4-[(6-Methoxy-benzothiazol-2-ylamino)-methyl]-benzoic Acid Methyl Ester | 503039-99-4

• 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-[(6-Methoxy-benzothiazol-2-ylamino)-methyl]-benzoic Acid Methyl Ester
• 英文别名: 4-[(6-Methoxy-benzothiazol-2-ylamino)-methyl]benzoic acid methyl ester；methyl 4-[[(6-methoxy-1,3-benzothiazol-2-yl)amino]methyl]benzoate
• CAS: 503039-99-4
• 化学式: C₁₇H₁₆N₂O₃S
• 分子量: 328.392
• InChiKey: SQHBNGOZAOEMFQ-UHFFFAOYSA-N

物化性质

• 沸点：
  505.8±60.0 °C(Predicted)
• 密度：
  1.322±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  23
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  88.7
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  4-[(6-Methoxy-benzothiazol-2-ylamino)-methyl]-benzoic Acid Methyl Ester 在 lithium hydroxide 作用下， 以 四氢呋喃 为溶剂， 生成 4-[[(6-methoxy-1,3-benzothiazol-2-yl)amino]methyl]benzoic acid
  参考文献：
  名称：

  4-(Heteroarylaminomethyl)-N-(2-aminophenyl)-benzamides and their analogs as a novel class of histone deacetylase inhibitors

  摘要：

  The synthesis and biological evaluation of a variety of 4-(heteroarylaminomethyl)-N-(2-aminophenyl)-benzamides and their analogs is described. Some of these compounds were shown to inhibit HDAC1 with IC50 values below the micromolar range, induce hyperacetylation of histones, upregulate expression of the tumor suppressor p21(WAF1/Cip1), and inhibit proliferation of human cancer cells. In addition, certain compounds of this class were active in several human tumor xenograft models in vivo. (c) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.12.057
• 作为产物：
  描述：

  2-氨基-6-甲氧基苯并噻唑 、 对甲酰基苯甲酸甲酯 在 三乙酰氧基硼氢化钠 作用下， 以 四氢呋喃 为溶剂， 生成 4-[(6-Methoxy-benzothiazol-2-ylamino)-methyl]-benzoic Acid Methyl Ester
  参考文献：
  名称：

  4-(Heteroarylaminomethyl)-N-(2-aminophenyl)-benzamides and their analogs as a novel class of histone deacetylase inhibitors

  摘要：

  The synthesis and biological evaluation of a variety of 4-(heteroarylaminomethyl)-N-(2-aminophenyl)-benzamides and their analogs is described. Some of these compounds were shown to inhibit HDAC1 with IC50 values below the micromolar range, induce hyperacetylation of histones, upregulate expression of the tumor suppressor p21(WAF1/Cip1), and inhibit proliferation of human cancer cells. In addition, certain compounds of this class were active in several human tumor xenograft models in vivo. (c) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.12.057

文献信息

• Inhibitors of histone deacetylase
  申请人：Delorme Daniel

  公开号：US06897220B2

  公开（公告）日：2005-05-24

  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药物组合物和方法。
• [EN] INHIBITORS OF HISTONE DEACETYLASE<br/>[FR] INHIBITEURS DE L'HISTONE DEACETYLASE
  申请人：METHYLGENE INC

  公开号：WO2004069823A1

  公开（公告）日：2004-08-19

  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.

  该发明涉及抑制组蛋白去乙酰化酶的技术。该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。该发明还提供了治疗细胞增殖性疾病和病症的组合物和方法。
• INHIBITORS OF HISTONE DEACETYLASE
  申请人：Methylgene, Inc.

  公开号：EP1590340A1

  公开（公告）日：2005-11-02
• US6897220B2
  申请人：——

  公开号：US6897220B2

  公开（公告）日：2005-05-24
• US7595343B2
  申请人：——

  公开号：US7595343B2

  公开（公告）日：2009-09-29