9-oxo-9-phenyl-nonanoic acid | 53702-23-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 9-oxo-9-phenyl-nonanoic acid
• 英文别名: 8-Oxo-8-phenyl-octan-carbonsaeure-(1)；9-Oxo-9-phenyl-nonansaeure；λ-Oxo-λ-phenyl-pelargonsaeure；η-Benzoyl-caprylsaeure；η-Benzoyl-octylsaeure；8-benzoyloctanoic acid；9-Oxo-9-phenylnonanoic acid
• CAS: 53702-23-1
• 化学式: C₁₅H₂₀O₃
• 分子量: 248.322
• InChiKey: BFUPULAAJVYXRI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  18
• 可旋转键数：
  9
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  54.4
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  9-oxo-9-phenyl-nonanoic acid 在 1-羟基苯并三唑一水物 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 盐酸羟胺 、 三乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 1.0h， 生成 N-Hydroxy-8-(benzoyl)octanamide
  参考文献：
  名称：

  Structurally Simple Trichostatin A-Like Straight Chain Hydroxamates as Potent Histone Deacetylase Inhibitors

  摘要：

  A series of new, structurally simple trichostatin A (TSA)-like straight chain hydroxamates were prepared and evaluated for their ability to inhibit partially purified human histone deacetylase 1 (HDAC-1). Some of these compounds such as 8m, 8n, 12, and 15b exhibited potent HDAC inhibitory activity with low nanomolar IC50 values, comparable to natural TSA. These compounds induce hyperacetylation of histones in T24 human cancer cells and significantly inhibit proliferation in. various human cancer cells. They also induce expression of p21 and cause cell cycle blocks in human cancer cells. in this paper, we describe the synthesis of these new compounds as well as structure-activity relationship results from enzyme inhibition and alterations in cellular function.

  DOI：

  10.1021/jm020154k
• 作为产物：
  描述：

  苯 在 三氯化铝 作用下， 生成 9-oxo-9-phenyl-nonanoic acid
  参考文献：
  名称：

  Raper; Wayne, Biochemical Journal, 1928, vol. 22, p. 193

  摘要：

  DOI：

文献信息

• Inhibitors of histone deacetylase
  申请人：——

  公开号：US20020115826A1

  公开（公告）日：2002-08-22

  The invention relates to the inhibition of histone deacetylase. The invention provides compounds and methods for inhibiting histone deacetylase enzymatic activity. The invention also provides compositions and methods for treating cell proliferative diseases and conditions.

  本发明涉及组蛋白去乙酰化酶的抑制。本发明提供了用于抑制组蛋白去乙酰化酶酶活性的化合物和方法。本发明还提供了用于治疗细胞增殖性疾病和状况的组合物和方法。
• Inhibitors of Histone Deacetylase
  申请人：Delorme Daniel

  公开号：US20090181971A1

  公开（公告）日：2009-07-16

  The invention relates to the inhibition of histone deacetylase. The invention provides compounds and methods for inhibiting histone deacetylase enzymatic activity. The invention also provides compositions and methods for treating cell proliferative diseases and conditions.

  本发明涉及抑制组蛋白去乙酰化酶的技术。本发明提供了抑制组蛋白去乙酰化酶酶活性的化合物和方法。本发明还提供了治疗细胞增殖性疾病和病状的组合物和方法。
• Coating compositions
  申请人：CIBA-GEIGY AG

