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FluocinoloneAcetonide-13C3

中文名称
——
中文别名
——
英文名称
FluocinoloneAcetonide-13C3
英文别名
12,19-difluoro-11-hydroxy-8-(2-hydroxyacetyl)-6,6,9,13-tetramethyl-5,7-dioxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-14,17-dien-16-one
FluocinoloneAcetonide-13C3化学式
CAS
——
化学式
C24H30F2O6
mdl
——
分子量
452.5
InChiKey
FEBLZLNTKCEFIT-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):
    2.5
  • 重原子数:
    32
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    93.1
  • 氢给体数:
    2
  • 氢受体数:
    8

文献信息

  • CORTICOSTEROID CONJUGATES AND USES THEREOF
    申请人:Teicher Martin H.
    公开号:US20100056488A1
    公开(公告)日:2010-03-04
    The invention features corticosteroids conjugated to either a charged group or a bulky group in a manner that resists in vivo cleavage, the resulting conjugate is a peripherally acting steroid with reduced activity in the central nervous system. The invention provides a method for treating a patient having an inflammatory disease by administering to the patient a corticosteroid conjugate.
  • Oligomer-Corticosteroid Conjugates
    申请人:Zhang Wen
    公开号:US20100286107A1
    公开(公告)日:2010-11-11
    The invention provides corticosteroids that are chemically modified by covalent attachment of a water soluble oligomer. A compound of the invention, when administered by any of a number of administration routes, exhibits a reduced biological membrane crossing rate as compared to the biological membrane crossing rate of the corticosteroid not attached to the water soluble oligomer.
  • IMPLANTABLE DRUG DEPOT FOR WEIGHT CONTROL
    申请人:King Vanja Margareta
    公开号:US20110027340A1
    公开(公告)日:2011-02-03
    The present invention is directed to an implantable drug depot for weight control. The drug depot includes at least one biodegradeable polymer and at least one biologically active agent. Through the administration of an effective amount of the biologically active agent at or near a target site, one can control weight gain and/or reduce, prevent or treat obesity. When appropriate formulations are provided within biodegradable polymers, weight control or treatment can be conducted for at least five days and up to one hundred and thirty-five days.
  • OLIGOMER-CORTICOSTEROID CONJUGATES
    申请人:NAKTAR THERAPEUTICS
    公开号:US20140309398A1
    公开(公告)日:2014-10-16
    The invention provides corticosteroids that are chemically modified by covalent attachment of a water-soluble oligomer. A compound of the invention, when administered by any of a number of administration routes, exhibits different properties compared to the properties of the corticosteroid not attached to the water-soluble oligomer.
  • Fluocinolone Formulations in a Biodegradable Polymer Carrier
    申请人:Warsaw Orthopedic, Inc.
    公开号:US20160022704A1
    公开(公告)日:2016-01-28
    Effective treatments of pain and inflammation are provided. Through the administration of an effective amount of fluocinolone at or near a target site, one can reduce, prevent or treat inflammation and pain and autoimmune disorders. In various embodiments, fluocinolone formulations may be provided within biodegradable polymers to reduce, prevent or treat sciatic pain and/or inflammation. In various embodiments, prevent transplant rejection for at least twenty-five days. In some embodiments, the pain relief can be for at least fifty days, at least one hundred days, at least one hundred and thirty-five days or at least one hundred and eighty days.
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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mass
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ir
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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