摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1-Butanaminium, N,N-dibutyl-N-propyl- | 29814-64-0

中文名称
——
中文别名
——
英文名称
1-Butanaminium, N,N-dibutyl-N-propyl-
英文别名
tributyl(propyl)azanium
1-Butanaminium, N,N-dibutyl-N-propyl-化学式
CAS
29814-64-0
化学式
C15H34N+
mdl
——
分子量
228.44
InChiKey
OTMZBTFLNZOUEP-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):
    4.9
  • 重原子数:
    16
  • 可旋转键数:
    11
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

文献信息

  • [EN] COMPOUNDS<br/>[FR] COMPOSÉS
    申请人:GLAXOSMITHKLINE IP DEV LTD
    公开号:WO2015113452A1
    公开(公告)日:2015-08-06
    The present invention relates to novel compounds that inhibit LRRK2 kinase activity, processes for their preparation, to compositions containing them and to their use in the treatment of or prevention of diseases characterized by LRRK2 kinase activity, for example Parkinson's disease, Alzheimer's disease and amyotrophic lateral sclerosis (ALS).
    本发明涉及抑制LRRK2激酶活性的新化合物,其制备方法,含有它们的组合物,以及它们在治疗或预防由LRRK2激酶活性特征的疾病中的应用,例如帕金森病、阿尔茨海默病和肌萎缩侧索硬化症(ALS)。
  • [EN] DPP-IV INHIBITORS<br/>[FR] INHIBITEURS DE LA DPP-IV
    申请人:GRAFFINITY PHARMACEUTICALS AG
    公开号:WO2005095343A1
    公开(公告)日:2005-10-13
    The invention relates to compounds of formula (I), Z-C(R<1>R<2>)-C(R<3>NH2)-C(R<4>R<5>)-X-N(R<6>R<7>), wherein Z, R<1-7> and X have the meaning as cited in the description and the claims. Said compounds are useful as DPP-lV inhibitors. The invention also relates to the preparation of such compounds as well as the production and use thereof as medicament.
    该发明涉及式(I)的化合物,其中Z-C(R1R2)-C(R3NH2)-C(R4R5)-X-N(R6R7),其中Z,R1-7和X的含义如描述和权利要求中所述。所述化合物可用作DPP-IV抑制剂。该发明还涉及制备此类化合物以及其作为药物的生产和使用。
  • Ionic liquids miscible with various polar/non-polar solvents and method of preparing the same
    申请人:Lim Myong Hoon
    公开号:US20090253924A1
    公开(公告)日:2009-10-08
    Provided are an ionic liquid and a method of preparing the same. The ionic liquid includes at least one type of compound represented by (Cat + )(R′COO − ). Here, the Cat + is a cation selected from the group consisting of quaternary ammonium, quaternary phosphonium, sulfonium, imidazolium, pyridinium, pyrazolium, piperidinium, pyrrolium, pyrrolidinium, triazolium, and a mixture of two or more thereof, and R′ is a hydrocarbon comprising at least one unsaturated bond, and having 4 to 30 carbon atoms. The ionic liquid is partially or completely miscible with various polar and/or non-polar solvents, and may be used as a solvent, a solvent additive, an electrolyte, a heat carrier, a charge carrier, a heat carrier additive, a charge career additive, or a phase transfer catalyst, at room temperatures and below. Furthermore, the cost of manufacturing the ionic liquid can be reduced.
    提供了一种离子液体及其制备方法。该离子液体包括至少一种由(Cat+)(R′COO−)表示的化合物类型。这里,Cat+是从季铵盐、季磷盐、砜、咪唑盐、吡啶盐、吡唑盐、哌啶盐、吡咯盐、吡咯啉盐、三唑盐和两种或更多以上混合物组成的阳离子中选择的,R′是含有至少一条不饱和键的碳氢化合物,具有4至30个碳原子。该离子液体部分或完全与各种极性和/或非极性溶剂相容,并可用作溶剂、溶剂添加剂、电解质、热载体、电荷载体、热载体添加剂、电荷载体添加剂或相转移催化剂,在室温及以下温度下使用。此外,可以降低制造该离子液体的成本。
  • DPP-IV inhibitors
    申请人:Santhera Pharmaceuticals (Schweiz) GmbH
    公开号:EP1702916A1
    公开(公告)日:2006-09-20
    The invention relates to compounds of formula (I) wherein Z, R1-7, X and n have the meaning as cited in the description and the claims. Said compounds are useful as DPP-IV inhibitors. The invention also relates to the preparation of such compounds as well as the production and use thereof as medicament.
    该发明涉及式(I)的化合物,其中Z、R1-7、X和n的含义如描述和权利要求中所述。所述化合物可用作DPP-IV抑制剂。该发明还涉及制备这种化合物以及其作为药物的生产和使用。
  • Dpp-Iv Inhibitors
    申请人:Edwards Paul John
    公开号:US20080275086A1
    公开(公告)日:2008-11-06
    The invention relates to compounds of formula (I) wherein Z, R 1-7 , X and n have the meaning as cited in the description and the claims. Said compounds are useful as DPP-IV inhibitors. The invention also relates to the preparation of such compounds as well as the production and use thereof as medicament.
    本发明涉及公式(I)的化合物,其中Z,R1-7,X和n的含义如描述和权利要求所述。所述化合物可用作DPP-IV抑制剂。本发明还涉及制备这种化合物以及作为药物的生产和使用。
查看更多

