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azidofluorescein

中文名称
——
中文别名
——
英文名称
azidofluorescein
英文别名
4-Azido-3',6'-dihydroxy-3H-spiro[isobenzofuran-1,9'-xanthen]-3-one;7-azido-3',6'-dihydroxyspiro[2-benzofuran-3,9'-xanthene]-1-one
azidofluorescein化学式
CAS
——
化学式
C20H11N3O5
mdl
——
分子量
373.324
InChiKey
OJZZBMSTESSSJH-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):
    4.4
  • 重原子数:
    28
  • 可旋转键数:
    1
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    90.4
  • 氢给体数:
    2
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    fluorescein amine亚硝酸正戊酯 在 sodium chloride 、 硫酸 作用下, 以 N-甲基乙酰胺 为溶剂, 生成 azidofluorescein
    参考文献:
    名称:
    Derivatives of fluorescein
    摘要:
    这项发明涉及荧光素衍生物及其生产。这些化合物在确定细胞内pH值方面具有价值。因此,可以获得具有相对稳定荧光水平的荧光活细胞。这种新型荧光素化合物可用于生物学和生物化学中的其他标记目的。
    公开号:
    US04609740A1
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文献信息

  • [EN] HYDROGELS WITH BIODEGRADABLE CROSSLINKING<br/>[FR] HYDROGELS À RÉTICULATION BIODÉGRADABLE
    申请人:PROLYNX LLC
    公开号:WO2013036847A1
    公开(公告)日:2013-03-14
    Hydrogels that degrade under appropriate conditions of pH and temperature by virtue of crosslinking compounds that cleave through an elimination reaction are described. The hydrogels may be used for delivery of various agents, such as pharmaceuticals. This invention provides hydrogels that degrade to smaller, soluble components in a non-enzymatic process upon exposure to physiological conditions and to methods to prepare them. The hydrogels are prepared from crosslinking agents that undergo elimination reactions under physiological conditions, thus cleaving the crosslinking agent from the backbone of the hydrogel. The invention also relates to the crosslinking agents themselves and intermediates in forming the hydro gels of the invention. The biodegradable hydro gels prepared according to the methods of the invention may be of use in diverse fields, including biomedical engineering, absorbent materials, and as carriers for drug delivery.
    描述了在适当的pH和温度条件下通过交联化合物裂解的水凝胶。这些水凝胶可用于传递各种药剂,如药物。该发明提供了在暴露于生理条件下会非酶催化降解为较小可溶性组分的水凝胶,以及制备它们的方法。这些水凝胶是由在生理条件下发生消除反应的交联剂制备而成,从而将交联剂从水凝胶的骨架中裂解出来。该发明还涉及交联剂本身以及形成该发明的水凝胶的中间体。根据该发明的方法制备的可生物降解水凝胶可用于各种领域,包括生物医学工程、吸收材料以及作为药物传递的载体。
  • HYDROGELS WITH BIODEGRADABLE CROSSLINKING
    申请人:ProLynx LLC
    公开号:US20170312368A1
    公开(公告)日:2017-11-02
    Hydrogels that degrade under appropriate conditions of pH and temperature by virtue of crosslinking compounds that cleave through an elimination reaction are described. The hydrogels may be used for delivery of various agents, such as pharmaceuticals.
    描述了在适当的pH和温度条件下,由于交联化合物通过消除反应而降解的水凝胶。这些水凝胶可以用于输送各种药剂,如药物。
  • [EN] CONJUGATES OF SOMATOSTATIN AND ITS ANALOGS<br/>[FR] CONJUGUÉS DE SOMATOSTATINE ET DE SES ANALOGUES
    申请人:PROLYNX LLC
    公开号:WO2015061503A1
    公开(公告)日:2015-04-30
    Conjugates of carriers and hydrogels for controlling the biological half-life of somatostatin and its analogs are disclosed.
    载体和水凝胶的共轭物用于控制生长抑素及其类似物的生物半衰期。
  • REACTIVE LABELLING COMPOUNDS AND USES THEREOF
    申请人:Academia Sinica
    公开号:US20150309041A1
    公开(公告)日:2015-10-29
    Provided are azido-BODIPY compounds of formula (I), cyclooctyne-based fluorogenic probes of formula (IV), and activity-based probes of formula (VI). These compounds undergo azide alkyne cycloadditions (AAC) with to form triazolyl products. The provided compounds are useful for detection and imaging of alkyne-, or azide-containing molecules. Methods for detection and imaging biomolecules using compounds of the present disclosure are disclosed.
    提供的是式(I)的叠氮基BODIPY化合物、式(IV)的环辛炔基荧光探针,以及式(VI)的活性探针。这些化合物通过叠氮-炔烃环加成反应(AAC)形成三唑基产物。提供的化合物可用于检测和成像含炔基或叠氮基的分子。本公开的方法揭示了利用本公开的化合物检测和成像生物分子的方法。
  • Chemoselective Fluorgenic Molecular Linkers and Methods for Their Preparation and Use
    申请人:Wang Qian
    公开号:US20070224695A1
    公开(公告)日:2007-09-27
    The present invention describes a bioconjugation strategy and compounds that are useful therein in which a fluorescent signal is produced when two molecular or supramolecular entities are linked by chemoselective combination of one linker having an azido or halide substituent group with another linker having a cyano or an alkyne substituent group. A kit is also provided.
    本发明描述了一种生物共轭策略和在其中有用的化合物,当两个分子或超分子实体通过一个含有偶氮基或卤素取代基的连接剂与另一个含有氰基或炔基取代基的连接剂进行化学选择性组合时,会产生荧光信号。同时还提供了一种试剂盒。
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