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Alvelestat (Synonyms: AZD9668)

Catalog No.GC14785

Alvelestat (AZD9668) est un inhibiteur sélectif et d'affinité biodisponible par voie orale de l'élastase des neutrophiles (NE) avec une valeur pIC50 de 7,9 nM, une valeur Ki de 9,4 nM et une valeur Kd de 9,5 nM.

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Alvelestat Chemical Structure

Cas No.: 848141-11-7

Taille Prix Stock Qté
10mM (in 1mL DMSO)
101,00 $US
En stock
1mg
28,00 $US
En stock
5mg
84,00 $US
En stock
10mg
147,00 $US
En stock
50mg
488,00 $US
En stock
100mg
713,00 $US
En stock

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

Alvelestat is an orally bioavailable inhibitor of neutrophil elastase (NE) with pIC50 value of 7.9[1].

The reversible NE inhibitor, alvelestat, is developed for treating the neutrophil-driven inflammatory lung diseases such as bronchiectasis and chronic obstructive pulmonary diseas. Alvelestat shows high affinity with human NE with a Ki value of 9.4nM. It is more than 600-fold selective for human NE over other serine proteases. In the whole-blood and cell- associated and explosive-release assays, alvelestat shows pIC50 values of 7.36, 7.32 and 7.3, respectively. In the acute lung injury model, administration of alvelestat significantly reduces the levels of hemoglobin and BAL hydroxyproline induced by human NE. In the smoke-induced airway inflammation model, alvelestat reduces both BAL neutrophils and IL-1β markedly. Furthermore, alvelestat can relieve inflammation and inhibit smoke-induced increases in lavage neutrophils and macrophages in a model of chronic smoke-induced inflammation and emphysema [1].

References:
[1] Stevens T, Ekholm K, Gränse M, et al. AZD9668: pharmacological characterization of a novel oral inhibitor of neutrophil elastase. Journal of Pharmacology and Experimental Therapeutics, 2011, 339(1): 313-320.

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Average Rating: 5 ★★★★★ (Based on Reviews and 25 reference(s) in Google Scholar.)

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