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2,3-二羟丙基十三烷酸酯 | 71958-74-2

中文名称
2,3-二羟丙基十三烷酸酯
中文别名
1-十三烷酸单甘油酯
英文名称
1-monomyristin
英文别名
3-tridecanoyloxy-propane-1,2-diol;3-Tridecanoyloxy-propan-1,2-diol;Glycerin-1.-tridecylat;1-Monotridecylin;2,3-Dihydroxypropyl tridecanoate
2,3-二羟丙基十三烷酸酯化学式
CAS
71958-74-2
化学式
C16H32O4
mdl
——
分子量
288.428
InChiKey
CLRCAFAXMVNJRH-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:
    411.2±25.0 °C(Predicted)
  • 密度:
    0.989±0.06 g/cm3(Predicted)
  • 溶解度:
    DMF:25mg/mL; DMF:PBS (pH 7.2) (1:2):0.3mg/mL;二甲基亚砜:20mg/mL;乙醇:15mg/mL
  • 物理描述:
    OtherSolid; PelletsLargeCrystals

计算性质

  • 辛醇/水分配系数(LogP):
    4.7
  • 重原子数:
    20
  • 可旋转键数:
    15
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.94
  • 拓扑面积:
    66.8
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    十三酸 、 alkaline earth salt of/the/ methylsulfuric acid 在 盐酸 作用下, 生成 2,3-二羟丙基十三烷酸酯
    参考文献:
    名称:
    Malkin; Riad el Shurbagy, Journal of the Chemical Society, 1936, p. 1630
    摘要:
    DOI:
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文献信息

