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2-Decyloxy-6-methyl-4H-3,1-benzoxazin-4-one | 282526-77-6

中文名称
——
中文别名
——
英文名称
2-Decyloxy-6-methyl-4H-3,1-benzoxazin-4-one
英文别名
2-Decoxy-6-methyl-3,1-benzoxazin-4-one
2-Decyloxy-6-methyl-4H-3,1-benzoxazin-4-one化学式
CAS
282526-77-6
化学式
C19H27NO3
mdl
——
分子量
317.428
InChiKey
XNXVOFLYSLWSPW-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

物化性质

  • 沸点:
    434.9±38.0 °C(Predicted)
  • 密度:
    1.07±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.5
  • 重原子数:
    23
  • 可旋转键数:
    10
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.58
  • 拓扑面积:
    47.9
  • 氢给体数:
    0
  • 氢受体数:
    4

文献信息

  • 2-Oxy-benzoxazinone derivatives for the treatment of obesity
    申请人:——
    公开号:US20030027821A1
    公开(公告)日:2003-02-06
    The use of a compound comprising formula (I): 1 (I) or a salt, ester, amide or prodrug therof in the inhibition of an enzyme whose preferred mode of action is to catalyse the hydrolysis of an ester functionality, e.g. in the control and inhibition of unwanted enzymes in products and processes. The compounds are also useful in medicine e.g. in the treatment of obesity and related conditions. The invention also relates to novel compounds within formula (I), to processes for preparing them and pharmaceutical compositions containing them. In formula (I) A is a 6-membered aromatic or heteroaromatic ring; and R 1 is a branched or unbranched alkyl (optionally interrupted by one or more oxygen atoms), alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, arylalkyl, reduced arylalkyl, arylalkenyl, heteroaryl, heteroarylalkyl, heteroarylalkenyl, reduced aryl, reduced heteroaryl, reduced heteroarylalkyl or a substituted derivative of any of the foregoing groups.
    公式(I)中包含的化合物的使用:1(I)或其盐、酯、酰胺或前药,在抑制一种首选作用模式是催化酯功能解的酶中的应用,例如在产品和过程中控制和抑制不需要的酶。这些化合物还在医学中有用,例如在肥胖和相关疾病的治疗中。本发明还涉及在公式(I)内的新化合物,用于制备它们的方法以及含有它们的药物组合物。在公式(I)中,A是一个6元芳香或杂芳环;R1是支链或直链烷基(可由一个或多个氧原子中断),烯烃基,炔烃基,环烷基,环烯烃基,芳基,芳基烷基,还原芳基烷基,芳基烯烃基,杂芳基,杂芳基烷基,杂芳基烯烃基,还原芳基,还原杂芳,还原杂芳烷基或上述任何一个基团的取代衍生物
  • Orlistat compositions
    申请人:——
    公开号:US20020035089A1
    公开(公告)日:2002-03-21
    A pharmaceutical combination or composition containing a lipase inhibitor, preferably orlistat, and a bile acid sequestrant is useful for treating obesity.
    一种含有脂肪酶抑制剂(最好是奥利司他)和胆酸螯合剂的药物组合或配方对治疗肥胖有效。
  • 2-Oxy-Benzoxazinone Derivatives for the Treatment of Obesity
    申请人:Hodson Harold Francis
    公开号:US20080161301A1
    公开(公告)日:2008-07-03
    The use of a compound comprising formula (I): or a salt, ester, amide or prodrug thereof in the inhibition of an enzyme whose preferred mode of action is to catalyse the hydrolysis of an ester functionality, e.g. in the control and inhibition of unwanted enzymes in products and processes. The compounds are also useful in medicine e.g. in the treatment of obesity and related conditions. The invention also relates to novel compounds within formula (I), to processes for preparing them and pharmaceutical compositions containing them. In formula (I) A is a 6-membered aromatic or heteroaromatic ring; and R 1 is a branched or unbranched alkyl (optionally interrupted by one or more oxygen atoms), alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, arylalkyl, reduced arylalkyl, arylalkenyl, heteroaryl, heteroarylalkyl, heteroarylalkenyl, reduced aryl, reduced heteroaryl, reduced heteroarylalkyl or a substituted derivative of any of the foregoing groups.
