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1,2-Dilauroyl-Sn-Glycero-3-Phosphate

中文名称
——
中文别名
——
英文名称
1,2-Dilauroyl-Sn-Glycero-3-Phosphate
英文别名
[(2R)-2-dodecanoyloxy-3-phosphonooxypropyl] dodecanoate
1,2-Dilauroyl-Sn-Glycero-3-Phosphate化学式
CAS
——
化学式
C27H53O8P
mdl
——
分子量
536.7
InChiKey
OKLASJZQBDJAPH-RUZDIDTESA-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):
    8.6
  • 重原子数:
    36
  • 可旋转键数:
    28
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.93
  • 拓扑面积:
    119
  • 氢给体数:
    2
  • 氢受体数:
    8

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

反应信息

点击查看最新优质反应信息

文献信息

  • FLUORESCENT ANTICANCER PLATINUM DRUGS
    申请人:INVICTUS ONCOLOGY PVT. LTD.
    公开号:US20180312534A1
    公开(公告)日:2018-11-01
    The present disclosure is in relation to the field of nanotechnology and cancer therapeutics. In particular, the present disclosure relates to fluorescent platinum based compounds. The disclosure further relates to synthesis of said fluorescent platinum based compounds, nanoparticles and compositions comprising said fluorescent platinum based compounds/nanoparticles. The disclosure also relates to methods of managing cancer by the fluorescence changes between aforesaid platinum based compounds and corresponding free ligands, nanoparticles and compositions.
    本公开涉及纳米技术和癌症治疗领域。具体而言,本公开涉及荧光铂基化合物。该公开进一步涉及合成所述荧光铂基化合物、纳米颗粒和包含所述荧光铂基化合物/纳米颗粒的组合物。该公开还涉及通过上述铂基化合物与相应的游离配体、纳米颗粒和组合物之间的荧光变化来管理癌症的方法。
  • HYDROPHILIC FLUORINATED MOLECULES FOR LIPOSOMAL 19F MRI PROBES WITH UNIQUE MR SIGNATURES
    申请人:TEXAS CHILDREN'S HOSPITAL
    公开号:US20180154025A1
    公开(公告)日:2018-06-07
    Readily available hydrophilic and small organofluorine moieties were condensed via “click chemistry” to generate nonionic hydrophilic fluorinated molecules with unique 19 F MR signatures. These were used to fabricate stable liposome formulations for imaging various tissue types. This approach was tailored to exploit the broad spectrum of organic 19 F molecular species and to generate probes with distinct 19 F MRI signatures for simultaneous assessment of multiple molecular targets within the same target volume.
    通过“点击化学”将易得的亲水性和小的有机氟基团缩合,生成具有独特的19F MR标记的非离子亲水性氟化分子。这些分子被用于制备稳定的脂质体配方,用于成像各种组织类型。这种方法旨在利用有机19F分子种类的广泛谱,生成具有不同19F MRI标记的探针,以同时评估同一目标体积内多个分子靶标。
  • [EN] COMPOSITIONS AND METHODS FOR DELIVERY OF NUCLEIC ACIDS<br/>[FR] COMPOSITIONS ET PROCÉDÉS D'ADMINISTRATION D'ACIDES NUCLÉIQUES
    申请人:POSEIDA THERAPEUTICS INC
    公开号:WO2022087148A1
    公开(公告)日:2022-04-28
    The present disclosure provides compositions and methods for the genetic modification of cells, including, but not limited to, resting T-cells and hepatocytes. The compositions and methods can comprise lipid nanoparticles, wherein the lipid nanoparticles comprise at least one multivalent cationic bolaform amphiphilic lipid, at least one structural lipid, at least one phospholipid and at least one PEGylated lipid.
    本公开提供了细胞基因修饰的组合物和方法,包括但不限于静止的T细胞和肝细胞。该组合物和方法可以包括脂质纳米粒子,其中脂质纳米粒子包括至少一种多价阳离子球形两亲性脂质、至少一种结构脂质、至少一种磷脂和至少一种PEG化脂质。
  • Modulation of release from dry powder formulations
    申请人:Basu K. Sujit
    公开号:US20050003003A1
    公开(公告)日:2005-01-06
    Particles which include a bioactive agent are prepared to have a desired matrix transition temperature. Delivery of the particles via the pulmonary system results in modulation of drug release from the particles. Sustained release and/or sustained pharmacologic action of the drug can be obtained by forming particles which include a combination of phospholipids that are miscible in one another and have a high matrix transition temperature.
    含有生物活性物质的微粒被制备成具有所需的基质转变温度。通过肺系统输送微粒会导致药物从微粒中释放的调节。通过形成包含彼此相溶且具有高基质转变温度的磷脂组合的微粒,可以获得药物的持续释放和/或持续药理作用。
  • Particles for inhalation having sustained release properties
    申请人:Basu Sujit K.
    公开号:US20080039366A1
    公开(公告)日:2008-02-14
    The invention generally relates to a method for pulmonary delivery of therapeutic, prophylactic and diagnostic agents to a patient wherein the agent is released in a sustained fashion, and to particles suitable for use in the method. In particular, the invention relates to a method for the pulmonary delivery of a therapeutic, prophylactic or diagnostic agent comprising administering to the respiratory tract of a patient in need of treatment, prophylaxis or diagnosis an effective amount of particles comprising a therapeutic, prophylactic or diagnostic agent or any combination thereof in association with a charged lipid, wherein the charged lipid has an overall net charge which is opposite to that of the agent upon association with the agent. Release of the agent from the administered particles occurs in a sustained fashion.
    本发明一般涉及一种将治疗、预防和诊断剂量形式送入患者肺部的方法,其中药剂以持续的方式释放,并且还涉及适用于该方法的颗粒。具体而言,本发明涉及一种肺部给药的方法,包括向需要治疗、预防或诊断的患者的呼吸道中投与有效量的颗粒,该颗粒包括治疗、预防或诊断剂量或其任何组合与带电脂质结合,其中带电脂质的总净电荷与其结合的药剂相反。所投与的颗粒中的药剂以持续的方式释放。
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同类化合物

