2-Thiaspiro<3.3>heptan | 174-76-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 硫杂环丁烷
• 英文名称: 2-Thiaspiro<3.3>heptan
• 英文别名: 2-thia-spiro[3.3]heptane；2-Thiaspiro[3.3]heptane
• CAS: 174-76-5
• 化学式: C₆H₁₀S
• 分子量: 114.211
• InChiKey: XDSXTVCYWYSQQN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  7
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  25.3
• 氢给体数：
  0
• 氢受体数：
  1

文献信息

• OXINDOLE COMPOUNDS CARRYING A CO-BOUND SPIRO SUBSTITUENT AND USE THEREOF FOR TREATING VASOPRESSIN-RELATED DISEASES
  申请人：AbbVie Deutschland GmbH & Co. KG

  公开号：US20150344489A1

  公开（公告）日：2015-12-03

  The present invention relates to novel substituted oxindole derivatives of formula I wherein the variables are as defined in the claims and the description. The invention further relates to pharmaceutical compositions comprising compounds I and their use for the treatment of vasopressin-related disorders.

  本发明涉及公式I的新型取代氧吲哚衍生物，其中变量如权利要求和描述中所定义。该发明还涉及包含化合物I的药物组合物，以及它们用于治疗与加压素相关的疾病。
• PYRROLO- AND PYRAZOLO-TRIAZOLODIAZEPINES AS BET-PROTEIN INHIBITORS FOR TREATING HYPERPROLIFERATIVE DISEASES
  申请人：BAYER PHARMA AKTIENGESELLSCHAFT

  公开号：US20160009725A1

  公开（公告）日：2016-01-14

  What is described are BET protein-inhibitory, especially BRD2-, BRD3- and BRD4-inhibitory, bicyclo- and spino-substituted pyrrolo- and pyrazolodiazepines of the general formula I in which X, Y, n, m, R 1 , R 2 , R 3 , R 4 and R 5 are each as defined in the description, to intermediates for preparation of the inventive compounds, to pharmaceutical compositions comprising the inventive compounds, and to the prophylactic and therapeutic use thereof for hyperproliferative disorders, especially for tumour disorders. Also described is the use of the compounds according to the invention as BET protein inhibitors for benign hyperplasias, for atherosclerotic disorders, for sepsis, for autoimmune disorders, for vascular disorders, for viral infections, for neurodegenerative disorders, for inflammatory disorders, for atherosclerotic disorders and for male fertility control.

  所描述的是BET蛋白抑制剂，特别是BRD2、BRD3和BRD4抑制剂，其为通式I的双环和螺环取代的吡咯烷和吡唑二氮杂环化合物，其中X、Y、n、m、R1、R2、R3、R4和R5如描述中所定义，以及用于制备本发明化合物的中间体，包含本发明化合物的制药组合物，以及其预防和治疗肿瘤性疾病等增生性疾病的用途。还描述了本发明化合物作为BET蛋白抑制剂用于良性增生、动脉硬化性疾病、败血症、自身免疫性疾病、血管疾病、病毒感染、神经退行性疾病、炎症性疾病、动脉硬化性疾病和男性生育控制的用途。
• [EN] MONOBACTAMS AND METHODS OF THEIR SYNTHESIS AND USE<br/>[FR] MONOBACTAMES ET PROCÉDÉS DE SYNTHÈSE ET D'UTILISATION DE CES DERNIERS
  申请人：HARVARD COLLEGE

  公开号：WO2015103583A1

  公开（公告）日：2015-07-09

  Described herein are monobactam antibiotics of Formula (I), (Ι'), (II), and (II'), along with methods and intermediates for preparing these compounds. Pharmaceutical compositions and methods of treating infectious diseases using the monobactams are also provided.

  本文描述了单环内酰胺抗生素的化学式(I)、(Ι')、(II)和(II')，以及制备这些化合物的方法和中间体。还提供了使用单环内酰胺治疗传染病的药物组合物和方法。
• PYRAZOLE COMPOUND AND PESTICIDAL MIXTURES COMPRISING A PYRAZOLE COMPOUND
  申请人：BASF SE

  公开号：US20150150257A1

  公开（公告）日：2015-06-04

  The present invention relates to pesticidal mixtures comprising as active compounds 1) at least one pyrazole compound A selected from the compounds of formula I: wherein the variables have the meaning as defined in the description, and 2) at least one further compound B selected from the compounds of the following groups A.1, A.2, A.3, A.4, A.5, A.6, A.7, A.8, A.9, A.10, A.11, A.12, A.13, A.14, A.15, A.16, A.17, F.1, F.2, F.3, F.4, F.5, F.6, F.7, F.8, F.9, F.10 and F.11 as defined in the specification. The present invention also relates to novel pyrazole compounds of the formula I. The present invention also relates to methods and use of these mixtures and novel compounds for combating invertebrate pests such as insects, arachnids or nematodes in and on plants, and for protecting such plants being infested with pests, especially also for protecting plant propagation material as like seeds.

  本发明涉及一种杀虫混合物，包括以下活性化合物：1）至少一种从式I化合物中选择的吡唑类化合物A，其中变量的含义如说明书所定义，以及2）至少一种从以下A.1、A.2、A.3、A.4、A.5、A.6、A.7、A.8、A.9、A.10、A.11、A.12、A.13、A.14、A.15、A.16、A.17、F.1、F.2、F.3、F.4、F.5、F.6、F.7、F.8、F.9、F.10和F.11化合物组中选择的进一步化合物B，如说明书中定义的。本发明还涉及式I的新的吡唑类化合物。本发明还涉及使用这些混合物和新化合物的方法，用于在植物内外对抗无脊椎动物害虫，例如昆虫、蜘蛛或线虫，并保护被害虫侵害的植物，特别是用于保护植物繁殖材料，例如种子。
• Acrylamide compounds for combating invertebrate pests
  申请人：BASF SE

  公开号：US20150065343A1

  公开（公告）日：2015-03-05

  The present invention relates to acrylamide compounds which are useful for combating or controlling invertebrate pests, in particular arthropod pests and nematodes, and to a method for producing them. The invention also relates to a method for controlling invertebrate pests by using these compounds and to plant propagation material and to an agricultural and a veterinary composition comprising said compounds.

  本发明涉及丙烯酰胺化合物，其可用于对抗或控制无脊椎动物害虫，特别是节肢动物害虫和线虫，并提供了一种生产它们的方法。本发明还涉及一种使用这些化合物控制无脊椎动物害虫的方法，以及包括该化合物的植物繁殖材料和农业和兽医组合物。