(4-hydroxy-3-methoxyphenyl)(phenyl)methanone | 51439-89-5

• 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: (4-hydroxy-3-methoxyphenyl)(phenyl)methanone
• 英文别名: 3-methoxy-4-hydroxybenzophenone；4-hydroxy-3-methoxybenzophenone；4-hydroxy-3-methoxy-benzophenone；4-Hydroxy-3-methoxy-benzophenon；1-(4-hydroxy-3-methoxyphenyl)phenyl-methanone；1-(4-hydroxy-3-methoxyphenyl)phenylmethanone；(4-Hydroxy-3-methoxyphenyl)phenylmethanone；(4-hydroxy-3-methoxyphenyl)-phenylmethanone
• CAS: 51439-89-5
• 化学式: C₁₄H₁₂O₃
• 分子量: 228.247
• InChiKey: BRCUPBLSVSOLOM-UHFFFAOYSA-N

物化性质

• 熔点：
  100–101°C5
• 沸点：
  405.1±35.0 °C(Predicted)
• 密度：
  1.201±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  46.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (4-hydroxy-3-methoxyphenyl)(phenyl)methanone 在 一水合肼 作用下， 生成 4-benzyl-2-methoxyphenol
  参考文献：
  名称：

  Richtzenhain; Alfredsson, Acta Chemica Scandinavica (1947), 1954, vol. 8, p. 1519,1528

  摘要：

  DOI：
• 作为产物：
  描述：

  4-(4-羟基-3-甲氧基-二苯亚甲基)-2-甲氧基-环己-2,5-二烯酮 在 sodium hydroxide 作用下， 生成 (4-hydroxy-3-methoxyphenyl)(phenyl)methanone
  参考文献：
  名称：

  Ioffe, Zhurnal Obshchei Khimii, 1950, vol. 20, p. 346,353;engl.Ausg.S.367,373

  摘要：

  DOI：

文献信息

• LTA4 Hydrolase inhibitors
  申请人：G.D. SEARLE & CO.

  公开号：EP1221441A2

  公开（公告）日：2002-07-10

  The present invention provides compounds of the formula Ar1-Q-Ar2-Y-R-Z and pharmaceutically acceptable salts thereof wherein Ar1 and Ar2 are optionally substituted aryl moieties, Z is an optionally substituted nitrogen-containing moiety which may be an acyclic, cyclic or bicyclic amine or an optionally substituted monocyclic or bicyclic nitrogen-containing heteroaromatic moiety; Q is a linking group capable of linking two aryl groups; R is an alkylene moiety; Y is a linking moiety capable of linking an aryl group to an alkylene moiety and wherein Z is bonded to R through a nitrogen atom. The compounds and pharmaceutical compositions of the present invention are useful in the treatment of inflammatory diseases which are mediated by LTB4 production, such as proriasis, ulcerative colitis, IBD and asthma.

  本发明提供了具有公式Ar1-Q-Ar2-Y-R-Z的化合物及其药用可接受的盐，其中Ar1和Ar2是可选地取代的芳基部分，Z是可选地取代的含氮部分，可以是环状、环状或双环状的胺，或可选地取代的单环或双环的含氮杂芳基部分；Q是能够连接两个芳基团的连接基团；R是烷基亚基；Y是能够连接芳基团和烷基亚基的连接基团，并且其中Z通过氮原子与R键合。本发明的化合物和药物组合物在治疗由LTB4产生介导的炎症性疾病中是有用的，例如银屑病、溃疡性结肠炎、炎症性肠病和哮喘。
• Structure−Activity Relationship Studies on 1-[2-(4-Phenylphenoxy)ethyl]pyrrolidine (SC-22716), a Potent Inhibitor of Leukotriene A₄ (LTA₄) Hydrolase
  作者：Thomas D. Penning、Nizal S. Chandrakumar、Barbara B. Chen、Helen Y. Chen、Bipin N. Desai、Stevan W. Djuric、Stephen H. Docter、Alan F. Gasiecki、Richard A. Haack、Julie M. Miyashiro、Mark A. Russell、Stella S. Yu、David G. Corley、Richard C. Durley、Brian F. Kilpatrick、Barry L. Parnas、Leslie J. Askonas、James K. Gierse、Elizabeth I. Harding、Maureen K. Highkin、James F. Kachur、Suzanne H. Kim、Gwen G. Krivi、Doreen Villani-Price、E. Yvonne Pyla、Walter G. Smith、Nayereh S. Ghoreishi-Haack

  DOI：10.1021/jm990496z

  日期：2000.2.1

  program, SC-22716 (1, 1-[2-(4-phenylphenoxy)ethyl]pyrrolidine) was identified as a potent inhibitor of LTA(4) hydrolase. Structure-activity relationship (SAR) studies around this structural class resulted in the identification of a number of novel, potent inhibitors of LTA(4) hydrolase, several of which demonstrated good oral activity in a mouse ex vivo whole blood assay.

