1-Ethyl-4-fluoro-2-methylpyrrolidine

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯烷类
• 英文名称: 1-Ethyl-4-fluoro-2-methylpyrrolidine
• 英文别名: 1-ethyl-4-fluoro-2-methylpyrrolidine
• 化学式: C₇H₁₄FN
• 分子量: 131.19
• InChiKey: KWXXXJKTYAHPHC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  9
• 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：
  3.2
• 氢给体数：
  0
• 氢受体数：
  2

文献信息

• [EN] SPIRO RING COMPOUND AS HEPATITIS C VIRUS (HCV) INHIBITOR AND USES THEREOF FIELD OF THE INVENTION<br/>[FR] COMPOSÉ DE TYPE NOYAU SPIRO UTILISABLE EN TANT QU'INHIBITEUR DU VIRUS DE L'HÉPATITE C (VHC) ET SES UTILISATIONS, DOMAINE DE L'INVENTION
  申请人：SUNSHINE LAKE PHARMA CO LTD

  公开号：WO2014082379A9

  公开（公告）日：2016-02-25
• SPIRO RING COMPOUNDS AS HEPATITIS C VIRUS (HCV) INHIBITORS
  申请人：Sunshine Lake Pharma Co., Ltd.

  公开号：EP2900656B1

  公开（公告）日：2017-05-17
• ETHER COMPOUNDS FOR TREATMENT OF COMPLEMENT MEDIATED DISORDERS
  申请人：Achillion Pharmaceuticals, Inc.

  公开号：US20160362433A1

  公开（公告）日：2016-12-15

  Compounds, methods of use, and processes for making inhibitors of complement factor D comprising Formula I, or a pharmaceutically acceptable salt or composition thereof wherein R 12 or R 13 on the A group is an ether (R 32 ) are provided. The inhibitors described herein target factor D and inhibit or regulate the complement cascade. The inhibitors of factor D described herein are capable of reducing the excessive activation of complement.
• PHOSPHONATE COMPOUNDS FOR TREATMENT OF COMPLEMENT MEDIATED DISORDERS
  申请人：Achillion Pharmaceuticals, Inc.

  公开号：US20170260219A1

  公开（公告）日：2017-09-14

  Compounds, methods of use, and processes for making inhibitors of complement factor D comprising Formula I, or a pharmaceutically acceptable salt or composition thereof wherein R 12 or R 13 on the A group is a phosphonate (R 32 ) are provided. The inhibitors described herein target factor D and inhibit or regulate the complement cascade at an early and essential point in the alternative complement pathway, and reduce factor D's ability to modulate the classical and lectin complement pathways. The inhibitors of factor D described herein are capable of reducing the excessive activation of complement, which has been linked to certain autoimmune, inflammatory, and neurodegenerative diseases, as well as ischemia-reperfusion injury and cancer.
• US9643986B2
  申请人：——

  公开号：US9643986B2

  公开（公告）日：2017-05-09