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荧光增白剂86

中文名称
荧光增白剂86
中文别名
——
英文名称
disodium;5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(E)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfonatophenyl]ethenyl]benzenesulfonate
英文别名
——
荧光增白剂86化学式
CAS
——
化学式
C40H42N12Na2O10S2
mdl
——
分子量
960.9
InChiKey
YJHDFAAFYNRKQE-YHPRVSEPSA-L
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):
    -3.4
  • 重原子数:
    66
  • 可旋转键数:
    20
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    344
  • 氢给体数:
    8
  • 氢受体数:
    22

文献信息

  • SUBSTITUTED QUINAZOLINE COMPOUNDS AND USES THEREOF FOR MODULATING GLUCOCEREBROSIDASE ACTIVITY
    申请人:Northwestern University
    公开号:US20170001976A1
    公开(公告)日:2017-01-05
    Disclosed are new small molecules having a substituted quinazoline core structure and the uses thereof for modulating glucocerebrosidase activity. Also disclosed are pharmaceutical compositions comprising the small molecules or activated glucocerebrosidase conjugated to the small molecules, which compositions may be administered in methods of treating diseases or disorders associated with glucocerebrosidase activity, including neurological diseases and disorders such as Gaucher's disease and Parkinson's disease.
    公开了具有取代喹唑啉核心结构的新小分子,以及它们用于调节葡萄糖苷脂酶活性的用途。还公开了包含这些小分子或与小分子结合的激活葡萄糖苷脂酶的药物组合物,这些组合物可以用于治疗与葡萄糖苷脂酶活性相关的疾病或失调,包括神经系统疾病和失调,如戈谢病和帕金森病。
  • [EN] PROBES FOR RAPID AND SPECIFIC DETECTION OF MYCOBACTERIA<br/>[FR] SONDES POUR LA DÉTECTION RAPIDE ET SPÉCIFIQUE DE MYCOBACTÉRIES
    申请人:UNIV LELAND STANFORD JUNIOR
    公开号:WO2017027062A1
    公开(公告)日:2017-02-16
    The compositions of the present disclosure provide novel fluorogenic probes for use in the specific imaging and detection of mycobacteria species, and in particular β-lactam- antibiotic resistant. Specificity for mycobacteria is conferred on these probes by incorporating a moiety that specifically targets the unique trapping mechanism of the DprE1 found in in mycobacteria. Accordingly, only Mycobacteria species that express both a β- lactamase and DprE1 enable both the activation of the caged fluorescent probe, and the affixing of the released fluorescent probes to the bacteria cells through the functioning reduction-covalent binding mechanism. Advantageously, such a probe is able, at its most sensitive, to allow single mycobacterium detection.
    本公开的组成提供了新颖的生色团探针,用于特定地成像和检测分枝杆菌种类,尤其是对β-内酰胺类抗生素具有抗药性的种类。这些探针通过引入一种特定针对分枝杆菌中DprE1独特捕获机制的基团,从而实现对分枝杆菌的特异性。因此,只有表达β-内酰胺酶和DprE1的分枝杆菌种类才能激活笼状荧光探针,并通过功能性还原-共价结合机制将释放的荧光探针固定到细菌细胞上。这种探针的一个显著优点是,在其最敏感的情况下,能够实现单个分枝杆菌的检测。
  • 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。
  • [EN] SUBSTITUTED 4-METHYL-PYRROLO[1.2-A]PYRIMIDINE-8-CARBOXAMIDE COMPOUNDS AND USES THEREOF FOR MODULATING GLUCOCEREBROSIDASE ACTIVITY<br/>[FR] COMPOSÉS DE 4-MÉTHYL-PYRROLO[1,2-A]PYRIMIDINE-8-CARBOXAMIDE SUBSTITUÉ ET LEURS UTILISATIONS POUR MODULER L'ACTIVITÉ DE LA GLUCOCÉRÉBROSIDASE
    申请人:UNIV NORTHWESTERN
    公开号:WO2017004408A1
    公开(公告)日:2017-01-05
    Disclosed are new small molecules having a 4-methylpyrrrolo[l,2-a]pyrimidine- 8-carboxamide core structure and the uses thereof for modulating glucocerebrosidase activity. Also disclosed are pharmaceutical compositions comprising the small molecules which may be administered in methods of treating diseases or disorders associated with glucocerebrosidase activity, including neurological diseases and disorders such as Gaucher's disease and Parkinson's disease. The small molecules may contain a fluorophore or may be conjugated to a fluorophore in order to prepare a fluorescent probe for use in high throughput screening methods to identify new modulators of glucocerebrosidase activity via fluorescence polarization.
    揭示了具有4-甲基吡咯并[1,2-a]嘧啶-8-羧酰胺核结构的新型小分子及其用途,用于调节葡萄糖乙酰硫脂酶活性。还揭示了包含这些小分子的药物组合物,可用于治疗与葡萄糖乙酰硫脂酶活性相关的疾病或疾病,包括神经系统疾病和障碍,如高雪氏病和帕金森病。这些小分子可能含有荧光团或与荧光团结合,以制备用于高通量筛选方法中的荧光探针,以通过荧光极化识别葡萄糖乙酰硫脂酶活性的新调节剂。
  • COMPOUNDS HAVING PHOTOCHEMICALLY REMOVABLE PROTECTING GROUPS BASED ON AN ELECTROCYCLIC REACTION BETWEEN A CHROMOPHORE ATTACHED VIA AN ANILIDE GROUP TO A BENZOTHIOPHENE RING
    申请人:MARQUETTE UNIVERSITY
    公开号:US20130231484A1
    公开(公告)日:2013-09-05
    Disclosed herein are compounds having photoremovable protecting groups which are removed after the compounds absorbs light of a given wavelength and undergo an electrocyclic reaction between a chromophore in the compound attached via an anilide to a benzothiophene ring.
    本文披露了一种化合物,其具有光可去保护基团,该基团在化合物吸收特定波长的光并在连接到苯并噻吩环的苯胺上的染料团之间发生电环反应后被去除。
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