(3S,4S)-3-Methyl-piperidin-4-ylamine | 473839-09-7

• 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: (3S,4S)-3-Methyl-piperidin-4-ylamine
• 英文别名: (3S,4S)-3-methylpiperidin-4-amine
• CAS: 473839-09-7
• 化学式: C₆H₁₄N₂
• 分子量: 114.19
• InChiKey: BCSXUVZTKVXBSD-WDSKDSINSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.2
• 重原子数：
  8
• 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：
  38
• 氢给体数：
  2
• 氢受体数：
  2

文献信息

• Generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, their preparation,compositions and use as medicaments
  申请人：WOCKHARDT LIMITED

  公开号：US20030216568A1

  公开（公告）日：2003-11-20

  This invention relates to new generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, to their optical isomers, diastereomers or enantiomers, as well as pharmaceutically acceptable salts, hydrates, prodrugs, polymorphs and pseudopolymorphs thereof, to their preparation, to their compositions and to their use.

  本发明涉及新一代三重靶向手性广谱抗菌7-取代哌啶酮羧酸衍生物，以及它们的光学异构体、对映异构体或对映体，以及其药学上可接受的盐、水合物、前药、多晶形和假多晶形，以及它们的制备、组成和用途。
• Generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-Quinolone carboxylic acid derivatives, their preparation, compositions and use as medicaments
  申请人：WOCKHARDT LIMITED

  公开号：US20030096812A1

  公开（公告）日：2003-05-22

  This invention relates to new generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, to their optical isomers, diastereomers or enantiomers, as well as pharmaceutically acceptable salts, hydrates, prodrugs, polymorphs and pseudopolymorphs thereof, to their preparation, to their compositions and to their use.

  本发明涉及新一代三重靶向手性广谱抗微生物7-取代哌啶酮羧酸衍生物，其光学异构体，对映异构体或对映体，以及其药学上可接受的盐，水合物，前药，多晶形和假多晶形，以及其制备，组成和使用。
• Generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, their preparation, compositions and use as medicaments
  申请人：De Souza John Noel

  公开号：US20050065164A1

  公开（公告）日：2005-03-24

  This invention relates to new generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, to their optical isomers, diastereomers or enantiomers, as well as pharmaceutically acceptable salts, hydrates, prodrugs, polymorphs and pseudopolymorphs thereof, to their preparation, to their compositions and to their use.

  本发明涉及新一代三重靶向、手性、广谱抗微生物的7-取代哌啶酮羧酸衍生物，以及它们的光学异构体、对映异构体或对映体、药学上可接受的盐、水合物、前药、多晶型和假多晶型，以及它们的制备、组合物和用途。
• New generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, their preparation, compositions and use as medicaments
  申请人：De Souza Noel John

  公开号：US20080214608A1

  公开（公告）日：2008-09-04

  This invention relates to new generation triple-targeting, chiral, broad-spectrum antimicrobial 7-substituted piperidino-quinolone carboxylic acid derivatives, to their optical isomers, diastereomers or enantiomers, as well as pharmaceutically acceptable salts, hydrates, prodrugs, polymorphs and pseudopolymorphs thereof, to their preparation, to their compositions and to their use.

  本发明涉及新一代三重靶向手性广谱抗微生物7-取代哌啶酮羧酸衍生物，以及它们的光学异构体、对映异构体或对映体，以及药学上可接受的盐、水合物、前药、多晶形和伪多晶形，以及它们的制备、组成和使用。
• [DE] PYRIMIDO[5,4-d]PYRIMIDINE, DIESE VERBINDUNGEN ENTHALTENDE ARZNEIMITTEL, DEREN VERWENDUNG UND VERFAHREN ZU IHRER HERSTELLUNG<br/>[EN] PYRIMIDO[5,4-D]PYRIMIDINES, MEDICAMENTS CONTAINING THESE COMPOUNDS, THEIR USE AND PROCESS FOR THEIR PRODUCTION<br/>[FR] PYRIMIDO[5,4-d]PYRIMIDINES, MEDICAMENTS CONTENANT CES COMPOSES, LEUR UTILISATION ET PROCEDE DE FABRICATION ASSOCIE
  申请人：DR. KARL THOMAE GMBH

  公开号：WO1997032880A1

  公开（公告）日：1997-09-12

  (DE) Die vorliegende Erfindung betrifft Pyrimido[5,4-d]pyrimidine der allgemeinen Formel (I), in der Ra bis Rc wie im Anspruch 1 definiert sind, deren Tautomeren, deren Stereoisomere und deren Salze, insbesonders deren physiologisch verträgliche Salze mit anorganischen oder organischen Säuren oder Basen, welche wertvolle pharmakologische Eigenschaften aufweisen, insbesondere eine Hemmwirkung auf die durch Tyrosinkinasen vermittelte Signaltransduktion, deren Verwendung zur Behandlung von Krankheiten, insbesondere von Tumorerkrankungen, und deren Herstellung.(EN) The present invention relates to pyrimido[5,4-d]pyrimidines of general formula (I) in which Ra to Rc are as defined in claim 1, their tautomers, stereoisomers and salts, especially their physiologically acceptable salts with inorganic or organic acids or bases exhibiting valuable pharmacological properties, especially an inhibitory effect on signal transduction produced by tyrosinkinases, their use in treating disorders, especially tumours, and their production.(FR) L'invention concerne des pyrimido[5,4-d]pyrimidines de formule générale (I), où Ra à Rc sont tels que définis dans la revendication 1; leurs tautomères, leurs stéréo-isomères et leur sels, notamment leurs sels physiologiquement acceptables avec des acides ou des bases inorganiques ou organiques, qui possèdent des propriétés pharmacologiques intéressantes, en particulier une action inhibitrice sur la transduction de signaux ayant pour médiation les tyrosine kinases; leur utilisation pour le traitement de maladies, notamment tumorales; et leur fabrication.

  该发明涉及5,4—双降欠碱性嘌呤核苷酸（Pyrimido[5,4-d]pyrimidine）的一般形式（I），其中Ra至Rc如同在要求1中所定义，它们的转变体、立体异构体及其盐，特别是与无机或有机酸或碱的生理相容性盐，具有重要药理性质，尤其是对通过酪氨酸激酶介导的信号传递产生抑制作用的性质，它们在治疗以及，尤其是癌症中的应用和生产的看法。