摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

ent-ruboxistaurine | 169940-29-8

中文名称
——
中文别名
——
英文名称
ent-ruboxistaurine
英文别名
(18R)-18-[(dimethylamino)methyl]-17-oxa-4,14,21-triazahexacyclo[19.6.1.17,14.02,6.08,13.022,27]nonacosa-1(28),2(6),7(29),8,10,12,22,24,26-nonaene-3,5-dione
ent-ruboxistaurine化学式
CAS
169940-29-8
化学式
C28H28N4O3
mdl
——
分子量
468.555
InChiKey
ZCBUQCWBWNUWSU-GOSISDBHSA-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:
    35
  • 可旋转键数:
    2
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    68.5
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    (R)-6,7,10,11-tetrahydro-9-[(dimethylamino)methyl]-5,21:12,17-dimetheno-9H-dibenzo[e,k]furo[3,4-h][1,4,13]oxadiazacyclohexadecine-18,20-dione 在 甲醇六甲基二硅氮烷 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 ent-ruboxistaurine
    参考文献:
    名称:
    Method of manufacturing ruboxistarin
    摘要:
    生产鲁博西他林的方法,包括以下步骤:制备L-2-去氧核糖-1-氰-3,4-二苯甲酸酯,然后去保护成为1-氰基L-2-去氧核糖,氧化断裂成(S)-4-羟基-2-(2-羟基乙氧基)-丁腈,并转化为甲磺酸(S)-3-氰基-3-(2-甲磺酰氧乙氧基)-丙基酯,然后与1-取代-3,4-双(3-吲哚基)马来酰亚胺偶联,得到9H,18H-5,21:12,17-二甲烯二苯并[e,k]吡咯并[3,4-h][1,4,13]噁二氮杂环十六烷-18,20(19H)-二酮,6,7,10,11-四氢-19-取代-9(S)-氰基,然后甲基化氨基团并去保护,形成5,21:12,17-二甲烯-9H-二苯并[e,k]呋喃[3,4-h][1,4,13]噁二氮杂环十六烷-18,20-二酮,6,7,10,11-四氢-9-[(二甲氨基)甲基]-,(S)- (9CI),最后一步是制备亚砜以形成鲁博西他林。
    公开号:
    EP2181999A1
点击查看最新优质反应信息

文献信息

  • Uses of chemicals to modulate GSK-3 signaling for treatment of bipolar disorder and other brain disorders
    申请人:Haggarty Stephen J.
    公开号:US20110008468A1
    公开(公告)日:2011-01-13
    Aspects of this invention are related, at least in part, to the use of chemical compounds able to inhibit GSK-3 and/or to stabilize β-catenin and formulations thereof. Some aspects of this invention relate to compositions comprising such compounds. Some aspects of the invention provide methods of using such compounds and/or compositions in the treatment of subjects having a neurological disease and/or psychiatric disorder. Some aspects of this invention provide methods of using ruboxistaurin, enzastaurin, sunitinib, midostaurin, lestaurtinib, 7-hydroxystaurosporine, and/or Chir99021 in the treatment of subjects having a neurological disease and/or psychiatric disorder. In some embodiments, compounds are administered in combination with Lithium.
  • METHODS OF TREATING HYPERPIGMENTATION DISORDERS
    申请人:CHROMADERM, INC.
    公开号:US20180185259A1
    公开(公告)日:2018-07-05
    Disclosed herein are compositions and methods of treating one or more symptom(s) related to a hyperpigmentation disorder.
  • US9265764B2
    申请人:——
    公开号:US9265764B2
    公开(公告)日:2016-02-23
  • [EN] METHODS OF TREATING HYPERPIGMENTATION DISORDERS<br/>[FR] MÉTHODES DE TRAITEMENT DE TROUBLES DE L'HYPERPIGMENTATION
    申请人:CHROMADERM INC
    公开号:WO2018118874A1
    公开(公告)日:2018-06-28
    Disclosed herein are compositions and methods of treating one or more symptom(s) related to a hyperpigmentation disorder.
  • Method of manufacturing ruboxistarin
    申请人:Zentiva, k.s.
    公开号:EP2181999A1
    公开(公告)日:2010-05-05
    Method of manufacturing ruboxistaurin, comprising the steps of preparation of L-2-deoxyribose 1-cyano-3,4-dibenzoate, followed by deprotection to 1-cyano L-2-deoxyribose, oxidative cleaving to (S)-4-hydroxy-2-(2-hydroxy-ethoxy)-butyronitrile and transformation to the methanesulfonic acid (S)-3-cyano-3-(2-methanesulfonyloxyethoxy)-propyl ester, then coupling with 1-substituted-3,4-bis(3-indolyl)maleimide leading to 9H,18H-5,21:12,17-dimethenodibenzo[e,k]pyrrolo[3,4-h][1,4,13] oxadiazacyclohexadecine-18,20(19H)-dione, 6,7,10,11-tetrahydro-19-substituted-9(S)-cyano, followed by methylation of the amino group and deprotection forming 5,21:12,17-dimetheno-9H-dibenzo[e,k]furo[3,4-h][1,4,13]oxadiazacyclohexadecine-18,20-dione, 6,7,10,11-tetrahydro-9-[(dimethylamino)methyl]-, (S)- (9CI), and the final step consisting of imido preparation to form ruboxistaurin.
    生产鲁博西他林的方法,包括以下步骤:制备L-2-去氧核糖-1-氰-3,4-二苯甲酸酯,然后去保护成为1-氰基L-2-去氧核糖,氧化断裂成(S)-4-羟基-2-(2-羟基乙氧基)-丁腈,并转化为甲磺酸(S)-3-氰基-3-(2-甲磺酰氧乙氧基)-丙基酯,然后与1-取代-3,4-双(3-吲哚基)马来酰亚胺偶联,得到9H,18H-5,21:12,17-二甲烯二苯并[e,k]吡咯并[3,4-h][1,4,13]噁二氮杂环十六烷-18,20(19H)-二酮,6,7,10,11-四氢-19-取代-9(S)-氰基,然后甲基化氨基团并去保护,形成5,21:12,17-二甲烯-9H-二苯并[e,k]呋喃[3,4-h][1,4,13]噁二氮杂环十六烷-18,20-二酮,6,7,10,11-四氢-9-[(二甲氨基)甲基]-,(S)- (9CI),最后一步是制备亚砜以形成鲁博西他林。
查看更多