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1-Isopropoxy-2-propanol, (R)- | 609847-70-3

中文名称
——
中文别名
——
英文名称
1-Isopropoxy-2-propanol, (R)-
英文别名
(2R)-1-propan-2-yloxypropan-2-ol
1-Isopropoxy-2-propanol, (R)-化学式
CAS
609847-70-3
化学式
C6H14O2
mdl
——
分子量
118.17
InChiKey
AFHJYKBGDDJSRR-ZCFIWIBFSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.4
  • 重原子数:
    8
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • NOVEL ISOXAZOLE DRIVATIVE
    申请人:Ishikawa Makoto
    公开号:US20110065739A1
    公开(公告)日:2011-03-17
    Disclosed is a compound represented by formula (I) or a pharmaceutically acceptable salt thereof, which has an agonistic activity on GPR120 and is therefore useful for the treatment of diabetes, obesity or hyperlipemia. [In formula (I), the A represents a phenyl group which may be substituted by a lower alkoxy group or the like; the 13 represents a bivalent group produced by removing two hydrogen atoms from a benzene ring which may be substituted by a halogen atom or the like; X represents a lower alkylene group having 2 to 4 carbon atoms in its main chain or the like, wherein a carbon atom constituting the main chain may be substituted by an oxygen atom or the like; and Y represents a hydrogen atom or the like.]
    揭示了一种由式(I)表示的化合物或其药学上可接受的盐,该化合物对GPR120具有激动活性,因此对于治疗糖尿病、肥胖或高脂血症是有用的。【在式(I)中,A代表可能被低烷氧基或类似物取代的苯基;13代表通过从苯环中去除两个氢原子而产生的二价基团,该苯环可能被卤素原子或类似物取代;X代表具有2至4个碳原子的低烷基基团或类似物,其中构成主链的碳原子可能被氧原子或类似物取代;Y代表氢原子或类似物。】
  • AZAINDOLIZINES AND METHODS OF USE
    申请人:Price Stephen
    公开号:US20110142826A1
    公开(公告)日:2011-06-16
    The invention relates to azaindolizines of formula I-a or I-b with anti-cancer and/or anti-inflammatory activity and more specifically to azaindolizines which inhibit MEK kinase activity. The invention provides compositions and methods useful for inhibiting abnormal cell growth or treating a hyperproliferative disorder, or treating an inflammatory disease in a mammal. The invention also relates to methods of using the compounds for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, or associated pathological conditions.
    本发明涉及具有抗癌和/或抗炎活性的公式I-a或I-b的氮杂吲哚咪唑,更具体地涉及抑制MEK激酶活性的氮杂吲哚咪唑。本发明提供了用于抑制异常细胞生长或治疗哺乳动物的增生性疾病或治疗炎症性疾病的组合物和方法。本发明还涉及使用该化合物进行哺乳动物细胞的体外、原位和体内诊断或治疗,或相关病理条件的方法。
  • SUBSTITUTED PYRIDINONE COMPOUNDS AS MEK INHIBITORS
    申请人:The Asan Foundation
    公开号:US20160108041A1
    公开(公告)日:2016-04-21
    The invention provides novel substituted heterocyclic compounds represented by Formula I and Formula II, or a pharmaceutically acceptable salt, solvate, polymorph, ester, tautomer or prodrug thereof, and a composition comprising these compounds. The compounds provided can be used as inhibitors of MEK and are useful in the treatment of inflammatory diseases, cancer and other hyperproliferative diseases. The invention further provides a method of treatment for inflammatory diseases, cancer and other hyperproliferative diseases in mammals, especially humans.
    本发明提供了一种新型取代杂环化合物,其由公式I和公式II表示,或其药学上可接受的盐、溶剂化合物、多晶形、酯、互变异构体或前药,以及包含这些化合物的组合物。所提供的化合物可用作MEK的抑制剂,并且在治疗炎症性疾病、癌症和其他增生性疾病方面非常有用。本发明还提供了一种治疗哺乳动物,特别是人类炎症性疾病、癌症和其他增生性疾病的方法。
  • NOVEL ISOXAZOLE DERIVATIVE
    申请人:MSD K.K.
    公开号:EP2298750A1
    公开(公告)日:2011-03-23
    Disclosed is a compound represented by formula (I) or a pharmaceutically acceptable salt thereof, which has an agonistic activity on GPR120 and is therefore useful for the treatment of diabetes, obesity or hyperlipemia. [In formula (I), the A represents a phenyl group which may be substituted by a lower alkoxy group or the like, or the like; the B represents a bivalent group produced by removing two hydrogen atoms from a benzene ring which may be substituted by a halogen atom or the like, or the like; X represents a lower alkylene group having 2 to 4 carbon atoms in its main chain or the like, wherein a carbon atom constituting the main chain may be substituted by an oxygen atom or the like; and Y represents a hydrogen atom or the like.]
    本发明公开了一种由式(I)代表的化合物或其药学上可接受的盐,该化合物对 GPR120 具有激动活性,因此可用于治疗糖尿病、肥胖症或高脂血症。式(I)中,A 代表苯基,可被低级烷氧基等取代;B 代表二价基团,通过从苯环中去除两个氢原子而产生,可被卤素原子等取代;X 代表低级亚烷基,其主链上有 2 至 4 个碳原子等,其中构成主链的一个碳原子可被氧原子等取代;Y 代表氢原子等。
  • POLYETHERS, METHODS OF MAKING SAME, AND USES THEREOF
    申请人:Coates Geoffrey W.
    公开号:US20140179895A1
    公开(公告)日:2014-06-26
    Isotactic polyethers, methods of making polyethers, and uses of polyethers. The polyethers have a chain transfer group formed from a chain transfer agent. The methods of making the polyethers use monoalcohol chain transfer agents or multifunctional chain transfer agents. The polyethers can be used in materials, such as polyurethanes, elastomers, thermoset plastics, and thermoplastics, and as non-ionic surfactants.
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