Found: 31
Select item for more details and to access through your institution.
Design and synthesis of imidazo[1,2‐a]pyridine‐chalcone conjugates as antikinetoplastid agents.
- Published in:
- Chemical Biology & Drug Design, 2024, v. 103, n. 1, p. 1, doi. 10.1111/cbdd.14400
- By:
- Publication type:
- Article
2‐Aroyl quinazolinone: Synthesis and in vitro anti‐parasitic activity.
- Published in:
- Chemical Biology & Drug Design, 2023, v. 102, n. 4, p. 763, doi. 10.1111/cbdd.14284
- By:
- Publication type:
- Article
Arylnitro monocarbonyl curcumin analogues: Synthesis and in vitro antitubercular evaluation.
- Published in:
- Chemical Biology & Drug Design, 2023, v. 101, n. 3, p. 717, doi. 10.1111/cbdd.14174
- By:
- Publication type:
- Article
Chalcone‐inspired rA<sub>1</sub>/A<sub>2A</sub> adenosine receptor ligands: Ring closure as an alternative to a reactive substructure.
- Published in:
- Chemical Biology & Drug Design, 2022, v. 99, n. 3, p. 416, doi. 10.1111/cbdd.13999
- By:
- Publication type:
- Article
Synthesis and evaluation of C3 substituted chalcone‐based derivatives of 7‐azaindole as protein kinase inhibitors.
- Published in:
- Chemical Biology & Drug Design, 2020, v. 96, n. 6, p. 1395, doi. 10.1111/cbdd.13748
- By:
- Publication type:
- Article
6‐Nitro‐1‐benzylquinolones exhibiting specific antitubercular activity.
- Published in:
- Chemical Biology & Drug Design, 2020, v. 96, n. 6, p. 1387, doi. 10.1111/cbdd.13747
- By:
- Publication type:
- Article
Evaluation of 2-benzylidene-1-tetralone derivatives as antagonists of A<sub>1</sub> and A<sub>2A</sub> adenosine receptors.
- Published in:
- Chemical Biology & Drug Design, 2018, v. 91, n. 1, p. 234, doi. 10.1111/cbdd.13074
- By:
- Publication type:
- Article
The Synthesis and Evaluation of C7-Substituted α-Tetralone Derivatives as Inhibitors of Monoamine Oxidase.
- Published in:
- Chemical Biology & Drug Design, 2015, v. 86, n. 4, p. 895, doi. 10.1111/cbdd.12508
- By:
- Publication type:
- Article
Betulin, a Newly Characterized Compound in Acacia auriculiformis Bark, Is a Multi-Target Protein Kinase Inhibitor.
- Published in:
- Molecules, 2021, v. 26, n. 15, p. 4599, doi. 10.3390/molecules26154599
- By:
- Publication type:
- Article
An Update on Development of Small-Molecule Plasmodial Kinase Inhibitors.
- Published in:
- Molecules, 2020, v. 25, n. 21, p. 5182, doi. 10.3390/molecules25215182
- By:
- Publication type:
- Article
Tractable Quinolone Hydrazides Exhibiting Sub‐Micromolar and Broad Spectrum Antitrypanosomal Activities.
- Published in:
- ChemMedChem, 2024, v. 19, n. 9, p. 1, doi. 10.1002/cmdc.202300667
- By:
- Publication type:
- Article
Nigella sativa L. and Its Active Compound Thymoquinone in the Clinical Management of Diabetes: A Systematic Review.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 20, p. 12111, doi. 10.3390/ijms232012111
- By:
- Publication type:
- Article
Synthesis and In Vitro Antibacterial Evaluation of Mannich Base Nitrothiazole Derivatives.
- Published in:
- Molbank, 2024, v. 2024, n. 1, p. M1793, doi. 10.3390/M1793
- By:
- Publication type:
- Article
Novel quinoline derivatives with broad‐spectrum antiprotozoal activities.
- Published in:
- Archiv der Pharmazie, 2024, v. 357, n. 6, p. 1, doi. 10.1002/ardp.202300319
- By:
- Publication type:
- Article
Synthesis and in vitro antiprotozoal evaluation of novel metronidazole–Schiff base hybrids.
- Published in:
- Archiv der Pharmazie, 2023, v. 356, n. 3, p. 1, doi. 10.1002/ardp.202200409
- By:
- Publication type:
- Article
Investigation of quinolone‐tethered aminoguanidine as novel antibacterial agents.
