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N-hydroxy-substituted 2-aryl acetamide analogs: A novel class of HIV-1 integrase inhibitors.
- Published in:
- Chemical Biology & Drug Design, 2017, v. 90, n. 4, p. 527, doi. 10.1111/cbdd.12974
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- Article
Design, synthesis and in vitro antiplasmodial activity of some bisquinolines against chloroquine-resistant strain.
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- Chemical Biology & Drug Design, 2017, v. 89, n. 6, p. 901, doi. 10.1111/cbdd.12914
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- Article
Synthesis, Biological Evaluation and Molecular Modeling Studies of New 2,3-Diheteroaryl Thiazolidin-4-Ones as NNRTIs.
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- Chemical Biology & Drug Design, 2015, v. 86, n. 5, p. 1285, doi. 10.1111/cbdd.12591
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- Article
Design, Synthesis, Biological Screening, and Molecular Docking Studies of Piperazine-Derived Constrained Inhibitors of DPP-IV for the Treatment of Type 2 Diabetes.
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- Chemical Biology & Drug Design, 2015, v. 85, n. 4, p. 439, doi. 10.1111/cbdd.12426
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- Article
Synthesis and Pharmacological Evaluation of Novel Arginine Analogs as Potential Inhibitors of Acetylcholine-Induced Relaxation in Rat Thoracic Aortic Rings.
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- Chemical Biology & Drug Design, 2012, v. 79, n. 4, p. 459, doi. 10.1111/j.1747-0285.2011.01286.x
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- Article
Anti-Stroke Profile of Thiazolidin-4-One Derivatives in Focal Cerebral Ischemia Model in Rat.
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- Chemical Biology & Drug Design, 2011, v. 78, n. 3, p. 445, doi. 10.1111/j.1747-0285.2011.01153.x
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- Article
Topological Features in Profiling the Antimalarial Activity Landscape of Anilinoquinolines: A Multipronged QSAR Study.
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- Journal of Chemistry, 2013, p. 1, doi. 10.1155/2013/154629
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- Article
EcoRV-T94V: a mutant restriction endonuclease with an altered substrate specificity towards modified oligodexynucleotides.
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- Protein Engineering, 1996, v. 9, n. 11, p. 1005, doi. 10.1093/protein/9.11.1005
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- Article