1239481-15-2Relevant academic research and scientific papers
Discovery of novel anti-angiogenesis agents. Part 10: Multi-target inhibitors of VEGFR-2, Tie-2 and EphB4 incorporated with 1,2,3-triazol
Pan, Xiaoyan,Liang, Liyuan,Si, Ru,Wang, Jin,Zhang, Qingqing,Zhou, Huaxin,Zhang, Lin,Zhang, Jie
, p. 1 - 9 (2018/12/04)
VEGFR-2, Tie-2, and EphB4 are essential for both angiogenesis and tumorigenesis. Herein, we developed a series of pyridines incorporated with 1,2,3-triazole as multi-target inhibitors based on the crystal structure alignment of the kinase domain of angiog
Pyridine compound and application
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Paragraph 0031; 0036; 0037; 0047, (2018/11/03)
The invention provides a pyridine compound and application. Based on the find of VEGFR-2 (Vascular Endothelial Growth Factor Receptor-2), EphB4 (Ephrin type-B receptor 4) and TIE-2 compensatory activation, biphenyl arylurea is used as a novel leading comp
A modular approach to catalytic synthesis using a dual-functional linker for Click and Suzuki coupling reactions
White, James R.,Price, Gareth J.,Schiffers, Stefanie,Raithby, Paul R.,Plucinski, Pawel K.,Frost, Christopher G.
supporting information; experimental part, p. 3913 - 3917 (2010/08/22)
The stable benzylazido-boronate ester 1 is presented as an example of a dual-functional linker that allows the synthetically valuable boronate motif to be clicked onto other molecules under mild conditions. The utility of the azido-boronate motif as a modular building block is demonstrated in the rapid synthesis of drug-like structures employing sequential catalytic azide-alkyne cycloaddition and Suzuki coupling reactions.
