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1-(3,4-dichlorophenyl)-4-(3-iodopropyl)piperazine | 1384298-69-4

中文名称
——
中文别名
——
英文名称
1-(3,4-dichlorophenyl)-4-(3-iodopropyl)piperazine
英文别名
——
1-(3,4-dichlorophenyl)-4-(3-iodopropyl)piperazine化学式
CAS
1384298-69-4
化学式
C13H17Cl2IN2
mdl
——
分子量
399.102
InChiKey
ONVUOKFFQPSSGK-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):
    4.6
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    6.5
  • 氢给体数:
    0
  • 氢受体数:
    2

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

  • Arginase inhibitors and methods of use thereof
    申请人:AstraZeneca AB
    公开号:US09447122B2
    公开(公告)日:2016-09-20
    The present invention includes arginase enzyme inhibitors, compositions comprising these arginase inhibitors, and methods of treating or diagnosing conditions characterized either by abnormally high arginase activity or abnormally low nitric oxide levels in a mammal, comprising administering compositions of the invention to the mammal.
    本发明涉及精氨酸酶抑制剂,包括这些精氨酸酶抑制剂的组合物,以及治疗或诊断哺乳动物中精氨酸酶活性异常高或一氧化氮平异常低的情况的方法,包括向哺乳动物投予本发明的组合物。
  • ARGINASE INHIBITORS AND METHODS OF USE THEREOF
    申请人:Corridor Pharmaceuticals, Inc.
    公开号:EP2658580A1
    公开(公告)日:2013-11-06
  • US8894970B2
    申请人:——
    公开号:US8894970B2
    公开(公告)日:2014-11-25
  • US9447122B2
    申请人:——
    公开号:US9447122B2
    公开(公告)日:2016-09-20
  • [EN] ARGINASE INHIBITORS AND METHODS OF USE THEREOF<br/>[FR] INHIBITEURS DE L'ARGINASE ET LEURS PROCÉDÉS D'UTILISATION
    申请人:CORRIDOR PHARMACEUTICALS INC
    公开号:WO2012091757A1
    公开(公告)日:2012-07-05
    Arginase enzyme inhibitors are disclosed for treating or diagnosing conditions characterized either by abnormally high arginase activity or abnormally low nitric oxide levels in a mammal, comprising administering compositions of the invention to the mammal. The invention includes a composition comprising an alpha-amino acid compound, or a derivative thereof, or a salt thereof, wherein a first substituent and a second substituent are linked to the alpha-carbon of the compound. The first substituent comprises a moiety selected from the group consisting of a boronic acid and N-hydroxy guanidine. The second substituent comprises a proximal nitrogen atom, wherein the proximal nitrogen is basic, further wherein the proximal nitrogen is separated from the alpha-carbon by a chain of two, three or four carbons, with the proviso that the compound is not 2-amino-6-borono-2-(3-(piperazin-1-yl)propyl)hexanoic acid, 2-(3-(4-acetylpiperazin- 1-yl)propyl)-2-aminb-6-boronohexanoic acid, 2-amino-6-borono-2-(3-(4-(4-cyanobenzoyl)piperazin-1-yl)propyl hexanoic acid, or 2-amino -6-borono-2-(3-(4-(3-methoxyphenylcarbamoyl)piperazin-1 -yljpropyl) hexanoic acid.
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