7 Results for "

polo-box domain

" in MedChemExpress (MCE) Product Catalog:
Products (7)

7 Results for "polo-box domain" in MCE Product Catalog:

3
3 Cited Publications
Cat. No.: HY-12134
CAS No.: 321688-88-4
Purity:  98.01%
Research Areas:  

Cancer

Poloxin is a non-ATP competitive Polo-like Kinase 1 (PLK1) inhibitor that targets the polo-box domain, with an IC50 of appr 4.8 μM.
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Cat. No.: HY-124761
CAS No.: 683808-78-8
Research Areas:  

Cancer

Poloppin is a potent, cell penetrant inhibitor of the mitotic Polo-like kinase (PLK) (IC50=26.9 μM) and prevents the protein-protein interaction via the Polo-box domain (PBD) (Kd= 29.5 μM). Poloppin selectively kills cells expressing mutant KRAS, enhancing death in mitosis. Poloppin is used for the study of KRAS-mutant cancers as single agents, or in combination with c-MET inhibitors .
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Cat. No.: HY-161521
CAS No.: 2991469-21-5
Research Areas:  

Cancer

PLK1-IN-10 (Compound 4Bb) is an orally active PLK1 PBD (polo-box domain) inhibitor. PLK1-IN-10 blocks the interaction of PLK1 with the cell division regulator protein 1 (PRC1) and decreases the protein expression of the CDK1-Cyclin B1 complex. PLK1-IN-10 reacts with glutathione (GSH) to increase cellular oxidative stress, ultimately leading to cell death .
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Cat. No.: HY-12135
CAS No.: 1239513-63-3
Research Areas:  

Cancer

Poloxipan is a pan-specific polo-like kinase (PLK) inhibitor that can inhibit a non-catalytic region at the C-terminus called the Polo-box domain (PBD) found in kinases. The IC50 values for Poloxipan against the PBDs of PLK-1/2/3 are 3.2 μM, 1.7 μM, and 3.0 μM, respectively. Poloxipan also inhibits other phospho-tyrosine binding domains, such as the forkhead-associated (FHA) domain of CHK-2, the WW domain of peptidyl-prolyl cis/trans isomerase (PIN1), and the phospho-tyrosine binding domains of STAT1/3/5 and lymphocyte-specific protein tyrosine kinase's SH2 domain. Poloxipan can be used in cancer research .
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Cat. No.: HY-W457608
CAS No.: 34330-04-6
Target:  

Drug Derivative

Research Areas:  

Cancer

CU7218 competitively binds to the phosphopeptide-binding pocket of 14-3-3ε and blocks its interaction with the 9J10 peptide. CU7218 can be used in cancer research .
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Cat. No.: HY-P702889
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: PLK3; Proliferation-Related Kinase; Prev. CNK; polo-Like Kinase 3; FNK; PLK-3; PRK; polo-Like Kinase 3 (Drosophila); Cytokine-Inducible Serine/Threonine-Protein Kinase; Cytokine-Inducible Kinase; Serine/Threonine-Protein Kinase PLK3; polo Like Kinase 3; F
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-181000
CAS No.: 3074520-74-1
Research Areas:  

Cancer

PROTAC PLK1 Degrader-3 (Compound DD-1) is a PLK1 PROTAC degrader based on the N-deglycosylation pathway, with a Kd value of 2.2 μM. The cell penetration ability of PROTAC PLK1 Degrader-3 is limited and a higher concentration is required to achieve significant degradation effects. PROTAC PLK1 Degrader-3 can be used for research on non-small cell lung cancer .
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