Proteasome Inhibitor II MF: C29H39N3O5
MW: 509.7
A potent, cell-permeable, and reversible proteasome inhibitor.

Proteasome Inhibitor II

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Nomes alternativos: Z-LLF-CHO
Aplicação Proteasome Inhibitor II is a potent, cell-permeable, and reversible proteasome inhibitor
Privada: ≥95%
Peso Molecular: 509.7
Separar por Funcao: C29H39N3O5
Para uso em exclusivo em pesquisa. Não se destina a uso em diagnostico e tratamento.
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Proteasome Inhibitor II is a potent, cell-permeable, reversible proteasome inhibitor. The compound has been shown to inhibit chymotrypsin-like activity of the pituitary multicatalytic proteinase complex (MPC; Ki = 460 nM). Proteasome Inhibitor II blocks the decay of IkB-a and IkB-b proteins in exponentially growing WEHI 231 cells. The chemical has been shown not to inhibit the peptidyl-glutamyl peptide hydrolyzing activity of MPC at concentrations as high as 200 µM.


Referencias

1. Orlowski, M., et al., 1993. Evidence for the presence of five distinct proteolytic components in the pituitary multicatalytic proteinase complex. Properties of two components cleaving bonds on the carboxyl side of branched chain and small neutral amino acids. Biochemistry. 32(6): 1563-72. PMID: 8431436
2. Orlowski, M., et al., 1997. Reactions of [14C]-3,4-dichloroisocoumarin with subunits of pituitary and spleen multicatalytic proteinase complexes (proteasomes). Biochemistry. 36(45): 13946-53. PMID: 9374874
3. Schauer, S L., et al., 1998. Dominant signals leading to inhibitor kappaB protein degradation mediate CD40 ligand rescue of WEHI 231 immature B cells from receptor-mediated apoptosis. Journal of immunology (Baltimore, Md. : 1950). 160(9): 4398-405. PMID: 9574544

Estado físico :
Solid
envie :
DMSO (5 mg/ml)
Manutencao :
Store at -20° C
Para uso em exclusivo em pesquisa. Não se destina a uso em diagnostico e tratamento.

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Proteasome Inhibitor II  Citacoes dos Produtos

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Citações 1 para 1 de 1 total

PMID: # 25461257  Aveic, S. et al. 2015. Exp. Hematol. 43: 180-190.e6.

Citações 1 para 1 de 1 total
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