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August 1, 2024Open Access

Figure S5 from A Selective FGFR1/2 PROTAC Degrader with Antitumor Activity

Ying Kong Xinyue Zhao Zhaofu Wang Siqi Yuan Sheng Chen Shidi Lou Shichao Ma Yunfeng Li Xinghao Wang Yangfeng Ge Guobin Li Hongbing Yang Mengxi Zhao Dandan Li Hailong Zhang Wenfu Tan Juan Wang

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Abstract

Binding affinity of BR-cpd7. A-C, Fluorescence polarization (FP) analysis of BR-cpd7 affinity for purified FGFR1/2/3 (n=3 replicates).

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Cite This Study

Kong et al. (2024) studied this question.

synapsesocial.com/papers/68e5e0e0b6db643587574c47 https://doi.org/10.1158/1535-7163.26423449

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Figure S4 from A Selective FGFR1/2 PROTAC Degrader with Antitumor Activity2024
2Figure S3 from A Selective FGFR1/2 PROTAC Degrader with Antitumor Activity2024
3Figure S2 from A Selective FGFR1/2 PROTAC Degrader with Antitumor Activity2024
4Table S2 from A Selective FGFR1/2 PROTAC Degrader with Antitumor Activity2024
5Table S2 from A Selective FGFR1/2 PROTAC Degrader with Antitumor Activity2024

Table S3 from A Selective FGFR1/2 PROTAC Degrader with Antitumor Activity2024
Table S3 from A Selective FGFR1/2 PROTAC Degrader with Antitumor Activity2024
Table S5 from A Selective FGFR1/2 PROTAC Degrader with Antitumor Activity2024