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GSK 461364 analogue II

 

CAS 929095-22-7

C27H27F3N4O3S  MW 544.59

Purity: 99% (optically pure)

 

 

 

 

Ordering Information:

 

Cat. No. Axon 1626

 

Qty1:  5 mg (research sample) / 135  $176

 

Qty3: 25 mg (research sample) / 505  $657

 

Qty4: on request

 

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Biological Activity:

 

Potent Polo-like kinase (PLK) inhibitor, selective at PLK1 (IC50: 2 nM) over PLK3 (IC50: 270 nM).

 

References:

 

TR Rheault et al. Heteroaryl-linked 5-(1H-benzimidazol-1-yl)-2-thiophene carboxamides: potent inhibitors of polo-like kinase 1 (PLK1) with improved drug-like properties. Bioorg. Med. Chem. Lett. 2010, 20(15), 4587-92. [online]

 

KA Emmitte et al. Design of potent thiophene inhibitors of polo-like kinase 1 with improved solubility and reduced protein binding. Bioorg. Med. Chem. Lett. 2009, 19(6), 1694-7. [online]

 

 

Chemical Name: (R)-5-(6-(1-methylpiperidin-4-yloxy)-1H-benzo[d]imidazol-1-yl)-3-(1-(2-(trifluoromethyl)phenyl)ethoxy)thiophene-2-carboxamide

 

GSK 461364 analogue II | PLK1 inhibitor | Axon Medchem | Axon 1626 | GSK461364 analogue II 

Axon Ligands TM - Research chemicals for biological study. Some high-profile samples could be provided under terms of contract research synthesis.

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Axon Ligands in the field:

 

BI 2536 | PLK1 inhibitor

BI 6727 | PLK1 inhibitor

GSK 461364 | PLK1 inhibitor

GSK 461364 analogue I | PLK1 inhibitor

GSK 461364 analogue II | PLK1 inhibitor

GW 843682X | PLK 1/3 inhibitor

 

 

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