1309666-82-7Relevant academic research and scientific papers
GPCR ligand dendrimer (GLiDe) conjugates: Adenosine receptor interactions of a series of multivalent xanthine antagonists
Kecskés, Angela,Tosh, Dilip K.,Wei, Qiang,Gao, Zhan-Guo,Jacobson, Kenneth A.
, p. 1115 - 1127 (2011)
Previously, G protein-coupled receptor (GPCR) agonists were tethered from polyamidoamine (PAMAM) dendrimers to provide high receptor affinity and selectivity. Here, we prepared GPCR ligand-dendrimer (GLiDe) conjugates from a potent adenosine receptor (AR)
Europium-labeled activity-based probe through click chemistry: Absolute serine protease quantification using 153Eu isotope dilution ICP/MS
Yan, Xiaowen,Luo, Yacui,Zhang, Zhubao,Li, Zhaoxin,Luo, Qiang,Yang, Limin,Zhang, Bo,Chen, Haifeng,Bai, Peiming,Wang, Qiuquan
, p. 3358 - 3363 (2012)
Click and analyze: The titled probe was synthesized by conjugating a sulfonyl fluoride and azido unit using click chemistry to give SF-Eu, which can react specifically with serine (Ser) in the active site of serine protease (SP). Combination of the method
A chemical "hub" for absolute quantification of a targeted protein: Orthogonal integration of elemental and molecular mass spectrometry
Yan, Xiaowen,Li, Zhaoxin,Liang, Yong,Yang, Limin,Zhang, Bo,Wang, Qiuquan
supporting information, p. 6578 - 6581 (2014/06/10)
A novel element-tagged activity-based photo-cleavable biotinylated chemical "Hub" was designed and synthesized to orthogonally integrate ICP-MS and ESI-MS for absolute targeted-protein quantification. This tetrafunctional chemical "hub" allowed us to quantify a targeted protein using species-unspecific isotope dilution ICP-MS and to know which protein is being quantified using ESI-IT-MS at the same time. This journal is the Partner Organisations 2014.
