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Next generation imidazothiazole and imidazooxazole derivatives as potential drugs against brain-eating amoebae.
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- Parasitology Research, 2024, v. 123, n. 6, p. 1, doi. 10.1007/s00436-024-08255-5
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- Article
Divergent Strategy for the Synthesis of Indolopyrazines Fused to Benzopyrimidinones and Benzimidazoles: Identification of Antiproliferative Molecules.
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- ChemistrySelect, 2023, v. 8, n. 46, p. 1, doi. 10.1002/slct.202303730
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- Article
Anti-proliferative activity of RIHMS-Qi-23 against MCF-7 breast cancer cell line is through inhibition of cell proliferation and senescence but not inhibition of targeted kinases.
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- BMC Cancer, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12885-023-11547-1
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- Article
The anti-amoebic potential of carboxamide derivatives containing sulfonyl or sulfamoyl moieties against brain-eating Naegleria fowleri.
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- Parasitology Research, 2023, v. 122, n. 11, p. 2539, doi. 10.1007/s00436-023-07953-w
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- Article
Complexity‐to‐Diversity and Pseudo‐Natural Product Strategies as Powerful Platforms for Deciphering Next‐Generation Therapeutics.
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- ChemMedChem, 2023, v. 18, n. 14, p. 1, doi. 10.1002/cmdc.202300117
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- Article
Design and synthesis of novel anti-urease imidazothiazole derivatives with promising antibacterial activity against Helicobacter pylori.
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- PLoS ONE, 2023, v. 17, n. 6, p. 1, doi. 10.1371/journal.pone.0286684
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- Article
Diastereoselective Synthesis of Camptothecin‐like Scaffolds: Construction of a New Class of Pseudo‐natural Products.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 13, p. 1, doi. 10.1002/ejoc.202300080
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- Article
Novel Anti-Acanthamoebic Activities of Irosustat and STX140 and Their Nanoformulations.
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- Antibiotics (2079-6382), 2023, v. 12, n. 3, p. 561, doi. 10.3390/antibiotics12030561
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- Article
Stereodivergent Transformation of Azepino[3,4,5‐cd]indoles En Route to Nature‐Inspired Scaffolds.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 9, p. 1, doi. 10.1002/ejoc.202201354
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- Article
Anti-amoebic activity of a series of benzofuran/benzothiophene derivatives against Acanthamoeba castellanii belonging to the T4 genotype.
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- Journal of Applied Microbiology, 2023, v. 134, n. 1, p. 1, doi. 10.1093/jambio/lxac030
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- Article
Imidazothiazole Derivatives Exhibited Potent Effects against Brain-Eating Amoebae.
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- Antibiotics (2079-6382), 2022, v. 11, n. 11, p. 1515, doi. 10.3390/antibiotics11111515
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- Article
Antiamoebic Activity of Imidazothiazole Derivatives against Opportunistic Pathogen Acanthamoeba castellanii.
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- Antibiotics (2079-6382), 2022, v. 11, n. 9, p. 1183, doi. 10.3390/antibiotics11091183
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- Article
Evaluation of Substituted Pyrazole-Based Kinase Inhibitors in One Decade (2011–2020): Current Status and Future Prospects.
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- Molecules, 2022, v. 27, n. 1, p. 1, doi. 10.3390/molecules27010330
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- Article
A Review of HER4 (ErbB4) Kinase, Its Impact on Cancer, and Its Inhibitors.
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- Molecules, 2021, v. 26, n. 23, p. 7376, doi. 10.3390/molecules26237376
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- Article
Evaluation of the Inhibitory Effects of Pyridylpyrazole Derivatives on LPS-Induced PGE 2 Productions and Nitric Oxide in Murine RAW 264.7 Macrophages.
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- Molecules, 2021, v. 26, n. 21, p. 6489, doi. 10.3390/molecules26216489
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- Article
Recent advances with alkaline phosphatase isoenzymes and their inhibitors.
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- Archiv der Pharmazie, 2020, v. 353, n. 5, p. 1, doi. 10.1002/ardp.202000011
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Mechanistic/mammalian target of rapamycin: Recent pathological aspects and inhibitors.
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- Medicinal Research Reviews, 2019, v. 39, n. 2, p. 631, doi. 10.1002/med.21535
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- Article
Synthesis of New Triarylpyrazole Derivatives Possessing Terminal Sulfonamide Moiety and Their Inhibitory Effects on PGE2 and Nitric Oxide Productions in Lipopolysaccharide-Induced RAW 264.7 Macrophages.
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- Molecules, 2018, v. 23, n. 10, p. 2556, doi. 10.3390/molecules23102556
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Synthesis of New Tricyclic and Tetracyclic Fused Coumarin Sulfonate Derivatives and Their Inhibitory Effects on LPS-Induced Nitric Oxide and PGE<sub>2</sub> Productions in RAW 264.7 Macrophages: Part 2.
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- Archiv der Pharmazie, 2016, v. 349, n. 11, p. 853, doi. 10.1002/ardp.201600243
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- Article
A New Series of Cycloalkane-fused Coumarin Sulfonates: Synthesis and In Vitro Antiproliferative Screening.
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- Bulletin of the Korean Chemical Society, 2016, v. 37, n. 2, p. 184, doi. 10.1002/bkcs.10651
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- Article
Cell-Based Biological Evaluation of a New Bisamide FMS Kinase Inhibitor Possessing Pyrrolo[3,2- c]pyridine Scaffold.
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- Archiv der Pharmazie, 2014, v. 347, n. 9, p. 635, doi. 10.1002/ardp.201400051
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- Article
Antiproliferative Diarylpyrazole Derivatives as Dual Inhibitors of the ERK Pathway and COX-2.
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- Chemical Biology & Drug Design, 2013, v. 82, n. 3, p. 336, doi. 10.1111/cbdd.12186
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FMS Kinase Inhibitors: Current Status and Future Prospects.
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- Medicinal Research Reviews, 2013, v. 33, n. 3, p. 599, doi. 10.1002/med.21258
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- Article
Design, Synthesis, and Antiproliferative Activity of 3,4-Diarylpyrazole-1-carboxamide Derivatives Against Melanoma Cell Line.
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- Archiv der Pharmazie, 2011, v. 344, n. 11, p. 745, doi. 10.1002/ardp.201000375
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Synthesis and in vitro antibacterial activity of new meropenem analogs.
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- Journal of Antibiotics, 2011, v. 64, n. 10, p. 687, doi. 10.1038/ja.2011.70
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- Article
Synthesis of 1 H-Pyrazole-1-carboxamide Derivatives and Their Antiproliferative Activity against Melanoma Cell Line.
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- Archiv der Pharmazie, 2011, v. 344, n. 3, p. 197, doi. 10.1002/ardp.201000057
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Radiosynthesis and in vitro evaluation of 1-(tetrahydro-5-hydroxy-6-(hydroxymethyl)-2H-pyran-3-yl)-5-[.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 2011, v. 54, n. 2, p. 93, doi. 10.1002/jlcr.1819
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- Article