(±)-4-ethyl-1-[4-(4-hydroxypiperidin-1-yl)phenyl]-7,8-dimethoxy-N-methyl-4,5-dihydro-3H-2,3-benzodiazepine-3-carboxamide

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: (±)-4-ethyl-1-[4-(4-hydroxypiperidin-1-yl)phenyl]-7,8-dimethoxy-N-methyl-4,5-dihydro-3H-2,3-benzodiazepine-3-carboxamide
• 英文别名: 4-ethyl-1-[4-(4-hydroxypiperidin-1-yl)phenyl]-7,8-dimethoxy-N-methyl-4,5-dihydro-2,3-benzodiazepine-3-carboxamide
• 化学式: C₂₆H₃₄N₄O₄
• 分子量: 466.58
• InChiKey: HTKJOKVOCZQUFF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  34
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  86.6
• 氢给体数：
  2
• 氢受体数：
  6

文献信息

• 2,3-BENZODIAZEPINES
  申请人：BAYER PHARMA AKTIENGESELLSCHAFT

  公开号：US20150203483A1

  公开（公告）日：2015-07-23

  What is described are BET protein-inhibitory, in particular BRD4-inhibitory 2,3-benzodiazepines of the general formula (I) in which R 1a , R 1b , R 1c , R 2 , R 3 , R 4 , R 5 , A and X have the meanings given in the description, intermediates for preparing the compounds according to the invention, pharmaceutical compositions comprising the compounds according to the invention and their prophylactic and therapeutic use for hyperproliferative disorders, in particular for tumour disorders. Also described is the use of BET protein inhibitors for benign hyperplasias, atherosclerotic disorders, sepsis, autoimmune disorders, vascular disorders, viral infections, for neurodegenerative disorders, for inflammatory disorders, for atherosclerotic disorders and for the control of male fertility.

  所描述的是一般式(I)的BET蛋白抑制剂，特别是BRD4抑制剂2,3-苯二氮䓬类化合物，其中R1a、R1b、R1c、R2、R3、R4、R5、A和X的含义如描述所示，用于制备本发明化合物的中间体，包括本发明化合物的药物组合物以及它们在高增殖性疾病，特别是肿瘤疾病的预防和治疗中的用途。还描述了BET蛋白抑制剂用于良性增生、动脉粥样硬化疾病、败血症、自身免疫性疾病、血管疾病、病毒感染、神经退行性疾病、炎症性疾病、动脉粥样硬化疾病和控制男性生育能力。
• 2,3-BENZODIAZEPINE
  申请人：Bayer Pharma Aktiengesellschaft

  公开号：EP2885286B1

  公开（公告）日：2017-03-22
• METHOD FOR STRATIFICATION OF MELANOMA PATIENTS BY DETERMINATION OF OXYGEN CONSUMPTION, PPARGC1A, PPARGC1B AND MITF LEVELS
  申请人：Bayer Pharma Aktiengesellschaft

  公开号：US20180164317A1

  公开（公告）日：2018-06-14

  The present invention refers to a method and kit for stratification of melanoma patients by determining the OCR and levels of PPARGC1A, PPARGC1B and MITF RNA, derived cDNA, or corresponding protein. Especially, the invention is related to stratification kits to determine whether a patient with melanoma will respond to treatment with a BET inhibitor. In a further aspect, the invention is related to the use of a BET inhibitor for the treatment of melanoma in a patient by stratifying a sample of body fluid or tumor tissue in vitro and determining whether a patient suffering from melanoma will respond to treatment with a BET inhibitor.
• US9890147B2
  申请人：——

  公开号：US9890147B2

  公开（公告）日：2018-02-13
• [DE] 2,3-BENZODIAZEPINE<br/>[EN] 2,3-BENZODIAZEPINES<br/>[FR] 2,3-BENZODIAZÉPINES
  申请人：BAYER PHARMA AG

  公开号：WO2014026997A1

  公开（公告）日：2014-02-20

  Es werden BET-proteininhibitorische, insbesondere BRD4-inhibitorische 2,3- Benzodiazepine der allgemeinen Formel (I), in der R1a, R1b, R1c, R2, R3, R4, R5, A und X die in der Beschreibung angegebenen Bedeutungen haben, Intermediate zur Herstellung der erfindungsgemäßen Verbindungen, pharmazeutische Mittel enthaltend die erfindungsgemäßen Verbindungen sowie deren prophylaktische und therapeutische Verwendung bei hyper-proliferativen Erkrankungen, insbesondere bei Tumorerkrankungen beschrieben. Desweiteren wird die Verwendung von BET-Proteininhibitoren in benignen Hyperplasien, atherosklerotische Erkrankungen, Sepsis, Autoimmunerkrankungen, Gefäßerkrankungen, viralen Infektionen, in neurodegenerativen Erkrankungen, in inflammatorischen Erkrankungen, in atherosklerotischen Erkrankungen und in der männlichen Fertilitätskontrolle beschrieben.