  公开号：EP0412933A1

  公开（公告）日：1991-02-13

  The present invention provides coating compositions comprising a) an organic film-forming binder; and b) a corrosion-inhibiting amount of a salt of i) a ketoacid having the formula (I): wherein a is 1,2,3,4 or 5; the R substituents are the same or different and each is hydrogen; halogen; nitro; cyano; CF₃; C₁-C₁₅ alkyl; C₅-C₁₂ cycloalkyl; C₂-C₁₅ alkenyl; C₁-C₁₂ halogenoalkyl; C₁-C₁₂ alkoxy; C₁-C₁₂ thioalkyl; C₆-C₁₂ aryl; C₆-C₁₀ aryloxy; C₇-C₁₂ alkaryl; -CO₂R₁ in which R₁ is a) hydrogen, b) C₁-C₂₀ alkyl optionally inter­rupted by one or more O-, N- or S-atoms, c) C₇-C₁₂ alkaryl or d) C₆-C₁₂ aryl optionally substituted with one or more carboxy groups; -COR₁ in which R₁ has its previous signi­ficance; NR₂R₃ in which R₂ and R₃ are the same or different and each is hydrogen or C₁-C₂₄ alkyl optionally interrupted by one or more O, S or NH moieties; or when a is 2, 3, 4 or 5, two adjacent groups R may be the atoms required to form a fused benzene or cyclo­hexyl ring; and n is an integer from 1 to 10; and ii) an amine of formula II: wherein X, Y and Z are the same or different, and are hydrogen; C₄-C₂₄ alkyl optionally interrupted by one or more O-atoms; phenyl; C₇-C₉ phenylalkyl; C₇-C₉ alkylphenyl; or two of X, Y and Z together with the N-atom to which they are attached form a 5-, 6- or 7-membered heterocyclic residue, which optionally contains a further oxygen, nitrogen or sulphur atom and which is optionally substituted by one or more C₁-C₄ alkyl, amino, hydroxy, carboxy or C₁-C₄ carboxy alkyl groups, and the other of X, Y and Z is hydrogen; provided that X, Y and Z are not simultaneously hydrogen. The salts derived from ketoacids of formula I and amines of formula II are new compounds.

  本发明提供的涂料组合物包括 a) 有机成膜粘合剂；和 b) 一种盐的腐蚀抑制剂。 i) 具有式(I)的酮酸： 其中 a 为 1、2、3、4 或 5；R 取代基相同或不同，且各自为氢；卤素；硝基；氰基；CF₃；C₁-C₁₅ 烷基；C₅-C₁₂ 环烷基；C₂-C₁₅ 烯基；C₁-C₁₂ 卤代烷基；C₁-C₁₂ 烷氧基；C₁-C₁₂ 硫代烷基；C₆-C₁₂ 芳基；C₆-C₁₀ 芳氧基； C₇-C₁₂ 烷芳基；-CO₂R₁，其中 R₁ a) 氢； b) C₁-C₂₀烷基，可选被一个或多个 O-、N- 或 S 原子间断、c) C₇-C₁₂烷芳基或 d) C₆-C₁₂芳基，可选地被一个或多个羧基取代；-COR₁，其中 R₁ 具有其先前的意义； NR₂R₃ ，其中 R₂ 和 R₃ 相同或不同，并且各自为氢或 C₁-C₂₄烷基，可选择被一个或多个 O、S 或 NH 分子打断；或当 a 为 2、3、4 或 5 时，两个相邻基团 R 可为形成融合苯环或环己基环所需的原子；且 n 为 1 至 10 的整数；以及 ii) 式 II 的胺 其中 X、Y 和 Z 相同或不同，并且是氢；C₄-C₂₄ 烷基，可选被一个或多个 O 原子打断；苯基；C₇-C₉ 苯基烷基；C₇-C₉ 烷基苯基；或 X、Y 和 Z 中的两个与它们所连接的 N 原子一起形成 5、6 或 7 元杂环残基，该残基可选地含有另一个氧原子、氮原子或硫原子，并可选地被一个或多个 C₁-C₄ 烷基、氨基、羟基、羧基或 C₁-C₄ 羧基烷基取代，而 X、Y 和 Z 中的另一个是氢；条件是 X、Y 和 Z 不能同时是氢。 由式 I 的酮酸和式 II 的胺衍生的盐是新化合物。
• Polyhydroxyalkanoate containing 3-hydroxybenzoylalkanoic acid as monomer unit, and method for producing the same
  申请人：CANON KABUSHIKI KAISHA

  公开号：EP1130042A2

  公开（公告）日：2001-09-05

  Microorganisms capable of producing novel polyalkanoates having 3-hydroxybenzoylalkanoic acids as monomer units by utilizing benzoylalkanoic acids as starting materials are cultured in media containing benzoylalkanoic acids and saccharides, and the polyhydroxyalkanoates produced in the culture cells are extracted and recovered.

  在含有苯甲酰烷酸和糖类的培养基中培养能够利用苯甲酰烷酸作为起始材料生产以 3-羟基苯甲酰烷酸为单体单元的新型聚烷酸酯的微生物，并提取和回收培养细胞中产生的聚羟基烷酸酯。
• Liquid crystalline properties of cholesteryl .omega.-arylalkanoates
  作者：Mitsuhiro Koden、Shiro Miyake、Shunsuke Takenaka、Shigekazu Kusabayashi

  DOI：10.1021/j150655a041

  日期：1984.5

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