Pages that link to "Q27662211"

The following pages link to Crystal Structures of TbCatB and Rhodesain, Potential Chemotherapeutic Targets and Major Cysteine Proteases of Trypanosoma brucei (Q27662211):

Displayed 23 items.

• In vivo protein crystallization opens new routes in structural biology (Q27644366) ‎ (← links)
• Natively Inhibited Trypanosoma brucei Cathepsin B Structure Determined by Using an X-ray Laser (Q27644494) ‎ (← links)
• Structural Basis for Inhibition of Cathepsin B Drug Target from the Human Blood Fluke, Schistosoma mansoni (Q27671668) ‎ (← links)
• Terpyridine platinum(II) complexes inhibit cysteine proteases by binding to active-site cysteine (Q27672388) ‎ (← links)
• Optimization of triazine nitriles as rhodesain inhibitors: structure-activity relationships, bioisosteric imidazopyridine nitriles, and X-ray crystal structure analysis with human cathepsin L (Q27684569) ‎ (← links)
• The Potential of Secondary Metabolites from Plants as Drugs or Leads against Protozoan Neglected Diseases-Part III: In-Silico Molecular Docking Investigations (Q28066944) ‎ (← links)
• In-silico investigation of antitrypanosomal phytochemicals from Nigerian medicinal plants (Q28481512) ‎ (← links)
• A global comparison of the human and T. brucei degradomes gives insights about possible parasite drug targets (Q28485518) ‎ (← links)
• Enzyme Tunnels and Gates As Relevant Targets in Drug Design. (Q36221405) ‎ (← links)
• Characterization of parasite-specific indels and their proposed relevance for selective anthelminthic drug targeting. (Q36679852) ‎ (← links)
• Drug targets in Leishmania (Q37869809) ‎ (← links)
• Suzuki-miyaura cross-coupling in acylation reactions, scope and recent developments (Q38076293) ‎ (← links)
• Molecular recognition in chemical and biological systems (Q38335784) ‎ (← links)
• In-silico Leishmania target selectivity of antiparasitic terpenoids. (Q39318097) ‎ (← links)
• Interactions of antiparasitic alkaloids with Leishmania protein targets: a molecular docking analysis (Q39328997) ‎ (← links)
• Dipeptidyl Enoates As Potent Rhodesain Inhibitors That Display a Dual Mode of Action (Q39412444) ‎ (← links)
• Identification of plakortide E from the Caribbean sponge Plakortis halichondroides as a trypanocidal protease inhibitor using bioactivity-guided fractionation (Q40539585) ‎ (← links)
• Design, synthesis and biological evaluation of potent azadipeptide nitrile inhibitors and activity-based probes as promising anti-Trypanosoma brucei agents (Q46954504) ‎ (← links)
• Inhibition of the Cysteine Protease Human Cathepsin L by Triazine Nitriles: Amide⋅⋅⋅Heteroarene π-Stacking Interactions and Chalcogen Bonding in the S3 Pocket. (Q51251348) ‎ (← links)
• Potent and Selective Inhibition of Cysteine Proteases fromPlasmodium falciparumandTrypanosoma brucei (Q61066420) ‎ (← links)
• Synthesis and Evaluation of 1,2,3-Triazole-Containing Vinyl and Allyl Sulfones as Anti-Trypanosomal Agents (Q61870451) ‎ (← links)
• Development of Novel Benzodiazepine-based Peptidomimetics as Inhibitors of Rhodesain of Trypanosoma brucei rhodesiense (Q93203118) ‎ (← links)
• Peptidyl Vinyl Ketones Irreversible Inhibitors of Rhodesain: Modifications of the P2 Fragment (Q96610549) ‎ (← links)