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Optimizing the use of CROs by academia and small companies.
- Published in:
- Nature Reviews Drug Discovery, 2013, v. 12, n. 7, p. 487, doi. 10.1038/nrd4057
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- Article
Substituted Aminoacetamides as Novel Leads for Malaria Treatment.
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- ChemMedChem, 2019, v. 14, n. 14, p. 1329, doi. 10.1002/cmdc.201900329
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- Article
Assessment of Pseudomonas aeruginosa N<sup>5</sup>,N<sup>10</sup>- Methylenetetrahydrofolate Dehydrogenase - Cyclohydrolase as a Potential Antibacterial Drug Target.
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- PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0035973
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- Article
IspE Inhibitors Identified by a Combination of In Silico and In Vitro High-Throughput Screening.
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- PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0035792
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- Article
N-myristoyltransferase inhibitors as new leads to treat sleeping sickness.
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- Nature, 2010, v. 464, n. 7289, p. 728, doi. 10.1038/nature08893
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- Article
The role of phosphotyrosine phosphatases in haematopoietic cell signal transduction.
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- BioEssays, 1997, v. 19, n. 5, p. 417, doi. 10.1002/bies.950190509
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- Article
Screening a protein kinase inhibitor library against Plasmodium falciparum.
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- Malaria Journal, 2017, v. 16, p. 1, doi. 10.1186/s12936-017-2085-4
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- Article
Discovery of Inhibitors of Trypanosoma brucei by Phenotypic Screening of a Focused Protein Kinase Library.
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- ChemMedChem, 2015, v. 10, n. 11, p. 1809, doi. 10.1002/cmdc.201500300
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- Article
Development of Small-Molecule Trypanosoma brucei N-Myristoyltransferase Inhibitors: Discovery and Optimisation of a Novel Binding Mode.
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- ChemMedChem, 2015, v. 10, n. 11, p. 1821, doi. 10.1002/cmdc.201500301
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- Article
Cover Picture: Development of Small-Molecule Trypanosoma brucei N-Myristoyltransferase Inhibitors: Discovery and Optimisation of a Novel Binding Mode (ChemMedChem 11/2015).
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- ChemMedChem, 2015, v. 10, n. 11, p. 1769, doi. 10.1002/cmdc.201500397
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- Article
Back Cover: From On-Target to Off-Target Activity: Identification and Optimisation of Trypanosoma brucei GSK3 Inhibitors and Their Characterisation as Anti- Trypanosoma brucei Drug Discovery Lead Molecules (ChemMedChem 7/2013).
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- ChemMedChem, 2013, v. 8, n. 7, p. 1228, doi. 10.1002/cmdc.201390029
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- Article
From On-Target to Off-Target Activity: Identification and Optimisation of Trypanosoma brucei GSK3 Inhibitors and Their Characterisation as Anti- Trypanosoma brucei Drug Discovery Lead Molecules.
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- ChemMedChem, 2013, v. 8, n. 7, p. 1127, doi. 10.1002/cmdc.201300072
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- Article
Design, Synthesis and Biological Evaluation of Trypanosoma brucei Trypanothione Synthetase Inhibitors.
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- ChemMedChem, 2012, v. 7, n. 1, p. 95, doi. 10.1002/cmdc.201100420
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- Article
Identification of Inhibitors of the Leishmania cdc2-Related Protein Kinase CRK3.
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- ChemMedChem, 2011, v. 6, n. 12, p. 2214, doi. 10.1002/cmdc.201100344
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- Article
Optimisation of the Anti- Trypanosoma brucei Activity of the Opioid Agonist U50488.
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- ChemMedChem, 2011, v. 6, n. 10, p. 1832, doi. 10.1002/cmdc.201100278
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- Article
Design, Synthesis and Biological Evaluation of Novel Inhibitors of Trypanosoma brucei Pteridine Reductase 1.
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- ChemMedChem, 2011, v. 6, n. 2, p. 302, doi. 10.1002/cmdc.201000450
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- Article
Cover Picture: Synthesis and Evaluation of Indatraline-Based Inhibitors for Trypanothione Reductase / Design, Synthesis and Biological Evaluation of Novel Inhibitors of Trypanosoma brucei Pteridine Reductase 1 / Modified 5′-Trityl Nucleosides as Inhibitors of Plasmodium falciparum dUTPase (ChemMedChem 2/2011)
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- ChemMedChem, 2011, v. 6, n. 2, p. 209, doi. 10.1002/cmdc.201190000
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- Article
Investigation of Trypanothione Reductase as a Drug Target in Trypanosoma brucei.
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- ChemMedChem, 2009, v. 4, n. 12, p. 2060, doi. 10.1002/cmdc.200900262
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- Article
Cover Picture: Improved Tricyclic Inhibitors of Trypanothione Reductase by Screening and Chemical Synthesis / Synthesis and Evaluation of 1-(1-(Benzo[ b]thiophen-2-yl)cyclohexyl)piperidine (BTCP) Analogues as Inhibitors of Trypanothione Reductase (ChemMedChem 8/2009)
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- ChemMedChem, 2009, v. 4, n. 8, p. 1209, doi. 10.1002/cmdc.200990035
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- Article
Synthesis and Evaluation of 1-(1-(Benzo[ b]thiophen-2-yl)cyclohexyl)piperidine (BTCP) Analogues as Inhibitors of Trypanothione Reductase.
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- ChemMedChem, 2009, v. 4, n. 8, p. 1341, doi. 10.1002/cmdc.200900098
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- Article
Lessons Learnt from Assembling Screening Libraries for Drug Discovery for Neglected Diseases.
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- ChemMedChem, 2008, v. 3, n. 3, p. 435, doi. 10.1002/cmdc.200700139
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- Article
A tyrosine-phosphorylated 110-120-kDa protein associates with the C-terminal SH2 domain of phosphotyrosine phosphatase-1D in T cell receptor-stimulated T cells.
- Published in:
- European Journal of Immunology, 1996, v. 26, n. 7, p. 1539, doi. 10.1002/eji.1830260720
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- Article