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9-methoxymappicine | 142727-79-5

中文名称
——
中文别名
——
英文名称
9-methoxymappicine
英文别名
(+/-)-1-Methoxy-7-(1-hydroxypropyl)-8-methylindolizino[1,2-b]quinolin-9(11H)-one;1-Methoxy-7-(1-hydroxypropyl)-8-methylindolizino[1,2-b]quinolin-9(11H)-one;7-(1-hydroxypropyl)-1-methoxy-8-methyl-11H-indolizino[1,2-b]quinolin-9-one
9-methoxymappicine化学式
CAS
142727-79-5
化学式
C20H20N2O3
mdl
——
分子量
336.39
InChiKey
JNCFAGIFKYMLEO-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):
    1.8
  • 重原子数:
    25
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    62.7
  • 氢给体数:
    1
  • 氢受体数:
    4

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    9-methoxymappicine 在 phosphate buffer 、 lipase Amano PS (Pseudomonas cepacia) 、 potassium carbonate 作用下, 以 四氢呋喃吡啶甲醇 为溶剂, 反应 74.0h, 生成 (S)-9-methoxymappicine
    参考文献:
    名称:
    Enantioselective synthesis of (S)- and (R)-mappicines and their analogues
    摘要:
    The naturally occurring alkaloids, camptothecin and mappicine ketone were converted to racemic mappicine acetate which was enantioselectively hydrolyzed to (S)- and (R)-mappicines in high optical purity using baker's yeast and a lipase, Amano PS. Treatment of the racemic acetate with baker's yeast afforded (S)-mappicine while with Amano PS yielded (R)-mappicine. 9-Methoxycamptothecin and 9-methoxymappicine ketone underwent similar conversion to (S)- and (R)-9-methxymappicines. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(99)00397-x
  • 作为产物:
    描述:
    9-甲氧基喜树碱 在 sodium tetrahydroborate 作用下, 以 甲醇 为溶剂, 反应 2.12h, 生成 9-methoxymappicine
    参考文献:
    名称:
    Enantioselective synthesis of (S)- and (R)-mappicines and their analogues
    摘要:
    The naturally occurring alkaloids, camptothecin and mappicine ketone were converted to racemic mappicine acetate which was enantioselectively hydrolyzed to (S)- and (R)-mappicines in high optical purity using baker's yeast and a lipase, Amano PS. Treatment of the racemic acetate with baker's yeast afforded (S)-mappicine while with Amano PS yielded (R)-mappicine. 9-Methoxycamptothecin and 9-methoxymappicine ketone underwent similar conversion to (S)- and (R)-9-methxymappicines. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(99)00397-x
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文献信息

  • Substituted indolizino\x9b1,2-b!quinolinones
    申请人:SmithKline Beecham Corporation
    公开号:US05883255A1
    公开(公告)日:1999-03-16
    The present invention provides a method of treating viral infections by using antiviral substituted indolizino\x9b1,2-b!quinolinone compounds, antiviral substituted indolizino\x9b1,2-b!quinolinone compounds, and pharmaceutical compositions thereof.
    本发明提供了一种使用抗病毒取代吲哚并咔啉酮化合物,抗病毒取代吲哚并咔啉酮化合物和其药物组合物治疗病毒感染的方法。
  • Das; Madhusudhan, Journal of Chemical Research - Part S, 2000, # 10, p. 476 - 477
    作者:Das、Madhusudhan
    DOI:——
    日期:——
  • US5883255A
    申请人:——
    公开号:US5883255A
    公开(公告)日:1999-03-16
  • [EN] SUBSTITUTED INDOLIZINO[1,2-b]QUINOLINONES<br/>[FR] INDOLIZINO[1,2-b]QUINOLINONES SUBSTITUEES
    申请人:SMITHKLINE BEECHAM CORPORATION
    公开号:WO1993020818A1
    公开(公告)日:1993-10-28
    (EN) The present invention provides a method of treating viral infections by using antiviral substituted indolizinol[1,2-b]quinolinone compounds, and pharmaceutical compositions thereof.(FR) La présente invention se rapporte à un procédé pour traiter les infections virales à l'aide de composés antiviraux d'indolizino[1,2-b]quinolinone substitués, et des compositions pharmaceutiques de ceux-ci.
  • Enantioselective synthesis of (S)- and (R)-mappicines and their analogues
    作者:Biswanath Das、P. Madhusudhan
    DOI:10.1016/s0040-4020(99)00397-x
    日期:1999.6
    The naturally occurring alkaloids, camptothecin and mappicine ketone were converted to racemic mappicine acetate which was enantioselectively hydrolyzed to (S)- and (R)-mappicines in high optical purity using baker's yeast and a lipase, Amano PS. Treatment of the racemic acetate with baker's yeast afforded (S)-mappicine while with Amano PS yielded (R)-mappicine. 9-Methoxycamptothecin and 9-methoxymappicine ketone underwent similar conversion to (S)- and (R)-9-methxymappicines. (C) 1999 Elsevier Science Ltd. All rights reserved.
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