1-(4-thio-3-methoxyphenyl)ethanone | 69114-75-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-(4-thio-3-methoxyphenyl)ethanone
• 英文别名: 4'-mercapto-3'-methoxyacetophenone；4-mercapto-3-methoxyacetophenone；2-methoxy-4-acetyl thiophenol；4-Acetyl-2-methoxy-thiophenol；1-(3-Methoxy-4-sulfanylphenyl)ethan-1-one；1-(3-methoxy-4-sulfanylphenyl)ethanone
• CAS: 69114-75-6
• 化学式: C₉H₁₀O₂S
• mdl: MFCD22565846
• 分子量: 182.243
• InChiKey: JSWOOQQBQYKDEW-UHFFFAOYSA-N

物化性质

• 沸点：
  310.2±32.0 °C(Predicted)
• 密度：
  1.156±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  12
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.222
• 拓扑面积：
  27.3
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  1-(4-thio-3-methoxyphenyl)ethanone 在 三溴化硼 、 potassium carbonate 作用下， 以 二氯甲烷 、 丙酮 为溶剂， 反应 4.0h， 生成 4'-benzylthio-3'-hydroxyacetophenone
  参考文献：
  名称：

  Carboxy-Substituted Cinnamides:  A Novel Series of Potent, Orally Active LTB₄ Receptor Antagonists

  摘要：

  A series of carboxy-substituted cinnamides were investigated as antagonists of the human cell surface leukotriene B-4 (LTB4) receptor. Binding was determined through measurement of [H-3]-LTB4 displacement from human neutrophils. Receptor antagonism was confirmed through a functional assay, which measures inhibition of Ca2+ release in human neutrophils. Potent antagonists were discovered through optimization of a random screening hit, a p-(alpha-methylbenzyloxy)cinnamide, having low-micromolar activity. Substantial improvement of in vitro potency was realized by the attachment of a carboxylic acid moiety to the cinnamide phenyl ring through a flexible tether, leading to identification of compounds with low-nanomolar potency. Modification of the benzyloxy substituent, either through ortho-substitution on the benzyloxy phenyl group or through replacement of the ether oxygen with a methylene or sulfur atom, produced achiral antagonists of equal or greater potency. The most potent compounds in vitro were assayed for oral activity using the arachidonic acid-induced mouse ear edema model of inflammation. Several compounds in this series were found to significantly inhibit edema formation and myeloperoxidase activity in this model up to 17 h after oral administration. Representatives of this series have been shown to be potent and long-acting orally active inhibitors of the LTB4 receptor.

  DOI：

  10.1021/jm980540v
• 作为产物：
  描述：

  香草乙酮 在 氢氧化钾 作用下， 以 四氢呋喃 、 乙二醇 为溶剂， 反应 2.5h， 生成 1-(4-thio-3-methoxyphenyl)ethanone
  参考文献：
  名称：

  Carboxy-Substituted Cinnamides:  A Novel Series of Potent, Orally Active LTB₄ Receptor Antagonists

  摘要：

  A series of carboxy-substituted cinnamides were investigated as antagonists of the human cell surface leukotriene B-4 (LTB4) receptor. Binding was determined through measurement of [H-3]-LTB4 displacement from human neutrophils. Receptor antagonism was confirmed through a functional assay, which measures inhibition of Ca2+ release in human neutrophils. Potent antagonists were discovered through optimization of a random screening hit, a p-(alpha-methylbenzyloxy)cinnamide, having low-micromolar activity. Substantial improvement of in vitro potency was realized by the attachment of a carboxylic acid moiety to the cinnamide phenyl ring through a flexible tether, leading to identification of compounds with low-nanomolar potency. Modification of the benzyloxy substituent, either through ortho-substitution on the benzyloxy phenyl group or through replacement of the ether oxygen with a methylene or sulfur atom, produced achiral antagonists of equal or greater potency. The most potent compounds in vitro were assayed for oral activity using the arachidonic acid-induced mouse ear edema model of inflammation. Several compounds in this series were found to significantly inhibit edema formation and myeloperoxidase activity in this model up to 17 h after oral administration. Representatives of this series have been shown to be potent and long-acting orally active inhibitors of the LTB4 receptor.

