Cystobactamids 920-1 and 920-2: Assignment of the Constitution and Relative Configuration by Total Synthesis.
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A. Kirschning | R. Müller | S. Hüttel | Jörg Fohrer | M. Norris | Liang-Liang Wang | Therese Planke | Franziska Gille | María Moreno | Maik Siebke
[1] Pieter C Dorrestein,et al. Total Synthesis and Biological Assessment of Novel Albicidins Discovered by Mass Spectrometric Networking. , 2017, Chemistry.
[2] D. Trauner,et al. Total Syntheses of Cystobactamids and Structural Confirmation of Cystobactamid 919-2. , 2017, Angewandte Chemie.
[3] A. Kirschning,et al. Discovery and Total Synthesis of Natural Cystobactamid Derivatives with Superior Activity against Gram-Negative Pathogens. , 2017, Angewandte Chemie.
[4] R. Süssmuth,et al. Synthesis of Albicidin Derivatives: Assessing the Role of N‐terminal Acylation on the Antibacterial Activity , 2016, ChemMedChem.
[5] Shunya Takahashi,et al. Isolation of Coralmycins A and B, Potent Anti-Gram Negative Compounds from the Myxobacteria Corallococcus coralloides M23. , 2016, Journal of natural products.
[6] R. Süssmuth,et al. Synthesis and Antimicrobial Activity of Albicidin Derivatives with Variations of the Central Cyanoalanine Building Block , 2016, ChemMedChem.
[7] R. Süssmuth,et al. The O-Carbamoyl-Transferase Alb15 Is Responsible for the Modification of Albicidin. , 2016, ACS chemical biology.
[8] R. Süssmuth,et al. The Albicidin Resistance Factor AlbD Is a Serine Endopeptidase That Hydrolyzes Unusual Oligoaromatic-Type Peptides. , 2015, Journal of the American Chemical Society.
[9] R. Süssmuth,et al. What makes Xanthomonas albilineans unique amongst xanthomonads? , 2015, Front. Plant Sci..
[10] R. Hartmann,et al. Synthesis and Biological Evaluation of Cystobactamid 507: A Bacterial Topoisomerase Inhibitor from Cystobacter sp. , 2015, Synlett.
[11] R. Süssmuth,et al. The gyrase inhibitor albicidin consists of p-aminobenzoic acids and cyanoalanine. , 2015, Nature chemical biology.
[12] Roderich D. Süssmuth,et al. Totalsynthese von Albicidin – eine Leitstruktur aus Xanthomonas albilineans für potente antibakterielle Gyrase‐Inhibitoren , 2015 .
[13] R. Müller,et al. Cystobactamids: myxobacterial topoisomerase inhibitors exhibiting potent antibacterial activity. , 2014, Angewandte Chemie.
[14] Richard A Friesner,et al. Accurate Force Field Development for Modeling Conjugated Polymers. , 2012, Journal of chemical theory and computation.
[15] C. Bertucci,et al. Conformational flexibility and absolute stereochemistry of (3R)-3-hydroxy-4-aryl-β-lactams investigated by chiroptical properties and TD-DFT calculations. , 2012, Chirality.
[16] Michael R. Shirts,et al. Modeling of Arylamide Helix Mimetics in the p53 Peptide Binding Site of hDM2 Suggests Parallel and Anti-Parallel Conformations Are Both Stable , 2012, PloS one.
[17] G. P. Johnson,et al. Comparison of different force fields for the study of disaccharides. , 2009, Carbohydrate research.
[18] Bert L de Groot,et al. Secondary structure propensities in peptide folding simulations: a systematic comparison of molecular mechanics interaction schemes. , 2009, Biophysical journal.
[19] Jeffrey P. Plante,et al. Oligobenzamide proteomimetic inhibitors of the p53–hDM2 protein–protein interaction , 2009, Chemical communications.
[20] Richard A. Friesner,et al. Integrated Modeling Program, Applied Chemical Theory (IMPACT) , 2005, J. Comput. Chem..
[21] Andreas F. M. Kilbinger,et al. Soluble oligoaramide precursors--a novel class of building blocks for rod-coil architectures. , 2005, Chemistry.
[22] K. Nicolaou,et al. A mild and selective method for the hydrolysis of esters with trimethyltin hydroxide. , 2005, Angewandte Chemie.
[23] A. Sudalai,et al. Asymmetric synthesis of l-DOPA and (R)-selegiline via, OsO4-catalyzed asymmetric dihydroxylation , 2004 .
[24] Jin-gen Deng. AN EFFICIENT SYNTHESIS OF ALTEROBACTIN A; A SUPER SIDEROPHORE OF MARINE ORIGIN , 1998 .
[25] Jin-gen Deng,et al. Total Synthesis of Alterobactin A, a Super Siderophore from an Open-Ocean Bacterium , 1995 .
[26] W. L. Jorgensen,et al. The OPLS [optimized potentials for liquid simulations] potential functions for proteins, energy minimizations for crystals of cyclic peptides and crambin. , 1988, Journal of the American Chemical Society.