Epoxomicin (Synonyms: BU 4061T) |
Katalog-Nr.GC12494 |
Epoxomicin is a selective proteasome inhibitor that effectively inhibits the chymotrypsin-like (CH-L) activity of the 20S proteasome, with an IC50 of approximately 40-80nM.
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Cas No.: 134381-21-8
Sample solution is provided at 25 µL, 10mM.
Epoxomicin is a selective proteasome inhibitor that effectively inhibits the chymotrypsin-like (CH-L) activity of the 20S proteasome, with an IC50 of approximately 40-80nM[1]. Epoxomicin covalently binds to the catalytic β subunits LMP 7, X, Z, and MECL 1 of the proteasome, leading to inhibition of the proteasome subunits' CH-L, T-L, and PGPH catalytic activities[2].
In vitro, Epoxomicin shows considerable cytotoxicity against B16-F10, HCT116, Moser, P388, and K562 cells, with IC50 values of 0.002μg/mL, 0.005μg/mL, 0.044μg/mL, 0.002μg/mL, and 0.037μg/mL, respectively[3]. Epoxymycin (0.2 and 2 μM) treated HEK293T cells for 1 hour, inhibiting the expression of proteasome beta-2 and beta-5 subunits in the cells[4]. Epoxomicin (100 nM) for 24 hours in Plasmodium falciparum cells results in a 77% reduction in gametocytes[5].
In vivo, Epoxymycin (0.5mg/kg), administered intraperitoneally, reduced polyubiquitination in GAS muscle of C57BL/6 mice by 23% and increased polyubiquitination in liver by 41%, the latter associated with The inhibitory effect of proteasome β5 is consistent [6]. Epoxymycin (0.5mg/kg/day) was administered to KI and WT mice for 1 week using a subcutaneously implanted osmotic minipump, which reduced the chymotrypsin-like activity of the mice by approximately 50%[7] .
References:
[1] Meng L , Mohan R , Kwok B H B ,et al.Epoxomicin, a potent and selective proteasome inhibitor, exhibits in vivo antiinflammatory activity[J]. Proceedings of the National Academy of Sciences, 1999, 96(18):10403-10408.
[2] Aboulaila M , Nakamura K , Govind Y ,et al.Evaluation of the in vitro growth-inhibitory effect of epoxomicin on Babesia parasites.[J].Veterinary Parasitology, 2010, 167(1):19-27.
[3] Hanada M, Sugawara K, Kaneta K, et al. Epoxomicin, a new antitumor agent of microbial origin.[J] Antibiot (Tokyo). 1992 Nov;45(11):1746-52.
[4] Fricker L D, Gelman J S, Castro L M, et al. Peptidomic analysis of HEK293T cells: effect of the proteasome inhibitor epoxomicin on intracellular peptides[J]. Journal of proteome research, 2012, 11(3): 1981-1990.
[5] Czesny B , Goshu S , Cook J L ,et al. The Proteasome Inhibitor Epoxomicin Has Potent Gametocytocidal Activity[J]. 2009.
[6]Jamart, Cécile, Gomes A V , Dewey S ,et al. Regulation of ubiquitin-proteasome and autophagy pathways after acute LPS and epoxomicin administration in mice[J].Bmc Musculoskeletal Disorders, 2014, 15(1):166.
[7]Schlossarek,Saskia,Singh,et al. Proteasome inhibition slightly improves cardiac function in mice with hypertrophic cardiomyopathy[J].Frontiers in Physiology, 2014.
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