3-acetylthio-piperidine | 1112922-38-9

• 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: 3-acetylthio-piperidine
• 英文别名: S-piperidin-3-yl ethanethioate
• CAS: 1112922-38-9
• 化学式: C₇H₁₃NOS
• 分子量: 159.252
• InChiKey: MIBHQPFCVIOBKT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.8
• 重原子数：
  10
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.86
• 拓扑面积：
  54.4
• 氢给体数：
  1
• 氢受体数：
  3

文献信息

• [EN] (AZA)INDAZOLYL-ARYL SULFONAMIDE AND RELATED COMPOUNDS AND THEIR USE IN TREATING MEDICAL CONDITIONS<br/>[FR] (AZA) INDAZOLYL-ARYLE SULFONAMIDE ET COMPOSÉS APPARENTÉS ET LEUR UTILISATION DANS LE TRAITEMENT D'ÉTATS MÉDICAUX
  申请人：HIBERCELL INC

  公开号：WO2020210828A1

  公开（公告）日：2020-10-15

  The invention provides (aza)indazolyl-aryl sulfonamide and related compounds, pharmaceutical compositions, and their use in the treatment of medical conditions, such as cancer, and in inhibiting GCN2 activity.

  这项发明提供了(aza)吲哚基芳基磺酰胺及相关化合物、药物组合物，以及它们在治疗医疗状况（如癌症）和抑制GCN2活性中的用途。
• SULFONYL-SUBSTITUTED CARBAPENEM COMPOUNDS
  申请人：Huang Zhenhua

  公开号：US20110046107A1

  公开（公告）日：2011-02-24

  The present invention relates to a compound of the formula (I), pharmaceutically acceptable salts, hydrolysable esters, isomers and hydrates thereof, and hydrates of the said esters or salts, wherein R 1 , R 2 , R 3 and are as defined in the description. The present invention further relates to a process for preparing the compounds, to pharmaceutical compositions comprising the compounds, and to the use of the compounds in the manufacture of a medicament for the treatment and/or prophylaxis of infectious diseases.

  本发明涉及式(I)的化合物、药用可接受的盐、可水解的酯、同分异构体和水合物，以及所述酯或盐的水合物，其中R1、R2、R3和R4如描述中定义。本发明进一步涉及制备这些化合物的方法、包含这些化合物的药物组合物，以及将这些化合物用于制造用于治疗和/或预防传染病的药物。
• (AZA)INDAZOLYL-ARYL SULFONAMIDE AND RELATED COMPOUNDS AND THEIR USE IN TREATING MEDICAL CONDITIONS
  申请人：HiberCell, Inc.

  公开号：US20220388964A1

  公开（公告）日：2022-12-08

  The invention provides (aza)indazolyl-aryl sulfonamide and related compounds, pharmaceutical compositions, and their use in the treatment of medical conditions, such as cancer, and in inhibiting GCN2 activity.