Pralsetinib (Blu667) |
| Catalog No.GC31780 |
프랄세티닙(Blu667)(BLU-667)은 매우 강력한 선택적 RET 억제제입니다. 프랄세티닙(Blu667)(BLU-667)은 각각 0.4, 0.3, 0.4, 0.4 및 0.4 nM의 IC50으로 WT RET, RET 돌연변이 V804L, V804M, M918T 및 CCDC6-RET 융합을 억제합니다.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 2097132-94-8
Sample solution is provided at 25 µL, 10mM.
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Pralsetinib (Blu667) is a highly potent and selective RET inhibitor with an IC50 of 0.4 nM for wild type RET kinase.
Pralsetinib (Blu667) is a RET inhibitor extracted from patent US20170121312A1, compound example 129[1]. Pralsetinib (Blu667) demonstrates more than 10-fold increased potency over approved MKIs against oncogenic RET variants and resistance mutants. Pralsetinib (Blu667) demonstrates potent activity (IC50=0.4 nM) against common oncogenic RET alterations, including RET M918T, an activating mutation found in MTC, as well as the CCDC6-RET fusion observed in PTC and NSCLC. Pralsetinib (Blu667) suppresses RET pathway signaling in a panel of RET-driven cell lines: LC2/ad (CCDC6-RET, NSCLC), MZ-CRC-1 (RET M918T, MTC), and TT (RET C634W, MTC)[2].
Pralsetinib (Blu667) potently inhibits growth of NSCLC and thyroid cancer xenografts driven by various RET mutations and fusions without inhibiting vascular endothelial growth factor receptor 2 (VEGFR-2). Pralsetinib (Blu667) showed potent dose dependent activity against both KIF5B-RET Ba/F3 and KIF5B-RET V804L Ba/F3 allograft tumors with doses as low as 10 mg/kg twice-daily[2].
[1]. Brumaker J, et al. Inhibitors of ret. US20170121312A1. [2]. Subbiah V, et al. Precision Targeted Therapy With BLU-667 for RET-Driven Cancers. American Association for Cancer Research. 10.1158/2159-8290.CD-18-0338.
Average Rating: 5 (Based on Reviews and 11 reference(s) in Google Scholar.)
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