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二油精 | 2465-32-9

中文名称
二油精
中文别名
生物柴油杂质;1,3-二精油;1,3-甘油二油酸酯
英文名称
1,3-diolein
英文别名
1,3-dioleoylglycerol;2-hydroxypropane-1,3-diyl dioleate;[2-hydroxy-3-[(Z)-octadec-9-enoyl]oxypropyl] (Z)-octadec-9-enoate
二油精化学式
CAS
2465-32-9;25637-84-7
化学式
C39H72O5
mdl
——
分子量
620.998
InChiKey
DRAWQKGUORNASA-CLFAGFIQSA-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

  • 溶解度:
    DMF:10mg/mL;乙醇:10mg/mL;乙醇:PBS (pH 7.2) (1:1): 0.5 mg/mL
  • 密度:
    0.89-0.92 g/cm3(Temp: 50 °C)
  • 熔点:
    12 °C
  • LogP:
    15.178 (est)
  • 物理描述:
    Liquid; OtherSolid

计算性质

  • 辛醇/水分配系数(LogP):
    14.3
  • 重原子数:
    44
  • 可旋转键数:
    36
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.85
  • 拓扑面积:
    72.8
  • 氢给体数:
    1
  • 氢受体数:
    5

安全信息

  • 危险品标志:
    Xi
  • 危险类别码:
    R36/37/38
  • WGK Germany:
    1

SDS

SDS:1ed85b6f02379f5d1662efa623a22076
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制备方法与用途

用途

二油酸甘油酯可用于治疗乳腺癌。

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量
    • 1
    • 2

反应信息

  • 作为反应物:
    描述:
    二油精2,6-二甲基吡啶 、 sodium iodide 作用下, 以 乙醚二氯甲烷丁酮 为溶剂, 反应 63.0h, 生成 N-[4-[2-(1,3-dioleoyloxy)propoxycarbonyl]butyl]-N,N,N-trimethylammonium iodide
    参考文献:
    名称:
    Symmetrical cationic triglycerides
    摘要:
    Some cationic triglycerides 1Aa-1Cb which have a symmetrical structure were effectively synthesized and formulated into cationic liposomes with the co-lipid dioleoylphosphatidylethanolamine (DOPE) and/or dilauroylphosphatidylcholine (DLPC). The plasmid encoding a luciferase was delivered into CHO cells by using these cationic liposomes. Our symmetrical cationic triglycerides showed high transfection activity when DOPE was used as a co-lipid. Among the symmetrical cationic triglycerides synthesized here, 1Ab and 1Ac, which have an oleoyl group at the 1- and 3-position in the glycerol backbone and also have a relatively long linker connecting the 2-hydroxy group in glycerol with the quaternary ammonium head group, were found to be the most suitable for gene delivery into cells. The transfection activity of the symmetrical cationic triglyceride 1Ab was comparable with that of its asymmetrical congener 6 and several times higher than that of Lipofectin(R). (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0968-0896(00)00242-x
  • 作为产物:
    描述:
    油酰氯吡啶 、 sodium tetrahydroborate 作用下, 以 四氢呋喃氯仿 为溶剂, 反应 0.25h, 生成 二油精
    参考文献:
    名称:
    [EN] LIPID PRODRUGS OF BTK INHIBITORS AND USES THEREOF
    [FR] PROMÉDICAMENTS LIPIDIQUES D'INHIBITEURS DE BTK ET LEURS UTILISATIONS
    摘要:
    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、紊乱或状况的方法,包括向需要的患者施用所述的脂质前药或其制药组合物。
    公开号:
    WO2020176868A1
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文献信息

