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Exploration of Pyrazolo[1,5‐a]pyrimidines as Membrane‐Bound Pyrophosphatase Inhibitors.
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- ChemMedChem, 2021, v. 16, n. 21, p. 3360, doi. 10.1002/cmdc.202100392
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- Article
Interaction between Retinoid Acid Receptor-Related Orphan Receptor Alpha (RORA) and Neuropeptide S Receptor 1 (NPSR1) in Asthma.
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- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0060111
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- Article
C1 Domain-Targeted Isophthalate Derivatives Induce Cell Elongation and Cell Cycle Arrest in HeLa Cells.
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- PLoS ONE, 2011, v. 6, n. 5, p. 1, doi. 10.1371/journal.pone.0020053
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C1 domain-targeted isophthalates as protein kinase C modulators: structure-based design, structure-activity relationships and biological activities.
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- Biochemical Society Transactions, 2014, v. 42, n. 6, p. 1543, doi. 10.1042/BST20140181
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- Article
Hydrophobic derivatives of 5-(hydroxymethyl)isophthalic acid that selectively induce apoptosis in leukemia cells but not in fibroblasts.
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- Drug Development Research, 2008, v. 69, n. 4, p. 185, doi. 10.1002/ddr.20116
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- Article
Stem cells are the most sensitive screening tool to identify toxicity of GATA4-targeted novel small-molecule compounds.
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- Archives of Toxicology, 2018, v. 92, n. 9, p. 2897, doi. 10.1007/s00204-018-2257-1
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- Article
Design, Synthesis, and Biological Activity of Urea Derivatives as Anaplastic Lymphoma Kinase Inhibitors.
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- ChemMedChem, 2011, v. 6, n. 9, p. 1680, doi. 10.1002/cmdc.201100168
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- Article
Total Synthesis of Bistramide A and Its 36( Z) Isomers: Differential Effect on Cell Division, Differentiation, and Apoptosis.
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- Chemistry - A European Journal, 2012, v. 18, n. 24, p. 7452, doi. 10.1002/chem.201102462
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- Article
Affinity chromatography reveals direct binding of the GATA4–NKX2-5 interaction inhibitor (3i-1000) with GATA4.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-59418-4
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- Article
Scaffold hopping from (5-hydroxymethyl) isophthalates to multisubstituted pyrimidines diminishes binding affinity to the C1 domain of protein kinase C.
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- PLoS ONE, 2018, v. 13, n. 4, p. 1, doi. 10.1371/journal.pone.0195668
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- Article
Orexin receptor agonist Yan 7874 is a weak agonist of orexin/hypocretin receptors and shows orexin receptor-independent cytotoxicity.
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- PLoS ONE, 2017, v. 12, n. 6, p. 1, doi. 10.1371/journal.pone.0178526
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- Article