6-[(4-phenylbenzoyl)amino]hexanoic acid | 251456-79-8

• 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: 6-[(4-phenylbenzoyl)amino]hexanoic acid
• CAS: 251456-79-8
• 化学式: C₁₉H₂₁NO₃
• 分子量: 311.381
• InChiKey: UMKXKCDEKNEPEN-UHFFFAOYSA-N

物化性质

• 熔点：
  169 °C
• 沸点：
  557.7±43.0 °C(Predicted)
• 密度：
  1.143±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  23
• 可旋转键数：
  8
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.26
• 拓扑面积：
  66.4
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  6-[(4-phenylbenzoyl)amino]hexanoic acid 在 盐酸 、 1-羟基苯并三唑 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 三乙胺 作用下， 以 甲醇 、 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 4.0h， 生成 N-[6-(hydroxyamino)-6-oxohexyl][1,1'-biphenyl]-4-carboxamide
  参考文献：
  名称：

  Il-6 production inhibitors

  摘要：

  一种IL-6产生抑制剂，包括式(I)的羟羟基酸衍生物（其中所有符号的含义与规范中定义的相同），其等效物，其非毒性盐或其前药作为活性成分。由于具有IL-6产生抑制活性，式(I)的化合物可能有助于预防和/或治疗各种炎症性疾病、败血症、多发性骨髓瘤、浆细胞白血病、骨质疏松症、消瘦症、牛皮癣、肾炎、肾细胞癌、卡波西肉瘤、类风湿性关节炎、高γ球蛋白血症（免疫球蛋白病）、卡斯尔曼病、心房内黏液瘤、糖尿病、自身免疫疾病、肝炎、结肠炎、移植物抗宿主病、传染病、子宫内膜异位症和实体癌症。

  公开号：

  US20050119305A1
• 作为产物：
  描述：

  methyl 6-(4-biphenylcarbonyl)aminocaproate 在 lithium hydroxide 作用下， 以 四氢呋喃 为溶剂， 反应 4.0h， 以80%的产率得到6-[(4-phenylbenzoyl)amino]hexanoic acid
  参考文献：
  名称：

  Amide Analogues of Trichostatin A as Inhibitors of Histone Deacetylase and Inducers of Terminal Cell Differentiation

  摘要：

  Inhibitors of histone deacetylase (HD) bear great potential as new drugs due to their ability to modulate transcription and to induce apoptosis or differentiation in cancer cells. We have described previously analogues of the complex natural HD inhibitors trapoxin B and trichostatin A with activities in the submicromolar range. Here we report structure-activity relationship analyses of further analogues of trichostatin A with respect to in vitro inhibition of maize HD-2 and their ability to induce terminal cell differentiation in Friend leukemic cells. This is the first report that shows the correlation between HD inhibitory activity and action on cancer cells on a larger series of similar compounds. Only the compounds that inhibit HD induce differentiation and/or exert antiproliferative activities in cell culture. Our studies support the use of in vitro systems as screening tools and provide structure-activity relationships that merit further investigation of this interesting target.

  DOI：

  10.1021/jm991091h

文献信息

• Amide Analogues of Trichostatin A as Inhibitors of Histone Deacetylase and Inducers of Terminal Cell Differentiation
  作者：Manfred Jung、Gerald Brosch、Doris Kölle、Hans Scherf、Clarissa Gerhäuser、Peter Loidl

  DOI：10.1021/jm991091h

  日期：1999.11.1

  Inhibitors of histone deacetylase (HD) bear great potential as new drugs due to their ability to modulate transcription and to induce apoptosis or differentiation in cancer cells. We have described previously analogues of the complex natural HD inhibitors trapoxin B and trichostatin A with activities in the submicromolar range. Here we report structure-activity relationship analyses of further analogues of trichostatin A with respect to in vitro inhibition of maize HD-2 and their ability to induce terminal cell differentiation in Friend leukemic cells. This is the first report that shows the correlation between HD inhibitory activity and action on cancer cells on a larger series of similar compounds. Only the compounds that inhibit HD induce differentiation and/or exert antiproliferative activities in cell culture. Our studies support the use of in vitro systems as screening tools and provide structure-activity relationships that merit further investigation of this interesting target.
• Il-6 production inhibitors
  申请人：Naka Masao

  公开号：US20050119305A1

  公开（公告）日：2005-06-02

  An IL-6 production inhibitor which comprises a hydroxamic acid derivative of formula (I) (wherein all the symbols have the same meanings as defined in the specification), an equivalent thereof, a non-toxic salt thereof or a prodrug thereof as an active ingredient. Because of having an IL-6 production inhibitory activity, the compound of formula (I) may be useful for the prevention and/or treatment of various inflammatory diseases, sepsis, multiple myeloma, plasma cell leukemia, osteoporosis, cachexia, psoriasis, nephritis, renal cell carcinoma, Kaposi's sarcoma, rheumatoid arthritis, hypergammaglobulinemia (gammophathy), Castleman's disease, intra-atrial myxoma, diabetes, autoimmune disease, hepatitis, colitis, graft-versus-host disease, infectious diseases, endometriosis and solid cancer.

  一种IL-6产生抑制剂，包括式(I)的羟羟基酸衍生物（其中所有符号的含义与规范中定义的相同），其等效物，其非毒性盐或其前药作为活性成分。由于具有IL-6产生抑制活性，式(I)的化合物可能有助于预防和/或治疗各种炎症性疾病、败血症、多发性骨髓瘤、浆细胞白血病、骨质疏松症、消瘦症、牛皮癣、肾炎、肾细胞癌、卡波西肉瘤、类风湿性关节炎、高γ球蛋白血症（免疫球蛋白病）、卡斯尔曼病、心房内黏液瘤、糖尿病、自身免疫疾病、肝炎、结肠炎、移植物抗宿主病、传染病、子宫内膜异位症和实体癌症。