(S)-glycidyl ether

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 环氧化物
• 英文名称: (S)-glycidyl ether
• 英文别名: (2S)-2-[[(2S)-oxiran-2-yl]methoxymethyl]oxirane
• 化学式: C₆H₁₀O₃
• 分子量: 130.144
• InChiKey: GYZLOYUZLJXAJU-PHDIDXHHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.5
• 重原子数：
  9
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  34.3
• 氢给体数：
  0
• 氢受体数：
  3

文献信息

• [EN] C-3 AND C-17 MODIFIED TRITERPENOIDS AS HIV-1 INHIBITORS<br/>[FR] TRITERPÉNOÏDES MODIFIÉS EN C-3 ET C-17 UTILISÉS COMME INHIBITEURS DU VIH-1
  申请人：VIIV HEALTHCARE UK (NO 5) LTD

  公开号：WO2017134596A1

  公开（公告）日：2017-08-10

  Compounds having drug and bio-affecting properties, their pharmaceutical compositions and methods of use are set forth. In particular, betulinic acid derivatives that possess unique antiviral activity are provided as HIV maturation inhibitors, as represented by compounds of Formula (I). These compounds are useful for the treatment of HIV and AIDS.

  具有药物和生物活性的化合物、其药物组合物及其用途被详细说明。特别是，提供了具有独特抗病毒活性的白桦酸衍生物，这些衍生物作为HIV成熟抑制剂，由公式(I)所示的化合物代表。这些化合物可用于治疗HIV和艾滋病。
• Compounds which mimic the chemical and biological properties of discodermolide
  申请人：——

  公开号：US20020103387A1

  公开（公告）日：2002-08-01

  Compounds which mimic the chemical and/or biological activity of discodermolide are provided and intermediates useful in their preparation.

  提供了模拟二十烷醇化合物的化学和/或生物活性的化合物，并提供了在其制备中有用的中间体。
• FUSED AMINODIHYDROTHIAZINE DERIVATIVES
  申请人：SUZUKI Yuichi

  公开号：US20090209755A1

  公开（公告）日：2009-08-20

  A compound represented by the general formula: or a pharmaceutically acceptable salt thereof or a solvate thereof, wherein Ring A is a C 6-14 aryl group or the like, L is —NR e CO— or the like (wherein R e is a hydrogen atom or the like), Ring B is a C 6-14 aryl group or the like, X is a C 1-3 alkylene group or the like, Y is a single bond or the like, Z is a C 1-3 alkylene group or the like, R 1 and R 2 are each independently a hydrogen atom or the like, and R 3 , R 4 , R 5 and R 6 are independently a hydrogen atom, a halogen atom or the like, has an Aβ production inhibitory effect or a BACE1 inhibitory effect and is useful as a prophylactic or therapeutic agent for a neurodegenerative disease caused by Aβ and typified by Alzheimer-type dementia.

  一个由以下通用公式表示的化合物：或其药用可接受的盐或其溶剂化物，其中环A是C6-14芳基或类似物，L是—NReCO—或类似物（其中Re是氢原子或类似物），环B是C6-14芳基或类似物，X是C1-3烷基烯基或类似物，Y是单键或类似物，Z是C1-3烷基烯基或类似物，R1和R2各自独立地是氢原子或类似物，而R3、R4、R5和R6各自独立地是氢原子、卤原子或类似物，具有Aβ产生抑制作用或BACE1抑制作用，并且可用作由Aβ引起的以阿尔茨海默型痴呆为特征的神经退行性疾病的预防或治疗剂。
• NOVEL FUSED AMINODIHYDROTHIAZINE DERIVATIVE
  申请人：Motoki Takafumi

  公开号：US20100093999A1

  公开（公告）日：2010-04-15

  A compound represented by the general formula: wherein Ring A is a C 6-14 aryl group or the like, L is —NR L CO— or the like (wherein R L is a hydrogen atom or the like), Ring B is a C 6-14 aryl group or the like, X is a C 1-3 alkylene group or the like, Y is a C 1-3 alkylene group or the like, Z is an oxygen atom or the like, R 1 and R 2 are each independently a hydrogen atom or the like, and R 3 , R 4 , R 5 and R 6 are independently a hydrogen atom, a halogen atom or the like, or a pharmaceutically acceptable salt thereof, or a solvate thereof, has an Aβ production inhibitory effect or a BACE1 inhibitory effect and is useful as a therapeutic agent for a neurodegenerative disease caused by Aβ and typified by Alzheimer-type dementia.

  一个由通式表示的化合物：其中环A是C6-14芳基或类似物，L是—NRLCO—或类似物（其中RL是氢原子或类似物），环B是C6-14芳基或类似物，X是C1-3烷基烯基或类似物，Y是C1-3烷基烯基或类似物，Z是氧原子或类似物，R1和R2分别是独立的氢原子或类似物，R3、R4、R5和R6独立地是氢原子、卤原子或类似物，或其药用可接受盐，或其溶剂化物，具有Aβ产生抑制作用或BACE1抑制作用，并且可用作治疗Aβ引起的以阿尔茨海默型痴呆为特征的神经退行性疾病的治疗剂。
• [EN] DIHYDROBENZOFURANYL ALKANAMINE DERIVATIVES AS 5HT2C AGONISTS<br/>[FR] DERIVES DE DIHYDROBENZOFURANYLE ALCANAMINE SERVANT D'AGONISTES DE 5HT2C
  申请人：WYETH CORP

  公开号：WO2005044812A1

  公开（公告）日：2005-05-19

  Compounds of Formula (I) or pharmaceutically acceptable salts thereof are provided: Formula (I) which are agonists or partial agonists of the 2C subtype of brain serotonin receptors. The compounds, and compositions containing the compounds, can be used to treat a variety of central nervous system disorders such as schizophrenia.

  提供了化合物的公式(I)或其药用可接受的盐：公式(I)的化合物，它们是脑血清素受体2C亚型的激动剂或部分激动剂。这些化合物和含有这些化合物的组合物可用于治疗多种中枢神经系统疾病，如精神分裂症。