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4-((2S)-2-{Benzyl[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]amino}-3-hydroxypropyl)phenol

中文名称
——
中文别名
——
英文名称
4-((2S)-2-{Benzyl[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]amino}-3-hydroxypropyl)phenol
英文别名
4-[(2S)-2-[benzyl-[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]amino]-3-hydroxypropyl]phenol
4-((2S)-2-{Benzyl[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]amino}-3-hydroxypropyl)phenol化学式
CAS
——
化学式
C24H26ClNO3
mdl
——
分子量
411.928
InChiKey
LEIDZKJNBONZDB-UPVQGACJSA-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):
    4.2
  • 重原子数:
    29
  • 可旋转键数:
    9
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    63.9
  • 氢给体数:
    3
  • 氢受体数:
    4

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • AMINOALCOHOL DERIVATIVES AND THEIR USE AS BETA 3 ADRENERGIC AGONISTS
    申请人:FUJISAWA PHARMACEUTICAL CO., LTD.
    公开号:EP1140849A1
    公开(公告)日:2001-10-10
  • [EN] AMINOALCOHOL DERIVATIVES AND THEIR USE AS BETA 3 ADRENERGIC AGONISTS<br/>[FR] AMINO-ALCOOLS ET LEUR UTILISATION COMME AGONISTES BETA-3 ADRENERGIQUES
    申请人:FUJISAWA PHARMACEUTICAL CO
    公开号:WO2000040560A1
    公开(公告)日:2000-07-13
    A compound of formula (I) wherein X1 is bond or -OCH2-; X2 is -(CH2)n-, in which n is 1, 2 or 3; X3 is bond, -O-, -S-, -OCH2-, or -NH-; R1 is phenyl or pyridyl each of which may have one or two substituent(s) selected from the group consisting of hydroxy, halogen, etc.; R2 is hydrogen, (lower)alkoxycarbonyl, etc.; R3 is hydroxy(lower)alkyl; halo(lower)alkyl, etc.; R4 is aryl or unsaturated heterocyclic group, each of which may have one or two substituent(s) selected from the group consisting of lower alkyl, hydroxy, carbamoyl, halogen, lower alkoxy, etc.; and a salt thereof which is useful as a medicament.
  • [EN] NEW AMINOALCOHOL DERIVATIVES<br/>[FR] NOUVEAUX DERIVES D'AMINOALCOOL
    申请人:FUJISAWA PHARMACEUTICAL CO
    公开号:WO2002000622A2
    公开(公告)日:2002-01-03
    The present invention relates to a compound of formula (I): wherein X1 is bond or -OCH2-; X2 is -(CH2)n-, in which n is 1 or 2; X3 is bond, -O- or -NH-; R1 is phenyl, indolyl or carbazolyl, each of which is optionally substituted with one or two substituent(s) selected from the group consisting of hydroxy, halogen, nitro, amino, formyl, (lower)alkylsulfonylamino, aryl(lower)alkoxy and hydroxy(lower)alkyl; R2 is hydrogen or aryl(lower)alkyl; R3 is hydrogen or hydroxy(lower)alkyl; R4 is aryl, 4-quinolyl, phthalazinyl, quinazolinyl, cinnolinyl or naphthyridinyl, each of which is optionally substituted with one or two substituent(s) defined in the specification, or a salt thereof. The compound (I) of the present invention and pharmaceutically acceptable salts thereof are useful for the prophylactic and/or the therapeutic treatment of pollakiurea or urinary incontinence.
  • Aminoalcohol derivatives and their use as beta 3 adrenergic agonists
    申请人:Fujisawa Pharmaceutical Co. Ltd.
    公开号:US20020143034A1
    公开(公告)日:2002-10-03
    A compound of the formula (I): 1 wherein X 1 is bond or —OCH 2 —; X 2 is —(CH 2 ) n —, in which n is 1, 2 or 3; X 3 is bond, —O—, —S—, —OCH 2 —, or —NH—; R 1 is phenyl or pyridyl each of which may have one or two substituent(s) selected from the group consisting of hydroxy, halogen, etc.; R 2 is hydrogen, (lower)alkoxycarbonyl, etc.; R 3 is hydroxy(lower)alkyl; halo(lower)alkyl, etc.; R 4 is aryl or unsaturated heterocyclic group, each of which may have one or two substituent(s) selected from the group consisting of lower alkyl, hydroxy, carbamoyl, halogen, lower alkoxy, etc.; and a salt thereof which is useful as a medicament.
    该化合物的结构式如下:其中X1是化学键或—OCH2—;X2是—(CH2)n—,其中n为1、2或3;X3是化学键,—O—,—S—,—OCH2—或—NH—;R1是苯基或吡啶基,每个基上可能有一个或两个亚基,如羟基、卤素等;R2是氢、(低)烷氧羰基等;R3是羟基(低)烷基、卤代(低)烷基等;R4是芳基或不饱和杂环基,每个基上可能有一个或两个亚基,如低烷基、羟基、氨基甲酰基、卤素、低烷氧基等;以及其盐,可用作药物。
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