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Structure−Activity Relationships for The Anti-HIV Activity of Flavonoids

https://doi.org/10.1021/ci020363d

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What this work says

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Use of Moment of Inertia in Comparative Molecular Field Analysis To Model Chromatographic Retention of Nonpolar Solutes

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Quantitative Structure−Activity Relationship of Flavonoid Analogues. 3. Inhibition of p56lck Protein Tyrosine Kinase

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Traditional topological indexes vs electronic, geometrical, and combined molecular descriptors in QSAR/QSPR research

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Quantitative Structure−Activity Relationship of Flavonoid p56lck Protein Tyrosine Kinase Inhibitors. A Neural Network Approach

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Hydrogen Bonding Parameters for QSAR: Comparison of Indicator Variables, Hydrogen Bond Counts, Molecular Orbital and Other Parameters

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Comparative QSAR: Toward a Deeper Understanding of Chemicobiological Interactions

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Use of physicochemical parameters in distance geometry and related three-dimensional quantitative structure-activity relationships: A demonstration using Escherichia coli dihydrofolate reductase inhibitors

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Synergistic Effect of Flavones and Flavonols Against Herpes Simplex Virus Type 1 in Cell Culture. Comparison with the Antiviral Activity of Propolis

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A Quantum Chemical Explanation of the Antioxidant Activity of Flavonoids

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Crystal structure of the Src family tyrosine kinase Hck

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Flavopiridol Inhibits Glycogen Phosphorylase by Binding at the Inhibitor Site

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Structure of quercetin dihydrate

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5-Hydroxyflavone

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Structure-Activity Relationship of Flavonoids in Suppressing Rat Liver Lipid Peroxidation

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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