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丙-2-基氧基环丙烷 | 5426-40-4

中文名称
丙-2-基氧基环丙烷
中文别名
——
英文名称
cyclopropyl isopropyl ether
英文别名
Propan-2-yloxycyclopropane
丙-2-基氧基环丙烷化学式
CAS
5426-40-4
化学式
C6H12O
mdl
——
分子量
100.161
InChiKey
VJWPDEOVRRJIGI-UHFFFAOYSA-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):
    1.4
  • 重原子数:
    7
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2909209000

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] ALLOSTERIC CHROMENONE INHIBITORS OF PHOSPHOINOSITIDE 3-KINASE (PI3K) FOR THE TREATMENT OF DISEASES ASSOCIATED WITH P13K MODULATION<br/>[FR] INHIBITEURS CHROMÉNONE ALLOSTÉRIQUES DE LA PHOSPHOINOSITIDE 3-KINASE (PI3K) POUR LE TRAITEMENT DE MALADIES ASSOCIÉES À LA MODULATION DE PI3K
    申请人:PETRA PHARMA CORP
    公开号:WO2021202964A1
    公开(公告)日:2021-10-07
    The disclosure relates to compounds of Formula (I) as allosteric chromenone inhibitors of phosphoinositide 3-kinase (PI3K) useful in the treatment of diseases or disorders associated with PI3K modulation, Formula (I), or a prodrug, solvate, enantiomer, stereoisomer, tautomer, or pharmaceutically acceptable salt thereof, wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, W, X, Y, s, and Ring A are as described herein.
    该披露涉及到式(I)的化合物,作为磷脂酰肌醇3-激酶(PI3K)的变构色酮抑制剂,在与PI3K调节相关的疾病或紊乱的治疗中有用,式(I),或其前药、溶剂化合物、对映体、立体异构体、互变异构体或其药学上可接受的盐,其中R1、R2、R3、R4、R5、R6、R7、R8、R9、W、X、Y、s和环A如本文所述。
  • ANTIVIRAL COMPOUNDS
    申请人:Alios BioPharma, Inc.
    公开号:US20160244460A1
    公开(公告)日:2016-08-25
    Disclosed herein are new antiviral compounds, together with pharmaceutical compositions that include one or more antiviral compounds, and methods of synthesizing the same. Also disclosed herein are methods of ameliorating and/or treating a paramyxovirus viral infection with one or more small molecule compounds. Examples of paramyxovirus infection include an infection caused by human respiratory syncytial virus (RSV).
    本文披露了新的抗病毒化合物,以及包括一个或多个抗病毒化合物的药物组合物,以及合成这些化合物的方法。本文还披露了使用一个或多个小分子化合物改善和/或治疗副粘病毒病毒感染的方法。副粘病毒感染的例子包括由人类呼吸道合胞病毒(RSV)引起的感染。
  • TETRAZOLINONE COMPOUND AND USE OF SAME
    申请人:Sumitomo Chemical Company, Limited
    公开号:US20160205935A1
    公开(公告)日:2016-07-21
    A tetrazolinone compound represented by formula (1): wherein R 1 , R 2 , R 3 , R 6 , R 7 , R 8 , R 9 , R 10 , and R 11 each independently represents a C1-C6 alkyl group optionally having one or more halogen atoms, etc.; R 4 , and R 5 each independently represents a hydrogen atom, etc.; Q represents any one group selected from Group P 2 (provided that the group optionally has one or more atoms or groups selected from Group P 1 ); and X represents an oxygen atom or a sulfur atom, has excellent control activity against pests.
    公式(1)所代表的四氮酮化合物: 其中R1、R2、R3、R6、R7、R8、R9、R10和R11分别独立地表示一个C1-C6烷基基团,可选地具有一个或多个卤素原子等;R4和R5分别独立地表示一个氢原子等;Q代表从P2组中选择的任一组(前提是该组可选地具有从P1组中选择的一个或多个原子或基团);X代表氧原子或硫原子,对害虫具有出色的控制活性。
  • PYRIDO[3,2-d]PYRIMIDINE PI3K DELTA INHIBITOR COMPOUNDS AND METHODS OF USE
    申请人:Castanedo Georgette
    公开号:US20110207713A1
    公开(公告)日:2011-08-25
    Formula I compounds, including stereoisomers, geometric isomers, tautomers, metabolites and pharmaceutically acceptable salts thereof, are useful for inhibiting the delta isoform of PI3K, and for treating disorders mediated by lipid kinases such as inflammation, immunological disorders, and cancer. Methods of using compounds of Formula I for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.
    Formula I 化合物,包括立体异构体、几何异构体、互变异构体、代谢物及其药学上可接受的盐,对抑制 PI3K 的δ异构体以及治疗由脂质激酶介导的疾病,如炎症、免疫性疾病和癌症,具有用途。公开了利用 Formula I 化合物在哺乳动物细胞中进行体外、体内和体内诊断、预防或治疗此类疾病,或相关病理条件的方法。
  • TETRAZOLINONE COMPOUNDS AND APPLICATIONS THEREOF
    申请人:SUMITOMO CHEMICAL COMPANY, LIMITED
    公开号:US20160150787A1
    公开(公告)日:2016-06-02
    A tetrazolinone compound represented by formula (1): wherein Q represents a 6-membered aromatic heterocyclic group optionally having one or more atoms or groups selected from Group P 1 , provided that a heteroatom constituting the heterocyclic group is a nitrogen atom, and the number of nitrogen atom is 1, 2, or 3; R 1 , R 2 , R 3 , and R 11 each represents a C1-C6 alkyl group optionally having one or more atoms or groups selected from Group P 2 ; R 4 and R 5 each represents a hydrogen atom, etc.; R 6 represents a C1-C6 alkyl group optionally having one or more halogen atoms, etc.; R 7 , R 8 , and R 9 each represents a hydrogen atom, etc.; and X represents an oxygen atom or a sulfur atom, has excellent control activity against pests.
    一种由式(1)表示的四唑酮化合物:其中Q代表一个6元芳香杂环基,可选地具有来自P1组的一个或多个原子或基团,前提是构成杂环基的杂原子为氮原子,且氮原子的数量为1、2或3;R1、R2、R3和R11分别代表一个C1-C6烷基基团,可选地具有来自P2组的一个或多个原子或基团;R4和R5各代表一个氢原子,等等;R6代表一个C1-C6烷基基团,可选地具有一个或多个卤原子,等等;R7、R8和R9各代表一个氢原子,等等;X代表一个氧原子或硫原子,对害虫具有出色的控制活性。
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