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1-methoxy-7,8,9,10-tetrahydro-6,11-dihydroxy-5,12-naphthacenequinone | 60314-06-9

中文名称
——
中文别名
——
英文名称
1-methoxy-7,8,9,10-tetrahydro-6,11-dihydroxy-5,12-naphthacenequinone
英文别名
6,11-Dihydroxy-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione
1-methoxy-7,8,9,10-tetrahydro-6,11-dihydroxy-5,12-naphthacenequinone化学式
CAS
60314-06-9
化学式
C19H16O5
mdl
——
分子量
324.333
InChiKey
DRMRBUBTZRGJST-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

  • 沸点:
    603.5±55.0 °C(Predicted)
  • 密度:
    1.430±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.6
  • 重原子数:
    24
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    83.8
  • 氢给体数:
    2
  • 氢受体数:
    5

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

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] PLATINUM-CONTAINING COMPOUNDS, AND RELATED COMPOSITIONS AND USES THEREOF<br/>[FR] COMPOSÉS CONTENANT DU PLATINE, COMPOSITIONS ASSOCIÉES ET LEURS UTILISATIONS
    申请人:MASSACHUSETTS INST TECHNOLOGY
    公开号:WO2020214436A1
    公开(公告)日:2020-10-22
    Platinum-containing compounds are generally described. Inventive compositions and uses thereof are also described.
    含铂化合物通常被描述。创新的组成和用途也被描述。
  • Synthesis, EPR, ENDOR and TRIPLE resonance investigations of anthracycline-related semiquinones
    作者:Hartmut B. Stegmann、Thomas Jülich、Ulrike Höfler、Paul Schuler、Wolfhard Koch、Karsten Krohn、Astrid Eickhoff
    DOI:10.1002/mrc.1260310510
    日期:1993.5
    substituted anthraquinones related to anthracyclines is described. One‐electron reduction of these compounds yields the corresponding semiquinones, which were characterized by EPR, ENDOR and TRIPLE resonance spectroscopy. The data indicate a rapid conformational interconversion of the cyclohexene moiety (ring A in the anthracyclines). The low‐temperature structures could be assigned to half‐chair conformers
    描述了与蒽环类相关的五种取代蒽醌的合成。这些化合物的单电子还原产生相应的半醌,其特征在于 EPR、ENDOR 和三重共振光谱。数据表明环己烯部分(蒽环类中的环 A)的快速构象相互转换。低温结构可以分配给半椅式构象异构体,其分裂常数和扭转角通过简单的计算得到。与已发表的结果相反,在 4 位引入取代基,扰乱了蒽醌的对称性,导致自旋密度分布发生显着变化。介绍了已知蒽醌自由基的重新解释和分配。
  • RECA INHIBITORS AND THEIR USES AS MICROBIAL INHIBITORS OR POTENTIATORS OF ANTIBIOTIC ACTIVITY
    申请人:Cottarel Guillaume
    公开号:US20110015137A1
    公开(公告)日:2011-01-20
    The present invention provides RecA inhibitors, compositions containing them, systems for identifying or characterizing them, and methods of using them.
  • CONJUGATES COMPRISING HYDROXYALKYL STARCH AND A CYTOTOXIC AGENT AND PROCESS FOR THEIR PREPARATION
    申请人:Knoller Helmut
    公开号:US20130178437A1
    公开(公告)日:2013-07-11
    The present invention relates to hydroxyalkyl starch (HAS) conjugates and to a method for preparing the hydroxyalkyl starch (HAS) conjugates, the hydroxyalkyl starch (HAS) conjugates comprising a hydroxyalkyl starch derivative and a cytotoxic agent, said conjugate having a structure according the following formula HAS′(-M) n wherein M is a residue of a cytotoxic agent, the cytotoxic agent comprising a carbonyl group, HAS′ is a residue of the hydroxyalkyl starch derivative comprising at least one functional group X, n is greater than or equal to 1, and wherein the cytotoxic agent is linked via the carbonyl function present in the cytotoxic agent to the functional group X comprised in the hydroxyalkyl starch derivative, wherein the linkage via the carbonyl function is a cleavable linkage, which is capable of being cleaved in vivo so as to release the cytotoxic agent.
  • [EN] DEGRADABLE COMPOUNDS AND METHODS OF USE THEREOF, PARTICULARLY WITH PARTICLE REPLICATION IN NON-WETTING TEMPLATES<br/>[FR] COMPOSÉS DÉGRADABLES ET LEURS PROCÉDÉS D'UTILISATION, IMPLIQUANT EN PARTICULIER UNE RÉPARTITION DES PARTICULES DANS DES MATRICES NON MOUILLANTES
    申请人:UNIV NORTH CAROLINA
    公开号:WO2009132265A2
    公开(公告)日:2009-10-29
    The present invention provides compounds that will degrade under specified conditions, methods of using such compounds, and compositions comprising such compounds. The degradable compounds of the invention may be characterized by the labile -Si-A-C- groups present in the compounds (A representing an atom, such as O, N, or S, or a group, such as C=O). The compounds may be incorporated into a composition that further may include a polymeric matrix and/or a cargo component. A wide variety of cargo components may also be used in the present invention. In particular embodiments, the cargo component comprises a drug or other therapeutic agent. Accordingly, the invention particularly provides pharmaceutical formulations and methods of delivering a drug or other therapeutic material.
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