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Angewandte Chemie (International Ed. in English)|November 29, 2023
Structure of Staphylococcus aureus ClpP Bound to the Covalent Active-Site Inhibitor Cystargolide AAstrid Illigmann, Marie-Theres Vielberg, Markus Lakemeyer, et al.Chemmedchem|May 19, 2010
Thiazolopyrimidine inhibitors of 2-methylerythritol 2,4-cyclodiphosphate synthase (IspF) from Mycobacterium tuberculosis and Plasmodium falciparumJulie G Geist, Susan Lauw, Victoria Illarionova, et al.Journal of Medicinal Chemistry|October 23, 2008
Leaving groups prolong the duration of 20S proteasome inhibition and enhance the potency of salinosporamidesRama Rao Manam, Katherine A McArthur, Ta-Hsiang Chao, et al.Science (New York, N.Y.)|March 21, 2024
Evolution-inspired engineering of nonribosomal peptide synthetasesKenan A J Bozhüyük, Leonard Präve, Carsten Kegler, et al.Journal of Medicinal Chemistry|July 10, 2014
Structure-based design of β1i or β5i specific inhibitors of human immunoproteasomesGerjan de Bruin, Eva M Huber, Bo-Tao Xin, et al.Nature Microbiology|March 19, 2026
Metronidazole and ether derivatives target Helicobacter pylori via simultaneous stress induction and inhibitionMichaela K Fiedler, Marianne S I Pandler, Ruolan Gong, et al.Journal of Medicinal Chemistry|January 19, 2019
Structure-Based Design of Inhibitors Selective for Human Proteasome β2c or β2i SubunitsBo-Tao Xin, Eva M Huber, Gerjan de Bruin, et al.Nature Chemistry|April 26, 2022
Global analysis of biosynthetic gene clusters reveals conserved and unique natural products in entomopathogenic nematode-symbiotic bacteriaYi-Ming Shi, Merle Hirschmann, Yan-Ni Shi, et al.Scientific Reports|April 15, 2018
Defective immuno- and thymoproteasome assembly causes severe immunodeficiencyIrina Treise, Eva M Huber, Tanja Klein-Rodewald, et al.Pageof 20