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Tetrahydroharman-1,3-dicarbonsaeure | 18070-61-6

中文名称
——
中文别名
——
英文名称
Tetrahydroharman-1,3-dicarbonsaeure
英文别名
1,2,3,4-Tetrahydro-harman-1,3-dicarbonsaeure;1-methyl-2,3,4,9-tetrahydro-1H-β-carboline-1,3-dicarboxylic acid;1-methyl-1,2,3,4-tetrahydronorharman-1,3-dicarboxylic acid;(1xi,3S)-1,2,3,4-Tetrahydro-1-methyl-beta-carboline-1,3-dicarboxylic acid;1-methyl-2,3,4,9-tetrahydropyrido[3,4-b]indole-1,3-dicarboxylic acid
Tetrahydroharman-1,3-dicarbonsaeure化学式
CAS
18070-61-6
化学式
C14H14N2O4
mdl
——
分子量
274.276
InChiKey
ZKGAKYZRRFOFGK-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

物化性质

  • 熔点:
    >192°C (dec.)
  • 沸点:
    595.5±50.0 °C(Predicted)
  • 密度:
    1.461±0.06 g/cm3(Predicted)
  • 溶解度:
    可溶于DMSO(少许)、甲醇(少许)
  • 物理描述:
    Solid

计算性质

  • 辛醇/水分配系数(LogP):
    -1.2
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    102
  • 氢给体数:
    4
  • 氢受体数:
    5

SDS

SDS:2d1d71f91d2857f9fdf2c2c2e20b8f44
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反应信息

  • 作为反应物:
    描述:
    Tetrahydroharman-1,3-dicarbonsaeure甲醇 为溶剂, 反应 24.0h, 生成 harman
    参考文献:
    名称:
    Electrochemistry of natural products. 7. Oxidative decarboxylation of some tetrahydro-.beta.-carbolinecarboxylic acids
    摘要:
    DOI:
    10.1021/jo01298a045
  • 作为产物:
    描述:
    DL-色氨酸丙酮酸硫酸 为溶剂, 反应 12.0h, 以62%的产率得到Tetrahydroharman-1,3-dicarbonsaeure
    参考文献:
    名称:
    Electrochemistry of natural products. 7. Oxidative decarboxylation of some tetrahydro-.beta.-carbolinecarboxylic acids
    摘要:
    DOI:
    10.1021/jo01298a045
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文献信息

  • METHODS FOR TREATING CANCER AND NON-NEOPLASTIC CONDITIONS
    申请人:Almstead Neil
    公开号:US20120202763A1
    公开(公告)日:2012-08-09
    Compounds that selectively inhibit pathological production of human vascular endothelial growth factor (VEGF) and compositions comprising such Compounds are described. Compounds that inhibit viral replication or the production of viral RNA or DNA or viral protein and compositions comprising such Compounds are described. Also described are methods of reducing VEGF using such Compounds and methods for treating cancer and non-neoplastic conditions involving the administration of such Compounds. Further described are methods of inhibiting viral replication or the production of viral RNA or DNA or viral protein using such Compounds and methods for treating viral infections involving the administration of such Compounds. The Compounds may be administered as a single agent therapy or in combination with one or more additional therapies to a human in need of such treatments.
    本文介绍了选择性抑制人类血管内皮生长因子(VEGF)病理性产生的化合物以及包含这些化合物的组合物。本文还介绍了抑制病毒复制或病毒RNA或DNA或病毒蛋白质产生的化合物以及包含这些化合物的组合物。同时,本文还介绍了使用这些化合物减少VEGF的方法以及使用这些化合物治疗癌症和非肿瘤性疾病的方法。本文还介绍了使用这些化合物抑制病毒复制或病毒RNA或DNA或病毒蛋白质产生的方法以及使用这些化合物治疗病毒感染的方法。这些化合物可以作为单一治疗剂或与一个或多个其他治疗剂联合使用,用于治疗需要这些治疗的人类。
  • USE OF DERIVATIVES OF TETRAHYDRO-BETA-CARBOLINES AS ANTIMETASTATIC AGENTS
    申请人:F. HOFFMANN-LA ROCHE AG
    公开号:EP0891187B1
    公开(公告)日:2002-01-30
  • METHODS FOR TREATING NEUROFIBROMATOSIS
    申请人:Cao Liangxian
    公开号:US20120157401A1
    公开(公告)日:2012-06-21
    Methods for treating neurofibromatosis involving the administration of a compound that selectively inhibits pathological production of human VEGF are described. The compound can be administered as a single-agent therapy or in combination with one or more additional therapies to a human in need of such treatment.
  • METHODS FOR TREATING KAPOSI SARCOMA
    申请人:Cao Liangxian
    公开号:US20120157400A1
    公开(公告)日:2012-06-21
    Methods for treating Kaposi's sarcoma involving the administration of a compound that selectively inhibits pathological production of human VEGF are described. The compound can be administered as a single-agent therapy or in combination with one or more additional therapies to a human in need of such treatment.
  • METHODS FOR TREATING BRAIN TUMORS
    申请人:Cao Liangxian
    公开号:US20120157402A1
    公开(公告)日:2012-06-21
    Methods for treating brain tumors involving the administration of a compound that selectively inhibits pathological production of human VEGF are described. The compound can be administered as a single agent therapy or in combination with one or more additional therapies to a human in need of such treatment.
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