Design of Gallinamide A Analogs as Potent Inhibitors of the Cysteine Proteases Human Cathepsin L and Trypanosoma cruzi Cruzain
Paul D. Boudreau
Bailey W. Miller
Laura-Isobel McCall
Jehad Almaliti
Raphael Reher
Ken Hirata
Thu Le
Jair L. Siqueira-Neto
Vivian Hook
William H. Gerwick
Raphael Reher
Reher Raphael
ORCID: 0000-0002-5858-1173
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Cell‐permeable high‐affinity tracers for G
q
proteins provide structural insights, reveal distinct binding kinetics and identify small molecule inhibitors
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Design of Gallinamide A Analogs as Potent Inhibitors of the Cysteine Proteases Human Cathepsin L and Trypanosoma cruzi Cruzain
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The genome analysis of C
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Burkholderia crenata reveals that secondary metabolism may be a key function of the A
rdisia crenata
leaf nodule symbiosis
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William Gerwick
Gerwick William
ORCID: 0000-0003-1403-4458
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A Multi-Omics Characterization of the Natural Product Potential of Tropical Filamentous Marine Cyanobacteria
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The Face of a Molecule
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Samholides, Swinholide-Related Metabolites from a Marine Cyanobacterium cf. Phormidium sp.
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Highly Convergent Total Synthesis and Assignment of Absolute Configuration of Majusculamide D, a Potent and Selective Cytotoxic Metabolite from Moorea sp.
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Nature's Combinatorial Biosynthesis Produces Vatiamides A–F
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Nature's Combinatorial Biosynthesis Produces Vatiamides A–F
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Cytotoxic Microcolin Lipopeptides from the Marine Cyanobacterium Moorea producens
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Design of Gallinamide A Analogs as Potent Inhibitors of the Cysteine Proteases Human Cathepsin L and Trypanosoma cruzi Cruzain
10.1021/acs.jmedchem.9b00294
Commensal oralRothia mucilaginosaproduces enterobactin – a metal chelating siderophore
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Correction to “Highly Convergent Total Synthesis and Assignment of Absolute Configuration of Majusculamide D, a Potent and Selective Cytotoxic Metabolite from Moorea sp.”
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The Chemistry, Biochemistry and Pharmacology of Marine Natural Products from Leptolyngbya, a Chemically Endowed Genus of Cyanobacteria
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jehad almaliti
almaliti jehad
ORCID: 0000-0002-3562-0846
Apratoxin Kills Cells by Direct Blockade of the Sec61 Protein Translocation Channel
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Dudawalamides A–D, Antiparasitic Cyclic Depsipeptides from the Marine Cyanobacterium Moorea producens
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Discovery and Synthesis of Caracolamide A, an Ion Channel Modulating Dichlorovinylidene Containing Phenethylamide from a Panamanian Marine Cyanobacterium cf. Symploca Species
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Development of a Potent Inhibitor of the Plasmodium Proteasome with Reduced Mammalian Toxicity
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Exploration of the carmaphycins as payloads in antibody drug conjugate anticancer agents
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Design of Gallinamide A Analogs as Potent Inhibitors of the Cysteine Proteases Human Cathepsin L and Trypanosoma cruzi Cruzain
10.1021/acs.jmedchem.9b00294
Largazole Analogues Embodying Radical Changes in the Depsipeptide Ring: Development of a More Selective and Highly Potent Analogue
10.1021/acs.jmedchem.6b01271