6 Results for "

MDMX/MDM2-IN-2

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "MDMX/MDM2-IN-2" in MCE Product Catalog:

Cat. No.: HY-149250
CAS No.: 3043723-74-3
Target:  

MDM-2/p53 Apoptosis

Research Areas:  

Cancer

MDMX/MDM2-IN-2 is a potent p53-MDM2/MDMX dual inhibitors with Kis of 0.23 μM and 2.45 μM for MDM2 and MDMX, respectively. MDMX/MDM2-IN-2 inhibits the binding of p53 and MDM2 proteins. MDMX/MDM2-IN-2 restores the function of p53 and enables cell cycle arrest and apoptosis. MDMX/MDM2-IN-2 inhibits cell migration and invasion. MDMX/MDM2-IN-2 has antitumor activity .
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Cat. No.: HY-123950
CAS No.: 430458-66-5
Purity:  ≥98.0%
Target:  

MDM-2/p53 Apoptosis

Research Areas:  

Cancer

MMRi64 disrupts Mdm2-MdmX interactions. MMRi64 downregulates Mdm2 and MdmX in leukemia cells. MMRi64 induces p53 accumulation, and induces the apoptotic arm of the p53 pathway in leukemia/lymphoma cells. MMRi64 can be used for cancer research .
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Cat. No.: HY-148106
CAS No.: 642072-49-9
Target:  

Ligands for E3 Ligase

Research Areas:  

Cancer

MEL23 is a MDM2 E3 ligase inhibitor that blocks the E3 ligase activity of the MDM2-MDMX complex. MEL23 inhibits Mdm2 and p53 ubiquitination in cells, reduce viability of cells with wild-type p53. MEL23 stabilizes MDM2 via a mechanism independent of p53 transcription .
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Cat. No.: HY-124791
CAS No.: 709009-15-4
Target:  

MDM-2/p53 PARP

Research Areas:  

Cancer

MMRi6 is a Mdm2-MdmX RING domain inhibitor that can disrupt Mdm2-MdmX RING-RING interaction in vitro. MMRi6 inhibits MdmX-stimulated Mdm2 autoubiquitination and Mdm2-MdmX-mediated p53 polyubiquitination in vitro without affecting NEDD4-1 autoubiquitination. MMRi6 induces p53 stabilization and accumulation and induces PARP cleavage in wt-p53 Emu-myc lymphoma cells. MMRi6 inhibits the growth of wt-p53 and p53-null Emu-myc lymphoma cells with IC50s of approximately 0.5 μM and 3 μM, respectively. MMRi6 can be used for the study of leukemia/lymphoma .
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Cat. No.: HY-164550
CAS No.: 2247210-09-7
Target:  

HDAC

Research Areas:  

Cancer

YF438 is an HDAC inhibitor with effective anticancer activity both in vitro and in vivo. YF438 inhibits the growth and metastasis of triple-negative breast cancer (TNBC) cells by blocking the interaction between HDAC and MDM2, inducing the dissociation of MDM2-MDMX, and promoting the degradation of MDM2 .
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Cat. No.: HY-163275
Target:  

MDM-2/p53 Apoptosis

Research Areas:  

Cancer

MDM2-IN-24 (compound A3f) exhibits MDM2-inhibiting and MDMX-activating properties in triple-negative breast cancer (TNBC) cells, with apoptotic and anti-proliferative activities .
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