SKPin C1
Discontinued Product
Chemical Name: 2-[4-Bromo-2-[[4-oxo-3-(3-pyridinylmethyl)-2-thioxo-5-thiazolidinylidene]methyl]phenoxy]acetic acid
Purity: ≥98%
Biological Activity
SKPin C1 is an inhibitor of Skp2-mediated p27 degradation. Induces p27 accumulation in metastatic melanoma cell lines. Promotes G1/S cell cycle arrest in T47D cells and LNCaP cells; induces G2/M cell cycle arrest in MCF-7 cells.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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Dual Inhibition of CDK4 and CDK2 via Targeting p27 Tyrosine Phosphorylation Induces a Potent and Durable Response in Breast Cancer Cells
P Patel, V Tsiperson, SRS Gottesman, J Somma, SW Blain
Mol. Cancer Res., 2018;0(0):. -
Skipping cancer: small molecule inhibitors of SKP2-mediated p27 degradation.
Rico-Bautista and Wolf
Chem.Biol., 2012;19:1497 -
Specific small molecule inhibitors of Skp2-mediated p27 degradation.
Wu et al.
Chem.Biol., 2012;19:1515
Product Datasheets
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Citations for SKPin C1
The citations listed below are publications that use Tocris products. Selected citations for SKPin C1 include:
2 Citations: Showing 1 - 2
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Identification of highly penetrant Rb-related synthetic lethal interactions in triple negative breast cancer.
Authors: Brough Et al.
Oncogene 2018;
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Proliferation and Survival of Embryonic Sympathetic Neuroblasts by MYCN and Activated ALK Signaling.
Authors: Kramer Et al.
J Neurosci 2016;36:10425
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