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ISA-2011B

中文名称
——
中文别名
——
英文名称
ISA-2011B
英文别名
(2S,8S)-2-(5-chloro-1H-indol-3-yl)-6-methyl-13,15-dioxa-3,6-diazatetracyclo-[8.7.0.0(3,8).0(12,16)]heptadeca-1(10),11,16-triene-4,7-dione;(2S,8S)-2-(5-chloro-1H-indol-3-yl)-6-methyl-13,15-dioxa-3,6-diazatetracyclo-[8.7.0.0(3,8)0.0(12,16)]heptadeca-1(10),11,16-triene-4,7-dione;(2S,8S)-2-(5-chloro-1H-indol-3-yl)-6-methyl-13,15-dioxa-3,6-diazatetracyclo[8.7.0.03,8.012,16]heptadeca-1(17),10,12(16)-triene-4,7-dione
ISA-2011B化学式
CAS
——
化学式
C22H18ClN3O4
mdl
——
分子量
423.856
InChiKey
FSEZESVJDPKRDS-UWJYYQICSA-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):
    2.9
  • 重原子数:
    30
  • 可旋转键数:
    1
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    74.9
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

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文献信息

  • Indolyl-Substituted Pyrazino-Quinolines and Their Use for the Treatment of Cancer
    申请人:Persson Jenny
    公开号:US20120157461A1
    公开(公告)日:2012-06-21
    There is provided compounds of formula I, wherein the wedged bonds, R 1 , R 2 , R 3 , R 4 , R 5 , R 5a , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 , X and Y have meanings given in the description, and pharmaceutically-acceptable salts thereof, which compounds are useful in the treatment of cancer and conditions affected by inhibition of angiogenesis.
    提供的是公式I的化合物,其中斜线键、R1、R2、R3、R4、R5、R5a、R6、R7、R8、R9、R10、R11、R12、R13、R14、X和Y的含义如描述中所述,以及药用可接受的盐,这些化合物在治疗癌症和受血管生成抑制影响的状态中有用。
  • INDOLYL-SUBSTITUTED PYRAZINO-QUINOLINES AND THEIR USE FOR THE TREATMENT OF CANCER
    申请人:Everest Biosciences, Inc.
    公开号:US20140235644A1
    公开(公告)日:2014-08-21
    The disclosure describes compounds of formula I, wherein the wedged bonds, R 1 , R 2 , R 3 , R 4 , R 5 , R 5a , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 , X and Y have meanings given in the description, and pharmaceutically-acceptable salts thereof; and methods of using such compounds useful in the treatment of cancer and conditions affected by inhibition of angiogenesis. Also provided, are processes for the preparation of formula I, by reacting formula I with other compounds; and processes for the preparation of a pharmaceutical formulation by bringing into association, a compound of formula I, with therapeutic agents and/or a pharmaceutically-acceptable adjuvant, diluent, or carrier.
    本公开说明了式I的化合物,其中楔形键,R1,R2,R3,R4,R5,R5a,R6,R7,R8,R9,R10,R11,R12,R13,R14,X和Y具有在说明书中给出的含义,以及其药学上可接受的盐;以及使用这种化合物在癌症治疗和抑制血管生成影响的疾病治疗中的方法。还提供了通过将式I与其他化合物反应的方法制备式I的过程;以及通过将式I的化合物与治疗剂和/或药学上可接受的佐剂,稀释剂或载体结合而制备制药配方的过程。
  • US8754086B2
    申请人:——
    公开号:US8754086B2
    公开(公告)日:2014-06-17
  • [EN] INDOLYL-SUBSTITUTED PYRAZINO-QUINOLINES AND THEIR USE FOR THE TREATMENT OF CANCER<br/>[FR] PYRAZINO-QUINOLINES À SUBSTITUTION INDOLYLE ET LEUR UTILISATION DANS LE TRAITEMENT DU CANCER
    申请人:ONCOREL AB
    公开号:WO2010149944A1
    公开(公告)日:2010-12-29
    There is provided compounds of formula I, wherein the wedged bonds, R1, R2, R3, R4, R5, R5a, R6, R7, R8, R9, R10, R11, R12, R13, R14, X and Y have meanings given in the description, and pharmaceutically- acceptable salts thereof, which compounds are useful in the treatment of cancer and conditions affected by inhibition of angiogenesis.
  • Synthesis of C-1 indol-3-yl substituted tetrahydroisoquinoline derivatives via a Pictet–Spengler approach
    作者:Rikard Larsson、Narda Blanco、Martin Johansson、Olov Sterner
    DOI:10.1016/j.tetlet.2012.07.017
    日期:2012.9
    A protocol for the diastereoselective synthesis of C-1 indol-3-yl substituted tetrahydroisoquinoline derivatives via Pictet–Spengler condensation with L-DOPA or l-DOPA derivatives and 1H-indole-3-carbaldehydes is presented. The protocol is used for the successful synthesis of several tetrahydroisoquinolines as well as diketopiperazine fused analogues.
    提出了通过Pictet-Spengler缩合与L -DOPA或1- DOPA衍生物和1 H-吲哚-3-甲醛进行非对映选择性合成C-1吲哚-3-基取代的四氢异喹啉衍生物的方案。该方案用于成功合成几种四氢异喹啉以及二酮哌嗪融合的类似物。
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