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Acefylline piperazine | 18833-13-1

中文名称
——
中文别名
——
英文名称
Acefylline piperazine
英文别名
2-(1,3-dimethyl-2,6-dioxopurin-7-yl)acetic acid;piperazine
Acefylline piperazine化学式
CAS
18833-13-1;1216768-50-1
化学式
C22H30N10O8
mdl
——
分子量
562.5
InChiKey
HAAJFUJFGYCCPU-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):
    -3.78
  • 重原子数:
    40
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    216
  • 氢给体数:
    4
  • 氢受体数:
    12

安全信息

  • 海关编码:
    2933990090

SDS

SDS:3d6493640d396f19ad1ce3632fd60a95
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文献信息

  • Drug production using non-cross reactive antibodies
    申请人:SYNBIOTICS CORPORATION
    公开号:EP0390612A1
    公开(公告)日:1990-10-03
    A method for producing low molecular weight compounds, which are capable of binding to a naturally occurring receptor and which can be used as drugs and which mimic the three dimensional surface structure of antibodies to drug molecules, are produced by first generating a non-cross reactive antibody to a drug and then producing a low molecular weight structural mimic of the antibody.
    一种生产低分子量化合物的方法,这些化合物能够与自然存在的受体结合,可用作药物,并且模仿抗体对药物分子的三维表面结构。这些化合物首先通过生成对药物的非交叉反应性抗体,然后生产出模仿抗体的低分子量结构模拟物。
  • 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。
  • 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。
  • CONTROLLED RELEASE PHARMACEUTICAL COMPOSITIONS FOR PROLONGED EFFECT
    申请人:Hemmingsen Pernille Hoyrup
    公开号:US20100239667A1
    公开(公告)日:2010-09-23
    Layered pharmaceutical composition suitable for oral use in the treatment of diseases where absorption takes place over a large part of the gastrointestinal tract. The composition comprising A) a solid inner layer comprising i) an active substance, and ii) one or more disintegrants/exploding agents, one of more effervescent agents or a mixture thereof. the solid inner layer being sandwiched between two outer layers B1) and B2), each outer layer comprising iii) a substantially water soluble and/or crystalline polymer or a mixture of substantially water soluble and/or crystalline polymers, the polymer being a polyglycol in the form of one of a) a homopolymer having a MW of at least about 100,000 daltons, and b) a copolymer having a MW of at least about 2,000 daltons, or a mixture thereof, and iv) an active substance, which is the same as in said solid inner layer A), and layer A being different from layer B, the layered composition being coated with a coating C) that has at least one opening exposing at least one surface of said outer layer, the coating being substantially insoluble in and impermeable to fluids and comprising a polymer, and the composition having a cylindrical form optionally with one or more tapered ends, wherein the ratio between the surface area of one end surface of the cylinder and the length of the cylinder is in a range of from 0.02 to 45 mm.
    分层制药组合物,适用于口服治疗吸收发生在胃肠道大部分的疾病。该组合物包括A) 一个固体内层,其中包括i) 一种活性物质,和ii) 一种或多种分散剂/爆炸剂,一种或多种泡腾剂或其混合物。该固体内层被夹在两个外层B1)和B2)之间,每个外层包括iii) 一种或多种溶性和/或结晶聚合物,或者溶性和/或结晶聚合物的混合物,聚合物为聚乙二醇,形式为a) 分子量至少为约100,000道尔顿的同聚物,和b) 分子量至少为约2,000道尔顿的共聚物,或其混合物,和iv) 一种活性物质,其与所述固体内层A)中的活性物质相同,且层A与层B不同,该分层组合物被涂覆有一种涂层C),该涂层具有至少一个开口,暴露出至少一个外层的表面,该涂层在液体中具有相当的不溶性和不透性,包括一种聚合物,该组合物具有圆柱形状,可选地具有一个或多个锥形端部,其中圆柱体的一个端面的表面积与圆柱体的长度之比在0.02至45毫米的范围内。
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