- Published in:
- Archiv der Pharmazie, 2022, v. 355, n. 10, p. 1, doi. 10.1002/ardp.202200172
- By:
- Publication type:
- Article
Recent Advances in Radical C−H Bond Functionalization of Imidazoheterocycles.
- Published in:
- Advanced Synthesis & Catalysis, 2020, v. 362, n. 20, p. 4226, doi. 10.1002/adsc.202000633
- By:
- Publication type:
- Article
Quinolone: a versatile therapeutic compound class.
- Published in:
- Molecular Diversity, 2023, v. 27, n. 3, p. 1501, doi. 10.1007/s11030-022-10581-8
- By:
- Publication type:
- Article
Exploration of 4-aminopyrrolo[2,3-d]pyrimidine as antitubercular agents.
- Published in:
- Molecular Diversity, 2023, v. 27, n. 2, p. 753, doi. 10.1007/s11030-022-10453-1
- By:
- Publication type:
- Article
New fused pyrroles with rA1/A2A antagonistic activity as potential therapeutics for neurodegenerative disorders.
- Published in:
- Molecular Diversity, 2022, v. 26, n. 4, p. 2211, doi. 10.1007/s11030-021-10327-y
- By:
- Publication type:
- Article
Correction to: Exploration of chalcones and related heterocycle compounds as ligands of adenosine receptors: therapeutics development.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Exploration of chalcones and related heterocycle compounds as ligands of adenosine receptors: therapeutics development.
- Published in:
- Molecular Diversity, 2022, v. 26, n. 3, p. 1779, doi. 10.1007/s11030-021-10257-9
- By:
- Publication type:
- Article
The evaluation of 1-tetralone and 4-chromanone derivatives as inhibitors of monoamine oxidase.
- Published in:
- Molecular Diversity, 2021, v. 25, n. 1, p. 491, doi. 10.1007/s11030-020-10143-w
- By:
- Publication type:
- Article
The monoamine oxidase inhibition properties of C6- and N1-substituted 3-methyl-3,4-dihydroquinazolin-2(1H)-one derivatives.
- Published in:
- Molecular Diversity, 2020, v. 24, n. 2, p. 391, doi. 10.1007/s11030-019-09960-5
- By:
- Publication type:
- Article
In-vitro transdermal penetration of cytarabine and its N4-alkylamide derivatives.
- Published in:
- Journal of Pharmacy & Pharmacology, 2010, v. 62, n. 6, p. 756, doi. 10.1211/jpp.62.06.0012
- By:
- Publication type:
- Article
3-Coumaranone derivatives as inhibitors of monoamine oxidase.
- Published in:
- Drug Design, Development & Therapy, 2015, v. 9, p. 5479, doi. 10.2147/DDDT.S89961
- By:
- Publication type:
- Article
2-acetylphenol analogs as potent reversible monoamine oxidase inhibitors.
- Published in:
- Drug Design, Development & Therapy, 2015, v. 9, p. 3635, doi. 10.2147/DDDT.S86225
- By:
- Publication type:
- Article
Seven Compounds from Turmeric Essential Oil Inhibit Three Key Proteins Involved in SARS-CoV-2 Cell Entry and Replication in silico.
- Published in:
- Journal of Computational Biophysics & Chemistry, 2021, v. 20, n. 8, p. 785, doi. 10.1142/S2737416521500484
- By:
- Publication type:
- Article
Synthesis and Adenosine RA<sub>1</sub>/A<sub>2A</sub> Receptor Affinity of Selected Aurones and 2-Benzylidene-1-Indanones.
- Published in:
- Pharmaceutical Chemistry Journal, 2023, v. 57, n. 5, p. 729, doi. 10.1007/s11094-023-02944-8
- By:
- Publication type:
- Article
Chemical Classes Presenting Novel Antituberculosis Agents Currently in Different Phases of Drug Development: A 2010–2020 Review.
- Published in:
- Pharmaceuticals (14248247), 2021, v. 14, n. 5, p. 461, doi. 10.3390/ph14050461
- By:
- Publication type:
- Article
Nitrothiazole‐Thiazolidinone Hybrids: Synthesis and in Vitro Antimicrobial Evaluation.
- Published in:
- Chemistry & Biodiversity, 2022, v. 19, n. 11, p. 1, doi. 10.1002/cbdv.202200729
- By:
- Publication type:
- Article