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Structure- and ligand-based drug design approaches for neglected tropical diseases.
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- Pure & Applied Chemistry, 2012, v. 84, n. 9, p. 1857, doi. 10.1351/PAC-CON-11-11-07
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- Article
Editorial: Antimalarial chemotherapy in the XXIst century.
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- Frontiers in Pharmacology, 2023, v. 13, p. 1, doi. 10.3389/fphar.2022.1118683
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- Article
Synthesis, Structure–Activity Relationships, and Parasitological Profiling of Brussonol Derivatives as New Plasmodium falciparum Inhibitors.
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- Pharmaceuticals (14248247), 2022, v. 15, n. 7, p. N.PAG, doi. 10.3390/ph15070814
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- Article
Pattern Recognition Techniques Applied to the Study of Leishmanial Glyceraldehyde-3-Phosphate Dehydrogenase Inhibition.
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- International Journal of Molecular Sciences, 2014, v. 15, n. 2, p. 3186, doi. 10.3390/ijms15023186
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- Article
Structural requirements for the collagenase and elastase activity of cathepsin K and its selective inhibition by an exosite inhibitor.
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- Biochemical Journal, 2015, v. 465, n. 1, p. 163, doi. 10.1042/BJ20140809
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- Article
Friedelin Synthase from Maytenus ilicifolia: Leucine 482 Plays an Essential Role in the Production of the Most Rearranged Pentacyclic Triterpene.
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- Scientific Reports, 2016, p. 36858, doi. 10.1038/srep36858
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- Article
Biliverdin targets enolase and eukaryotic initiation factor 2 (eIF2α) to reduce the growth of intraerythrocytic development of the malaria parasite Plasmodium falciparum.
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- Scientific Reports, 2016, p. 22093, doi. 10.1038/srep22093
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- Article
The Methionine 549 and Leucine 552 Residues of Friedelin Synthase from Maytenus ilicifolia Are Important for Substrate Binding Specificity.
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- Molecules, 2021, v. 26, n. 22, p. 6806, doi. 10.3390/molecules26226806
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- Article
Molecular Cloning and Biochemical Characterization of Iron Superoxide Dismutase from Leishmania braziliensis.
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- Molecular Biotechnology, 2018, v. 60, n. 8, p. 595, doi. 10.1007/s12033-018-0095-2
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- Article
Crystal structure of Zika virus NS5 RNA-dependent RNA polymerase.
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- Nature Communications, 2017, v. 8, n. 3, p. 14764, doi. 10.1038/ncomms14764
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- Article
QSAR studies on benzothiophene derivatives as Plasmodium falciparum N‐myristoyltransferase inhibitors: Molecular insights into affinity and selectivity.
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- Drug Development Research, 2022, v. 83, n. 2, p. 264, doi. 10.1002/ddr.21646
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- Article
Editorial: Antimalarial chemotherapy in the XXIst century, volume II.
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- Frontiers in Pharmacology, 2023, p. 1, doi. 10.3389/fphar.2023.1229764
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- Article
Non-Toxic Dimeric Peptides Derived from the Bothropstoxin-I Are Potent SARS-CoV-2 and Papain-like Protease Inhibitors.
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- Molecules, 2021, v. 26, n. 16, p. 4896, doi. 10.3390/molecules26164896
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- Article
Identification of Electronic and Structural Descriptors of Adenosine Analogues Related to Inhibition of Leishmanial Glyceraldehyde-3-Phosphate Dehydrogenase.
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- Molecules, 2013, v. 18, n. 5, p. 5032, doi. 10.3390/molecules18055032
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- Article
Optimization of Plasmodium vivax infection of colonized Amazonian Anopheles darlingi.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-44556-y
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- Article
A composite docking approach for the identification and characterization of ectosteric inhibitors of cathepsin K.
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- PLoS ONE, 2017, v. 12, n. 11, p. 1, doi. 10.1371/journal.pone.0186869
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- Article
The (5 Z)-5-Pentacosenoic and 5-Pentacosynoic Acids Inhibit the HIV-1 Reverse Transcriptase.
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- Lipids, 2015, v. 50, n. 10, p. 1043, doi. 10.1007/s11745-015-4064-2
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- Article