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2,4-dichloro-3-(2,4-dimethyl-quinolin-8-yloxymethyl)-N-{1-[4-(2-piperidin-4-yl-ethyl)-piperazine-1-carbonyl]-cyclopentyl}-benzenesulfonamide | 635697-34-6

中文名称
——
中文别名
——
英文名称
2,4-dichloro-3-(2,4-dimethyl-quinolin-8-yloxymethyl)-N-{1-[4-(2-piperidin-4-yl-ethyl)-piperazine-1-carbonyl]-cyclopentyl}-benzenesulfonamide
英文别名
2,4-dichloro-3-[(2,4-dimethylquinolin-8-yl)oxymethyl]-N-[1-[4-(2-piperidin-4-ylethyl)piperazine-1-carbonyl]cyclopentyl]benzenesulfonamide
2,4-dichloro-3-(2,4-dimethyl-quinolin-8-yloxymethyl)-N-{1-[4-(2-piperidin-4-yl-ethyl)-piperazine-1-carbonyl]-cyclopentyl}-benzenesulfonamide化学式
CAS
635697-34-6
化学式
C35H45Cl2N5O4S
mdl
——
分子量
702.745
InChiKey
KHIYBOHDGQYXDT-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):
    5.7
  • 重原子数:
    47
  • 可旋转键数:
    10
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    112
  • 氢给体数:
    2
  • 氢受体数:
    8

文献信息

  • [EN] BASIC NON-PEPTIDE BRADYKININ ANTAGONISTS AND PHARMACEUTICAL COMPOSITIONS THEREFROM<br/>[FR] ANTAGONISTES DE BRADYKININE NON PEPTIDIQUE DE BASE ET COMPOSITIONS PHARMACEUTIQUES A BASE DESDITS ANTAGONISTES
    申请人:MENARINI RICERCHE SPA
    公开号:WO2003103671A1
    公开(公告)日:2003-12-18
    Non-peptide compounds of formula (I) having activity as specific antagonists of bradykinin (BK) B2 receptor. The compounds are chemically characterized by the presence of an alpha, alpha-disubstituted amino acid at least one amino group, free or salified, or the corresponding ammonium quaternary salt. These BK receptor antagonists are a novel class of medicaments which can be used in all the disorders in which said receptors are involved.
    化学式为(I)的非肽类化合物具有作为布雷肽(BK) B2受体特异性拮抗剂的活性。这些化合物在化学上的特征是至少有一个基团存在α,α-二取代氨基酸,自由或盐化,或相应的盐。这些BK受体拮抗剂是一类新型药物,可用于所有涉及该受体的疾病中。
  • Basic non-peptide bradykinin antagonists and pharmaceutical compositions therefrom
    申请人:Calvani Federico
    公开号:US20060205712A1
    公开(公告)日:2006-09-14
    Non-peptide compounds of formula (I) having activity as specific antagonists of bradykinin (BK) B2 receptor. The compounds are chemically characterized by the presence of an alpha, alpha-disubstituted amino acid at least one amino group, free or salified, or the corresponding ammonium quaternary salt. These BK receptor antagonists are a novel class of medicaments which can be used in all the disorders in which said receptors are involved
    具有缓激肽(BK)B2 受体特异性拮抗剂活性的式(I)非肽化合物。这些化合物的化学特征是含有至少一个α-α-二取代氨基酸基团(游离的或盐化的)或相应的季盐。这些 BK 受体拮抗剂是一类新型药物,可用于治疗所有涉及上述受体的疾病。
  • BASIC NON-PEPTIDE BRADYKININ ANTAGONISTS AND PHARMACEUTICAL COMPOSITIONS THEREFROM
    申请人:Menarini Ricerche S.p.A.
    公开号:EP1513531A1
    公开(公告)日:2005-03-16
  • US7491825B2
    申请人:——
    公开号:US7491825B2
    公开(公告)日:2009-02-17
  • [EN] DIAGNOSIS, MONITORING, PROGNOSIS, PREVENTION AND TREATMENT OF ANEURYSMS<br/>[FR] DIAGNOSTIC, CONTRÔLE, PRONOSTIC, PRÉVENTION ET TRAITEMENT DES ANÉVRYSMES
    申请人:UNIV JAMES COOK
    公开号:WO2010127381A1
    公开(公告)日:2010-11-11
    The present invention relates generally to altering levels of components in the kallikrein-kinin system (KKS) to assist in preventing or treating aneurysms in an individual, and also to detecting the presence, determining the prognosis or monitoring the progression of an aneurysm by detecting aberrant expression of one or more genes in the kallikrein-kinin system (KKS). The invention also relates to methods for identifying agents that antagonise the KKS, and methods of producing agents comprising KKS antagonists for preventing or treating aneurysms.
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