1,3,3-Trimethylpiperidin-4-amine | 1369161-64-7

• 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: 1,3,3-Trimethylpiperidin-4-amine
• CAS: 1369161-64-7
• 化学式: C₈H₁₈N₂
• 分子量: 142.24
• InChiKey: NQAINYVXJLGSMR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  10
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  29.3
• 氢给体数：
  1
• 氢受体数：
  2

文献信息

• TRICYCLIC GYRASE INHIBITORS
  申请人：Bensen Daniel

  公开号：US20120238751A1

  公开（公告）日：2012-09-20

  Disclosed herein are compounds having the structure of Formula I and pharmaceutically suitable salts, esters, and prodrugs thereof that are useful as antibacterially effective tricyclic gyrase inhibitors. Related pharmaceutical compositions, uses and methods of making the compounds are also contemplated.

  本文披露了具有式I结构的化合物，以及作为抗菌有效的三环酶抑制剂的药用盐、酯和前药，相关的药物组合物、用途和制备该化合物的方法也在考虑之中。
• [EN] ENANTIOMERICALLY PURE ADAMANTANE DERIVATIVES FOR THE TREATMENT OF FILOVIRUS INFECTION<br/>[FR] DÉRIVÉS ÉNANTIOMÉRIQUEMENT PURS D'ADAMATANE POUR LE TRAITEMENT D'INFECTIONS À FILOVIRUS
  申请人：ARISAN THERAPEUTICS INC

  公开号：WO2019018185A1

  公开（公告）日：2019-01-24

  The compounds of the invention as shown by general structure I, as shown below, are effective in treating filovirus infections. Structure I X is selected from the group consisting of O and H; R1 is selected from (C6 to C10) aryl and (C2 to C9) heteroaryl, and R2 is selected from (C1 to C10) alkyl, (C1 to C10) alkenyl, (C1 to C10) alkynyl, (C3 to C10) cycloalkyi, and (C5 to C10) cycloalkenyl, and NR3aR3b is defined in the specification. These compounds are effective in treating filovirii infections including Ebolavirus and Marburgvirus.

  本发明的化合物如一般结构I所示，如下所示，对于治疗丝状病毒感染具有有效性。 结构I中X的选择来自于O和H的群组; R1的选择来自于（C6到C10）芳基和（C2到C9）杂环芳基，而R2的选择来自于（C1到C10）烷基，（C1到C10）烯基，（C1到C10）炔基，（C3到C10）环烷基和（C5到C10）环烯基，而NR3aR3b在规范中被定义。 这些化合物对于治疗丝状病毒感染包括埃博拉病毒和马尔堡病毒具有有效性。
• Tricyclic Gyrase inhibitors
  申请人：MERCK SHARP & DOHME CORP.

  公开号：US10865216B2

  公开（公告）日：2020-12-15

  Disclosed herein are compounds having the structure of Formula I and pharmaceutically suitable salts, esters, and prodrugs thereof that are useful as antibacterially effective tricyclic gyrase inhibitors. In addition, species of tricyclic gyrase inhibitors compounds are also disclosed herein. Related pharmaceutical compositions, uses and methods of making the compounds are also contemplated.

  本文公开了具有式 I 结构的化合物及其药学上适用的盐、酯和原药，它们可作为抗菌有效的三环回旋酶抑制剂。此外，本文还公开了三环回旋酶抑制剂化合物的种类。 还考虑了相关的药物组合物、用途和化合物的制造方法。
• Tricyclic gyrase inhibitors
  申请人：Merck Sharp & Dohme Corp.

  公开号：US10858360B2

  公开（公告）日：2020-12-08

  Disclosed herein are compounds having the structure of Formula I and pharmaceutically suitable salts, esters, and prodrugs thereof that are useful as antibacterially effective tricyclic gyrase inhibitors. Related pharmaceutical compositions, uses and methods of making the compounds are also contemplated.

  本文公开了具有式 I 结构的化合物及其药学上适用的盐、酯和原药，它们可作为抗菌有效的三环回旋酶抑制剂。 还考虑了相关的药物组合物、用途和化合物的制造方法。
• US9732083B2
  申请人：——

  公开号：US9732083B2

  公开（公告）日：2017-08-15