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Broad-Spectrum Anticancer Activity and Pharmacokinetic Properties of a Prenyloxy-Substituted Indeno[1,2- b ]indole Derivative, Discovered as CK2 Inhibitor.
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- Pharmaceuticals (14248247), 2021, v. 14, n. 6, p. 542, doi. 10.3390/ph14060542
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- Article
Self-Assembled Supramolecular Nanoparticles Improve the Cytotoxic Efficacy of CK2 Inhibitor THN7.
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- Pharmaceuticals (14248247), 2018, v. 11, n. 1, p. 10, doi. 10.3390/ph11010010
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- Article
Unexpected Binding Mode of a Potent Indeno[1,2-b]indole-Type Inhibitor of Protein Kinase CK2 Revealed by Complex Structures with the Catalytic Subunit CK2α and Its Paralog CK2α'.
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- Pharmaceuticals (14248247), 2017, v. 10, n. 4, p. 98, doi. 10.3390/ph10040098
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Development of Pharmacophore Model for Indeno[1,2-b]indoles as Human Protein Kinase CK2 Inhibitors and Database Mining.
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- Pharmaceuticals (14248247), 2017, v. 10, n. 1, p. 8, doi. 10.3390/ph10010008
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Synthesis, Biological Evaluation and Molecular Modeling of Substituted Indeno[1,2-b]indoles as Inhibitors of Human Protein Kinase CK2.
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- Pharmaceuticals (14248247), 2015, v. 8, n. 2, p. 279, doi. 10.3390/ph8020279
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- Article
DMAP as a new efficient catalyst for the one-pot synthesis of condensed phthalazines.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2017, v. 72, n. 5, p. 361, doi. 10.1515/znb-2016-0262
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- Article
Microwave-accelerated multicomponent synthesis and X-ray characterization of novel benzothiadiazinone dioxide derivatives, analogues of Monastrol.
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- Research on Chemical Intermediates, 2021, v. 47, n. 4, p. 1359, doi. 10.1007/s11164-020-04378-3
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- Article
Methyl 3-(Quinolin-2-yl)indolizine-1-carboxylate.
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- Molbank, 2016, v. 2016, n. 1, p. m883, doi. 10.3390/M883
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Synthesis, proton NMR stereochemical study and diels-alder reaction of ( E)-7-arylidene-2 H,6 H-naphtho[1,8- bc]furan-2,6-diones.
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- Journal of Heterocyclic Chemistry, 1993, v. 30, n. 1, p. 41, doi. 10.1002/jhet.5570300108
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- Article
Synthesis of Carbazolequinone Derivatives as Inhibitors of Toxoplasma gondii Purine Nucleoside Phosphorylase.
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- European Journal of Organic Chemistry, 2002, v. 2002, n. 11, p. 1834, doi. 10.1002/1099-0690(200206)2002:11<1834::AID-EJOC1834>3.0.CO;2-K
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- Article
Mechanistic basis of breast cancer resistance protein inhibition by new indeno[1,2-b]indoles.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-020-79892-w
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- Article
Phenolic indeno[1,2-b]indoles as ABCG2-selective potent and non-toxic inhibitors stimulating basal ATPase activity.
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- Drug Design, Development & Therapy, 2015, v. 9, p. 3481, doi. 10.2147/DDDT.S84982
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- Article
Phenolic indeno[1,2-b]indoles as ABCG2-selective potent and non-toxic inhibitors stimulating basal ATPase activity.
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- Drug Design, Development & Therapy, 2015, v. 9, p. 3481, doi. 10.2147/DDDT.S84982
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- Article
QSAR Model of Indeno[1,2-b]indole Derivatives and Identification of N-isopentyl-2-methyl-4,9-dioxo-4,9-Dihydronaphtho[2,3-b]furan-3-carboxamide as a Potent CK2 Inhibitor.
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- Molecules, 2020, v. 25, n. 1, p. 97, doi. 10.3390/molecules25010097
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- Article
Synthesis, Spectroscopic Characterization, and In Vitro Antibacterial Evaluation of Novel Functionalized Sulfamidocarbonyloxyphosphonates.
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- Molecules, 2018, v. 23, n. 7, p. 1682, doi. 10.3390/molecules23071682
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- Article