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2-Methyl-2-(piperazin-1-yl)propan-1-ol dihydrochloride | 873066-14-9

中文名称
——
中文别名
——
英文名称
2-Methyl-2-(piperazin-1-yl)propan-1-ol dihydrochloride
英文别名
2-methyl-2-piperazin-1-ylpropan-1-ol;dihydrochloride
2-Methyl-2-(piperazin-1-yl)propan-1-ol dihydrochloride化学式
CAS
873066-14-9
化学式
C8H20Cl2N2O
mdl
MFCD18917291
分子量
231.16
InChiKey
APPDNESLCCLETD-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):
    -0.34
  • 重原子数:
    13
  • 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:
    35.5
  • 氢给体数:
    4
  • 氢受体数:
    3

文献信息

  • NOVEL THIENOPYRROLE COMPOUNDS
    申请人:Wishart Neil
    公开号:US20110152243A1
    公开(公告)日:2011-06-23
    The invention provides a compound of Formula (I) pharmaceutically acceptable salts, pro-drugs, biologically active metabolites, stereoisomers and isomers thereof wherein the variable are defined herein. The compounds of the invention are useful for treating immunological and oncological conditions.
    该发明提供了公式(I)的化合物,包括药用盐、前药、生物活性代谢物、立体异构体和同分异构体,其中变量在此处定义。该发明的化合物可用于治疗免疫和肿瘤疾病。
  • Substituted N-arylsulfonylheterocyclic amines as gamma-secretase inhibitors
    申请人:Josien B. Hubert
    公开号:US20060040936A1
    公开(公告)日:2006-02-23
    This invention discloses novel gamma secretase inhibitors of the formula: wherein: L is —O—, —N(R 6 )—, —S—, —S(O)—, or —S(O 2 )—; R 1 is selected from the group consisting of aryl and heteroaryl; R 2 is selected from the group consisting of alkyl, —C(O)—Y, —X—C(O)—Y, -alkylene-X—C(O)—Y, -alkylene-C(O)—Y, -alkylene-cycloalkylene-X—C(O)—Y, -alkylene-cycloalkylene-C(O)—Y, -cycloalkylene-alkylene-X—C(O)—Y, -cycloalkylene-alkylene-C(O)—Y, -cycloalkylene-X—C(O)—Y, -cycloalkylene-C(O)—Y, -alkylene-cycloalkylene-alkylene-X—C(O)—Y, -alkylene-cycloalkylene-alkylene-C(O)—Y, aryl, and heteroaryl; R 3 is selected from the group consisting of aryl, heteroaryl, alkyl, cycloalkyl, arylalkyl, arylcycloalkyl, heteroarylalkyl, heteroarylcycloalkyl, arylheterocycloalkyl, and alkoxyalkyl; each R 4 and R 5 is independently selected from the group consisting of H and alkyl; and Y is selected from the group consisting of —NR 8 R 9 , —N(R 6 )—(CH 2 ) b —NR 8 R 9 , aryl, heteroaryl, alkyl, cycloalkyl, arylalkyl, arylcycloalkyl, heteroarylalkyl, heteroarylcycloalkyl, and arylheterocycloalkyl; or Y is selected from the group consisting of: One or more compounds of formula I, or formulations comprising such compounds, may be useful, e.g. in treating Alzheimer's Disease.
    本发明公开了式如下的新型γ 分泌酶抑制剂: 其中 L是-O-、-N(R 6 )-、-S-、-S(O)-或-S(O 2 )-; R 1 选自由芳基和杂芳基组成的组; R 2 选自由烷基、-C(O)-Y、-X-C(O)-Y、-亚烷基-X-C(O)-Y、-亚烷基-C(O)-Y、-亚烷基-环亚烷基-X-C(O)-Y、-亚烷基-环亚烷基-C(O)-Y、-环亚烷基-亚烷基-X-C(O)-Y-环亚烷基-亚烷基-C(O)-Y、-环亚烷基-亚烷基-X-C(O)-Y、-环亚烷基-亚烷基-X-C(O)-Y、-亚烷基-环亚烷基-亚烷基-C(O)-Y、芳基和杂芳基; R 3 选自由芳基、杂芳基、烷基、环烷基、芳基烷基、芳基环烷基、杂芳基烷基、杂芳基环烷基、芳基杂环烷基和烷氧基烷基组成的组; 每个 R 4 和 R 5 独立选自由 H 和烷基组成的组;以及 Y 选自 -NR 8 R 9 、-N(R 6 )-(CH 2 ) b -NR 8 R 9 、芳基、杂芳基、烷基、环烷基、芳基烷基、芳基环烷基、杂芳基烷基、杂芳基环烷基和芳基杂环烷基;或 Y 选自以下组成的组 一种或多种式 I 化合物或包含此类化合物的制剂可用于治疗阿尔茨海默病等。
  • SUBSTITUTED N-ARYLSULFONYLHETEROCYCLIC AMINES AS GAMMA-SECRETASE INHIBITORS
    申请人:Schering Corporation
    公开号:EP1789404B1
    公开(公告)日:2010-03-24
  • Substituted N-Arylsulfonylheterocyclic Amines As Gamma-Secretase Inhibitors
    申请人:Josien Hubert B.
    公开号:US20100087425A1
    公开(公告)日:2010-04-08
    This invention discloses novel gamma secretase inhibitors of the formula: wherein: L is —O—, —N(R 6 )—, —S—, —S(O)—, or —S(O 2 )—; R 1 is selected from the group consisting of aryl and heteroaryl; R 2 is selected from the group consisting of alkyl, —C(O)—Y, —X—C(O)—Y, -alkylene-X—C(O)—Y, -alkylene-C(O)—Y, -alkylene-cycloalkylene-X—C(O)—Y, -alkylene-cycloalkylene-C(O)—Y, -cycloalkylene-alkylene-X—C(O)—Y, -cycloalkylene-alkylene-C(O)—Y, -cycloalkylene-X—C(O)—Y, -cycloalkylene-C(O)—Y, -alkylene-cycloalkylene-alkylene-X—C(O)—Y, -alkylene-cycloalkylene-alkylene-C(O)—Y, aryl, and heteroaryl; R 3 is selected from the group consisting of aryl, heteroaryl, alkyl, cycloalkyl, arylalkyl, arylcycloalkyl, heteroarylalkyl, heteroarylcycloalkyl, arylheterocycloalkyl, and alkoxyalkyl; each R 4 and R 5 is independently selected from the group consisting of H and alkyl; and Y is selected from the group consisting of —NR 8 R 9 , —N(R 6 )—(CH 2 ) b —NR 8 R 9 , aryl, heteroaryl, alkyl, cycloalkyl, arylalkyl, arylcycloalkyl, heteroarylalkyl, heteroarylcycloalkyl, and aryl heterocycloalkyl; or Y is selected from the group consisting of: One or more compounds of formula I, or formulations comprising such compounds, may be useful, e.g. in treating Alzheimer's Disease.
  • US7763613B2
    申请人:——
    公开号:US7763613B2
    公开(公告)日:2010-07-27
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