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SCH 529074

Katalog-Nr.GC14561

SCH 529074 ist ein potenter und oral aktiver p53-Aktivator. SCH 529074 bindet spezifisch und konformationsabhängig an p53 DBD (DNA-Bindungsdomäne) mit einem Ki von 1–2 μM in sättigbarer Weise. SCH 529074 stellt die Funktion von mutiertem p53 wieder her und unterbricht die HDM2-vermittelte Ubiquitinierung von Wildtyp-p53. SCH 529074 kann für die Untersuchung des nicht-kleinzelligen Lungenkarzinoms (NSCLC) verwendet werden.

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SCH 529074 Chemische Struktur

Cas No.: 922150-11-6

Größe Preis Lagerbestand Menge
1mg
38,00 $
Auf Lager
5mg
195,00 $
Auf Lager
10mg
324,00 $
Auf Lager
25mg
649,00 $
Auf Lager

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

SCH 529074 is a small molecule activator of p53, a tumor suppressor that is mutated or non-functional in 50% of human tumors.[1] SCH 529074 restores DNA binding activity and increases DNA binding affinity of two recombinant GST fusion mutant p53 DNA binding domains (R273H and R249S) in an electrophoretic mobility shift assay with Kd values of 0.6740 and 0.4313, respectively. It also stimulates DNA binding activity and prevents human double minute-2 (Hdm-2) ubiquitination of wild-type p53 in vitro. SCH 29074 reduces proliferation of tumor cell lines with mutant and wild-type p53 (EC50s = 400-3,700 nM), with the p53 mutant cell lines being the most sensitive. In vivo, SCH 529074 reduces tumor growth in a DLD-1 human colorectal cancer xenograft model in mice in a dose-dependent manner.

Reference:
[1]. Demma, M., Maxwell, E., Ramos, R., et al. SCH529074, a small molecule activator of mutant p53, which binds p53 DNA binding domain (DBD), restores growth-suppressive function to mutant p53 and interrupts HDM2-mediated ubiquitination of wild type p53. J. Biol. Chem. 285(14), 10198-10212 (2010).

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Average Rating: 5 ★★★★★ (Based on Reviews and 23 reference(s) in Google Scholar.)

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