324521 Sigma-AldrichEeyarestatin I - CAS 412960-54-4 - Calbiochem
A cell-permeable oxo-imidazolidinyl-hydroxyurea that localizes to ER, where it interacts with AAA ATPase p97 via its nitrofuran-containing moiety, without exhibiting affinity toward Hsp70 / ATPase NSF
More>> A cell-permeable oxo-imidazolidinyl-hydroxyurea that localizes to ER, where it interacts with AAA ATPase p97 via its nitrofuran-containing moiety, without exhibiting affinity toward Hsp70 / ATPase NSF Less<<Sinónimos: 1-(4-Chloro-phenyl)-3-(3-(4-chloro-phenyl)-5,5-dimethyl-1-(3-(5-nitro-furan-2-yl)-allyldiene-hydrazinocarbonylmethyl)-2-oxo-imidazolidin-4-yl)-1-hydroxyl-urea, EerI, ES1, Valosin-containing Protein Inhibitor II, VCP Inhibitor II, ERAD Inhibitor II, p97 Inhibitor II
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Descripción
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Tabla espec. clave
CAS # | Empirical Formula |
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412960-54-4 | C₂₇H₂₅Cl₂N₇O₇ |
Products
Número de referencia | Embalaje | Cant./Env. | |
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324521-25MG | Frasco de vidrio | 25 mg |
Description | |
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Overview | A cell-permeable oxo-imidazolidinyl-hydroxyurea that preferentially localizes to ER, where it interacts with AAA (ATPase associated with diverse cellular activities) ATPase p97 (Kd = 5 - 10 µM) via its nitrofuran-containing moiety, without exhibiting affinity toward Hsp70 or AAA ATPase NSF (N-methylmaleimide-sensitive factor). Evidence indicates that EerI cellular metabolite, but not EerI itself, is responsible for the inhibition of ER membrane translocon sec61 complex-mediated transfer of newly synthesized polypeptide, resulting in a blockage of ER-mediated posttranslational glycosylation and signal peptide removal (Effective conc. = 8 µM in HepG2 and HeLa cultures). Ether independent or as a consequence of the early effect on sec61 complex, EerI culture treatment also induces a selective dissociation of an 180 kDa protein from the atx3-containing p97/VCP (Valosin-containing protein) complex and a blockage of the complex-associated deubiquitination of ERAD (ER-associated protein degradation) substrates in a reversible manner, resulting in an accumulation of polyubiquitinated proteins (Effective conc. = 10 µM in A9 and 293T cultures). EerI culture treatment (10 µM) is also demonstrated to selectively induce cytotoxicity in lymphoid cell lines, BJAB, HBL-2, JEKO-1, Jurkat, KMS-12, MINO, as well as primary leukemia cells from CLL (chronic lymphocytic leukemia) patients, but not PBMC from healthy donors, by upregulating the BH3-only pro-apoptotic protein NOXA in cancer cells via ATF3/4 activation and a downregulation of H2A ubiquitination. Unlike DBeQ (Cat. No. 506190), EeRI does not inhibit p97 ATPase activity. |
Catalogue Number | 324521 |
Brand Family | Calbiochem® |
Synonyms | 1-(4-Chloro-phenyl)-3-(3-(4-chloro-phenyl)-5,5-dimethyl-1-(3-(5-nitro-furan-2-yl)-allyldiene-hydrazinocarbonylmethyl)-2-oxo-imidazolidin-4-yl)-1-hydroxyl-urea, EerI, ES1, Valosin-containing Protein Inhibitor II, VCP Inhibitor II, ERAD Inhibitor II, p97 Inhibitor II |
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CAS number | 412960-54-4 |
Form | Light yellow-orange solid |
Hill Formula | C₂₇H₂₅Cl₂N₇O₇ |
Chemical formula | C₂₇H₂₅Cl₂N₇O₇ |
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Quality Level | MQ100 |
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Purity | ≥90% by HPLC |
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Packaged under inert gas | Packaged under inert gas |
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Número de referencia | GTIN |
324521-25MG | 04055977197358 |
Documentation
Eeyarestatin I - CAS 412960-54-4 - Calbiochem Ficha datos de seguridad (MSDS)
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Eeyarestatin I - CAS 412960-54-4 - Calbiochem Certificados de análisis
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324521 |
Referencias bibliográficas
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Chou, T.F., et al. 2011. Proc. Natl. Acad. Sci. USA 108, 4834. Wang. Q, et al. 2010. PLoS ONE 5, e15479. Cross, B.C.S., et al. 2009. J. Cell. Sci. 122, 4393. Wang, Q., et al. 2009. Proc. Natl. Acad. Sci. USA 106, 2200. Wang, Q., et al. 2008. J. Biol. Chem. 283, 7445. Fiebiger, E., et al. 2004. Mol. Biol. Cell 15, 1635. |