N-Ethyltetrahydro-2-furanamine | 887590-74-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 氧唑烯
• 英文名称: N-Ethyltetrahydro-2-furanamine
• 英文别名: N-ethyloxolan-2-amine
• CAS: 887590-74-1
• 化学式: C₆H₁₃NO
• 分子量: 115.17
• InChiKey: RTXDVVBGOHPKEJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  8
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  21.3
• 氢给体数：
  1
• 氢受体数：
  2

文献信息

• PYRROLOPYRAZINE INHIBITORS OF KINASES
  申请人：Penning Thomas D.

  公开号：US20110015172A1

  公开（公告）日：2011-01-20

  The present invention relates to compounds of formula (I) or pharmaceutical acceptable salts, wherein R 1a , R 1b , X, and Y are defined in the description. The present invention relates also to compositions containing said compounds which are useful for inhibiting kinases such as Cdc7 and methods of treating diseases such as cancer.

  本发明涉及式(I)的化合物或药用可接受的盐，其中R1a、R1b、X和Y在描述中有定义。本发明还涉及含有上述化合物的组合物，用于抑制Cdc7等激酶并治疗癌症等疾病的方法。
• [EN] B-RAF KINASE INHIBITORS<br/>[FR] INHIBITEURS DE KINASE B-RAF
  申请人：BOEHRINGER INGELHEIM INT

  公开号：WO2011117381A1

  公开（公告）日：2011-09-29

  The present invention encompasses compounds of general formula (1) where in the groups R0to R3 and L are defined as in claim 1, which are suitable for the 5 treatment of diseases characterised by excessive or abnormal cell proliferation, pharmaceutical preparations which contain compounds of this kind and their use as medicaments.

  本发明涵盖了一般式（1）中的化合物，其中基团R0至R3和L的定义如权利要求书中所述，这些化合物适用于治疗以细胞过度或异常增殖为特征的疾病，包含这种化合物的药物制剂以及它们作为药物的用途。
• Protein Kinase Inhibitors (Variants), Use Thereof in Treating Oncological Diseases and a Pharmaceutical Composition Based Thereon
  申请人：Obshchestvo s ogranichennoy otvetstvennostyou "Fusion Pharma"

  公开号：US20140213592A1

  公开（公告）日：2014-07-31

  The present invention relates to the treatment of oncological, chronic inflammatory and similar diseases with the aid of new families of chemical compounds having improved efficiency with regard to the inhibition of Abl kinase and mutant forms thereof, as well as other therapeutically significant kinases. It describes protein kinase inhibitors in the form of compounds of general formula (I) and compounds of general formula (II), or a tautomer, an individual isomer, a mixture of isomers, a pharmaceutically acceptable salt, a solvate or a hydrate thereof.

  本发明涉及使用新的化学化合物家族辅助治疗肿瘤、慢性炎症和类似疾病，这些化合物家族在抑制Abl激酶及其突变形式以及其他具有治疗意义的激酶方面具有提高的效率。本发明描述了蛋白激酶抑制剂，其形式为通式(I)和通式(II)的化合物，或其互变异构体、单个异构体、异构体混合物、药学上可接受的盐、溶剂或其水合物。
• B-RAF KINASE INHIBITORS
  申请人：Steurer Steffen

  公开号：US20130190286A1

  公开（公告）日：2013-07-25

  The present invention encompasses compounds of general formula (1) where in the groups R 0 to R 3 and L are defined as in claim 1 , which are suitable for the 5 treatment of diseases characterised by excessive or abnormal cell proliferation, pharmaceutical preparations which contain compounds of this kind and their use as medicaments.

  本发明涵盖了通式（1）的化合物，其中R0到R3和L的定义如权利要求1所述，适用于治疗由过度或异常细胞增殖所特征的疾病，包含这种化合物的制药制剂以及它们作为药物的使用。
• PYRIDYLTRIAZOLES
  申请人：Ettmayer Peter

  公开号：US20130225562A1

  公开（公告）日：2013-08-29

  The present invention encompasses compounds of general formula (1) wherein the groups R 0 to R 3 and L are defined as in claim 1 , which are suitable for the treatment of diseases characterised by excessive or abnormal cell proliferation, pharmaceutical preparations which contain such compounds and their use as medicaments.

  本发明涵盖通式（1）的化合物，其中R0至R3和L基团的定义如权利要求1所述，适用于治疗由过度或异常细胞增殖特征的疾病，包含这种化合物的制药制剂以及它们作为药物的用途。