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N-(5-chloro-2-methoxyphenyl)-3,5-bis(trifluoromethyl)benzene carbohydrazonamide | 202822-41-1

中文名称
——
中文别名
——
英文名称
N-(5-chloro-2-methoxyphenyl)-3,5-bis(trifluoromethyl)benzene carbohydrazonamide
英文别名
N-(5-Chloro-2-methoxyphenyl)-3,5-bis(trifluoromethyl) benzene carbohydrazonamide;N-amino-N'-(5-chloro-2-methoxyphenyl)-3,5-bis(trifluoromethyl)benzenecarboximidamide
N-(5-chloro-2-methoxyphenyl)-3,5-bis(trifluoromethyl)benzene carbohydrazonamide化学式
CAS
202822-41-1
化学式
C16H12ClF6N3O
mdl
——
分子量
411.734
InChiKey
JJTLMQIYPPPEAA-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):
    4.7
  • 重原子数:
    27
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    59.6
  • 氢给体数:
    2
  • 氢受体数:
    9

反应信息

  • 作为反应物:
    参考文献:
    名称:
    4,5-Diphenyltriazol-3-ones:  Openers of Large-Conductance Ca2+-Activated Potassium (Maxi-K) Channels
    摘要:
    A series of diphenyl-substituted heterocycles were synthesized and evaluated by electrophysiological techniques as openers of the cloned mammalian large-conductance, Call-activated potassium (maxi-K) channel. The series was designed from deannulation of known benzimidazolone maxi-K opener NS-004 (2) thereby providing an effective template for obtaining structure-activity-related information. The triazolone ring system was the most studied wherein 4,5-diphenyltriazol-3-one 6d (maxi-K = 158%) was identified as the optimal maxi-K channel opener.
    DOI:
    10.1021/jm010569q
  • 作为产物:
    参考文献:
    名称:
    4,5-Diphenyltriazol-3-ones:  Openers of Large-Conductance Ca2+-Activated Potassium (Maxi-K) Channels
    摘要:
    A series of diphenyl-substituted heterocycles were synthesized and evaluated by electrophysiological techniques as openers of the cloned mammalian large-conductance, Call-activated potassium (maxi-K) channel. The series was designed from deannulation of known benzimidazolone maxi-K opener NS-004 (2) thereby providing an effective template for obtaining structure-activity-related information. The triazolone ring system was the most studied wherein 4,5-diphenyltriazol-3-one 6d (maxi-K = 158%) was identified as the optimal maxi-K channel opener.
    DOI:
    10.1021/jm010569q
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文献信息

  • Diphenyl oxadiazolones as potassium channel modulators
    申请人:Bristol-Myers Squibb Company
    公开号:US05869509A1
    公开(公告)日:1999-02-09
    Novel compounds of Formula 1 are useful to treat disorders responsive to openers of the large conductance calcium-activated potassium channels: ##STR1## wherein "Het" is one of a select group of heterocyclic moieties; Z is independently for each occurrence selected from O or S; R.sup.a, R.sup.b and R.sup.c each are independently selected from hydrogen, halogen, OH, CF.sub.3, ##STR2## provided R.sup.c is not hydrogen; and when R.sup.a and R.sup.b are hydrogen, R.sup.c may be a heterocyclic moiety selected from the group consisting of imidazol-1-yl, morpholinomethyl, N-methylimidazol- 2-yl, and pyridinyl; R.sup.d and R.sup.e each are independently selected from hydrogen, halogen, CF.sub.3, NO.sub.2 or imidazol-1-yl; m, n and p each are independently selected from an integer of O or 1; and R.sup.f and R.sup.g each are independently hydrogen; C.sub.1-4 alkyl; or R.sup.f and R.sup.g, taken together with the nitrogen atom to which they are attached, is a heterocyclic moiety selected from the group consisting of N-methylpiperazine, morpholine, thiomorpholine, N-benzylpiperazine and imidazolinone.
    化合物1的新型化合物可用于治疗对大导电性钙激活钾通道开放剂反应的疾病:其中"Het"是一组特定的杂环基团之一;Z独立地为每次出现选择O或S;R.sup.a,R.sup.b和R.sup.c各自独立地选择氢,卤素,OH,CF.sub.3,provided R.sup.c不是氢;当R.sup.a和R.sup.b为氢时,R.sup.c可以是从咪唑-1-yl,morpholinomethyl,N-甲基咪唑-2-yl和吡啶基中选择的杂环基团之一;R.sup.d和R.sup.e各自独立地选择氢,卤素,CF.sub.3,NO.sub.2或咪唑-1-yl;m,n和p各自独立地选择O或1的整数;而R.sup.f和R.sup.g各自独立地选择氢;C.sub.1-4烷基;或R.sup.f和R.sup.g与它们所连接的氮原子一起选择从N-甲基哌嗪,morpholine,thiomorpholine,N-苄基哌嗪和咪唑啉酮中选择的杂环基团之一。
  • US06077861
    申请人:——
    公开号:——
    公开(公告)日:——
  • DIPHENYL HETEROCYCLES AS POTASSIUM CHANNEL MODULATORS
    申请人:Bristol-Myers Squibb Company
    公开号:EP0915856A1
    公开(公告)日:1999-05-19
  • EP0915856A4
    申请人:——
    公开号:EP0915856A4
    公开(公告)日:2006-04-12
  • US5869509A
    申请人:——
    公开号:US5869509A
    公开(公告)日:1999-02-09
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