钙(2R)-2,3-二(棕榈酰氧基)丙基磷酸酯 辛酸(1R)-1-[(磷酰氧基)甲基]-1,2-乙二基酯单钠盐 血小板活化因子 (C18) 血小板-活化因子C18 苯甲醇,2-甲氧基-5-甲基-a-[1-(甲基氨基)乙基]- 苯甲基(2R)-2-(羟甲基)吡咯烷-1-羧酸酯 苯(甲)醛,2-甲基-4-硝基- 胞苷二磷酸甘油酯 胞苷-5’-二磷酸甘油酯二钠盐 肉豆蔻酰基溶血磷脂胆碱 聚乙二醇单甲醚-2000-二十八烷基磷脂酰乙醇胺 磷酸二氢1,3-羟基-2-丙酯 磷酸,单[3-(十八烷氧基)-2-(苯基甲氧基)丙基]单[2-(1-吡咯烷基)乙基]酯 磷酯酰乙醇胺 磷脂酰胆碱(大豆) 磷脂酰肌醇 磷脂酰乙醇胺(牛脑) 磷脂酰乙醇胺(大豆) 磷脂酰丝氨酸 硬脂酰溶血卵磷脂 甲氧基聚乙二醇-二棕榈酰磷酯酰乙醇胺 甘磷酸胆碱 甘油磷酸镁 甘油磷酸锌 甘油磷酸铁 甘油磷酸钾 甘油磷酸钾 甘油磷酸钠 甘油磷酸钙盐 甘油磷酸酯镍(2+)盐 甘油磷酸酯锰盐 甘油磷酸酯 甘油磷酸水和物 甘油磷酸-N-花生四烯酸乙醇胺 甘油磷酸-N-油酰基乙醇胺 甘油磷酸-N-棕榈酰乙醇胺 甘油磷酰丝氨酸 琥珀酸)氢21-羟基-5&#x3B2-孕烷-3,20-二酮21-( 焦磷酸甘油油酰甘油(铵盐) 溶血磷脂酰胆碱(鸡蛋) 溶血卵磷脂(猪或牛肝) 氨基甲酰-PAF(C16) 氢化磷脂酰胆碱 氢化卵磷脂 月桂酰溶血磷酰脂 心磷脂(钠盐或铵盐) 大豆卵磷脂 外消旋-1,2-二月桂酰-甘油-3-磷酰-胆碱 叔-丁氧基羰基-脯氨酰-氨基琥珀酰<丁二酰>-甘氨酰-丙氨酸甲基酯 反-N-(1-(2-乙氧基乙基)-3-甲基-4-哌啶基)-N-苯基苯酰胺