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Aclacinomycin A hydrochloride

Catalog No.GC35238

Chlorhydrate d'aclacinomycine A (chlorhydrate d'aclarubicine), une molécule fluorescente et le premier inhibiteur non peptidique décrit présentant une spécificité discrète pour l'activité CTRL (chymotrypsine-like) du protéasome 20S. Le chlorhydrate d'aclacinomycine A est également un double inhibiteur de la topoisomérase I et II. Un agent chimiothérapeutique anthracycline efficace pour les cancers hématologiques et les tumeurs solides.

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Aclacinomycin A hydrochloride Chemical Structure

Cas No.: 75443-99-1

Taille Prix Stock Qté
10mM (in 1mL DMSO)
415,00 $US
En stock
5mg
260,00 $US
En stock
10mg
445,00 $US
En stock
25mg
908,00 $US
En stock
50mg
1 483,00 $US
En stock

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

Aclacinomycin A hydrochloride (Aclarubicin hydrochloride), a fluorescent molecule and the first described non-peptidic inhibitor showing discrete specificity for the CTRL (chymotrypsin-like) activity of the 20S proteasome[1]. Aclacinomycin A hydrochloride is also a dual inhibitor of topoisomerase I and II[2]. An effective anthracycline chemotherapeutic agent for hematologic cancers and solid tumors[3]. 20S proteasome[1].Topoisomerase I and II[2].

[1]. Isoe T, et al. Inhibition of different steps of the ubiquitin system by CDDP and aclarubicin. Biochim Biophys Acta. 1992 Sep 15;1117(2):131-5. [2]. Hajji N, et al. Induction of genotoxic and cytotoxic damage by aclarubicin, a dual topoisomerase inhibitor. Mutat Res. 2005 May 2;583(1):26-35. [3]. Iihoshi H, et al. Aclarubicin, an anthracycline anti-cancer drug, fluorescently contrasts mitochondria and reduces the oxygen consumption rate in living human cells. Toxicol Lett. 2017 Aug 5;277:109-114.

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Average Rating: 5 ★★★★★ (Based on Reviews and 13 reference(s) in Google Scholar.)

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