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罗索哌隆 | 2804-00-4

中文名称
罗索哌隆
中文别名
罗颂哌酮
英文名称
8-[4-(4-fluoro-phenyl)-4-oxo-butyl]-2-methyl-2,8-diaza-spiro[4.5]decane-1,3-dione
英文别名
Roxoperone;8-[4-(4-fluorophenyl)-4-oxobutyl]-2-methyl-2,8-diazaspiro[4.5]decane-1,3-dione
罗索哌隆化学式
CAS
2804-00-4
化学式
C19H23FN2O3
mdl
——
分子量
346.402
InChiKey
YJPFLFAWBYRCEH-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:
    205.2°C (rough estimate)
  • 密度:
    1.1708 (estimate)

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    25
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    57.7
  • 氢给体数:
    0
  • 氢受体数:
    5

安全信息

  • 海关编码:
    2933990090

SDS

SDS:c889a34b90a18c66e9b5d6ecf9bb3390
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文献信息

  • Diagnostic/therapeutic agents
    申请人:NYCOMED IMAGING AS
    公开号:US20040141922A1
    公开(公告)日:2004-07-22
    Targetable diagnostic and/or therapeutically active agents, e.g. ultrasound contrast agents, having reporters comprising gas-filled microbubbles stabilised by monolayers of film-forming surfactants, the reporter being coupled or linked to at least one vector.
    可定向诊断和/或治疗活性剂,例如超声对比剂,具有由单分子层膜形成表面活性剂稳定的充气微泡构成的报告物,该报告物与至少一个载体耦合或链接。
  • Controlled absorption water-soluble pharmaceutically active organic compound formulation for once-daily administration
    申请人:Counts David F.
    公开号:US10463611B2
    公开(公告)日:2019-11-05
    The present disclosure provides a once-daily water-soluble pharmaceutically active formulation for oral administration. In certain embodiments, the composition comprises a water-soluble pharmaceutically active organic compound incorporated into a small particulate, each particulate having a core of the water-soluble pharmaceutically active organic compound or an acceptable salt thereof in reversible association with a pharmaceutically acceptable drug-binding polymer. The core of the composition being surrounded by an insoluble water permeable membrane that is capable of delaying the dissolution of the pharmaceutically active compound therewithin and providing for extended release of the pharmaceutically active compound. In some embodiments, the formulation of the invention are designed to extend release of the pharmaceutically active organic compound for about 3 hours to about 8 hours, thereby enabling preparation of an extended release formulation for any pharmaceutically active compound with a half-life of from about 16 hours to about 21 hours.
    本公开提供了一种用于口服的每日一次溶性药用活性制剂。在某些实施方案中,该组合物包括掺入小颗粒中的溶性药用活性有机化合物,每个颗粒都有一个溶性药用活性有机化合物或其可接受盐的核心,该核心与药学上可接受的药物结合聚合物可逆结合。组合物的核心由不溶性透膜包围,该膜能够延迟其中的药用活性化合物的溶解,并延长药用活性化合物的释放时间。在某些实施方案中,本发明的制剂可将药用活性有机化合物的释放时间延长约 3 小时至约 8 小时,从而能够制备半衰期为约 16 小时至约 21 小时的任何药用活性化合物的缓释制剂。
  • LYOPHILIZATION PROCESS AND PRODUCTS OBTAINED THEREBY
    申请人:Scidose, Llc
    公开号:EP1954244A1
    公开(公告)日:2008-08-13
  • CONTROLLED ABSORPTION WATER-SOLUBLE PHARMACEUTICALLY ACTIVE ORGANIC COMPOUND FORMULATION FOR ONCE-DAILY ADMINISTRATION
    申请人:STI Pharma, LLC
    公开号:EP2717860A1
    公开(公告)日:2014-04-16
  • Methods and devices for the treatment of ocular conditions
    申请人:deJuan Eugene
    公开号:US20060110428A1
    公开(公告)日:2006-05-25
    Featured is a method for instilling one or more bioactive agents into ocular tissue within an eye of a patient for the treatment of an ocular condition, the method comprising concurrently using at least two of the following bioactive agent delivery methods (A)-(C): (A) implanting a sustained release delivery device comprising one or more bioactive agents in a posterior region of the eye so that it delivers the one or more bioactive agents into the vitreous humor of the eye; (B) instilling (e.g., injecting or implanting) one or more bioactive agents subretinally; and (C) instilling (e.g., injecting or delivering by ocular iontophoresis) one or more bioactive agents into the vitreous humor of the eye.
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