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≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
WF-47-JS03 is a potent and selective RET kinase inhibitor with IC 50 s of 1.7 nM and 5.3 nM for KIF5B-RET transfected Ba/F3 cells and CCDC6-RET transfected LC-2/ad lung cancer cells, respectively. WF-47-JS03 demonstrates >500-fold selectivity against kina
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In Vitro:WF-47-JS03 inhibits Tel-KDR transfected Ba/F3 cells and Ba/F3 wild-type cell lines with IC 50 s of 0.99 and 1.5 μM, respectively. MCE has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo:WF-47-JS03 significantly inhibits tumor growth in RIE KIF5B-RET xenograft mice and is well tolerated at 1, 3, and 10mg/kg in the 10 day study. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Mod
Biological Activity:WF-47-JS03 is a potent and selective RET kinase inhibitor with IC 50 s of 1.7 nM and 5.3 nM for KIF5B-RET transfected Ba/F3 cells and CCDC6-RET transfected LC-2/ad lung cancer cells, respectively. WF-47-JS03 demonstrates >500-fold selectivity against kina
| Sonrisas canónicas | NC(N1C(N=C2NC3CC(C)(C)N(C)C(C)(C)C3)=C(C4=CC(OC)=C(OC)C=C4)C=N1)=C2C5=CC=CC=C5 |
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| Peso molecular | 514.66 |
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View spec sheet →| Solubilidad | DMSO : 62.5 mg/mL (121.44 mM; Need ultrasonic) |
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