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丙二醇月桂酸酯 | 37321-62-3

中文名称
丙二醇月桂酸酯
中文别名
——
英文名称
Dodecanoic acid, ester with 1,2-propanediol
英文别名
dodecanoic acid;propane-1,2-diol
丙二醇月桂酸酯化学式
CAS
37321-62-3
化学式
C15H32O4
mdl
——
分子量
276.41
InChiKey
LLRANSBEYQZKFY-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:
    138-141 °C(Press: 0.6 Torr)
  • 密度:
    0.913 at 20℃
  • LogP:
    4.63-11.09 at 20℃

计算性质

  • 辛醇/水分配系数(LogP):
    3.35
  • 重原子数:
    19
  • 可旋转键数:
    11
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.93
  • 拓扑面积:
    77.8
  • 氢给体数:
    3
  • 氢受体数:
    4

安全信息

  • WGK Germany:
    3

反应信息

  • 作为产物:
    参考文献:
    名称:
    PHARMACEUTICAL COMPOSITION FOR ORAL ADMINISTRATION OF A PYRAZOLE-3-CARBOXAMIDE DERIVATIVE
    摘要:
    本发明揭示和声明了一种药物组合物,其为液体或半液体形式,在水介质中自我乳化或自我微乳化,用于口服吡唑-3-羧酰胺衍生物,其中所述衍生物溶解在含有一种或多种脂溶剂和非离子亲水性表面活性剂的两性分子混合物中。
    公开号:
    US20060264469A1
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文献信息

  • [EN] PHENOTHIAZINE DERIVATIVES AND USES THEREOF<br/>[FR] DÉRIVÉS DE PHÉNOTHIAZINE ET LEURS UTILISATIONS
    申请人:CAMP4 THERAPEUTICS CORP
    公开号:WO2019195789A1
    公开(公告)日:2019-10-10
    The present invention provides phenothiazine compounds, processes for their preparation, pharmaceutical compositions comprising the compounds, and the use of the compounds or the compositions in the treatment of various diseases or conditions, for example ribosomal disorders and ribosomopathies, e.g. Diamond Blackfan anemia (DBA).
    本发明提供了吩噻嗪化合物,其制备方法,包含该化合物的药物组合物,以及在治疗各种疾病或症状中使用该化合物或组合物,例如核糖体紊乱和核糖体病,例如钻石-布莱克范贫血(DBA)。
  • Controlled-release compositions containing opioid agonist and antagonist
    申请人:——
    公开号:US20020010127A1
    公开(公告)日:2002-01-24
    Controlled-release dosage forms containing an opioid agonist; an opioid antagonist; and a controlled release material release during a dosing interval an analgesic or sub-analgesic amount of the opioid agonist along with an amount of said opioid antagonist effective to attenuate a side effect of said opioid agonist. The dosage form provides analgesia for at least about 8 hours when administered to human patients. In other embodiments, the dose of antagonist released during the dosing interval enhances the analgesic potency of the opioid agonist.
    含有阿片激动剂、阿片拮抗剂和受控释放材料的控释剂型,其在给药间隔期间释放阿片激动剂的镇痛或亚镇痛量以及足以减轻所述阿片激动剂的副作用的阿片拮抗剂的量。当给予人类患者时,该剂型提供至少约8小时的镇痛作用。在其他实施例中,给药间隔期释放的拮抗剂剂量增强了阿片激动剂的镇痛效力。
  • [EN] LYMPHATIC SYSTEM-DIRECTING LIPID PRODRUGS<br/>[FR] PROMÉDICAMENTS LIPIDIQUES ORIENTANT VERS LE SYSTÈME LYMPHATIQUE
    申请人:ARIYA THERAPEUTICS INC
    公开号:WO2019046491A1
    公开(公告)日:2019-03-07
    The present invention provides lymphatic system-directing lipid prodrugs, pharmaceutical compositions thereof, methods of producing such prodrugs and compositions, as well as methods of improving the bioavailability or other properties of a therapeutic agent that comprises part of the lipid prodrug. The present invention also provides methods of treating a disease, disorder, or condition such as those disclosed herein, comprising administering to a patient in need thereof a provided lipid prodrug or a pharmaceutical composition thereof.
    本发明提供了淋巴系统定向脂质前药,其制药组合物,制备这种前药和组合物的方法,以及改善作为脂质前药一部分的治疗剂的生物利用度或其他性质的方法。本发明还提供了治疗疾病、紊乱或症状的方法,包括向需要的患者施用所提供的脂质前药或其制药组合物。
  • 3-AMINOXALYL-AMINOBENZAMIDE DERIVATIVES AND INSECTICIDAL AND MITICIDAL AGENTS CONTAINING SAME AS ACTIVE INGREDIENT
    申请人:Usui Shuichi
    公开号:US20120022263A1
    公开(公告)日:2012-01-26
    The present invention herein provides a 3-aminooxalylaminobenzamide derivative which is used as an insecticide or miticide. The 3-aminooxalylaminobenzamide derivative is one represented by the following general formula [1]: (R 1 and R 2 each represent, for instance, a C 1 to C 3 alkoxy group or a C 1 to C 3 haloalkoxy group; R 3 and R 4 each represent, for instance, a C 1 to C 8 alkyl group or a C 1 to C 8 haloalkyl group; R 5 represents, for instance, a C 1 to C 5 haloalkyl group; R 6 and R 7 each represent, for instance, a hydrogen atom or a C 1 to C 5 alkyl group; Y represents, for instance, a hydrogen atom or a halogen atom; Z represents, for instance, a hydrogen atom; n is an integer ranging from 0 to 4 and m is an integer ranging from 0 to 2).
    本发明提供了一种用作杀虫剂杀螨剂的3-基草酰胺基苯甲酰衍生物。 3-基草酰胺基苯甲酰衍生物由以下通用式[1]表示: (R1和R2分别表示,例如,C1到C3烷氧基或C1到C3卤代烷氧基;R3和R4分别表示,例如,C1到C8烷基或C1到C8卤代烷基;R5表示,例如,C1到C5卤代烷基;R6和R7分别表示,例如,氢原子或C1到C5烷基;Y表示,例如,氢原子或卤原子;Z表示,例如,氢原子;n是一个范围从0到4的整数,m是一个范围从0到2的整数)。
  • [EN] BIPHENYL SUBSTITUTED 1,3-DIHYDRO-BENZOIMIDAZOL-2-YLIDENEAMINE DERIVATIVES<br/>[FR] DÉRIVÉS DE 1,3-DIHYDRO-BENZOIMIDAZOL-2-YLIDÈNE-AMINE À SUBSTITUTION BIPHÉNYLE
    申请人:NOVARTIS AG
    公开号:WO2011157787A1
    公开(公告)日:2011-12-22
    The invention relates to new derivatives of formula (I), wherein the substituents are as defined in the specification; to processes for the preparation of such derivatives; pharmaceutical compositions comprising such derivatives; such derivatives as a medicament; such derivatives for the treatment of one or more IGF-1 R mediated disorders or diseases.
    这项发明涉及公式(I)的新衍生物,其中取代基如规范中所定义;制备这种衍生物的方法;包括这种衍生物的药物组合物;将这种衍生物用作药物;将这种衍生物用于治疗一个或多个IGF-1 R介导的疾病。
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