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A Versatile Class of 1,4,4-Trisubstituted Piperidines Block Coronavirus Replication In Vitro.
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- Pharmaceuticals (14248247), 2022, v. 15, n. 8, p. 1021, doi. 10.3390/ph15081021
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- Article
Small Molecule–Peptide Conjugates as Dimerization Inhibitors of Leishmania infantum Trypanothione Disulfide Reductase.
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- Pharmaceuticals (14248247), 2021, v. 14, n. 7, p. 689, doi. 10.3390/ph14070689
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- Article
Molecular and structural basis of oligopeptide recognition by the Ami transporter system in pneumococci.
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- PLoS Pathogens, 2024, v. 20, n. 6, p. 1, doi. 10.1371/journal.ppat.1011883
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- Article
Age-Related Effects on Right Femoral Bone of Male Wistar Rats: A Morphometric and Biomechanical Study.
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- Journal of Health & Allied Sciences NU, 2022, v. 12, n. 1, p. 67, doi. 10.1055/s-0041-1730107
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- Article
The Effects of Aging on the Femoral Bone Mass, Bone Stiffness and Maximum Resistance Strength - Assessed in a Rat Model.
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- Journal of Morphological Sciences, 2021, v. 38, p. 85, doi. 10.51929/jms.38.15.2021
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- Article
Synthesis of Tri- and Tetracyclic Condensed Quinoxalin-2-ones Fused Across the C-3-N-4 Bond.
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- European Journal of Organic Chemistry, 2003, v. 2003, n. 12, p. 2314, doi. 10.1002/ejoc.200300028
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Reactivity of the 4-Amino-5 H-1,2-Oxathiole-2,2-Dioxide Heterocyclic System: A Combined Experimental and Theoretical Study.
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- Chemistry - A European Journal, 2008, v. 14, n. 31, p. 9620, doi. 10.1002/chem.200800433
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(F)uridylylated Peptides Linked to VPg1 of Foot-and- Mouth Disease Virus (FMDV): Design, Synthesis and X-Ray Crystallography of the Complexes with FMDV RNA-Dependent RNA Polymerase.
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- Molecules, 2019, v. 24, n. 13, p. 2360, doi. 10.3390/molecules24132360
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Design, Synthesis, and Biological Evaluation of Unconventional Aminopyrimidine, Aminopurine, and Amino-1,3,5-triazine Methyloxynucleosides.
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- ChemMedChem, 2015, v. 10, n. 2, p. 321, doi. 10.1002/cmdc.201402465
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- Article
From β-Amino-γ-sultone to Unusual Bicyclic Pyridine and Pyrazine Heterocyclic Systems: Synthesis and Cytostatic and Antiviral Activities.
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- ChemMedChem, 2011, v. 6, n. 4, p. 686, doi. 10.1002/cmdc.201000546
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- Article
The N137 and P140 amino acids in the p51 and the P95 amino acid in the p66 subunit of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase are instrumental to maintain catalytic activity and to design new classes of anti-HIV-1 drugs
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- FEBS Letters, 2005, v. 579, n. 11, p. 2294, doi. 10.1016/j.febslet.2005.02.077
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Design, synthesis and structure-activity relationship (SAR) studies of an unusual class of non-cationic fatty amine-tripeptide conjugates as novel synthetic antimicrobial agents.
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- Frontiers in Pharmacology, 2024, p. 1, doi. 10.3389/fphar.2024.1428409
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- Article