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(2,5-dioxopyrrolidin-1-yl) 4-[[1-[4-[3,5-bis[[(12aS)-8-methoxy-6-oxo-12a,13-dihydroindolo[2,1-c][1,4]benzodiazepin-9-yl]oxymethyl]-N-[2-[2-(2-methoxyethoxy)ethoxy]ethyl]anilino]butanoyl-methylamino]-2-methylpropan-2-yl]disulfanyl]butanoate | 1239586-83-4

中文名称
——
中文别名
——
英文名称
(2,5-dioxopyrrolidin-1-yl) 4-[[1-[4-[3,5-bis[[(12aS)-8-methoxy-6-oxo-12a,13-dihydroindolo[2,1-c][1,4]benzodiazepin-9-yl]oxymethyl]-N-[2-[2-(2-methoxyethoxy)ethoxy]ethyl]anilino]butanoyl-methylamino]-2-methylpropan-2-yl]disulfanyl]butanoate
英文别名
——
(2,5-dioxopyrrolidin-1-yl) 4-[[1-[4-[3,5-bis[[(12aS)-8-methoxy-6-oxo-12a,13-dihydroindolo[2,1-c][1,4]benzodiazepin-9-yl]oxymethyl]-N-[2-[2-(2-methoxyethoxy)ethoxy]ethyl]anilino]butanoyl-methylamino]-2-methylpropan-2-yl]disulfanyl]butanoate化学式
CAS
1239586-83-4
化学式
C66H75N7O14S2
mdl
——
分子量
1254.49
InChiKey
GZOSQCCAEDYTPH-GTMCEHENSA-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):
    5.5
  • 重原子数:
    89
  • 可旋转键数:
    32
  • 环数:
    10.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    268
  • 氢给体数:
    0
  • 氢受体数:
    19

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

  • 作为产物:
    描述:
    N-羟基丁二酰亚胺4-[[1-[4-[3,5-bis[[(12aS)-8-methoxy-6-oxo-12a,13-dihydroindolo[2,1-c][1,4]benzodiazepin-9-yl]oxymethyl]-N-[2-[2-(2-methoxyethoxy)ethoxy]ethyl]anilino]butanoyl-methylamino]-2-methylpropan-2-yl]disulfanyl]butanoic acid盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下, 以 二氯甲烷 为溶剂, 以45%的产率得到(2,5-dioxopyrrolidin-1-yl) 4-[[1-[4-[3,5-bis[[(12aS)-8-methoxy-6-oxo-12a,13-dihydroindolo[2,1-c][1,4]benzodiazepin-9-yl]oxymethyl]-N-[2-[2-(2-methoxyethoxy)ethoxy]ethyl]anilino]butanoyl-methylamino]-2-methylpropan-2-yl]disulfanyl]butanoate
    参考文献:
    名称:
    [EN] NOVEL BENZODIAZEPINE DERIVATIVES
    [FR] NOUVEAUX DÉRIVÉS DE BENZODIAZÉPINE
    摘要:
    该发明涉及具有抗增殖活性的新型苯二氮䓬啶衍生物,更具体地涉及具有式(I)和(II)的新型苯二氮䓬啶化合物,其中二氮䓬啶环(B)与杂环环(CD)融合,其中杂环环是双环的或式(III)的化合物,其中二氮䓬啶环(B)与杂环环(C)融合,其中杂环环是单环的。该发明提供了这些化合物的细胞毒性二聚体。该发明还提供了单体和二聚体的结合物。该发明进一步提供了使用该发明的化合物或结合物抑制异常细胞生长或治疗哺乳动物增殖性疾病的有效组合物和方法。该发明还涉及使用该发明的化合物或结合物进行体外、原位和体内诊断或治疗哺乳动物细胞或相关病理条件的方法。
    公开号:
    WO2010091150A1
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文献信息