同类化合物

(N-(2-甲基丙-2-烯-1-基)乙烷-1,2-二胺) (4-(苄氧基)-2-(哌啶-1-基)吡啶咪丁-5-基)硼酸 (11-巯基十一烷基)-,,-三甲基溴化铵 鼠立死 鹿花菌素 鲸蜡醇硫酸酯DEA盐 鲸蜡硬脂基二甲基氯化铵 鲸蜡基胺氢氟酸盐 鲸蜡基二甲胺盐酸盐 高苯丙氨醇 高箱鲀毒素 高氯酸5-(二甲氨基)-1-({(E)-[4-(二甲氨基)苯基]甲亚基}氨基)-2-甲基吡啶正离子 高氯酸2-氯-1-({(E)-[4-(二甲氨基)苯基]甲亚基}氨基)-6-甲基吡啶正离子 高氯酸2-(丙烯酰基氧基)-N,N,N-三甲基乙铵 马诺地尔 马来酸氢十八烷酯 马来酸噻吗洛尔EP杂质C 马来酸噻吗洛尔 马来酸倍他司汀 顺式环己烷-1,3-二胺盐酸盐 顺式氯化锆二乙腈 顺式吡咯烷-3,4-二醇盐酸盐 顺式双(3-甲氧基丙腈)二氯铂(II) 顺式3,4-二氟吡咯烷盐酸盐 顺式1-甲基环丙烷1,2-二腈 顺式-二氯-反式-二乙酸-氨-环己胺合铂 顺式-二抗坏血酸(外消旋-1,2-二氨基环己烷)铂(II)水合物 顺式-N,2-二甲基环己胺 顺式-4-甲氧基-环己胺盐酸盐 顺式-4-环己烯-1.2-二胺 顺式-4-氨基-2,2,2-三氟乙酸环己酯 顺式-2-甲基环己胺 顺式-2-(苯基氨基)环己醇 顺式-2-(氨基甲基)-1-苯基环丙烷羧酸盐酸盐 顺式-1,3-二氨基环戊烷 顺式-1,2-环戊烷二胺 顺式-1,2-环丁腈 顺式-1,2-双氨甲基环己烷 顺式--N,N'-二甲基-1,2-环己二胺 顺式-(R,S)-1,2-二氨基环己烷铂硫酸盐 顺式-(2-氨基-环戊基)-甲醇 顺-2-戊烯腈 顺-1,3-环己烷二胺 顺-1,3-双(氨甲基)环己烷 顺,顺-丙二腈 非那唑啉 靛酚钠盐 靛酚 霜霉威盐酸盐 霜脲氰