5 Results for "

SU-DHL-10

" in MedChemExpress (MCE) Product Catalog:
Products (5)

5 Results for "SU-DHL-10" in MCE Product Catalog:

Cat. No.: HY-160945
CAS No.: 3032302-70-5
Research Areas:  

Cancer

NMT-IN-7 is a N-myristoyl transferase (NMT) inhibitor, with IC50s of 2.1 nM for HsNMT1M, 0.6 nM for SU-DHL-10 cell. NMT-IN-7 can be used as a ADC cytotoxin .
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Cat. No.: HY-170762
CAS No.: 2155856-87-2
Target:  

Apoptosis Bcl-2 Family

Research Areas:  

Cancer

Mcl-1 inhibitor 21 (Example 1-36) is a Mcl-1 inhibitor with an IC50 of 328 nM. Mcl-1 inhibitor 21 exhibits proapototic and anti-proliferation activities against SUDHL5 and SUDHL10 cell lines and can be utilized in cancer research .
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Cat. No.: HY-170762A
CAS No.: 2157421-23-1
Target:  

Apoptosis Bcl-2 Family

Research Areas:  

Cancer

(+)-Mcl-1 inhibitor 21 (Example 1-37) is a Mcl-1 inhibitor with an IC50 of 172 nM. (+)-Mcl-1 inhibitor 21 exhibits proapototic and anti-proliferation activities against SUDHL5 and SUDHL10 cell lines and can be utilized in cancer research .
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Cat. No.: HY-170762B
CAS No.: 2157421-24-2
Target:  

Apoptosis Bcl-2 Family

Research Areas:  

Cancer

(-)-Mcl-1 inhibitor 21 (Example 1-38) is a Mcl-1 inhibitor with an IC50 of 7.51 μM. (-)-Mcl-1 inhibitor 21 exhibits proapototic and anti-proliferation activities against SUDHL5 and SUDHL10 cell lines and can be utilized in cancer research .
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Cat. No.: HY-181459
CAS No.: 3109617-69-5
PARP1-IN-55 is a potent and selective PARP1 inhibitor with an IC50 value of 0.019 μM. PARP1-IN-55 exhibits anti-proliferative selective activity against MCF-7 breast cancer cells (IC50 = 3.6 μM). PARP1-IN-55 inhibits the PARP1-mediated DNA damage repair pathway, induces ROS accumulation, disrupts mitochondrial membrane potential, induced apoptosis and suppresses cancer cell migration, invasion, and colony formation. PARP1-IN-55 can be used for the study of breast cancer .
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