3,3,3-trifluoro-1-[4-(3H-pyrrolo[3,2-f][1,7]naphthyridin-9-yl)piperazin-1-yl]propan-1-one | 1401444-03-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 英文名称: 3,3,3-trifluoro-1-[4-(3H-pyrrolo[3,2-f][1,7]naphthyridin-9-yl)piperazin-1-yl]propan-1-one
• CAS: 1401444-03-8
• 化学式: C₁₇H₁₆F₃N₅O
• 分子量: 363.342
• InChiKey: FJPCGKSVLVEFDO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  26
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.35
• 拓扑面积：
  65.1
• 氢给体数：
  1
• 氢受体数：
  7

文献信息

• Nucleotide mimics and their prodrugs
  申请人：Cook D. Phillip

  公开号：US20070259832A1

  公开（公告）日：2007-11-08

  The present invention relates to nucleoside diphosphate mimics and nucleoside triphosphate mimics, which contain diphosphate or triphosphate moiety mimics and optionally sugar-modifications and/or base-modifications. The nucleotide mimics of the present invention, in a form of a pharmaceutically acceptable salt, a pharmaceutically acceptable prodrug, or a pharmaceutical formulation, are useful as antiviral, antimicrobial, and anticancer agents. The present invention provides a method for the treatment of viral infections, microbial infections, and proliferative disorders. The present invention also relates to pharmaceutical compositions comprising the compounds of the present invention optionally in combination with other pharmaceutically active agents.

  本发明涉及核苷酸二磷酸类似物和核苷酸三磷酸类似物，其包含二磷酸或三磷酸基类似物，以及可选的糖修饰和/或碱基修饰。本发明的核苷酸类似物以药学上可接受的盐、药学上可接受的前药或制剂形式，可用作抗病毒、抗微生物和抗癌药物。本发明提供了一种治疗病毒感染、微生物感染和增殖性疾病的方法。本发明还涉及包含本发明化合物的制药组合物，可选地与其他药学活性剂组合使用。
• SUBSTITUTED FUSED TRICYCLIC COMPOUNDS, COMPOSITIONS AND MEDICINAL APPLICATIONS THEREOF
  申请人：Advinus Therapeutics Limited

  公开号：EP2688890B1

  公开（公告）日：2017-08-30
• US9115133B2
  申请人：——

  公开号：US9115133B2

  公开（公告）日：2015-08-25
• [EN] SUBSTITUTED FUSED TRICYCLIC COMPOUNDS, COMPOSITIONS AND MEDICINAL APPLICATIONS THEREOF<br/>[FR] COMPOSÉS TRICYCLIQUES SUBSTITUÉS; COMPOSITIONS ET APPLICATIONS MÉDICINALES CORRESPONDANTES
  申请人：ADVINUS THERAPEUTICS LTD

  公开号：WO2012127506A1

  公开（公告）日：2012-09-27

  The present invention relates to substituted fused tricyclic compounds of formula (I) or (Ia), their tautomers, polymorphs, stereoisomers, prodrugs, solvates, co-crystals, pharmaceutically acceptable salts, pharmaceutical compositions containing them and methods of treating conditions and diseases that are mediated by JAK activity. The compounds of the present invention are useful in the treatment, prevention or suppression of diseases and disorders mediated by JAK activity. Such conditions include, but not limited to, arthritis, Alzheimer's disease, autoimmune thyroid disorders, cancer, diabetes, leukemia, T-cell prolymphocytic leukemia, lymphoma, myleoproliferation disorders, lupus, multiple myeloma, multiple sclerosis, osteoarthritis, sepsis, psoriatic arthritis, prostate cancer, T-cell autoimmune disease, inflammatory diseases, chronic and acute allograft transplant rejection, bone marrow transplant, stroke, asthma, chronic obstructive pulmonary disease, allergy, bronchitis, viral diseases, or Type I diabetes, complications from diabetes, rheumatoid arthritis, asthma, Crohn's disease, dry eye, uveitis, inflammatory bowel disease, organ transplant rejection, psoriasis and ulcerative colitis. The present disclosure also relates to process for the preparation of such compounds, and to pharmaceutical compositions containing them.