1-methyl-piperidine-3-thiol | 98278-56-9

• 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: 1-methyl-piperidine-3-thiol
• 英文别名: 1-Methyl-piperidin-3-thiol；1-Methylpiperidine-3-thiol
• CAS: 98278-56-9
• 化学式: C₆H₁₃NS
• 分子量: 131.242
• InChiKey: XSNHICJZIUNEOS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 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：
  4.2
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  alkaline earth salt of/the/ methylsulfuric acid 在 sodium hydroxide 、 水 作用下， 生成 1-methyl-piperidine-3-thiol
  参考文献：
  名称：

  N-substituted-3-thiol piperidines and thioesters thereof

  摘要：

  公开号：

  US02834785A1

文献信息

• [EN] BIFUNCTIONAL COMPOUNDS FOR DEGRADING BTK VIA UBIQUITIN PROTEOSOME PATHWAY<br/>[FR] COMPOSÉS BIFONCTIONNELS POUR LA DÉGRADATION DE LA BTK PAR L'INTERMÉDIAIRE DE LA VOIE DE L'UBIQUITINE-PROTÉOSOME
  申请人：NURIX THERAPEUTICS INC

  公开号：WO2021113557A1

  公开（公告）日：2021-06-10

  This disclosure relates to compounds useful for degrading BTK via a ubiquitin proteolytic pathway. The description also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compositions in the treatment of various disease, conditions, or disorders.

  本公开涉及通过泛素蛋白酶途径降解BTK的化合物。描述还提供了包括这些化合物的药学上可接受的组合物，以及使用这些组合物治疗各种疾病、状况或障碍的方法。
• [EN] ANALOGOUS COMPOUNDS OF STROBILURINES AND THEIR USE AS ACARICIDES AND INSECTICIDES<br/>[FR] COMPOSES ANALOGUES AUX STROBILURINES ET LEUR UTILISATION EN TANT QU'ACARICIDES ET INSECTICIDES
  申请人：ISAGRO RICERCA SRL

  公开号：WO2003087032A1

  公开（公告）日：2003-10-23

  Compounds are described, having general formula (I) and their use as acaricides, insecticides and/or fungicides.

  描述了通式（I）的化合物，并且它们被用作杀螨剂、杀虫剂和/或杀菌剂。
• Substituted guanidine derivatives
  申请人：——

  公开号：US20030018056A1

  公开（公告）日：2003-01-23

  A compound represented by the following formula: 1 wherein R is a substituted or unsubstituted benzene ring, a fused polycyclic hydrocarbon ring which is substituted or unsubstituted, a monocyclic heterocyclic ring which is substituted or unsubstituted, a polycyclic heterocyclic ring which is substituted or unsubstituted, A and E are independently a single bond, a lower alkylene group or the like, G is a single bond, an oxygen atom or the like, and Y is a —SO 3 H group or the like, a prodrug of said compound, or a pharmaceutically acceptable salt of said compound or prodrug is useful as a therapeutic or prophylactic agent for diseases caused by the acceleration of the sodium/proton exchange transport system.

  以下化合物的化学式：1其中R是取代或未取代的苯环，取代或未取代的融合多环碳氢环，取代或未取代的单环杂环环，取代或未取代的多环杂环环，A和E分别是单键，低碳烷基或类似物，G是单键，氧原子或类似物，Y是—SO3H基团或类似物，该化合物的前药，或该化合物或前药的药学可接受的盐对于由于钠/质子交换转运系统加速引起的疾病是有用的治疗或预防剂。
• Substituted guanidine derivatives, process for production thereof, and pharmaceutical uses thereof
  申请人：SUMITOMO PHARMACEUTICALS COMPANY, LIMITED

  公开号：EP0787728A1

  公开（公告）日：1997-08-06

  A compound which is a substituted guanidine derivative of formula (1): wherein each of R1, R2, R3 and R4, which are the same or different, is hydrogen or an organic group; each of Y1, Y2, Y3, Y4, Y5, Y6 and Y7, which are the same or different, is a single bond, -CH2-, -O-,-CO-, -C(=C(R11)R12- -S(O)n- or -N(R10)-, or any pairs represented by Y1 and Y2, Y2 and Y3, Y3 and Y4, Y4 and Y5, Y5 and Y6 or Y6 and Y7 represent -CH=CH- , and wherein at least two of Y1, Y2, Y3, Y4, Y5, Y6 and Y7 is other than a single bond; m is 0 or an integer of 1 to 5; and Z, each of which are the same or different when m is an integer of 2 to 5, is an organic substituent, or a pharmaceutically acceptable acid addition salt thereof, is useful as a therapeutic or prophylactic agent for diseases cause by acceleration of the sodium/proton (Na+/H+) exchange transport system such as hyperpiesia, arrhythmia, angina pectoris, hypercardia, diabetes, organopathies due to ischemia or ischemia re-perfusion, conditions due to cerebral ischemia, diseases caused by cell over-proliferation and diseases caused by trouble with endothelial cells.

  一种化合物，其为式（1）的取代的鸟氨酸衍生物：其中R1、R2、R3和R4中的每一个，相同或不同，均为氢或有机基团；Y1、Y2、Y3、Y4、Y5、Y6和Y7中的每一个，相同或不同，均为单键，-CH2-，-O-，-CO-，-C（=C（R11）R12-，-S（O）n-或-N（R10）-，或由Y1和Y2，Y2和Y3，Y3和Y4，Y4和Y5，Y5和Y6或Y6和Y7表示的任何一对均表示-CH=CH-，其中至少有两个Y1、Y2、Y3、Y4、Y5、Y6和Y7不是单键；m为0或1到5的整数；当m为2到5的整数时，Z均为有机取代基，或其药学上可接受的酸加成盐，用于治疗或预防由钠/质子（Na+/H+）交换转运系统加速引起的疾病，如高血压、心律失常、心绞痛、心肌过度收缩、糖尿病、缺血或再灌注引起的器官病变、脑缺血引起的疾病、细胞过度增殖引起的疾病以及内皮细胞问题引起的疾病。
• Analogous compounds of strobilurines and their use as acaricides and insecticides
  申请人：Venturini Isabella

  公开号：US20060235075A1

  公开（公告）日：2006-10-19

  Compounds are described, having general formula (I) and their use as acaricides, insecticides and/or fungicides.

  描述了具有通式（I）的化合物，并且它们被用作杀螨剂、杀虫剂和/或杀菌剂。