  白三烯B（4）（LTB（4））是促炎性介质，已与包括炎症性肠病（IBD）和牛皮癣在内的多种疾病的发病机制有关。由于LTA（4）水解酶的作用是LTB（4）生产的限速步骤，因此该酶代表了抑制LTB（4）生产的诱人药理学目标。通过内部筛选程序，SC-22716（1，1- [2-（4-苯基苯氧基）乙基]吡咯烷）被确定为LTA（4）水解酶的有效抑制剂。围绕此结构类别的结构活性关系（SAR）研究导致鉴定了许多新型的，有效的LTA（4）水解酶抑制剂，其中几种在小鼠离体全血试验中表现出良好的口服活性。
• 1-(arylthioalkyl, arylaminoalkyl or arylmethylenealkyl)-4-(heteroaryl)
  申请人：Hoechst Roussel Pharmaceuticals, Inc.

  公开号：US05605913A1

  公开（公告）日：1997-02-25

  Heteroarylpiperidines, pyrrolidines, and piperazines are useful as antipsychotic and analgesic agents. the compounds are especially useful for treating psychoses by administering to a mammal a psychoses-treating effective amount of one of the compounds. Depot derivatives of the compounds are useful for providing long acting effects of the compounds. The compounds are also useful as analgesics by administering a pain-relieving effective amount of one of the compounds to a mammal.

  杂芳基哌啶、吡咯烷和哌嗪作为抗精神病和镇痛剂是有用的。这些化合物特别适用于通过向哺乳动物施用治疗精神病有效量的其中一种化合物来治疗精神病。这些化合物的长效衍生物对于提供这些化合物的长期作用是有用的。通过向哺乳动物施用镇痛有效量的其中一种化合物，这些化合物也作为镇痛剂有用。
• Heteroarylpiperidines, pyrrolidines and piperazines and their use as
  申请人：Hoechst-Roussel Pharmaceuticals, Inc.

  公开号：US05364866A1

  公开（公告）日：1994-11-15

  Heteroarylpiperidines, pyrrolidines, and piperazines are useful as antipsychotic and analgesic agents. The compounds are especially useful for treating psychoses by administering to a mammal a psychoses-treating effective amount of one of the compounds. The compounds are also useful as analgesics by administering a pain-relieving effective amount of one of the compounds to a mammal.

  吡啶基哌啶、吡咯烷和哌嗪等杂环哌啶类化合物可用作抗精神病和镇痛剂。这些化合物特别适用于通过向哺乳动物施用其中一种化合物的抗精神病有效量来治疗精神病。这些化合物也可通过向哺乳动物施用其中一种化合物的镇痛有效量来用作镇痛剂。
• An eco-friendly Co(OAc)2-catalyzed aerobic oxidation of 4-benzylphenols into 4-hydroxybenzophenones
  作者：Jian-Gang Huang、Ying Guo、Jian-An Jiang、Hong-Wei Liu、Ya-Fei Ji

  DOI：10.1007/s11164-014-1801-8

  日期：2015.10

  An undecorated Co(OAc)2-catalyzed aerobic oxidation system has been reported that enables direct transformation of 4-benzylphenols into the corresponding 4-hydroxybenzophenones. The procedure is especially suitable for electron-withdrawing group-containing substrates, which are commonly inefficient to conduct this category of oxidation. Based on well-defined p-benzoquinone methides and the confirmed ethereal intermediate, a plausible mechanism was depicted.

  一种未修饰的Co(OAc)2催化的好氧氧化系统已被报道，它能够将4-苄基苯酚直接转化为相应的4-羟基苯基酮。该方法尤其适用于含有电子吸引基团的底物，因为这类底物通常在进行此类氧化时效率较低。基于明确的对苯醌甲基和确认的醚中间体，提出了一种合理的机制。