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Privileged Scaffold Hybridization in the Design of Carbonic Anhydrase Inhibitors.
- Published in:
- Molecules, 2024, v. 29, n. 18, p. 4444, doi. 10.3390/molecules29184444
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- Article
Evaluation of the performance of 3D virtual screening protocols: RMSD comparisons, enrichment assessments, and decoy selection—What can we learn from earlier mistakes?
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- Journal of Computer-Aided Molecular Design, 2008, v. 22, n. 3/4, p. 213, doi. 10.1007/s10822-007-9163-6
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- Article
Site directed mutagenesis studies on HIV-1 reverse transcriptase (RT) shed light on the mechanism of action of a new Ribonuclease H/DNA polymerase RT dual inhibitor.
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- 2013
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- Publication type:
- Abstract
A Novel Series of 3,4-Disubstituted Dihydropyrazoles: Synthesis and Evaluation for MAO Enzyme Inhibition.
- Published in:
- Journal of Heterocyclic Chemistry, 2013, v. 50, p. E87, doi. 10.1002/jhet.1072
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- Publication type:
- Article
Synthesis and characterization of new phthalhydrazothiazole derivatives: A preliminary investigation on their activity against hepatocellular carcinoma.
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- Journal of Heterocyclic Chemistry, 2009, v. 46, n. 4, p. 674, doi. 10.1002/jhet.138
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- Publication type:
- Article
Exploring New Scaffolds for the Dual Inhibition of HIV-1 RT Polymerase and Ribonuclease Associated Functions.
- Published in:
- Molecules, 2021, v. 26, n. 13, p. 3821, doi. 10.3390/molecules26133821
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- Publication type:
- Article
Targeting HIV-1 RNase H: N'-(2-Hydroxy-benzylidene)-3,4,5-Trihydroxybenzoylhydrazone as Selective Inhibitor Active against NNRTIs-Resistant Variants.
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- Viruses (1999-4915), 2020, v. 12, n. 7, p. 729, doi. 10.3390/v12070729
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- Article
Molecular interaction fields in drug discovery: recent advances and future perspectives.
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- WIREs: Computational Molecular Science, 2013, v. 3, n. 6, p. 594, doi. 10.1002/wcms.1150
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- Publication type:
- Article
Isonicotinoylhydrazothiazoles and isonicotinoyl-N<sup>4</sup>-substituted thiosemicarbazides: Synthesis, characterization, and anti-mycobacterial activity.
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- Journal of Heterocyclic Chemistry, 2006, v. 43, n. 5, p. 1337, doi. 10.1002/jhet.5570430529
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- Article
Structure-Based Virtual Screening of Novel Natural Alkaloid Derivatives as Potential Binders of h-telo and c-myc DNA G-Quadruplex Conformations.
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- Molecules, 2015, v. 20, n. 1, p. 206, doi. 10.3390/molecules20010206
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- Publication type:
- Article
Alizarine derivatives as new dual inhibitors of the HIV-1 reverse transcriptase-associated DNA polymerase and RNase H activities effective also on the RNase H activity of non-nucleoside resistant reverse transcriptases.
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- FEBS Journal, 2011, v. 278, n. 9, p. 1444, doi. 10.1111/j.1742-4658.2011.08057.x
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- Publication type:
- Article
Predicting Cyclooxygenase Inhibition by Three-Dimensional Pharmacophoric Profiling. Part I: Model Generation, Validation and Applicability in Ethnopharmacology.
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- Molecular Informatics, 2010, v. 29, n. 1/2, p. 75, doi. 10.1002/minf.200900071
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- Publication type:
- Article
Studies on Cycloheptathiophene-3-carboxamide Derivatives as Allosteric HIV-1 Ribonuclease H Inhibitors.
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- ChemMedChem, 2016, v. 11, n. 16, p. 1709, doi. 10.1002/cmdc.201600015
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- Publication type:
- Article
Hit Identification of a Novel Dual Binder for h-telo/c-myc G-Quadruplex by a Combination of Pharmacophore Structure-Based Virtual Screening and Docking Refinement.
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- ChemMedChem, 2016, v. 11, n. 16, p. 1721, doi. 10.1002/cmdc.201600053
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- Publication type:
- Article
Back Cover: Hit Identification of a Novel Dual Binder for h-telo/c-myc G-Quadruplex by a Combination of Pharmacophore Structure-Based Virtual Screening and Docking Refinement (ChemMedChem 16/2016).
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- ChemMedChem, 2016, v. 11, n. 16, p. 1875, doi. 10.1002/cmdc.201600393
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- Article
Cover Picture: Studies on Cycloheptathiophene-3-carboxamide Derivatives as Allosteric HIV-1 Ribonuclease H Inhibitors (ChemMedChem 16/2016).
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- ChemMedChem, 2016, v. 11, n. 16, p. 1669, doi. 10.1002/cmdc.201600392
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- Publication type:
- Article
Design, Synthesis, and Biological Evaluation of 1,3-Diarylpropenones as Dual Inhibitors of HIV-1 Reverse Transcriptase.
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- ChemMedChem, 2014, v. 9, n. 8, p. 1869, doi. 10.1002/cmdc.201402015
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- Publication type:
- Article
2-(2-Methyl-2-nitrovinyl)furan but Not Furvina Interfere with Staphylococcus aureus Agr Quorum-Sensing System and Potentiate the Action of Fusidic Acid against Biofilms.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 2, p. 613, doi. 10.3390/ijms22020613
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- Article
5-Nitro-3-(2-(4-phenylthiazol-2- yl)hydrazineylidene)indolin-2- one derivatives inhibit HIV-1 replication by a multitarget mechanism of action.
- Published in:
- Frontiers in Cellular & Infection Microbiology, 2023, p. 1, doi. 10.3389/fcimb.2023.1193280
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- Publication type:
- Article
Ribonuclease H/DNA Polymerase HIV-1 Reverse Transcriptase Dual Inhibitor: Mechanistic Studies on the Allosteric Mode of Action of Isatin-Based Compound RMNC6.
- Published in:
- PLoS ONE, 2016, v. 11, n. 1, p. 1, doi. 10.1371/journal.pone.0147225
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- Publication type:
- Article