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(S)-2-[4-(4-benzyloxyphenoxy)phenoxy]-1-methylethylamine | 1204483-90-8

中文名称
——
中文别名
——
英文名称
(S)-2-[4-(4-benzyloxyphenoxy)phenoxy]-1-methylethylamine
英文别名
(2S)-1-[4-(4-phenylmethoxyphenoxy)phenoxy]propan-2-amine
(S)-2-[4-(4-benzyloxyphenoxy)phenoxy]-1-methylethylamine化学式
CAS
1204483-90-8
化学式
C22H23NO3
mdl
——
分子量
349.43
InChiKey
TXJNQDNQCYKYSX-KRWDZBQOSA-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):
    4.4
  • 重原子数:
    26
  • 可旋转键数:
    8
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    53.7
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • 9-membered fused ring derivative
    申请人:Shionogi & Co., Ltd.
    公开号:US10233156B2
    公开(公告)日:2019-03-19
    The purpose of the present invention is to provide novel compounds having ACC2 selective inhibitory activity. In addition, the present invention provides a pharmaceutical composition comprising the compound. A compound of Formula: or its pharmaceutically acceptable salt, wherein, R1 is substituted or unsubstituted fused aromatic heterocyclyl represented by Formula: wherein, ring B is 5-membered ring, ring C is 6-membered ring; ring A is substituted or unsubstituted non-aromatic carbocycle or the like; —L1— is —O—(CR6R7)m— or the like; —L2— is —O—(CR6R7)n— or the like; each R6 is independently hydrogen or the like; each R7 is independently hydrogen or the like; each m is independently an integer of 0, 1, 2 or 3; each n is independently an integer of 1, 2 or 3; R2 is substituted or unsubstituted alkyl; R3 is hydrogen or substituted or unsubstituted alkyl; R4 is substituted or unsubstituted alkylcarbonyl or the like.
    本发明的目的是提供具有 ACC2 选择性抑制活性的新型化合物。此外,本发明还提供了一种包含该化合物的药物组合物。 式的化合物: 或其药学上可接受的盐、 其中,R1 是由式表示的取代或未取代的融合芳香杂环基: 其中 环 B 是 5 元环,环 C 是 6 元环; 环 A 是取代或未取代的非芳香族碳环或类似物; -L1-是-O-(CR6R7)m-或类似物; -L2-是-O-(CR6R7)n-或类似物; 每个 R6 独立地为氢或类似物 每个 R7 独立地为氢或类似物; 每个 m 独立地为 0、1、2 或 3 的整数 每个 n 独立地为 1、2 或 3 的整数; R2 是取代或未取代的烷基; R3 是氢或取代或未取代的烷基; R4 是取代或未取代的烷基羰基或类似物。
  • [EN] HETEROCYCLIC COMPOUNDS, PROCESSES FOR THEIR PREPARATION, MEDICAMENTS COMPRISING THESE COMPOUNDS, AND THE USE THEREOF<br/>[FR] COMPOSÉS HÉTÉROCYCLIQUES, LEURS PROCÉDÉS DE PRÉPARATION, MÉDICAMENTS COMPRENANT LESDITS COMPOSÉS ET LEUR UTILISATION
    申请人:SANOFI AVENTIS
    公开号:WO2010003624A3
    公开(公告)日:2010-04-22
  • 9-MEMBERED FUSED RING DERIVATIVE
    申请人:Shionogi & Co., Ltd.
    公开号:US20180079727A1
    公开(公告)日:2018-03-22
    The purpose of the present invention is to provide novel compounds having ACC2 selective inhibitory activity. In addition, the present invention provides a pharmaceutical composition comprising the compound. A compound of Formula: or its pharmaceutically acceptable salt, wherein, R 1 is substituted or unsubstituted fused aromatic heterocyclyl represented by Formula: wherein, ring B is 5-membered ring, ring C is 6-membered ring; ring A is substituted or unsubstituted non-aromatic carbocycle or the like; -L 1 - is —O—(CR 6 R 7 )m- or the like; -L 2 - is —O—(CR 6 R 7 )n- or the like; each R 6 is independently hydrogen or the like; each R 7 is independently hydrogen or the like; each m is independently an integer of 0, 1, 2 or 3; each n is independently an integer of 1, 2 or 3; R 2 is substituted or unsubstituted alkyl; R 3 is hydrogen or substituted or unsubstituted alkyl; R 4 is substituted or unsubstituted alkylcarbonyl or the like.
  • US8470841B2
    申请人:——
    公开号:US8470841B2
    公开(公告)日:2013-06-25
  • HETEROCYCLIC COMPOUNDS, PROCESSES FOR THEIR PREPARATION, MEDICAMENTS COMPRISING THESE COMPOUNDS, AND THE USE THEREOF
    申请人:Zoller Gerhard
    公开号:US20110183998A1
    公开(公告)日:2011-07-28
    Heterocyclic derivatives, processes for their preparation, medicaments comprising these compounds, and the use thereof. The invention relates to compounds of the formula I in which the radicals R1, R2, R3, R4, W, A, B, D, E, G, L, M, R, T and Y have the stated meanings, and to the physiologically tolerated salts thereof. The compounds are suitable for example for the treatment of the metabolic syndrome, insulin resistance, obesity and diabetes.
    杂环衍生物、其制备方法、包含这些化合物的药物和其用途。本发明涉及式I中的化合物,其中基团R1、R2、R3、R4、W、A、B、D、E、G、L、M、R、T和Y具有所述的含义,并且其生理上可耐受的盐。该化合物适用于例如代谢综合征、胰岛素抵抗、肥胖和糖尿病的治疗。
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