methyl 3-amino-5-tert-butyl-1-methylpyrrole-2carboxylate | 216574-70-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯
• 英文名称: methyl 3-amino-5-tert-butyl-1-methylpyrrole-2carboxylate
• 英文别名: methyl 3-amino-1-methyl-5-t-butylpyrrole-2-carboxylate；methyl 3-amino-5-tert-butyl-1-methylpyrrole-2-carboxylate
• CAS: 216574-70-8
• 化学式: C₁₁H₁₈N₂O₂
• 分子量: 210.276
• InChiKey: XGUABPXHAFXZBI-UHFFFAOYSA-N

物化性质

• 沸点：
  320.2±42.0 °C(Predicted)
• 密度：
  1.08±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.55
• 拓扑面积：
  57.2
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  methyl 3-amino-5-tert-butyl-1-methylpyrrole-2carboxylate 生成 5-tert-butyl-1-methyl-3-(3-p-tolyl-ureido)-1H-pyrrole-2-carboxylic acid methyl ester
  参考文献：
  名称：

  p38 Kinase inhibitors for the treatment of arthritis and osteoporosis: thienyl, furyl, and pyrrolyl ureas

  摘要：

  Inhibitors of the MAP kinase p38 are potentially useful for the treatment for osteoporosis, arthritis, and other inflammatory diseases. A series of thienyl, furyl, and pyrrolyl ureas has been identified as potent p38 inhibitors, displaying in vitro activity in the nanomolar range. (C) 2000 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(00)00574-6

文献信息

• Inhibition of p38 kinase activity by aryl ureas
  申请人：Bayer Corporation

  公开号：US06344476B1

  公开（公告）日：2002-02-05

  This invention relates to the use of a group of aryl ureas in treating cytokine mediated diseases other than cancer and proteolytic enzyme mediated diseases other than cancer, and pharmaceutical compositions for use in such therapy.

  本发明涉及一组芳香脲在治疗非癌症的细胞因子介导疾病和非癌症的蛋白水解酶介导疾病中的用途，以及用于此类治疗的药物组合物。
• Raf kinase inhibitors
  申请人：BAYER CORPORATION and ONYX PHARMACEUTICALS West Haven, CT and Richmond, CA, respectively

  公开号：US20010006975A1

  公开（公告）日：2001-07-05

  Methods of treating tumors mediated by raf kinase, with substituted urea compounds, and such compounds per se.

  通过使用替代尿素化合物和这些化合物本身，治疗由Raf激酶介导的肿瘤的方法。
• Raf Kinase Inhibitors
  申请人：WOOD Jill E.

  公开号：US20100063088A1

  公开（公告）日：2010-03-11

  Methods of treating tumors mediated by raf kinase, with substituted urea compounds, and such compounds per se.

  使用替代尿素类化合物治疗由Raf激酶介导的肿瘤的方法，以及这些化合物本身。
• INHIBITION OF P38 KINASE ACTIVITY BY ARYL UREAS
  申请人：RANGES Gerald

  公开号：US20100160371A1

  公开（公告）日：2010-06-24

  This invention relates to the use of a group of aryl ureas in treating cytokine mediated diseases other than cancer and proteolytic enzyme mediated diseases other than cancer, and pharmaceutical compositions for use in such therapy.

  本发明涉及使用一组芳基脲类化合物治疗细胞因子介导的疾病和蛋白酶酶介导的疾病，但不包括癌症，并提供了用于该疗法的制药组合物。
• ARYL UREAS FOR THE TREATMENT OF INFLAMMATORY OR IMMUNOMODULATORY DISEASES
  申请人：Bayer Corporation

  公开号：EP1019040B1

  公开（公告）日：2004-09-29