N,3-dimethylcyclopentan-1-amine | 252854-33-4

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: N,3-dimethylcyclopentan-1-amine
• CAS: 252854-33-4
• 化学式: C₇H₁₅N
• mdl: MFCD03412911
• 分子量: 113.2
• InChiKey: KYMXBBBWJVWQSX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  8
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  12
• 氢给体数：
  1
• 氢受体数：
  1

文献信息

• Pyrrolo[2,3-d]pyrimidine compounds
  申请人：——

  公开号：US20020019526A1

  公开（公告）日：2002-02-14

  A compound of the formula 1 wherein R 1 , R 2 and R 3 are as defined above, which are inhibitors of the enzyme protein tyrosine kinases such as Janus Kinase 3 and as such are useful therapy as immunosuppressive agents for organ transplants, lupus, multiple sclerosis, rheumatoid arthritis, psoriasis, Type I diabetes and complications from diabetes, cancer, asthma, atopic dermatitis, autoimmune thyroid disorders, ulcerative colitis, Crohn's disease, Alzheimer's disease, Leukemia and other autoimmune diseases.

  一种化合物的结构式，其中R1、R2和R3如上所定义，它们是蛋白酪氨酸激酶的抑制剂，如Janus激酶3，因此可作为免疫抑制剂用于器官移植、狼疮、多发性硬化、类风湿性关节炎、牛皮癣、1型糖尿病和糖尿病并发症、癌症、哮喘、特应性皮炎、自身免疫性甲状腺疾病、溃疡性结肠炎、克罗恩病、阿尔茨海默病、白血病和其他自身免疫疾病的治疗。
• [EN] HETEROBIFUNCTIONAL COMPOUNDS WITH IMPROVED SPECIFICITYFOR THE BROMODOMAIN OF BRD4<br/>[FR] COMPOSÉS HÉTÉROBIFONCTIONNELS PRÉSENTANT UNE SPÉCIFICITÉ AMÉLIORÉE POUR LE BROMODOMAINE DE BRD4
  申请人：DANA FARBER CANCER INST INC

  公开号：WO2019079701A1

  公开（公告）日：2019-04-25

  Disclosed are heterobifunctional compounds that effectuate selective degradation of a target protein, and which include a targeting ligand that binds a target protein and at least one other protein, a ligand that binds an E3 ubiquitin ligase or a component of E3 ubiquitin ligase, and a specificity modulating linker that links the first ligand and the second ligand. Pharmaceutical compositions containing the compounds, and methods of using and making the compounds are also disclosed.

  本文披露了一种异源双功能化合物，可以实现对目标蛋白的选择性降解。该化合物包括一个结合目标蛋白和至少另一种蛋白的靶向配体，一个结合E3泛素连接酶或E3泛素连接酶组分的配体，以及一个调节特异性的连接子，连接第一配体和第二配体。此外，还披露了含有这些化合物的药物组合物，以及使用和制备这些化合物的方法。
• [EN] COMPOUNDS FOR THE TREATMENT OF BOVINE OR SWINE RESPIRATORY DISEASE<br/>[FR] COMPOSÉS POUR LE TRAITEMENT D'UNE MALADIE RESPIRATOIRE BOVINE OU PORCINE
  申请人：INTERVET INT BV

  公开号：WO2020002238A1

  公开（公告）日：2020-01-02

  The present invention provides compounds of formula (I) for use in the treatment of respiratory diseases of animals, especially Bovine or Swine Respiratory disease (BRD and SRD).

  本发明提供了用于治疗动物呼吸道疾病，特别是牛或猪呼吸道疾病（BRD和SRD）的化合物（I）的公式。
• Pyrrolo [2,3-D] pyrimidine compounds
  申请人：Pfizer Inc.

  公开号：US20030212273A1

  公开（公告）日：2003-11-13

  A compound of the formula 1 wherein R 1 , R 2 and R 3 are as defined above, which are inhibitors of the enzyme protein tyrosine kinases such as Janus Kinase 3 and as such are useful therapy as immunosuppressive agents for organ transplants, lupus, multiple sclerosis, rheumatoid arthritis, psoriasis, Type I diabetes and complications from diabetes, cancer, asthma, atopic dermatitis, autoimmune thyroid disorders, ulcerative colitis, Crohn's disease, Alzheimer's disease, Leukemia and other autoimmune diseases.

  化合物的公式为1，其中R1，R2和R3的定义如上所述，它们是蛋白酪氨酸激酶的抑制剂，例如Janus Kinase 3，并且作为免疫抑制剂用于器官移植，狼疮，多发性硬化症，类风湿性关节炎，牛皮癣，1型糖尿病和糖尿病并发症，癌症，哮喘，特应性皮炎，自身免疫性甲状腺疾病，溃疡性结肠炎，克罗恩病，阿尔茨海默病，白血病和其他自身免疫性疾病的有用治疗方法。
• 4-IMIDAZOLIN-2-ONE COMPOUNDS
  申请人：Kubo Akira

  公开号：US20090088422A1

  公开（公告）日：2009-04-02

  The present invention relates to a compound of the formula [I]: wherein G 1 is an alkyl which is substituted by a halogen atom or an alkoxy, or a group of the formula: wherein ring B is benzene ring which may be substituted, etc., Q1 and Q2 may be the same or different, and each is hydrogen atom, a halogen atom or an alkyl, n is 0, 1, 2, 3 or 4, R 1 is hydrogen atom, an alkyl which may be substituted, a cycloalkyl which may be substituted, a phenyl which may be substituted, etc., Z 1 , Z 2 , Z 3 and Z 4 may be the same or different, and each is CH or N, provided that 3 or more of Z 1 , Z 2 , Z 3 and Z 4 should not be N at the same time, G 2 is hydrogen atom, —NR 3 R 4 , —OR 5 , etc., where R 3 to R 8 each is independently hydrogen atom, an alkyl which may be substituted, an alkenyl, an alkynyl, etc., or a pharmaceutically acceptable salt thereof.

  本发明涉及一种式[I]的化合物：其中，G1是被卤素原子或烷氧基取代的烷基，或者是式的基团：其中环B是苯环，可能被取代等，Q1和Q2可以相同也可以不同，且每个是氢原子、卤素原子或烷基，n为0、1、2、3或4，R1是氢原子、可能被取代的烷基、可能被取代的环烷基、可能被取代的苯基等，Z1、Z2、Z3和Z4可以相同也可以不同，且每个是CH或N，但应满足Z1、Z2、Z3和Z4中至少有3个不为N，G2是氢原子、-NR3R4、-OR5等，其中R3至R8各自独立地是氢原子、可能被取代的烷基、烯基、炔基等，或者其药学上可接受的盐。