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product description:NSC 95397 is a potent, selective Cdc25 dual specificity phosphatase inhibitor with Ki of 32 nM, 96 nM, 40 nM for Cdc25A, Cdc25B and Cdc25C, respectively. NSC 95397 has IC50 of 22.3 nM, 56.9
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NSC 95397 is a 1,4-naphthoquinone-based irreversible inhibitor of Cdc25 dual-specificity phosphatases (Ki = 32, 96 and 40 nM for inhibition of Cdc25A, -B and -C respectively). NSC 95397 exhibits 125-180-fold selectivity over VH1-related dual-specificity phosphatase
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Image Search Results
Journal: Cell Biology and Toxicology
Article Title: CtBP1–LSD1 complex drives ErbB2 activation via H3K9me2 demethylation in DRGs during paclitaxel-induced neuropathic pain
doi: 10.1007/s10565-025-10122-7
Figure Lengend Snippet: PTX-induced CtBP1 upregulation requires interaction with transcription partners to regulate ErbB2 transcription/expression in DRG neurons.. Diagram of the timeline of this experiment. Paclitaxel, PTX. Vehicle, VEH. DMSO, vehicle. NSC, NSC95397, CtBP1-protein partner interaction inhibitor.. (C) The paw mechanical threshold measured on day 14 in PTX or VEH rats in response to intrathecal injection NSC95397 (NSC; inhibit the CtBP1-protein partner interaction; 1, 10 and 30 nM; 10 μL, administered twice daily for three consecutive days from day 11 to 13 after PTX treatment) or VEH (vehicle). Each group: 6 rats. B, One-way ANOVA, F (5, 30) = 14.97, p < 0.0001. D, One-way ANOVA, F (2, 12) = 0.1286, p = 0.8805. ** p < 0.01 vs. VEH 14D. ## p < 0.01 vs. PTX 14D.. The paw mechanical latency measured on day 14 in PTX rats in response to intrathecal injection NSC95397 (NSC; inhibit the CtBP1-protein partner interaction; 30 nM; 10 μL, administered twice daily for three consecutive days from day 11 to 13 after PTX treatment) or VEH (vehicle). Each group: 6 rats. C, One-way ANOVA, F (3, 16) = 62.20, p < 0.0001.** p < 0.01 vs. VEH 14D. ## p < 0.01 vs. PTX 14D.. Representative qPCR statistical analyses of ErbB2 mRNA abundances in the DRGs at day 14 of PTX rats in response to intrathecal injection NSC95397 (NSC; inhibit the CtBP1-protein partner interaction; 30 nM; 10 μL, administered twice daily for three consecutive days from day 11 to 13 after PTX treatment) or or VEH (vehicle). Relative quantification (RQ) = 2 −△△CT . Each group has 5 rats. One-way ANOVA, F (3, 16) = 19.32, p < 0.0001. ** p < 0.01 vs. VEH 14D. ## p < 0.01 vs. PTX 14D. Representative Western blot and statistical analyses (normalized to GAPDH) of CtBP1 and ErbB2 abundances in the DRGs at day 14 of PTX rats in response to intrathecal injection NSC95397 (NSC; inhibit the CtBP1-protein partner interaction; 30 nM; 10 μL, administered twice daily for three consecutive days from day 11 to 13 after PTX treatment) or or VEH (vehicle). Each group has 5 rats. CtBP1, One-way ANOVA, F (3, 16) = 24.92, p < 0.0001. ErbB2, One-way ANOVA, F (3, 16) = 35.69, p < 0.0001.** p < 0.01 vs. VEH 14D. ## p < 0.01 vs. PTX 14D.. ChIP-qPCR assay of the abundance of the CtBP1-precipitated ErbB2 promoter fragments at day at day 14 of PTX rats in response to intrathecal injection NSC95397 (NSC; inhibit the CtBP1-protein partner interaction; 30 nM; 10 μL, administered twice daily for three consecutive days from day 11 to 13 after PTX treatment) or or VEH (vehicle) Each group: 5 rats. CtBP1, One-way ANOVA, F (3, 16) = 33.00, p < 0.0001. IgG, One-way ANOVA, F (3, 16) = 0.17, p = 0.9140. ** p < 0.01 vs. VEH 14D. ## p < 0.01 vs. PTX 14D
Article Snippet: AG825 (an ErbB2 inhibitor; 1, 30, and 100 nM; 10 μL; Tocris Bioscience, Bristol, UK),
Techniques: Expressing, Injection, Quantitative Proteomics, Western Blot, ChIP-qPCR