    使用式(I)的化合物或其盐、酯、酰胺或前药在抑制一种首选模式为催化酯官能团解的酶方面具有应用,例如在产品和过程中控制和抑制不需要的酶。该化合物也在医学上有用,例如在肥胖和相关疾病的治疗中。该发明还涉及式(I)内的新化合物,以及制备它们的过程和含有它们的药物组成物。 在式(I)中,A是6元芳香或杂芳香环;而R1是支链或非支链烷基(可选地被一个或多个氧原子打断)、烯基、炔基、环烷基、环烯基、芳基、芳基烷基、还原芳基烷基、芳基烯基、杂芳基、杂芳基烷基、杂芳基烯基、还原芳基、还原杂芳基、还原杂芳基烷基或上述任何基团的取代衍生物
  • 2-OXY-BENZOXAZINONE DERIVATIVES FOR THE TREATMENT OF OBESITY
    申请人:Hodson Harold Francis
    公开号:US20110065697A1
    公开(公告)日:2011-03-17
    The use of a compound comprising formula (I): or a salt, ester, amide or prodrug thereof in the inhibition of an enzyme whose preferred mode of action is to catalyse the hydrolysis of an ester functionality, e.g. in the control and inhibition of unwanted enzymes in products and processes. The compounds are also useful in medicine e.g. in the treatment of obesity and related conditions. The invention also relates to novel compounds within formula (I), to processes for preparing them and pharmaceutical compositions containing them. In formula (I) A is a 6-membered aromatic or heteroaromatic ring; and R 1 is a branched or unbranched alkyl (optionally interrupted by one or more oxygen atoms), alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, arylalkyl, reduced arylalkyl, arylalkenyl, heteroaryl, heteroarylalkyl, heteroarylalkenyl, reduced aryl, reduced heteroaryl, reduced heteroarylalkyl or a substituted derivative of any of the foregoing groups.
    使用公式(I)的化合物或其盐,酯,酰胺或前药在抑制其首选作用方式为催化酯官能团解的酶中的应用,例如在产品和过程中控制和抑制不需要的酶。该化合物在医学上也很有用,例如在肥胖和相关疾病的治疗中。该发明还涉及公式(I)内的新化合物、制备它们的过程以及含有它们的制药组合物。在公式(I)中,A是6元芳香或杂芳香环;R1是支链或直链烷基(可选地由一个或多个氧原子中断),烯基,炔基,环烷基,环烯基,芳基,芳基烷基,还原芳基烷基,芳基烯基,杂芳基,杂芳基烷基,杂芳基烯基,还原芳基,还原杂芳基,还原杂芳基烷基或任何上述基团的取代衍生物
  • Process for preparing a pharmaceutical composition
    申请人:——
    公开号:US20020018812A1
    公开(公告)日:2002-02-14
    A method for the preparation of compositions, preferably pharmaceutical compositions, in form of expanded, mechanically stable, lamellar, porous, sponge-like or foam structures out of solutions and dispersions results in a favored pharmaceutical product. This method comprises the steps of a) preparing a solution or a homogeneous dispersion of a liquid and a compound selected from the group consisting of one or more pharmaceutically active compounds, one or more pharmaceutically suitable excipients, and mixtures thereof, followed by b) the expansion of the solution or the homogeneous dispersion without boiling.
    一种从溶液和分散液中制备膨化的、机械稳定的、片状的、多孔的、海绵状的或泡沫状 的组合物(最好是药物组合物)的方法,可以制备出受青睐的药物产品。该方法包括以下步骤:a) 制备溶液或液体与选自一种或多种药用活性化合物、一种或多种药用赋形剂及其混合物的化合物的均匀分散液;b) 不经沸腾使溶液或均匀分散液膨胀。
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