4 Results for "

SHP2-IN-26

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

4 Results for "SHP2-IN-26" in MCE Product Catalog:

Cat. No.: HY-157888
Target:  

SHP2 Phosphatase

Research Areas:  

Cancer

SHP2-IN-26 (Compound 4b) is a highly selective SHP2 allosteric inhibitor with a IC50 value of 3.2 nM. SHP2-IN-26 inhibits the phosphorylation of ERK and AKT in NCI-H358 cells. SHP2-IN-26 has antitumor activity .
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1
1 Cited Publications
Cat. No.: HY-145162
CAS No.: 2458219-65-1
Purity:  95.83%
Research Areas:  

Cancer

SHP2-D26 is a SHP2 PROTAC degrader with DC50 values of 6.0 nM (KYSE520 cells) and 2.6 nM (MV4;11 cells), respectively. SHP2-D26 inhibits ERK phosphorylation, upregulates Bim levels, downregulates Mcl-1 levels, and induces cell cycle arrest and apoptosis. SHP2-D26 can be used in studies related to esophageal cancer, acute myeloid leukemia and non-small cell lung cancer .
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Cat. No.: HY-145703
CAS No.: 2740582-16-3
Purity:  99.76%
Target:  

PROTACs Drug Isomer

Research Areas:  

Others

SHP2-D26 isomer-1 (Compound 26) is an isomer of SHP2-D26 (HY-145162). SHP2-D26 is the first highly potent SHP2 PROTAC degrader. The induction of SHP2 degradation by SHP2-D26 requires binding to VHL-1 and SHP2 proteins, and is dependent on ubiquitin-like modification and the proteasome. SHP2-D26 can be used in the research of esophageal cancer and acute myeloid leukemia .
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Cat. No.: HY-176796
CAS No.: 2458219-45-7
Research Areas:  

Cancer

SHP2-IN-43 (Compound 5) is a SHP2 inhibitor with an IC50 of 98.7 nM. SHP2-IN-43 can be used as a PROTAC target ligand in the synthesis of SHP2-D26 (HY-145162) .
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