  • [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。
  • [EN] LIPID PRODRUGS OF JAK INHIBITORS AND USES THEREOF<br/>[FR] PROMÉDICAMENTS LIPIDIQUES D'INHIBITEURS DE JAK ET LEURS UTILISATIONS
    申请人:PURETECH LYT INC
    公开号:WO2020176859A1
    公开(公告)日:2020-09-03
    The present invention provides lymphatic system-directing lipid prodrugs, pharmaceutical compositions thereof, methods of producing such prodrugs and compositions, and 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 disclosed lipid prodrug or a pharmaceutical composition thereof.
    本发明提供了淋巴系统定向脂质前药,其药物组成物,生产这种前药和组成物的方法,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、紊乱或状况的方法,例如本文所披露的那些,包括向需要的患者施用所披露的脂质前药或其药物组成物。
  • [EN] TREATMENT OF NEURODEGENERATIVE CONDITIONS<br/>[FR] TRAITEMENT D'ETATS NEURODEGENERATIFS
    申请人:BTG INT LTD
    公开号:WO2005018632A1
    公开(公告)日:2005-03-03
    A method is provided for treating a patient in need of therapy for a neurodegenerative disease comprising administering to that patient a therapeutically effective dose of a lipid glyceride comprising a glycerol moiety and a fatty acid moiety, the fatty acid moiety being selected from the group consisting of Ϝ-linolenic acid, dihomo-Ϝ-linolenic acid and arachidonic acid characterised in that the selected fatty acid moiety is attached to the glycerol moiety at its sn-2 position. Preferably the method is that wherein the lipid is administered for a duration and at a dose sufficient to maintain or elevate TGF-β1 levels in the patient to therapeutic levels.
    提供了一种治疗神经退行性疾病患者的方法,包括向该患者施用含有甘油基团和脂肪酸基团的治疗有效剂量的脂质甘油酯,所述脂肪酸基团选自Ϝ-亚麻酸、二油酸和花生四烯酸组成的群体,其特点在于所选的脂肪酸基团附着在甘油基团的sn-2位置。最好的方法是,脂质被施用的持续时间和剂量足以维持或提高患者体内TGF-β1水平至治疗水平。
  • 1-O-Alkyl (di)glycerol ethers synthesis from methyl esters and triglycerides by two pathways: catalytic reductive alkylation and transesterification/reduction
    作者:Marc Sutter、Wissam Dayoub、Estelle Métay、Yann Raoul、Marc Lemaire
    DOI:10.1039/c3gc36907b
    日期:——
    esters, monoglycerides or oleic sunflower refined oil, the corresponding 1-O-alkyl (di)glycerol ethers were obtained in both high yields and selectivity by two different pathways. With methyl esters, a reductive alkylation with (di)glycerol was realized under 50 bar hydrogen pressure in the presence of 1 mol% of Pd/C and an acid co-catalyst. A second two step procedure was evaluated from methyl esters
    从可用的和生物来源的甲酯中, 甘油单酸酯或油酸向日葵精制油,通过两种不同途径以高收率和选择性获得了相应的1- O-烷基(二)甘油醚。对于甲酯,在1mol%的Pd / C和酸助催化剂的存在下,在50巴的氢气压力下,实现了与(二)甘油的还原性烷基化。从甲酯或三油精 包括第一次酯交换反应成相应的 甘油单酸酯与BaO / Al 2 O 3 催化剂,然后 减少在H 2压力下,用可循环利用的非均相催化体系Pd / C和Amberlyst 35合成所需的甘油单醚。另外,还提出了反应机理。
  • [EN] LIPID PRODRUGS OF PREGNANE NEUROSTEROIDS AND USES THEREOF<br/>[FR] PROMÉDICAMENTS LIPIDIQUES DE NEUROSTÉROÏDES DE PRÉGNANE ET LEURS UTILISATIONS
    申请人:PURETECH HEALTH LLC
    公开号:WO2020028787A1
    公开(公告)日:2020-02-06
    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 disclosed lipid prodrug or a pharmaceutical composition thereof.
    本发明提供了淋巴系统定向脂质前药,以及其制药组合物、生产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述的脂质前药或其制药组合物。
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