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1-benzyl-1,2,3,4-tetrahydro-8-methoxy-β-carboline-1-carboxylic acid | 29573-13-5

中文名称
——
中文别名
——
英文名称
1-benzyl-1,2,3,4-tetrahydro-8-methoxy-β-carboline-1-carboxylic acid
英文别名
1-benzyl-6-methoxy-2,3,4,9-tetrahydro-1H-β-carboline-1-carboxylic acid;1-Benzyl-6-methoxy-2,3,4,9-tetrahydropyrido[3,4-b]indole-1-carboxylic acid
1-benzyl-1,2,3,4-tetrahydro-8-methoxy-β-carboline-1-carboxylic acid化学式
CAS
29573-13-5
化学式
C20H20N2O3
mdl
——
分子量
336.39
InChiKey
YRUJFNBUZZDZPP-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):
    0.8
  • 重原子数:
    25
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    74.4
  • 氢给体数:
    3
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    重氮甲烷1-benzyl-1,2,3,4-tetrahydro-8-methoxy-β-carboline-1-carboxylic acid盐酸 作用下, 以 甲醇乙醚 为溶剂, 反应 24.0h, 生成 1-benzyl-1-carbomethoxy-1,2,3,4-tetrahydro-8-methoxy-β-carboline
    参考文献:
    名称:
    Improved synthesis and characterization of Pictet-Spengler adducts of phenylpyruvic acid and biogenic amines
    摘要:
    DOI:
    10.1021/jo00321a047
  • 作为产物:
    描述:
    5-甲氧基色胺(Z)-2-hydroxy-3-phenylacrylic acid乙醇 为溶剂, 反应 48.0h, 以93%的产率得到1-benzyl-1,2,3,4-tetrahydro-8-methoxy-β-carboline-1-carboxylic acid
    参考文献:
    名称:
    Improved synthesis and characterization of Pictet-Spengler adducts of phenylpyruvic acid and biogenic amines
    摘要:
    DOI:
    10.1021/jo00321a047
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文献信息

  • Beta-carboline compounds and analogues thereof as mitogen-activated protein kinase-activated protein kinase-2 inhibitors
    申请人:Anderson R. David
    公开号:US20050137220A1
    公开(公告)日:2005-06-23
    A method is described for inhibiting mitogen activated protein kinase-activated protein kinase-2 in a subject in need of such inhibition, where the method involves administering to the subject a beta-carboline MK-2 inhibiting compound, or a pharmaceutically acceptable salt thereof.
    本文描述了一种用于抑制需要这种抑制的受试者中的有丝分裂原活化蛋白激酶激活蛋白激酶-2的方法,其中该方法涉及向受试者施用一种β-喀啉MK-2抑制化合物或其药学上可接受的盐。
  • HUDLICKY T.; KUTCHAN T. M.; SHEN G.; SUTLIFF V. E.; COSCIA C. J., J. ORG. CHEM., 1981, 46, NO 8, 1738-1741
    作者:HUDLICKY T.、 KUTCHAN T. M.、 SHEN G.、 SUTLIFF V. E.、 COSCIA C. J.
    DOI:——
    日期:——
  • [EN] BETA-CARBOLINE COMPOUNDS AND ANALOGUES THEREOF AND THEIR USE AS MITOGEN-ACTIVATED PROTEIN KINASE-ACTIVATED PROTEIN KINASE-2 INHIBITORS<br/>[FR] COMPOSES DE BETA-CARBOLINE AINSI QUE LEURS ANALOGUES ET LEUR UTILISATION EN TANT QU'INHIBITEURS DE PROTEINE KINASE-2 ACTIVEE PAR PROTEINE KINASE ACTIVEE PAR DES MITOGENES
    申请人:PHARMACIA CORP
    公开号:WO2005009370A2
    公开(公告)日:2005-02-03
    Novel methods and compositions are described for inhibiting mitogen activated protein kinase-activated protein kinase-2 in a subject. The method involves administering to the subject a beta-carboline MK-2 inhibiting compound, or a pharmaceutically acceptable salt, or isomer thereof. The novel compositions are capable of inhibiting mitogen activated protein kinase-activated protein kinase-2 and analogues thereof. Pharmaceutical compositions and kits that include these compounds are also described.
  • Improved synthesis and characterization of Pictet-Spengler adducts of phenylpyruvic acid and biogenic amines
    作者:Tomas Hudlicky、Toni M. Kutchan、Grace Shen、Vincent E. Sutliff、Carmine J. Coscia
    DOI:10.1021/jo00321a047
    日期:1981.4
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