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2-[Ethyl(methyl)amino]ethyl methyl hydrogen phosphate

中文名称
——
中文别名
——
英文名称
2-[Ethyl(methyl)amino]ethyl methyl hydrogen phosphate
英文别名
2-[ethyl(methyl)amino]ethyl methyl hydrogen phosphate
2-[Ethyl(methyl)amino]ethyl methyl hydrogen phosphate化学式
CAS
——
化学式
C6H16NO4P
mdl
——
分子量
197.17
InChiKey
MEESWILPYBNBPX-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

计算性质

  • 辛醇/水分配系数(LogP):
    -2.9
  • 重原子数:
    12
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    59
  • 氢给体数:
    1
  • 氢受体数:
    5

文献信息

  • [EN] TLR-AGONIST-CONJUGATED ANTIBODY RECRUITING MOLECULES (TLR_ARMS)<br/>[FR] MOLÉCULES DE RECRUTEMENT D'ANTICORPS CONJUGUÉS À UN AGONISTE DE TLR)
    申请人:UNIV YALE
    公开号:WO2013166110A1
    公开(公告)日:2013-11-07
    The present invention relates to chimeric chemical compounds which are used to recruit antibodies to cancer cells, in particular, prostate cancer cells or metastasized prostate cancer cells. The compounds according to the present invention comprise an antibody binding terminus (ABT) moiety covalently bonded to a cell binding terminus (CBT) and Toll-like receptor agonist (TLR) through a linker and a multifunctional connector group or molecule.
    本发明涉及嵌合化学化合物,用于招募抗体到癌细胞,特别是前列腺癌细胞或转移的前列腺癌细胞。根据本发明的化合物包括一个与细胞结合末端(CBT)和通过连接物和多功能连接组或分子共价结合的抗体结合末端(ABT)基团和Toll样受体激动剂(TLR)。
  • [EN] SMALL MOLECULE BASED ANTIBODY-RECRUITING COMPOUNDS FOR CANCER TREATMENT<br/>[FR] COMPOSÉS DE RECRUTEMENT D'ANTICORPS À BASE DE PETITES MOLÉCULES POUR LE TRAITEMENT DU CANCER
    申请人:UNIV YALE
    公开号:WO2017023994A1
    公开(公告)日:2017-02-09
    The present invention relates to chimeric (including bifunctional) compounds, compositions comprising those compounds and methods of treating cancer in a patient or subject, especially including metastatic cancer where cancer cells exhibit overexpression (heightened expression) of cell surface urokinase-type plasminogen activator receptor (urokinase receptor) compared to normal (non-cancerous) cells. The compounds bind to the urokinase-type plasminogen activator receptor (uPAR) on the surface of a cancer cell, including a metastatic cancer cell, and consequently recruit native antibodies of the patient or subject where the antibodies can selectively degrade and/or deactivate targeted cancer cells through antibody-dependent cellular phagocytosis and antibody-dependent cellular cytotoxicity (ADCC) and/or complement dependent cytotoxicity (CDC) against a large number and variety of cancers, thus providing cancer cell death and an inhibition of growth, elaboration and/or metastasis of the cancer, including remission and cure of the patient's cancer.
    本发明涉及嵌合(包括双功能)化合物,包含这些化合物的组合物以及治疗患者或受试者癌症的方法,特别是包括转移性癌症,其中癌细胞相对于正常(非癌细胞)细胞表现出细胞表面尿激酶型纤溶酶原激活剂受体(尿激酶受体)的过表达(增强表达)。这些化合物与癌细胞表面的尿激酶型纤溶酶原激活剂受体(uPAR)结合,包括转移性癌细胞,从而招募患者或受试者的天然抗体,这些抗体可以通过抗体依赖性细胞吞噬和抗体依赖性细胞毒性(ADCC)和/或补体依赖性细胞毒性(CDC)选择性地降解和/或使靶向的癌细胞失活,针对大量和各种癌症,从而提供癌细胞死亡并抑制癌症的生长、扩散和/或转移,包括患者癌症的缓解和治愈。
  • FLUORESCENT PHOSPHOLIPID ETHER COMPOUNDS, COMPOSITIONS, AND METHODS OF USE
    申请人:Cellectar, Inc.
    公开号:EP2429591B1
    公开(公告)日:2015-08-26
  • HYDROGEL-BASED DECONTAMINATION OF AQUEOUS SAMPLES CONTAINING NANOPARTICLES
    申请人:UNIVERSITE DE BORDEAUX
    公开号:US20150076062A1
    公开(公告)日:2015-03-19
    The present invention relates to the use of a supramolecular system in order to remove particles from a liquid medium containing same. According to the invention, the supramolecular system includes at least one molecule having a low molecular weight and/or an organic compound from living organisms, preferably from jellyfish, said compound being selected from among collagen, a polysaccharide, a proteoglycan or a mixture of two of said organic compounds, and said molecule having a low molecular weight and formula (I) as defined herein. The invention also relates to a method for removing particles from a liquid medium containing same. The invention is particularly suitable for use in water decontamination and biotechnology.
  • LONG-LIVED GADOLINIUM BASED TUMOR TARGETED IMAGING AND THERAPY AGENTS
    申请人:WISCONSIN ALUMNI RESEARCH FOUNDATION
    公开号:US20170128572A1
    公开(公告)日:2017-05-11
    Alkylphosphocholine analogs incorporating a chelating moiety that is chelated to gadolinium are disclosed herein. The alkylphophocholine analogs are compounds having the formula: or a salt thereof. R 1 includes a chelating agent that is chelated to a gadolinium atom; a is 0 or 1; n is an integer from 12 to 30; m is 0 or 1; Y is —H, —OH, —COOH, —COOX, —OCOX, or —OX, wherein X is an alkyl or an arylalkyl; R 2 is —N + H 3 , —N + H 2 Z, —N + HZ 2 , or —N + Z 3 , wherein each Z is independently an alkyl or an aroalkyl; and b is 1 or 2. The compounds can be used to detect solid tumors or to treat solid tumors. In detection/imaging applications, the gadolinium emits signals that are detectable using magnetic resonance imaging. In therapeutic treatment, the gadolinium emits tumor-targeting charged particles when exposed to epithermal neutrons.
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