Pages that link to "Item:Q1029762"
From MaRDI portal
The following pages link to Application to QSAR studies of 2-furylethylene derivatives (Q1029762):
Displaying 14 items.
- Quantitative structure-activity relationship studies of boron-containing dipeptide proteasome inhibitors using calculated mathematical descriptors (Q626470) (← links)
- Variation effect on the insecticide activity of DDT analogues. A chemometric approach (Q696461) (← links)
- Predictive models for maximum recommended therapeutic dose of antiretroviral drugs (Q764174) (← links)
- QSAR analysis of 1,4-dihydro-4-oxo-1-(2-thiazolyl)-1,8-naphthyridines exhibiting anticancer activity by optimal SMILES-based descriptors (Q848189) (← links)
- QSAR modeling of human catechol \(O\)-methyltransferase enzyme kinetics (Q1029742) (← links)
- Molecular modeling of wine polyphenols (Q1037483) (← links)
- MIA-QSAR based model for bioactivity prediction of flavonoid derivatives as acetylcholinesterase inhibitors (Q1712878) (← links)
- Characterization of structure-antioxidant activity relationship of peptides in free radical systems using QSAR models: key sequence positions and their amino acid properties (Q1715094) (← links)
- Aug-MIA-QSAR based strategy in bioactivity prediction of a series of flavonoid derivatives as HIV-1 inhibitors (Q1739235) (← links)
- The application of conformal prediction to the drug discovery process (Q2352377) (← links)
- SMILES as an alternative to the graph in QSAR modelling of bee toxicity (Q2373281) (← links)
- 3D quantitative structure-activity relationships study on anti-gastric cancer of chrysin derivatives (Q2696383) (← links)
- Quantitative structure activity relationship study of inhibitory activities of 5-lipoxygenase and design new compounds by different chemometrics methods (Q4617565) (← links)
- Quantitative Structure-Activity Relationships: Linear Regression Modelling and Validation Strategies by Example (Q5738281) (← links)