  DOI：

  10.1021/jm980540v

文献信息

• 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。
• Aryl-substituted acrylamides with Leukotriene B4 (LTB-4) receptor antagonist activity
  申请人：Novartis AG

  公开号：US06291530B1

  公开（公告）日：2001-09-18

  Disclosed are compounds of formula (I) wherein W is CH or N; R is (mono- or di cabocyclic or heterocyclic aryl)-lower alkyl; R1 is hydrogen or lower alkyl; R2 and R3 are hydrogen, lower alkyl, lower alkoxy-lower alkyl or aryl-lower alkyl; or R2 and R3 joined together represent lower alkylene optionally interrupted by O, NH, N-lower alkyl or S so as to form a ring with the amide nitrogen; X is O, S, SO, S2 or a direct bond; X1 is O, S, SO, SO2 or a direct bond; Y is a direct bond, lower alkylene or lower alkylidene; and Z is carboxyl, 5-tetrazolyl,, hydroxymethyl or carboxyl derivatized in the form of a pharmaceutically acceptable ester, and pharmaceutically acceptable salts thereof; which arm useful as LTB-4 antagonists.

  本发明涉及一种式子（I）的化合物，其中W为CH或N；R为（单环或双环芳基或杂环芳基）-较低烷基；R1为氢或较低烷基；R2和R3为氢、较低烷基、较低烷氧基-较低烷基或芳基-较低烷基；或者R2和R3结合在一起，用较低烷基烷基可选地中断的O、NH、N-较低烷基或S表示，以形成与酰胺氮原子形成环的环；X为O、S、SO、S2或直接键；X1为O、S、SO、SO2或直接键；Y为直接键、较低烷基或较低烷基亚甲基；Z为羧基、5-四唑基、羟甲基或以药学上可接受的酯形式衍生的羧基，并且其药学上可接受的盐；它们有用作LTB-4拮抗剂。
• Golf ball
  申请人：Dunlop Sports Co., Ltd.

  公开号：EP2668976A1

  公开（公告）日：2013-12-04

  A golf ball 2 includes a core 4, a mid layer 6, and a cover 10. The core 4 includes a center 16, a first envelope layer 18, and a second envelope layer 20. The first envelope layer 18 is formed by a first rubber composition being crosslinked. The second envelope layer 20 is formed by a second rubber composition being crosslinked. The first rubber composition and/or the second rubber composition include: a base rubber; a co-crosslinking agent; a crosslinking initiator; and an acid and/or a salt. The co-crosslinking agent is (1) an α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms; and/or (2) a metal salt of an α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms.

  高尔夫球 2 包括球芯 4、中层 6 和外层 10。球芯 4 包括中心 16、第一包胶层 18 和第二包胶层 20。第一包层 18 由交联的第一橡胶成分形成。第二包胶层 20 由交联的第二橡胶组合物形成。第一橡胶组合物和/或第二橡胶组合物包括：基础橡胶；共交联剂；交联引发剂；酸和/或盐。共交联剂是（1）具有 3 至 8 个碳原子的 α，β-不饱和羧酸；和/或（2）具有 3 至 8 个碳原子的 α，β-不饱和羧酸的金属盐。
• GOLF BALL
  申请人：Dunlop Sports Co., Ltd.

  公开号：EP3156441A1

  公开（公告）日：2017-04-19

  A golf ball 2 includes a core 4, a first mid layer 6, a second mid layer 8, and a cover 12. The core 4 includes a center 18 and an envelope layer 20. The center 18 is formed by crosslinking a first rubber composition, and the envelope layer 20 is formed by crosslinking a second rubber composition. The first rubber composition or the second rubber composition includes a base rubber, a co-crosslinking agent, a crosslinking initiator, and an acid and/or a salt. The co-crosslinking agent is: (1) an α, β-unsaturated carboxylic acid having 3 to 8 carbon atoms; and/or (2) a metal salt of an α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms. A hardness Hm2 of the second mid layer 8 is greater than a hardness Hm1 of the first mid layer 6. The hardness Hm2 is greater than a hardness Hc of the cover 12.

  高尔夫球 2 包括球芯 4、第一中层 6、第二中层 8 和外层 12。球芯 4 包括中心 18 和包层 20。中心 18 由第一种橡胶组合物交联形成，包层 20 由第二种橡胶组合物交联形成。第一种橡胶组合物或第二种橡胶组合物包括基础橡胶、共交联剂、交联引发剂以及酸和/或盐。共交联剂为 (1) 具有 3 至 8 个碳原子的 α、β-不饱和羧酸；和/或 (2) 具有 3 至 8 个碳原子的 α、β-不饱和羧酸的金属盐。 第二中间层 8 的硬度 Hm2 大于第一中间层 6 的硬度 Hm1。硬度 Hm2 大于盖板 12 的硬度 Hc。