  • NOVEL BENZODIAZEPINE DERIVATIVES
    申请人:Li Wei
    公开号:US20100203007A1
    公开(公告)日:2010-08-12
    The invention relates to novel benzodiazepine derivatives with antiproliferative activity and more specifically to novel benzodiazepines of formula (I) and (II), in which the diazepine ring (B) is fused with a heterocyclic ring (CD), wherein the heterocyclic ring is bicyclic or a compound of formula (III), in which the diazepine ring (B) is fused with a heterocyclic ring (C), wherein the heterocyclic ring is monocyclic. The invention provides cytotoxic dimers of these compounds. The invention also provides conjugates of the monomers and the dimers. The invention further provides compositions and methods useful for inhibiting abnormal cell growth or treating a proliferative disorder in a mammal using the compounds or conjugates of the invention. The invention further relates to methods of using the compounds or conjugates for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, or associated pathological conditions.
    本发明涉及具有抗增殖活性的新型苯二氮平衍生物,更具体地涉及公式(I)和(II)的新型苯二氮平,其中二氮平环(B)与杂环环(CD)融合,其中杂环环为双环或公式(III)的化合物,其中二氮平环(B)与杂环环(C)融合,其中杂环环为单环。本发明提供这些化合物的细胞毒性二聚体。本发明还提供单体和二聚体的结合物。本发明还提供使用该发明的化合物或结合物抑制异常细胞生长或治疗哺乳动物增殖性疾病的组合物和方法。本发明还涉及使用该化合物或结合物进行哺乳动物细胞的体外、原位和体内诊断或治疗,或相关病理条件的方法。
  • Benzodiazepine derivatives
    申请人:ImmunoGen, Inc.
    公开号:US10208127B2
    公开(公告)日:2019-02-19
    The invention relates to novel benzodiazepine derivatives with antiproliferative activity and more specifically to novel benzodiazepines of formula (I) and (II), in which the diazepine ring (B) is fused with a heterocyclic ring (CD), wherein the heterocyclic ring is bicyclic or a compound of formula (III), in which the diazepine ring (B) is fused with a heterocyclic ring (C), wherein the heterocyclic ring is monocyclic. The invention provides cytotoxic dimers of these compounds. The invention also provides conjugates of the monomers and the dimers. The invention further provides compositions and methods useful for inhibiting abnormal cell growth or treating a proliferative disorder in a mammal using the compounds or conjugates of the invention. The invention further relates to methods of using the compounds or conjugates for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, or associated pathological conditions.
    本发明涉及具有抗增殖活性的新型苯并二氮杂卓衍生物,更具体地说,涉及式(I)和(II)的新型苯并二氮杂卓,其中二氮杂卓环(B)与杂环(CD)融合,其中杂环为双环;或式(III)的化合物,其中二氮杂卓环(B)与杂环(C)融合,其中杂环为单环。本发明提供了这些化合物的细胞毒性二聚体。本发明还提供了单体和二聚体的共轭物。本发明进一步提供了使用本发明化合物或共轭物抑制哺乳动物异常细胞生长或治疗增殖性疾病的组合物和方法。本发明进一步涉及使用本发明化合物或共轭物体外、原位和体内诊断或治疗哺乳动物细胞或相关病理状况的方法。
  • US8426402B2
    申请人:——
    公开号:US8426402B2
    公开(公告)日:2013-04-23
  • US9550787B2
    申请人:——
    公开号:US9550787B2
    公开(公告)日:2017-01-24
  • [EN] NOVEL BENZODIAZEPINE DERIVATIVES<br/>[FR] NOUVEAUX DÉRIVÉS DE BENZODIAZÉPINE
    申请人:IMMUNOGEN INC
    公开号:WO2010091150A1
    公开(公告)日:2010-08-12
    The invention relates to novel benzodiazepine derivatives with antiproliferative activity and more specifically to novel benzodiazepines of formula (I) and (II), in which the diazepine ring (B) is fused with a heterocyclic ring (CD), wherein the heterocyclic ring is bicyclic or a compound of formula (III), in which the diazepine ring (B) is fused with a heterocyclic ring (C), wherein the heterocyclic ring is monocyclic. The invention provides cytotoxic dimers of these compounds. The invention also provides conjugates of the monomers and the dimers. The invention further provides compositions and methods useful for inhibiting abnormal cell growth or treating a proliferative disorder in a mammal using the compounds or conjugates of the invention. The invention further relates to methods of using the compounds or conjugates for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, or associated pathological conditions.
    该发明涉及具有抗增殖活性的新型苯二氮䓬啶衍生物,更具体地涉及具有式(I)和(II)的新型苯二氮䓬啶化合物,其中二氮䓬啶环(B)与杂环环(CD)融合,其中杂环环是双环的或式(III)的化合物,其中二氮䓬啶环(B)与杂环环(C)融合,其中杂环环是单环的。该发明提供了这些化合物的细胞毒性二聚体。该发明还提供了单体和二聚体的结合物。该发明进一步提供了使用该发明的化合物或结合物抑制异常细胞生长或治疗哺乳动物增殖性疾病的有效组合物和方法。该发明还涉及使用该发明的化合物或结合物进行体外、原位和体内诊断或治疗哺乳动物细胞或相关病理条件的方法。
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