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Echelon Biosciences
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compound 7 comp 7 - by Bioz Stars,
2026-08
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PF-543 Citrate (Sphingosine Kinase 1 Inhibitor II Citrate) is a potent, selective, reversible and sphingosine-competitive SPHK1 inhibitor with an IC50 of 2 nM and a Ki of 3.6 nM. PF-543 Citrate is >100-fold selectivity for
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Selleck Chemicals
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pf 543 - by Bioz Stars,
2026-08
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Tocris
sphingosine kinase 1 sphk1 inhibitor pf 543 hydrochloride ![]() Sphingosine Kinase 1 Sphk1 Inhibitor Pf 543 Hydrochloride, supplied by Tocris, used in various techniques. Bioz Stars score: 89/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/pf+543/pmc08220815-48-38-45?v=Tocris Average 89 stars, based on 1 article reviews
sphingosine kinase 1 sphk1 inhibitor pf 543 hydrochloride - by Bioz Stars,
2026-08
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Merck KGaA
pf-543 ![]() Pf 543, supplied by Merck KGaA, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/pf+543/pmc06265344-31-3-11?v=Merck+KGaA Average 90 stars, based on 1 article reviews
pf-543 - by Bioz Stars,
2026-08
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Pfizer Inc
pf 543 ![]() Pf 543, supplied by Pfizer Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/pf+543/pm41860929-54-0-8?v=Pfizer+Inc Average 86 stars, based on 1 article reviews
pf 543 - by Bioz Stars,
2026-08
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PF 543 is a potent inhibitor of sphingosine kinase 1 SPHK1 IC 2 nM that inhibits sphingosine 1 phosphate S1P binding to human recombinant SPHK1 K 3 6 nM It is selective for SPHK1 over
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Image Search Results
Journal: Frontiers in Cell and Developmental Biology
Article Title: Ceramide Kinase Inhibition Blocks IGF-1-Mediated Survival of Otic Neurosensory Progenitors by Impairing AKT Phosphorylation
doi: 10.3389/fcell.2021.678760
Figure Lengend Snippet: Inhibition of endogenous SPHK1 has no effect on early inner ear development. (A) Morphological aspect of organotypic cultures after 20 h in serum-free medium (SFM), 1 μM PF-543, 10 nM IGF-1, IGF-1 plus PF-543. Immunostaining with TUNEL (cyan) and PH3 (red) of at least 5 otic vesicle per condition. Scale bar: 150 μm. (B) Quantification of otic vesicle area, (C) TUNEL-positive or (D) PH3-labeled cells in the presence or absence of PF-543 (0.25 and 1 μM) and IGF-1 (10 nM). (E) SOX2 intensity (F) and Tuj-1 intensity as neurogenesis markers normalized to data for SFM. Data are represented as mean ± SEM from at least n = 4 otic vesicles per condition. Statistical significance was calculated by one-way ANOVA followed by Bonferroni’s (B,E) or Dunnett’s T3 post hoc test (C) . * p < 0.05, ** p < 0.01, *** p < 0.001 vs control.
Article Snippet: Culture treatments included serum-free medium (SFM, control condition), 10 nM IGF-1 (recombinant IGF-I; Roche Molecular Biochemicals, Basel, Switzerland), the CERK inhibitor adamantane-1-carboxylic acid (2-benzoylamino-benzothiazol-6-yl)amide (NVP-231, hereafter called CKi) (Tocris Bioscience, Bristol, United Kingdom) prepared in DMSO, and the
Techniques: Inhibition, Immunostaining, TUNEL Assay, Labeling, Control