  • NOVEL COMPOUNDS AS DIACYLGLYCEROL ACYLTRANSFERASE INHIBITORS
    申请人:GlaxoSmithKline LLC
    公开号:US20140148437A1
    公开(公告)日:2014-05-29
    This invention relates to novel compounds which are inhibitors of acyl coenzyme A: diacylglycerol acyltransferase 1 (DGAT-1), to pharmaceutical compositions containing them, to processes for their preparation, and to their use in therapy, alone or in combination with weight management therapies or other triglyceride lowering therapy for the prevention or treatment of diseases related to DGAT-1 dysfunction or where modulation of DGAT-1 activity may have therapeutic benefit including but not limited to obesity, obesity related disorders, genetic (Type 1, Type 5 hyperlipidemia) and acquired forms of hypertriglyceridemia or hyperlipoproteinemia-related disorders, caused by but not limited to lipodystrophy, hypothyroidism, medications (beta blockers, thiazides, estrogen, glucocorticoids, transplant) and other factors (pregnancy, alcohol intake), hyperlipoproteinemia, chylomicronemia, dyslipidemia, non-alcoholic steatohepatitis, diabetes, insulin resistance, metabolic syndrome, cardiovascular outcomes, angina, excess hair growth (including syndromes associated with hirsutism), nephrotic syndrome, fibrosis such as myocardial, renal and liver fibrosis, hepatitis C virus infection and acne or other skin disorders.
    这项发明涉及一种新型化合物,它们是酰辅酶A:二酰基甘油酰基转移酶1(DGAT-1)的抑制剂,以及含有它们的药物组合物,它们的制备方法,以及它们在治疗中的使用,单独或与体重管理疗法或其他降甘油三酯疗法结合,用于预防或治疗与DGAT-1功能障碍相关的疾病,或者调节DGAT-1活性可能具有治疗益处的疾病,包括但不限于肥胖、与肥胖相关的疾病、遗传性(1型、5型高脂血症)和获得性高三酰甘油脂或高脂蛋白血症相关疾病,由脂肪萎缩、甲状腺功能减退、药物(β受体阻滞剂、噻嗪类药物、雌激素、糖皮质激素、移植)和其他因素(怀孕、饮酒)引起,高脂蛋白血症、乳糜微粒血症、血脂异常、非酒精性脂肪肝炎、糖尿病、胰岛素抵抗、代谢综合征、心血管结果、心绞痛、多毛(包括与多毛症相关的综合征)、肾病综合征、纤维化如心肌、肾脏和肝脏纤维化、丙型肝炎病毒感染和痤疮或其他皮肤疾病。
  • [EN] NOVEL COMPOUNDS AS DIACYLGLYCEROL ACYLTRANSFERASE INHIBITORS<br/>[FR] NOUVEAUX COMPOSÉS EN TANT QU'INHIBITEURS DE DIACYLGLYCÉROL ACYLTRANSFÉRASE
    申请人:GLAXOSMITHKLINE LLC
    公开号:WO2012162129A1
    公开(公告)日:2012-11-29
    This invention relates to novel compounds which are inhibitors of acyl coenzymeA: diacylglycerol acyltransferase 1 (DGAT-1), to pharmaceutical compositions containing them, to processes for their preparation, and to their use in therapy for the prevention or treatment of diseases related to DGAT-1 dysfunction or where modulation of DGAT-1 activity may have therapeutic benefit including but not limited to obesity, obesity related disorders, hypertriglyceridemia, hyperlipoproteinemia, chylomicronemia, dyslipidemia, non-alcoholic steatohepatitis, diabetes, insulin resistance, metabolic syndrome, hepatitis C virus infection and acne or other skin disorders.
    这项发明涉及一种新型化合物,它们是酰辅酶A:二酰基甘油酰基转移酶1(DGAT-1)的抑制剂,以及含有它们的药物组合物,它们的制备方法,以及它们在治疗中的应用,用于预防或治疗与DGAT-1功能障碍相关的疾病,或者调节DGAT-1活性可能具有治疗益处的疾病,包括但不限于肥胖,与肥胖相关的疾病,高三酰甘油血症,高脂蛋白血症,乳糜微粒血症,脂质代谢异常,非酒精性脂肪肝炎,糖尿病,胰岛素抵抗,代谢综合征,丙型肝炎病毒感染,痤疮或其他皮肤疾病。
  • Novel Compounds as Diacylglycerol Acyltransferase Inhibitors
    申请人:CHRISTENSEN Rowena
    公开号:US20150307445A1
    公开(公告)日:2015-10-29
    This invention relates to novel compounds which are inhibitors of acyl coenzymeA: diacylglycerol acyltransferase 1 (DGAT-1), to pharmaceutical compositions containing them, to processes for their preparation, and to their use in therapy for the prevention or treatment of diseases related to DGAT-1 dysfunction or where modulation of DGAT-1 activity may have therapeutic benefit including but not limited to obesity, obesity related disorders, hypertriglyceridemia, hyperlipoproteinemia, chylomicronemia, dyslipidemia, non-alcoholic steatohepatitis, diabetes, insulin resistance, metabolic syndrome, hepatitis C virus infection and acne or other skin disorders.
    这项发明涉及一种新型化合物,它们是酰辅酶A:二酰基甘油酰基转移酶1(DGAT-1)的抑制剂,以及含有它们的药物组合物,它们的制备方法,以及它们在治疗中的应用,用于预防或治疗与DGAT-1功能障碍相关的疾病,或者调节DGAT-1活性可能具有治疗益处的疾病,包括但不限于肥胖、与肥胖相关的疾病、高三酸甘油酯血症、高脂蛋白血症、乳糜微粒血症、脂质代谢异常、非酒精性脂肪肝、糖尿病、胰岛素抵抗、代谢综合征、丙型肝炎病毒感染、痤疮或其他皮肤疾病。
  • Inhibitors of diacylglycerol O-acyltransferase type 1 enzyme
    申请人:Kym R. Philip
    公开号:US20080015227A1
    公开(公告)日:2008-01-17
    The present invention relates to compounds of formula (I). wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , m, n, p and q are defined herein Pharmaceutical compositions and methods for treating DGAT-1 related diseases or conditions are also disclosed.
    本发明涉及式(I)的化合物。其中R1、R2、R3、R4、R5、R6、m、n、p和q在此处定义。还公开了用于治疗DGAT-1相关疾病或症状的药物组合物和方法。
  • [EN] NOVEL COMPOUNDS AS DIACYLGLYCEROL ACYLTRANSFERASE INHIBITORS<br/>[FR] NOUVEAUX COMPOSÉS UTILISÉS COMME INHIBITEURS DE DIACYLGLYCÉROL ACYLTRANSFÉRASE
    申请人:GLAXOSMITHKLINE LLC
    公开号:WO2014081994A1
    公开(公告)日:2014-05-30
    This invention relates to novel compounds which are inhibitors of acyl coenzyme A: diacylglycerol acyltransferase 1 (DGAT-1 ), to pharmaceutical compositions containing them, to processes for their preparation, and to their use in therapy, alone or in combination with weight management therapies or other triglyceride lowering therapy for the prevention or treatment of diseases related to DGAT-1 dysfunction or where modulation of DGAT-1 activity may have therapeutic benefit.
    本发明涉及一种新型化合物,它们是酰基辅酶A:二酰基甘油酰基转移酶1(DGAT-1)的抑制剂,以及含有它们的药物组合物,其制备方法,以及它们在治疗中的使用,单独或与体重管理疗法或其他三酸甘油酯降低疗法结合使用,用于预防或治疗与DGAT-1功能障碍相关的疾病或调节DGAT-1活性可能具有治疗益处的疾病。
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