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Identification and structure activity relationship of novel flavone derivatives that inhibit the production of nitric oxide and PGE2 in LPS-induced RAW 264.7 cells. |
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Total synthesis and bioactivity of unique flavone desmosdumotin B and its analogs. |
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Beneficial effects of different flavonoids, on functional recovery after ischemia and reperfusion in isolated rat heart. |
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Flavones and structurally related 4-chromenones inhibit carbonic anhydrases by a different mechanism of action compared to coumarins. |
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Inhibitory potential of flavonoids on PtdIns(3,4,5)P3 binding with the phosphoinositide-dependent kinase 1 pleckstrin homology domain. |
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Synthesis, characterization, and estrogen receptor binding affinity of flavone-, indole-, and furan-estradiol conjugates. |
2007 |
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Relationship between the structures of flavonoids and their NF-κB-dependent transcriptional activities. |
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99mTc/Re complexes based on flavone and aurone as SPECT probes for imaging cerebral β-amyloid plaques. |
2010 |
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3D QSAR and docking study of flavone derivatives as potent inhibitors of influenza H1N1 virus neuraminidase. |
2011 |
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Design, synthesis and biological evaluation of new arylpiperazine derivatives bearing a flavone moiety as α1-adrenoceptor antagonists. |
2011 |
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Non-covalent inhibitors of rhinovirus 3C protease. |
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Synthetic chalcones, flavanones, and flavones as antitumoral agents: biological evaluation and structure-activity relationships. |
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Synthesis of caged 2,3,3a,7a-tetrahydro-3,6-methanobenzofuran-7(6H)-ones: Evaluating the minimum structure for apoptosis induction by gambogic acid. |
2008 |
Bioorg. Med. Chem. |
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Design and synthesis of aminoester heterodimers containing flavone or chromone moieties as modulators of P-glycoprotein-based multidrug resistance (MDR). |
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Synthesis and potent antimicrobial activity of some novel 2-phenyl or methyl-4H-1-benzopyran-4-ones carrying amidinobenzimidazoles. |
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Synthesis of antiproliferative flavones from calycopterin, major flavonoid of Calycopteris floribunda Lamk. |
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Bioorg. Med. Chem. |
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Synthesis of C(7) modified chrysin derivatives designing to inhibit beta-ketoacyl-acyl carrier protein synthase III (FabH) as antibiotics. |
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