Thiol-ene Enabled Chemical Synthesis of Truncated S-Lipidated Teixobactin Analogs
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[1] Sung‐Hyun Yang,et al. Replacement of the Acrid tert -Butylthiol and an Improved Isolation Protocol for Cysteine Lipidation on a Peptide or Amino Acid (CLipPA) , 2020 .
[2] M. Brimble,et al. Direct synthesis of cyclic lipopeptides using intramolecular native chemical ligation and thiol-ene CLipPA chemistry. , 2020, Organic & biomolecular chemistry.
[3] M. Brimble,et al. Synthesis of Antimicrobial Lipopeptides Using the "CLipPA" Thiol-Ene Reaction. , 2020, Methods in molecular biology.
[4] Xuechen Li,et al. Establishing the structure-activity relationship of teixobactin , 2019, Chinese Chemical Letters.
[5] D. S. Reddy,et al. Total synthesis of Met10-teixobactin , 2019, Tetrahedron Letters.
[6] Xiuyun Sun,et al. Developing Equipotent Teixobactin Analogues against Drug-Resistant Bacteria and Discovering a Hydrophobic Interaction between Lipid II and Teixobactin. , 2018, Journal of Medicinal Chemistry.
[7] M. Oggioni,et al. Lipopeptidomimetics derived from teixobactin have potent antibacterial activity against Staphylococcus aureus. , 2018, Chemical communications.
[8] Xuechen Li,et al. Synthesis and antibacterial studies of teixobactin analogues with non-isostere substitution of enduracididine. , 2018, Bioorganic & medicinal chemistry.
[9] R. Beuerman,et al. Design and Syntheses of Highly Potent Teixobactin Analogues against Staphylococcus aureus, Methicillin-Resistant Staphylococcus aureus (MRSA), and Vancomycin-Resistant Enterococci (VRE) in Vitro and in Vivo. , 2018, Journal of medicinal chemistry.
[10] Yahya E. Jad,et al. Teixobactin as a scaffold for unlimited new antimicrobial peptides: SAR study. , 2017, Bioorganic & medicinal chemistry.
[11] M. Brimble,et al. Synthesis and biological evaluation of novel teixobactin analogues. , 2017, Organic & biomolecular chemistry.
[12] J. Nowick,et al. Alanine scan reveals modifiable residues in teixobactin. , 2017, Chemical communications.
[13] E. Breukink,et al. Teixobactin analogues reveal enduracididine to be non-essential for highly potent antibacterial activity and lipid II binding† †Electronic supplementary information (ESI) available: Peptide synthesis, HPLC, LC-MS analysis, NMR spectra, microbiological data (MIC, MBC, time kill kinetics), lipid II an , 2017, Chemical science.
[14] Xuechen Li,et al. Synthesis and structure-activity relationship of teixobactin analogues via convergent Ser ligation. , 2017, Bioorganic & medicinal chemistry.
[15] F. Albericio,et al. Converting Teixobactin into a Cationic Antimicrobial Peptide (AMP). , 2017, Journal of medicinal chemistry.
[16] A. Madder,et al. Syntheses of potent teixobactin analogues against methicillin-resistant Staphylococcus aureus (MRSA) through the replacement of l-allo-enduracididine with its isosteres. , 2017, Chemical communications.
[17] J. Ziller,et al. X-ray crystallographic structure of a teixobactin analogue reveals key interactions of the teixobactin pharmacophore. , 2017, Chemical communications.
[18] E. Breukink,et al. Defining the molecular structure of teixobactin analogues and understanding their role in antibacterial activities. , 2017, Chemical communications.
[19] Z. Pan,et al. Synthesis and structure–activity relationship studies of teixobactin analogues , 2017 .
[20] Yahya E. Jad,et al. Lysine Scanning of Arg10–Teixobactin: Deciphering the Role of Hydrophobic and Hydrophilic Residues , 2016, ACS omega.
[21] M. Brimble,et al. Enduracididine, a rare amino acid component of peptide antibiotics: Natural products and synthesis , 2016, Beilstein journal of organic chemistry.
[22] Ebrahim H Ghazvini Zadeh,et al. Total synthesis of teixobactin , 2016, Nature Communications.
[23] M. Moloney. Natural Products as a Source for Novel Antibiotics. , 2016, Trends in pharmacological sciences.
[24] Kevin H. Chen,et al. Elucidation of the Teixobactin Pharmacophore. , 2016, ACS chemical biology.
[25] Roger G. Linington,et al. Total Synthesis of Teixobactin. , 2016, Organic letters.
[26] Sung‐Hyun Yang,et al. Lipidation of Cysteine or Cysteine-Containing Peptides Using the Thiol-Ene Reaction (CLipPA) , 2016 .
[27] A. Madder,et al. Efficient total syntheses and biological activities of two teixobactin analogues. , 2016, Chemical communications.
[28] Yahya E. Jad,et al. Synthesis and Biological Evaluation of a Teixobactin Analogue. , 2015, Organic letters.
[29] K. Lewis,et al. A new antibiotic kills pathogens without detectable resistance , 2015, Nature.
[30] M. Brimble,et al. Direct peptide lipidation through thiol-ene coupling enables rapid synthesis and evaluation of self-adjuvanting vaccine candidates. , 2013, Angewandte Chemie.
[31] Miriam Góngora-Benítez,et al. Handles for Fmoc solid-phase synthesis of protected peptides. , 2013, ACS combinatorial science.
[32] J. McMurray,et al. The synthesis of cyclic peptides using fmoc solid-phase chemistry and the linkage agent 4-(4-Hydroxymethyl-3-methoxyphenoxy)-butyric acid , 1993 .
[33] R. B. Merrifield,et al. Quantitative monitoring of solid-phase peptide synthesis by the ninhydrin reaction. , 1981, Analytical biochemistry.