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(9S)-9-ethyl-9-hydroxy-1-pentyl-2-propyl-1H,12H-pyrano[3",4":6',7']indolizino-[1',2':6,5]pyrido[4,3,2-de]quinazoline-10,13(9H,15H)-dione | 538374-81-1

中文名称
——
中文别名
——
英文名称
(9S)-9-ethyl-9-hydroxy-1-pentyl-2-propyl-1H,12H-pyrano[3",4":6',7']indolizino-[1',2':6,5]pyrido[4,3,2-de]quinazoline-10,13(9H,15H)-dione
英文别名
(10S)-10-ethyl-10-hydroxy-23-pentyl-22-propyl-8-oxa-4,15,21,23-tetrazahexacyclo[14.7.1.02,14.04,13.06,11.020,24]tetracosa-1,6(11),12,14,16(24),17,19,21-octaene-5,9-dione
(9S)-9-ethyl-9-hydroxy-1-pentyl-2-propyl-1H,12H-pyrano[3",4":6',7']indolizino-[1',2':6,5]pyrido[4,3,2-de]quinazoline-10,13(9H,15H)-dione化学式
CAS
538374-81-1
化学式
C29H32N4O4
mdl
——
分子量
500.597
InChiKey
UTGPCZXENDNUBY-LJAQVGFWSA-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):
    2.7
  • 重原子数:
    37
  • 可旋转键数:
    7
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    95.3
  • 氢给体数:
    1
  • 氢受体数:
    6

文献信息

  • Novel hexacyclic compounds
    申请人:——
    公开号:US20030144304A1
    公开(公告)日:2003-07-31
    The present invention relates to hexacyclic compound of the formula [1], 1 wherein Z, R 3 and R 4 are as identified therein, and pharmaceutically acceptable salts thereof. These compounds are useful in the treatment of cell proliferative disorders.
    本发明涉及公式[1]中的六环化合物,其中Z、R3和R4如所述,以及其药用可接受的盐。这些化合物可用于治疗细胞增殖性疾病。
  • Novel process for the preparation of hexacyclic compounds
    申请人:Fukuda Hiroshi
    公开号:US20060178376A1
    公开(公告)日:2006-08-10
    This invention relates to novel processes for the preparation of compounds of the formula [1], wherein R1, R2, R3 and R4 are as defined in the claims and description as well as pharmaceutically acceptable salts thereof. The compounds of the formula [1] are hexacyclic compounds having potent anti-tumor activity.
    本发明涉及一种制备公式[1]化合物的新型工艺,其中R1,R2,R3和R4如权利要求和说明书中所定义,并且它们的药学上可接受的盐。公式[1]化合物是具有强大的抗肿瘤活性的六环化合物。
  • Novel Process for the Preparation of Hexacyclic Compounds
    申请人:FUKUDA HIROSHI
    公开号:US20090312554A1
    公开(公告)日:2009-12-17
    This invention relates to novel processes for the preparation of compounds of the formula [1], wherein R 1 , R 2 , R 3 and R 4 are as defined in the claims and description as well as pharmaceutically acceptable salts thereof. The compounds of the formula [ 1 ] are hexacyclic compounds having potent anti-tumor activity.
    本发明涉及一种新的制备式[1]化合物的方法,其中R1、R2、R3和R4如权利要求和说明书中所定义,以及其药学上可接受的盐。式[1]化合物是具有强效抗肿瘤活性的六环化合物。
  • HEXACYCLIC COMPOUNDS
    申请人:CHUGAI SEIYAKU KABUSHIKI KAISHA
    公开号:EP1480984B9
    公开(公告)日:2009-03-11
  • CONDENSED CAMPTOTHECINS AS ANTITUMOR AGENTS
    申请人:CHUGAI SEIYAKU KABUSHIKI KAISHA
    公开号:EP1480984B1
    公开(公告)日:2008-06-11
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