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(6Z,9Z,27Z,30Z)-pentatriaconta-6,9,27,30-tetraen-18-one | 1192363-14-6

中文名称
——
中文别名
——
英文名称
(6Z,9Z,27Z,30Z)-pentatriaconta-6,9,27,30-tetraen-18-one
英文别名
(6Z,9Z,27Z,30Z)-hexatriaconta-6,9,27,30-tetraen-18-one
(6Z,9Z,27Z,30Z)-pentatriaconta-6,9,27,30-tetraen-18-one化学式
CAS
1192363-14-6
化学式
C36H64O
mdl
——
分子量
512.904
InChiKey
CTMQDMMCQGNIRX-MAZCIEHSSA-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):
    14.1
  • 重原子数:
    37
  • 可旋转键数:
    29
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] IMPROVED AMINO LIPIDS AND METHODS FOR THE DELIVERY OF NUCLEIC ACIDS<br/>[FR] LIPIDES AMINÉS AMÉLIORÉS ET PROCÉDÉS D'ADMINISTRATION D'ACIDES NUCLÉIQUES
    申请人:TEKMIRA PHARMACEUTICALS CORP
    公开号:WO2010042877A1
    公开(公告)日:2010-04-15
    The present invention provides superior compositions and methods for the delivery of therapeutic agents to cells. In particular, these include novel lipids and nucleic acid-lipid particles that provide efficient encapsulation of nucleic acids and efficient delivery of the encapsulated nucleic acid to cells in vivo. The compositions of the present invention are highly potent, thereby allowing effective knock-down of specific target proteins at relatively low doses. In addition, the compositions and methods of the present invention are less toxic and provide a greater therapeutic index compared to compositions and methods previously known in the art.
    本发明提供了用于将治疗剂传递给细胞的优越组合物和方法。具体来说,这些包括新型脂质和核酸-脂质颗粒,能够有效地封装核酸并有效地将封装的核酸传递给体内的细胞。本发明的组合物具有高度的效力,因此可以以相对较低的剂量有效地降低特定靶蛋白的表达。此外,本发明的组合物和方法与先前在艺术领域中已知的组合物和方法相比,毒性更低,并提供更大的治疗指数。
  • CATIONIC LIPIDS AND USES THEREOF
    申请人:Dande Prasad A.
    公开号:US20100104629A1
    公开(公告)日:2010-04-29
    Cationic lipids, cationic lipid based drug delivery systems, ways to make them and methods of treating diseases using them are disclosed.
    本发明揭示了阳离子脂质、基于阳离子脂质的药物传递系统、制备它们的方法以及使用它们治疗疾病的方法。
  • COMPOSITIONS AND METHODS FOR THE DELIVERY OF NUCLEIC ACIDS
    申请人:Hope Michael J.
    公开号:US20110117125A1
    公开(公告)日:2011-05-19
    The present invention provides compositions and methods for the delivery of therapeutic agents to cells. In particular, these include novel lipids and nucleic acid-lipid particles that provide efficient encapsulation of nucleic acids and efficient delivery of the encapsulated nucleic acid to cells in vivo. The compositions of the present invention are highly potent, thereby allowing effective knock-down of specific target protein at relatively low doses. In addition, the compositions and methods of the present invention are less toxic and provide a greater therapeutic index compared to compositions and methods previously known in the art.
    本发明提供了递送治疗剂到细胞的组合物和方法。特别地,这些包括新型脂质和核酸-脂质颗粒,它们提供了核酸的高效封装和封装的核酸在体内细胞中的高效递送。本发明的组合物非常有效,因此可以在相对较低的剂量下有效地降低特定靶蛋白的表达。此外,本发明的组合物和方法比先前在艺术领域中已知的组合物和方法毒性更小,提供更大的治疗指数。
  • AMINO LIPIDS AND METHODS FOR THE DELIVERY OF NUCLEIC ACIDS
    申请人:Hope Michael J.
    公开号:US20110256175A1
    公开(公告)日:2011-10-20
    The present invention provides superior compositions and methods for the delivery of therapeutic agents to cells. In particular, these include novel lipids and nucleic acid-lipid particles that provide efficient encapsulation of nucleic acids and efficient delivery of the encapsulated nucleic acid to cells in vivo. The compositions of the present invention are highly potent, thereby allowing effective knock-down of specific target proteins at relatively low doses. In addition, the compositions and methods of the present invention are less toxic and provide a greater therapeutic index compared to compositions and methods previously known in the art.
    本发明提供了优越的组合物和方法,用于将治疗剂传递到细胞。特别是,这些包括新型脂质和核酸-脂质颗粒,可有效地封装核酸,并将封装的核酸高效地传递到体内的细胞中。本发明的组合物具有高度的效力,因此可以在相对较低的剂量下有效地敲低特定靶蛋白。此外,本发明的组合物和方法与先前已知的组合物和方法相比,毒性更小,提供更大的治疗指数。
  • IMPROVED AMINO LIPIDS AND METHODS FOR THE DELIVERY OF NUCLEIC ACIDS
    申请人:Arbutus Biopharma Corporation
    公开号:EP3225621A1
    公开(公告)日:2017-10-04
    The present invention provides superior compositions and methods for the delivery of therapeutic agents to cells. In particular, these include novel lipids and nucleic acid-lipid particles that provide efficient encapsulation of nucleic acids and efficient delivery of the encapsulated nucleic acid to cells in vivo. The compositions of the present invention are highly potent, thereby allowing effective knock-down of specific target proteins at relatively low doses. In addition, the compositions and methods of the present invention are less toxic and provide a greater therapeutic index compared to compositions and methods previously known in the art.
    本发明提供了向细胞输送治疗剂的优良组合物和方法。其中特别包括新型脂质和核酸-脂质颗粒,它们能有效封装核酸,并在体内将封装的核酸高效递送至细胞。本发明的组合物具有很高的效力,因此能以相对较低的剂量有效地敲除特定的靶蛋白。此外,与本领域以前已知的组合物和方法相比,本发明的组合物和方法毒性更低,治疗指数更高。
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