QSAR Analysis of Some TIBO Derivatives As HIV-1 Reverse Transcriptase Inhibitors

References (20)

1. 1 Quantum-Chemical Descriptors in QSAR/QSPR Studies [DOI]
2. 2 On the rank deficiency and rank augmentation of the spectral measurement matrix [DOI]
3. 3 Quantum Molecular Similarity. 3. QTMS Descriptors [DOI]
4. 4 Estimation of Binding Affinities for HEPT and Nevirapine Analogues with HIV-1 Reverse Transcriptase via Monte Carlo Simulations [DOI]
5. 5 Three-Dimensional Quantitative Structure-Activity Relationship (QSAR) of HIV Integrase Inhibitors: A Comparative Molecular Field Analysis (CoMFA) Study [DOI]
6. 6 QSAR models based on quantum topological molecular similarity [DOI]
7. 7 Quantum topological molecular similarity. Part 4.See ref. 7 for Part 3. A QSAR study of cell growth inhibitory properties of substituted (E)-1-phenylbut-1-en-3-ones [DOI]
8. 8 Computational Studies on Tetrahydropyrimidine-2-one HIV-1 Protease Inhibitors: Improving Three-Dimensional Quantitative Structure−Activity Relationship Comparative Molecular Field Analysis Models by Inclusion of Calculated Inhibitor- and Receptor-Based Properties [DOI]
9. 9 QSAR analysis of caffeoyl naphthalene sulfonamide derivatives as HIV-1 integrase inhibitors [DOI]
10. 10 QSAR study of novel 1,1,3-trioxo[1,2,4]-thiadiazine (TTDs) analogues as potent anti-HIV agents [DOI]
11. 11 Three-Dimensional Structure-Activity Analysis of a Series of Porphyrin Derivatives with Anti-HIV-1 Activity Targeted to the V3 Loop of the gp120 Envelope Glycoprotein of the Human Immunodeficiency Virus Type 1 [DOI]
12. 12 Computational Studies on HIV-1 Protease Inhibitors: Influence of Calculated Inhibitor−Enzyme Binding Affinities on the Statistical Quality of 3D-QSAR CoMFA Models [DOI]
13. 13 Predicting anti-HIV activity of PETT derivatives: CoMFA approach [DOI]
14. 14 5 Inhibitors of HIV Proteinase [DOI]
15. 15 QSAR study on some arylsulfonamides as anti-HIV agents [DOI]
16. 16 Comparative molecular similarity indices analysis for predicting anti-HIV activity of phenyl ethyl thiourea (PET) derivatives [DOI]
17. 17 The Art of 'HAART': Researchers Probe the Potential and Limits of Aggressive HIV Treatments [DOI]
18. 18 Non-nucleoside anti-HIV-1 reverse transcriptase inhibitors (NNRTIs): a chemical survey from lead compounds to selected drugs for clinical trials.
19. 19 Three-dimensional quantitative structure–activity relationships study on HIV-1 reverse transcriptase inhibitors in the class of dipyridodiazepinone derivatives, using comparative molecular field analysis [DOI]
20. 20 Pharmacophoric features of nucleosidic HIV-1RT inhibitors [DOI]

Cited by 2

Related research

• Saponin: Properties, Methods of Evaluation and Applications — shares topic coverage
• Pharmacological and Therapeutic Activities of Kigelia africana (Lam.) Benth — shares topic coverage
• Facile Preparation of a Nanostructured Silver Oxide from a Mixed Ligand Coordination Polymer: Characterization and Biological Activity — shares topic coverage
• QSAR Study of Series of HEPT (1-[(2-hydroxyethoxy) methyl]-6-(phenylthio)thyio)thymine) Derivatives Using Genetic Function Approximation as Anti-HIV-1 Agents — shares topic coverage
• Determination of Total Protein, Superoxide Dismutase, Catalase Activity and Lipid Peroxidation in Soil Macro-fauna (Earthworm) from Onitsha Municipal Open Waste Dump — shares topic coverage