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(2-Hexadecanoyloxy-3-hydroxypropyl) octadec-9-enoate

中文名称
——
中文别名
——
英文名称
(2-Hexadecanoyloxy-3-hydroxypropyl) octadec-9-enoate
英文别名
——
(2-Hexadecanoyloxy-3-hydroxypropyl) octadec-9-enoate化学式
CAS
——
化学式
C37H70O5
mdl
——
分子量
594.9
InChiKey
DOZKMFVMCATMEH-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):
    14.2
  • 重原子数:
    42
  • 可旋转键数:
    35
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    72.8
  • 氢给体数:
    1
  • 氢受体数:
    5

文献信息

  • Pharmaceutical compositions having a modified vehicle
    申请人:——
    公开号:US20040170650A1
    公开(公告)日:2004-09-02
    A composition comprising: (a) one to three bioactive agents; and (b) a vehicle comprising; (i) a modified liquid carrier, and (ii) an unmodified liquid carrier wherein the ratio by volume of the modified liquid carrier to the unmodified liquid carrier is between 0.00001:99.99999 to less than 0.01:99.99, that provide the composition with predictable sustained-release properties and wherein immediately after manufacture of the composition, said composition can be administered to a host such that the one to three bioactive agents is released to the host on a sustained basis.
    一种组合物,包括 (a) 一至三种生物活性剂;和 (b) 一种载体,包括 (i) 改性液体载体,和 (ii) 未改性液体载体 其中,改性液体载体与未改性液体载体的体积比介于 0.00001:99.99999 至小于 0.01:99.99 之间,从而使该组合物具有可预测的持续释放特性,并且在制造该组合物后,可立即将所述组合物施用到宿主体内,从而使一至三种生物活性剂持续释放到宿主体内。
  • USE OF DIACYLOLYCEROLS FOR INCREASING THE MELANIN CONTENT IN MELANOCYTES
    申请人:TRUSTEES OF BOSTON UNIVERSITY
    公开号:EP0655907B1
    公开(公告)日:1999-04-28
  • PROCESS FOR THE PRODCUTION OF GLYCERIDES WITH LIPASES
    申请人:NIPPON SUISAN KAISHA, LTD.
    公开号:EP1300470B1
    公开(公告)日:2010-09-15
  • PHARMACEUTICAL COMPOSITIONS HAVING A MODIFIED VEHICLE
    申请人:Zoetis Services LLC
    公开号:EP1569693B1
    公开(公告)日:2016-12-28
  • Methods of measuring the dissolution rate of an analyte in a non-aqueous liquid composition
    申请人:——
    公开号:US20040115822A1
    公开(公告)日:2004-06-17
    The present invention provides a method of characterizing the transfer of an analyte from a non-aqueous liquid composition to an aqueous medium and in particular to an in vitro method for measuring the dissolution of a drug from a sustained release dosage form.
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