BI-1347

10mM in DMSO

Reagent Code: #142640
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CAS Number 2163056-91-3

science Other reagents with same CAS 2163056-91-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 356.42 g/mol
Formula C₂₂H₂₀N₄O
inventory_2 Storage & Handling
Storage -20°C

description Product Description

BI-1347 is a potent and selective inhibitor of the fibroblast growth factor receptor (FGFR) family, particularly FGFR1. It is primarily used in research settings to study signaling pathways involved in cell proliferation, survival, and differentiation. Due to its ability to block aberrant FGFR signaling, it has shown promise in preclinical studies for the treatment of cancers driven by FGFR gene amplifications, mutations, or fusions, such as certain types of bladder, lung, and breast cancers. The compound is employed in in vitro and in vivo models to evaluate tumor response and mechanism of resistance to FGFR inhibition. Its high selectivity helps minimize off-target effects, making it a valuable tool for validating FGFR as a therapeutic target. BI-1347 is also used in combination studies with other anticancer agents to assess synergistic effects and improve therapeutic outcomes in resistant tumor types.

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inventory 1ml
10-20 days ฿6,480.00

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BI-1347
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BI-1347 is a potent and selective inhibitor of the fibroblast growth factor receptor (FGFR) family, particularly FGFR1. It is primarily used in research settings to study signaling pathways involved in cell proliferation, survival, and differentiation. Due to its ability to block aberrant FGFR signaling, it has shown promise in preclinical studies for the treatment of cancers driven by FGFR gene amplifications, mutations, or fusions, such as certain types of bladder, lung, and breast cancers. The compound is employed in in vitro and in vivo models to evaluate tumor response and mechanism of resistance to FGFR inhibition. Its high selectivity helps minimize off-target effects, making it a valuable tool for validating FGFR as a therapeutic target. BI-1347 is also used in combination studies with other anticancer agents to assess synergistic effects and improve therapeutic outcomes in resistant tumor types.
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