2H-Indol-2-one, 4-(aminomethyl)-1,3-dihydro- | 214759-48-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 2H-Indol-2-one, 4-(aminomethyl)-1,3-dihydro-
• 英文别名: 4-(aminomethyl)-1,3-dihydroindol-2-one
• CAS: 214759-48-5
• 化学式: C₉H₁₀N₂O
• 分子量: 162.19
• InChiKey: UTNSTHVHICXSPF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.5
• 重原子数：
  12
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  55.1
• 氢给体数：
  2
• 氢受体数：
  2

文献信息

• THIAZOLE AND THIOPHENE COMPOUNDS
  申请人：Gillespie Paul

  公开号：US20120238569A1

  公开（公告）日：2012-09-20

  Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of inflammatory diseases and disorders such as, for example, asthma and COPD.

  本文提供的是式(I)的化合物及其药学上可接受的盐，其中取代基如规范中所披露的那样。这些化合物及含有它们的药物组合物对于治疗炎症性疾病和紊乱，例如哮喘和慢性阻塞性肺病，是有用的。
• [EN] SELECTIVE KINASE INHIBITORS<br/>[FR] INHIBITEURS SÉLECTIFS DE KINASES
  申请人：PORTOLA PHARM INC

  公开号：WO2013078468A1

  公开（公告）日：2013-05-30

  Provided are pyrimidine compounds for inhibiting of Syk kinase, intermediates used in making such compounds, methods for their preparation, pharmaceutical compositions thereof, methods for inhibition Syk kinase activity, and methods for treating conditions mediated at least in part by Syk kinase activity.

  提供了用于抑制Syk激酶的嘧啶化合物，用于制备这些化合物的中间体，其制备方法，药物组合物，抑制Syk激酶活性的方法，以及治疗至少部分由Syk激酶活性介导的疾病的方法。
• [EN] PYRAZOLO[4,3-D]PYRIMIDINES AS KINASE INHIBITORS<br/>[FR] PYRAZOLO[4,3-D]PYRIMIDINES UTILES EN TANT QU'INHIBITEURS DE KINASES
  申请人：ORIGENIS GMBH

  公开号：WO2014060112A1

  公开（公告）日：2014-04-24

  The present invention relates to novel compounds of formula (I) that are capable of inhibiting one or more kinases, especially SYK (Spleen Tyrosine Kinase), LRRK2 (Leucine-rich repeat kinase 2) and/or MYLK (Myosin light chain kinase) or mutants thereof. The compounds find applications in the treatment of a variety of diseases. These diseases include autoimmune diseases, inflammatory diseases, bone diseases, metabolic diseases, neurological and neurodegenerative diseases, cancer, cardiovascular diseases, allergies, asthma, alzheimer's disease, parkinson's disease, skin disorders, eye diseases, infectious diseases and hormone-related diseases.

  本发明涉及具有式（I）的新化合物，其能够抑制一个或多个激酶，特别是SYK（脾酪氨酸激酶）、LRRK2（富含亮氨酸重复的激酶2）和/或MYLK（肌球蛋白轻链激酶）或其突变体。这些化合物可用于治疗多种疾病。这些疾病包括自身免疫疾病、炎症性疾病、骨疾病、代谢性疾病、神经和神经退行性疾病、癌症、心血管疾病、过敏、哮喘、阿尔茨海默病、帕金森病、皮肤疾病、眼部疾病、传染病和激素相关疾病。
• [EN] OXINDOLOPYRIMIDINE AS IGF1R RECEPTOR INHIBITORS<br/>[FR] OXINDOLEPYRIMIDINES UTILISÉES EN TANT QU'INHIBITEURS DU RÉCEPTEUR IGF-1R
  申请人：BOEHRINGER INGELHEIM INT

  公开号：WO2012085126A1

  公开（公告）日：2012-06-28

  The present invention encompasses compounds of general formula (I) wherein the groups R5 to R10, A, L1, B, m and p 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.

  本发明涵盖了一般式(I)的化合物，其中R5至R10、A、L1、B、m和p的定义如权利要求书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。
• Diaminopropionic acid derivatives
  申请人：Fotouhi Nader

  公开号：US20070155671A1

  公开（公告）日：2007-07-05

  A compound of formula 1a which is useful for treating reperfusion injury, and salts, prodrugs, and related compounds.

  化合物1a的公式，对于治疗再灌注损伤是有用的，包括盐类、前药和相关化合物。