced appearance of wrinkles and aged skin, improved skin color, treatment of photodamaged skin, improvement in skin's radiance and clarity and finish, and an overall healthy and youthful appearance of the skin, involving aberrant angiogenesis and hyperplasia employing one or more benzo[c]chromen-6-one derivatives.

  本文描述了一种预防和/或治疗皮肤疾病的组合物和方法，包括但不限于银屑病和特应性皮炎，以及提供抗衰老效益，从而减少皱纹和老化皮肤的出现，改善皮肤颜色，治疗光损伤皮肤，改善皮肤的光泽度和清晰度，以及整体健康和年轻的外观，涉及异常血管生成和增生，并采用一种或多种苯并[c]色酮衍生物。