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piperazinium(1+) hydrogen-L-tartrate | 133-36-8

中文名称
——
中文别名
——
英文名称
piperazinium(1+) hydrogen-L-tartrate
英文别名
piperitol;piperazine; mesotartrate;Piperazin; Mesotartrat;piperazine tartrate;Piperazin-tartrat;Piperate Tartrate;2,3-dihydroxybutanedioic acid;piperazine
piperazinium(1+) hydrogen-L-tartrate化学式
CAS
133-36-8
化学式
C4H6O6*C4H10N2
mdl
——
分子量
236.225
InChiKey
VNFVKWMKVDOSKT-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):
    -2.94
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    139
  • 氢给体数:
    6
  • 氢受体数:
    8

安全信息

  • 海关编码:
    2933599090

SDS

SDS:fb0850864fb5f1bb510b45b9d37f3b42
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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。
  • Azaindole derivatives as inhibitors of p38 kinase
    申请人:Mavunkel J. Babu
    公开号:US20050288299A1
    公开(公告)日:2005-12-29
    The invention is directed to methods to inhibit p38 kinase, preferably p38-α using compounds which are azaindoles wherein the azaindoles are coupled through a piperidine or piperazine type linker to another cyclic moiety.
    本发明涉及抑制p38激酶的方法,优选抑制p38-α,使用的化合物是氮杂吲哚,其中氮杂吲哚通过哌啶或哌嗪型连接剂与另一个环状基团耦合。
  • 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。
  • Transdermal drug delivery device including an occlusive backing
    申请人:Noven Pharmaceuticals, Inc.
    公开号:US10231938B2
    公开(公告)日:2019-03-19
    A transdermal drug delivery system for the topical application of one or more active agents contained in one or more polymeric and/or adhesive carrier layers, proximate to a non-drug containing polymeric backing layer which can control the delivery rate and profile of the transdermal drug delivery system by adjusting the moisture vapor transmission rate of the polymeric backing layer.
    一种透皮给药系统,用于局部应用一种或多种活性剂,这些活性剂包含在一个或多个聚合物和/或粘合剂载体层中,靠近一个不含药物的聚合物背层,该背层可通过调节聚合物背层的湿气透过率来控制透皮给药系统的给药速率和概况。
  • Technology for preparation of macromolecular microspheres
    申请人:Ansun Biopharma, Inc.
    公开号:US10583086B2
    公开(公告)日:2020-03-10
    Microspheres are produced by contacting an aqueous solution of a protein or other macromolecule with an organic solvent and a counterion, and chilling the solution. The microspheres are useful for preparing pharmaceuticals of defined dimensions.
    微球是通过将蛋白质或其他大分子的水溶液与有机溶剂和反离子接触,然后将溶液冷却而制成的。微球可用于制备特定尺寸的药物。
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