4 Results for "

kinase-panel selectivity

" in MedChemExpress (MCE) Product Catalog:
Products (4)

4 Results for "kinase-panel selectivity" in MCE Product Catalog:

Cat. No.: HY-149075
CAS No.: 3027761-24-3
Research Areas:  

Cancer

MR22 is a potent pan-SIK (salt-inducible kinase) inhibitor. MR22 no longer exhibits activity on STE group kinases and displays excellent selectivity in a representative kinase panel. MR22-dependent SIK inhibition led to centrosome dissociation and subsequent cell-cycle arrest in ovarian cancer cells .
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Cat. No.: HY-179599
CAS No.: 1448757-02-5
Target:  

DYRK EGFR

Research Areas:  

Neurological Disease Cancer

Dyrk1A-IN-15 is a selective, brain-penetrant and ATP-competitive Dyrk1A inhibitor with a IC50 of 19 nM. Dyrk1A-IN-15 displays high selectivity across a broad kinase panel (specific for DYRK kinases) with nanomolar potency. Dyrk1A-IN-15 impairs neurosphere self-renewal, cell invasion, and EGFR stability in vitro. Dyrk1A-IN-15 inhibits tumor growth and prolongs survival in vivo. Dyrk1A-IN-15 has potential for glioblastoma (GBM) research .
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Cat. No.: HY-179600
CAS No.: 2805339-74-4
Target:  

DYRK EGFR

Research Areas:  

Neurological Disease Cancer

Dyrk1A-IN-16 is a selective, brain-penetrant and ATP-competitive Dyrk1A inhibitor with a IC50 of 53 nM. Dyrk1A-IN-16 displays high selectivity across a broad kinase panel (specific for DYRK kinases) with nanomolar potency. Dyrk1A-IN-16 impairs neurosphere self-renewal, cell invasion, and EGFR stability in vitro. Dyrk1A-IN-16 inhibits tumor growth and prolongs survival in vivo. Dyrk1A-IN-16 has potential for glioblastoma (GBM) research .
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Cat. No.: HY-189673
Target:  

FLT3 STAT Akt ERK PDGFR Apoptosis

Research Areas:  

Cancer

FLT3-ITD-IN-4 is an orally active FLT3-ITD inhibitor. FLT3-ITD-IN-4 targets FLT3-ITD with an IC50 of 1.1 nM, blocking autophosphorylation and downstream STAT, AKT, and ERK signaling. FLT3-ITD-IN-4 shows weaker inhibition of wild-type FLT3, with PDGFRβ as the primary off-target, demonstrating selectivity across a broad kinase panel. FLT3-ITD-IN-4 induces cell cycle arrest, apoptosis, and DNA damage response. FLT3-ITD-IN-4 can be used for research on acute myeloid leukemia .
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