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二甲基四碘 | 7601-55-0

中文名称
二甲基四碘
中文别名
——
英文名称
Metocurine Iodide
英文别名
(1S,16R)-9,10,21,25-tetramethoxy-15,15,30,30-tetramethyl-7,23-dioxa-15,30-diazoniaheptacyclo[22.6.2.23,6.18,12.118,22.027,31.016,34]hexatriaconta-3(36),4,6(35),8(34),9,11,18(33),19,21,24,26,31-dodecaene;diiodide
二甲基四碘化学式
CAS
7601-55-0
化学式
C40H48I2N2O6
mdl
——
分子量
906.6
InChiKey
DIGFQJFCDPKEPF-OIUSMDOTSA-L
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

  • 比旋光度:
    D22 +148 to +158° (c = 0.25)
  • 熔点:
    267-270

计算性质

  • 辛醇/水分配系数(LogP):
    1.46
  • 重原子数:
    50
  • 可旋转键数:
    4
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    55.4
  • 氢给体数:
    0
  • 氢受体数:
    8

ADMET

毒理性
  • 蛋白质结合
35% 在血浆中
35% in plasma
来源:DrugBank

安全信息

  • 危险等级:
    6.1(b)
  • 包装等级:
    III
  • 危险类别:
    6.1(b)
  • 危险品运输编号:
    UN 3249

SDS

SDS:0c0002f50f674a06e128ca076fe72ef1
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文献信息

  • PRODRUG COMPOSITIONS, PRODRUG NANOPARTICLES, AND METHODS OF USE THEREOF
    申请人:Washington University
    公开号:US20160279060A1
    公开(公告)日:2016-09-29
    The present invention encompasses prodrug compositions, nanoparticles comprising one or more prodrugs, and methods of use thereof.
    本发明涵盖了前药组合物、包含一种或多种前药的纳米粒子,以及其使用方法。
  • [EN] PRODRUG COMPOSITIONS AND METHODS OF TREATMENT<br/>[FR] COMPOSITIONS DE PROMÉDICAMENT ET PROCÉDÉS DE TRAITEMENT
    申请人:AQUESTIVE THERAPEUTICS INC
    公开号:WO2021087359A1
    公开(公告)日:2021-05-06
    Pharmaceutical compositions include a prodrug of epinephrine are described.
    药物组合物包括表述的肾上腺素前药。
  • Multi-functional ionic liquid compositions for overcoming polymorphism and imparting improved properties for active pharmaceutical, biological, nutritional, and energetic ingredients
    申请人:Rogers D. Robin
    公开号:US20070093462A1
    公开(公告)日:2007-04-26
    Disclosed are ionic liquids and methods of preparing ionic liquid compositions of active pharmaceutical, biological, nutritional, and energetic ingredients. Also disclosed are methods of using the compositions described herein to overcome polymorphism, overcome solubility and delivery problems, to control release rates, add functionality, enhance efficacy (synergy), and improve ease of use and manufacture.
    揭示了离子液体及制备活性药物、生物、营养和能量成分的离子液体组合物的方法。还揭示了利用本文描述的组合物的方法,以克服多型性、克服溶解度和输送问题、控制释放速率、增加功能性、增强功效(协同作用)以及改善易用性和制造工艺。
  • Physical, chemical, and isotopic (atomic) labels
    申请人:Pearl Technology Holdings, LLC.
    公开号:US20040258617A1
    公开(公告)日:2004-12-23
    Chemical or isotopic labels are added to, e.g., a potentially lethal drug formulation, to generate a unique chemical fingerprint. Combinations of chemical additives are mixed with the drug to aid in their isolation and identification, especially when such drugs are used for illicit purposes. When stable isotopes are incorporated into lethal drugs, the labeling process conveys a very unique internal chemical signature and greatly aids in the identification of the parent drug in body fluids and tissues. When heath-care providers become aware that certain drugs can now be easily tracked and identified in a victim, individuals may be reluctant to utilize these agents for ill purposes.
    化学或同位素标记被添加到例如潜在致命的药物配方中,以生成独特的化学指纹。化学添加剂的组合与药物混合在一起,以帮助其隔离和识别,尤其是当这些药物被用于非法目的时。当稳定同位素被纳入致命药物中时,标记过程传达了非常独特的内部化学签名,并极大地帮助在体液和组织中识别母药。当医疗保健提供者意识到某些药物现在可以轻松跟踪和识别受害者时,个人可能会不愿意将这些药物用于不良目的。
  • Anticoagulant contrast media
    申请人:Melton J. Laura
    公开号:US20050281746A1
    公开(公告)日:2005-12-22
    The present invention provides novel anticoagulant contrast agents, which comprise an organic scaffolding moiety, an organic anticoagulant moiety, and an imaging moiety. The invention also provides anticoagulant contrast media and methods of visualizing internal structures utilizing the novel anticoagulant contrast agents and anticoagulant contrast media.
    本发明提供了一种新型抗凝对比剂,包括有机支架基团、有机抗凝基团和成像基团。该发明还提供了抗凝对比介质和利用新型抗凝对比剂和抗凝对比介质来可视化内部结构的方法。
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