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[(E)-octadec-9-enyl] 2,3-dihydroxypropanoate

中文名称
——
中文别名
——
英文名称
[(E)-octadec-9-enyl] 2,3-dihydroxypropanoate
英文别名
——
[(E)-octadec-9-enyl] 2,3-dihydroxypropanoate化学式
CAS
——
化学式
C21H40O4
mdl
——
分子量
356.5
InChiKey
JPJYKWFFJCWMPK-MDZDMXLPSA-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:
    25
  • 可旋转键数:
    19
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    66.8
  • 氢给体数:
    2
  • 氢受体数:
    4

文献信息

  • Compositions and methods for delivery of biologically active agents
    申请人:Khoo Shui-Mei
    公开号:US20070108405A1
    公开(公告)日:2007-05-17
    The present invention provides methods and compositions for the delivery of a biologically active agent to a biological system. The compositions include the active agent and a lyotropic phase and release of the active agent to the biological system is modified by the lyotropic phase.
    本发明提供了将生物活性物质传递到生物系统的方法和组合物。这些组合物包括活性物质和亲疏相,而亲疏相可以调节活性物质在生物系统中的释放。
  • Urea-, glycerate- and, hydroxyamide-headed hydrocarbon chain lyotropic phases forming surfactants
    申请人:Boyd James Benjamin
    公开号:US20050249665A1
    公开(公告)日:2005-11-10
    The invention provides a compound containing a head group based on urea, glycerol or glycerate and a tail selected from the group consisting of a branched alkyl chain, a branched alkyloxy chain or an alkenyl chain. The compounds may be used as surfactants to form a lyotropic phase that is stable in excess polar solution.
    本发明提供了一种化合物,其头部基团为尿素甘油甘油酸酯,尾部基团选自支链烷基、支链烷氧基或烯基。这些化合物可用作表面活性剂,形成在过量极性溶液中稳定的溶解相。
  • COMPOSITIONS AND METHODS FOR DELIVERY OF BIOLOGICALLY ACTIVE AGENTS
    申请人:FH Faulding & Co. Limited
    公开号:EP1667656A1
    公开(公告)日:2006-06-14
  • MODIFIED RELEASE DRUG POWDER COMPOSITION COMPRISING GASTRO-RETENTIVE RAFT FORMING SYSTEMS HAVING TRIGGER PULSE DRUG RELEASE
    申请人:Tris Pharma, Inc.
    公开号:US20220241189A1
    公开(公告)日:2022-08-04
    An orally administrable drug powder composition which forms a gastro-retentive RAFT having at least two trigger pulses is provided. The composition contains, at a minimum, (a) at least one drug in an immediate release pulse release form; (b) at least one drug in a delayed trigger release form; (c) at least one non-toxic gas generating agent and (d) a RAFT system, wherein following oral ingestion, the composition provides a self-assembling gastro-retentive RAFT having entrapped therein, the at least one drug of (a) and (b) and the gas generated in situ by the non-toxic gas generating agent, thereby providing a floating gastro-retentive RAFT having a dual pulse system wherein at least the second pulse is a trigger pulse and which retains the at least one drug in the stomach for at least about 3 hours, provided that the composition does not include a gamma hydroxybutyrate and its salts, hydrates, tautomers, or solvates, or complexes thereof.
  • [EN] COMPOSITIONS AND METHODS FOR DELIVERY OF BIOLOGICALLY ACTIVE AGENTS<br/>[FR] COMPOSITIONS ET PROCEDES POUR LA DELIVRANCE D'AGENTS BIOLOGIQUEMENT ACTIFS
    申请人:DBL AUSTRALIA PTY LTD
    公开号:WO2005021046A1
    公开(公告)日:2005-03-10
    The present invention provides methods and compositions for the delivery of a biologically active agent to a biological system. The compositions include the active agent and a lyotropic phase and release of the active agent to the biological system is modified by the lyotropic phase.
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