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双萘醋丙酯哌嗪 | 5061-22-3

中文名称
双萘醋丙酯哌嗪
中文别名
萘非维林;双萘丙酰氧乙哌嗪;萘维林;双萘酯哌嗪
英文名称
meso-1.4-Bis-<2-(2--propionyloxy)-ethyl>-piperazin
英文别名
Nafiverin;rac.-1.4-Bis-<2-(2--propionyloxy)-ethyl>-piperazin;2-naphthalen-1-yl-propionic acid 2,2'-piperazine-1,4-diyl-diethyl ester;Nafiverine;2-[4-[2-(2-naphthalen-1-ylpropanoyloxy)ethyl]piperazin-1-yl]ethyl 2-naphthalen-1-ylpropanoate
双萘醋丙酯哌嗪化学式
CAS
5061-22-3
化学式
C34H38N2O4
mdl
——
分子量
538.687
InChiKey
ZLFQARCCMWUSQE-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):
    6.7
  • 重原子数:
    40
  • 可旋转键数:
    12
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    59.1
  • 氢给体数:
    0
  • 氢受体数:
    6

文献信息

  • Technology for the Preparation of Microparticles
    申请人:Malakhov Michael
    公开号:US20090098207A1
    公开(公告)日:2009-04-16
    Microspheres are produced by contacting a solution of a macromolecule or small molecule in a solvent with an antisolvent and a counterion, and chilling the solution. The microspheres are useful for preparing pharmaceuticals, nutraceuticals, cosmetic products and the like of defined dimensions.
    微球是通过将溶液中的大分子或小分子与抗溶剂和对离子接触,并冷却溶液而制备的。这些微球可用于制备具有明确定义尺寸的药物、营养保健品、化妆品等产品。
  • Thiazolidinone, oxazolidinone, and imidazolone derivatives for treating non-inflammatory gastrointestinal tract disorders
    申请人:Fraser Oliver Matthew
    公开号:US20050113421A1
    公开(公告)日:2005-05-26
    A method is provided for using Cav2.2 subunit calcium channel modulators, particularly thiazolidinone, oxazolidinone, and imidazolone derivatives, to treat non-inflammatory gastrointestinal tract disorders.
    提供了一种方法,用于使用Cav2.2亚单位通道调节剂,特别是噻唑啉酮、噁唑啉酮和咪唑啉酮衍生物,来治疗非炎症性胃肠道疾病。
  • Compositions and methods to effect the release profile in the transdermal administration of active agents
    申请人:——
    公开号:US20020004065A1
    公开(公告)日:2002-01-10
    Compositions and methods for the transdermal delivery of active agents up to a period of seven days or more at substantially a zero-order release rate comprising a pharmaceutically acceptable adhesive matrix and a polymeric plastic material that provides a release rate regulating effect on the active agents.
    本发明涉及一种用于经皮递送活性药剂的组合物和方法,该组合物和方法能够在持续时间为七天或更长时间内以几乎零阶释放速率递送活性药剂,包括一种药学上可接受的粘合基质和一种聚合物塑料材料,该聚合物塑料材料对活性药剂具有释放速率调节作用。
  • Diagnostic/therapeutic agents
    申请人:Klaveness Jo
    公开号:US20050002865A1
    公开(公告)日:2005-01-06
    Targetable diagnostic and/or therapeutically active agents, e.g. ultrasound contrast agents, comprising a suspension in an aqueous carrier liquid of a reporter comprising gas-containing or gas-generating material, said agent being capable of forming at least two types of binding pairs with a target.
    可定位的诊断和/或治疗活性剂,例如超声对比剂,包括悬浮在载体液中的报告物,该报告物包含含气体或生成气体的材料,该剂能够与目标形成至少两种结合对。
  • METHODS FOR FINE PARTICLE MANUFACTURE
    申请人:Board of Regents, The University of Texas System
    公开号:US20150050345A1
    公开(公告)日:2015-02-19
    Processes for preparing micronized particles comprising a poorly water soluble bioactive agent are provided. The processes utilize a superheated aqueous phase which can serve as the continuous phase of an emulsion. The superheated aqueous phase can be used to melt poorly water soluble bioactive agents and/or matrix materials which them form molten droplets dispersed within the superheated aqueous phase. The size and size distribution of the molten droplets can be controlled using a variety of suitable methods. The molten droplets can then be cooled to form micronized particles comprising the poorly water soluble bioactive agent. If desired, the cooling rate can be selected to control the crystalline morphology of the resulting micronized particles.
    提供了制备含有难溶性生物活性剂的微粒子的过程。该过程利用超热相,可以作为乳液的连续相。超热相可以用于熔化难溶性生物活性剂和/或基质材料,形成分散在超热相中的熔融液滴。可以使用各种适当的方法来控制熔融液滴的大小和大小分布。然后,可以将熔融液滴冷却以形成含有难溶性生物活性剂的微粒子。如果需要,可以选择冷却速率来控制所得微粒子的晶体形态。
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