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tert-butyl-[(1S,2R)-1-(1,4-dihydro-2,3-benzoxazine-3-carbonyl)-2-phenylcyclopropyl]carbamic acid

中文名称
——
中文别名
——
英文名称
tert-butyl-[(1S,2R)-1-(1,4-dihydro-2,3-benzoxazine-3-carbonyl)-2-phenylcyclopropyl]carbamic acid
英文别名
——
tert-butyl-[(1S,2R)-1-(1,4-dihydro-2,3-benzoxazine-3-carbonyl)-2-phenylcyclopropyl]carbamic acid化学式
CAS
——
化学式
C23H26N2O4
mdl
——
分子量
394.5
InChiKey
WYPKZGRXBZXMJC-XXBNENTESA-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):
    3.2
  • 重原子数:
    29
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    70.1
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • NOVEL BINDER-DRUG CONJUGATES (ADCs) AND USE OF SAME
    申请人:SEATTLE GENETICS, INC.
    公开号:US20150246136A1
    公开(公告)日:2015-09-03
    The present patent application relates to novel binder-drug conjugates (ADCs) of N,N-dialkylauristatins directed against the target epidermal growth factor receptor (EGFR, gene ID 1956), effective metabolites of these ADCs, methods for producing these ADCs, use of these ADCs for treatment and or prevention of diseases as well as the use of these ADCs to produce pharmaceutical drugs for treatment and/or prevention of diseases, in particular hyperproliferative and/or angiogenic diseases such as cancer, for example. Such treatments may be administered as monotherapy or in combination with other pharmaceutical drugs or other therapeutic measures.
    本专利申请涉及针对靶向表皮生长因子受体(EGFR,基因ID 1956)的新型结合物-药物共轭物(ADCs)N,N-二烷基月桂酰基蛋白酶抑制剂,这些ADCs的有效代谢物,生产这些ADCs的方法,利用这些ADCs治疗和/或预防疾病,以及利用这些ADCs生产用于治疗和/或预防疾病的药物,特别是治疗高增殖和/或血管生成性疾病,如癌症。这种治疗可以作为单药疗法或与其他药物或其他治疗措施联合使用。
  • Novel Binder-Drug Conjugates (ADCs) and Use of Same
    申请人:Lerchen Hans-Georg
    公开号:US20140127240A1
    公开(公告)日:2014-05-08
    The present patent application relates to novel binder-drug conjugates (ADCs) of N,N-dialkylauristatins directed against the target epidermal growth factor receptor (EGFR, gene ID 1956), effective metabolites of these ADCs, methods for producing these ADCs, use of these ADCs for treatment and or prevention of diseases as well as the use of these ADCs to produce pharmaceutical drugs for treatment and/or prevention of diseases, in particular hyperproliferative and/or angiogenic diseases such as cancer, for example. Such treatments may be administered as monotherapy or in combination with other pharmaceutical drugs or other therapeutic measures.
    本专利申请涉及针对表皮生长因子受体(EGFR,基因ID 1956)的新型结合物-药物共轭物(ADCs)N,N-二烷基月桂酰基蛋白酶抑制剂,这些ADCs的有效代谢物,生产这些ADCs的方法,利用这些ADCs治疗和/或预防疾病以及利用这些ADCs生产用于治疗和/或预防疾病的药物,特别是治疗高增殖和/或血管生成性疾病,如癌症。这种治疗可以作为单药疗法或与其他药物或其他治疗措施联合使用。
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