4-Methyl-7H-cyclopenta[B]pyridine | 91598-35-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: 4-Methyl-7H-cyclopenta[B]pyridine
• CAS: 91598-35-5
• 化学式: C₉H₉N
• 分子量: 131.17
• InChiKey: BBXGHAKTWHZIBP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  10
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  12.9
• 氢给体数：
  0
• 氢受体数：
  1

文献信息

• NITROGEN-CONTAINING SPIROCYCLIC COMPOUNDS AND PHARMACEUTICAL USES THEREOF
  申请人：Noji Satoru

  公开号：US20110136778A1

  公开（公告）日：2011-06-09

  A compound of the following general formula [I]: wherein each symbol has the same meaning as defined herein, or a pharmaceutically acceptable salt thereof, or a solvate thereof, and a pharmaceutical use of the same in treating organ transplant rejection, graft versus host reaction after transplantation, autoimmune disease, allergic disease and chronic myeloproliferative disease.

  以下通用公式[I]的化合物：其中每个符号具有本文中定义的相同含义，或其药用可接受盐，或其溶剂化合物，并且其在治疗器官移植排斥、移植后移植物抗宿主反应、自身免疫疾病、过敏疾病和慢性骨髓增生性疾病中的药用。
• HETEROARYL COMPOUNDS, COMPOSITIONS, AND METHODS OF USE IN CANCER TREATMENT
  申请人：Turcotte Sandra

  公开号：US20110105436A1

  公开（公告）日：2011-05-05

  Provided herein are novel heteroaryl compounds, compositions comprising the compounds, and methods of treatment or prevention comprising administration of the compounds. The compounds are effective in the targeting of cells defective in the von Hippel-Lindau gene and in inducing autophagic cell death. The methods are directed to treating or preventing diseases such as cancer, and in particular cancers resulting from von Hippel-Lindau disease. The compounds of the invention may be administered in combination with another therapeutic agent.

  本文提供了新型的杂环芳基化合物、包含这些化合物的组合物以及治疗或预防方法，包括给予这些化合物。这些化合物能够有效地针对von Hippel-Lindau基因缺陷的细胞，并诱导自噬性细胞死亡。这些方法旨在治疗或预防癌症等疾病，特别是由von Hippel-Lindau病引起的癌症。本发明的化合物可以与另一种治疗药物联合使用。
• Thiazole derivatives
  申请人：Banno Hiroshi

  公开号：US20110003807A1

  公开（公告）日：2011-01-06

  The present invention relates to a compound represented by the formula (I) or (I′): wherein each symbol is as defined in the specification, or a salt thereof, and a PI3K and(or) mTOR inhibitor containing the compound or a prodrug thereof.

  本发明涉及一种由式(I)或(I')所表示的化合物：其中每个符号如规范中所定义，或其盐，以及含有该化合物或其前药的PI3K和/或mTOR抑制剂。
• Heteroaryls and uses thereof
  申请人：Hirose Masaaki

  公开号：US20110003806A1

  公开（公告）日：2011-01-06

  This invention provides compounds of formula IA or IB: wherein R 1 , R 2 , G 1 and HY are as described in the specification. The compounds are inhibitors of PI3K and/or mTor and are thus useful for treating proliferative, inflammatory, or cardiovascular disorders.

  该发明提供了式IA或IB的化合物：其中R1、R2、G1和HY如规范中所述。这些化合物是PI3K和/或mTor的抑制剂，因此可用于治疗增殖性、炎症性或心血管疾病。
• US9090601B2
  申请人：——

  公开号：US9090601B2

  公开（公告）日：2015-07-28