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AP-III-a4

Cat. No. M14421

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AP-III-a4 Structure
Synonym:

ENOblock

Size Price Availability Quantity
1mg USD 60 In stock
5mg USD 150 In stock
10mg USD 240 In stock
25mg USD 450 In stock
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Quality Control & Documentation
Biological Activity

ENOblock(AP-III-a4) is a novel small molecule which is the first, nonsubstrate analogue that directly binds to enolase and inhibits its activity (IC50=0.576 uM); inhibit cancer cell metastasis in vivo. IC50 value: 0.576 uM Target: enolase Enolase is a component of the glycolysis pathway and a “moonlighting” protein, with important roles in diverse cellular processes that are not related to its function in glycolysis. However, small molecule tools to probe enolase function have been restricted to crystallography or enzymology. In this study, we report the discovery of the small molecule “ENOblock”, which is the first, nonsubstrate analogue that directly binds to enolase and inhibits its activity. ENOblock was isolated by small molecule screening in a cancer cell assay to detect cytotoxic agents that function in hypoxic conditions, which has previously been shown to induce drug resistance. Further analysis revealed that ENOblock can inhibit cancer cell metastasis in vivo. Moreover, an unexpected role for enolase in glucose homeostasis was revealed by in vivo analysis. Thus, ENOblock is the first reported enolase inhibitor that is suitable for biological assays. This new chemical tool may also be suitable for further study as a cancer and diabetes drug candidate. A Unique Small Molecule Inhibitor of Enolase Clarifies Its Role in Fundamental Biological Processes By Jung, Da-Woon; Kim, Woong-Hee; Park, Si-Hwan; Lee, Jinho; Kim, Jinmi; Su, Dongdong; Ha, Hyung-Ho; Chang, Young-Tae; Williams, Darren R. From ACS Chemical Biology (2013), 8(6), 1271-1282.

Chemical Information
Molecular Weight 594.72
CAS Number 1177827-73-4
Form Solid
Solubility (25°C) DMSO 62.5 mg/mL
Storage 2-8°C, protect from light
References

[1] Ting Yang, et al. Cell Death Dis. Enolase 1 regulates stem cell-like properties in gastric cancer cells by stimulating glycolysis

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Keywords: AP-III-a4, ENOblock supplier, inhibitors, activators

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