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Design, Synthesis, and Biological Evaluation of Indole-2-carboxamides as Potential Multi-Target Antiproliferative Agents.
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- Pharmaceuticals (14248247), 2023, v. 16, n. 7, p. 1039, doi. 10.3390/ph16071039
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Design, Synthesis, and Antiproliferative Activity of New 5-Chloro-indole-2-carboxylate and Pyrrolo[3,4- b ]indol-3-one Derivatives as Potent Inhibitors of EGFR T790M /BRAF V600E Pathways.
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- Molecules, 2023, v. 28, n. 3, p. 1269, doi. 10.3390/molecules28031269
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A ribosomally synthesised and post-translationally modified peptide containing a β-enamino acid and a macrocyclic motif.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32774-3
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Synthesis and Biological Evaluation of Indole-2-Carboxamides with Potent Apoptotic Antiproliferative Activity as EGFR/CDK2 Dual Inhibitors.
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- Pharmaceuticals (14248247), 2022, v. 15, n. 8, p. 1006, doi. 10.3390/ph15081006
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Discovery and Biosynthetic Investigation of a New Antibacterial Dehydrated Non‐Ribosomal Tripeptide.
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- Angewandte Chemie, 2021, v. 133, n. 6, p. 3266, doi. 10.1002/ange.202012902
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Discovery and Biosynthetic Investigation of a New Antibacterial Dehydrated Non‐Ribosomal Tripeptide.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 6, p. 3229, doi. 10.1002/anie.202012902
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- Article
Productive Syntheses of Privileged Scaffolds Inspired by the Recognition of a Diels–Alder Pattern Common to Three Classes of Natural Products.
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- Chemistry - A European Journal, 2020, v. 26, n. 67, p. 15477, doi. 10.1002/chem.202002372
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A Weakened Immune Response to Synthetic Exo-Peptides Predicts a Potential Biosecurity Risk in the Retrieval of Exo-Microorganisms.
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- Microorganisms, 2020, v. 8, n. 7, p. 1066, doi. 10.3390/microorganisms8071066
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Structure-Based Design, Synthesis and Bioactivity of a New Anti-TNFα Cyclopeptide.
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- Molecules, 2020, v. 25, n. 4, p. 922, doi. 10.3390/molecules25040922
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- Article
Berichtigung: A Unique Tryptophan C-Prenyltransferase from the Kawaguchipeptin Biosynthetic Pathway.
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- Angewandte Chemie, 2017, v. 129, n. 2, p. 446, doi. 10.1002/ange.201609949
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Corrigendum: A Unique Tryptophan C-Prenyltransferase from the Kawaguchipeptin Biosynthetic Pathway.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 2, p. 433, doi. 10.1002/anie.201609949
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- Article
A Unique Tryptophan C-Prenyltransferase from the Kawaguchipeptin Biosynthetic Pathway.
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- Angewandte Chemie, 2016, v. 128, n. 11, p. 3660, doi. 10.1002/ange.201509920
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- Article
A Unique Tryptophan C-Prenyltransferase from the Kawaguchipeptin Biosynthetic Pathway.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 11, p. 3596, doi. 10.1002/anie.201509920
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- Article
Discovery of a Single Monooxygenase that Catalyzes Carbamate Formation and Ring Contraction in the Biosynthesis of the Legonmycins.
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- Angewandte Chemie, 2015, v. 127, n. 43, p. 12888, doi. 10.1002/ange.201502902
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Rücktitelbild: Discovery of a Single Monooxygenase that Catalyzes Carbamate Formation and Ring Contraction in the Biosynthesis of the Legonmycins (Angew. Chem. 43/2015).
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- Angewandte Chemie, 2015, v. 127, n. 43, p. 13016, doi. 10.1002/ange.201506192
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- Article
Discovery of a Single Monooxygenase that Catalyzes Carbamate Formation and Ring Contraction in the Biosynthesis of the Legonmycins.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 43, p. 12697, doi. 10.1002/anie.201502902
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- Article
Back Cover: Discovery of a Single Monooxygenase that Catalyzes Carbamate Formation and Ring Contraction in the Biosynthesis of the Legonmycins (Angew. Chem. Int. Ed. 43/2015).
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- Angewandte Chemie International Edition, 2015, v. 54, n. 43, p. 12824, doi. 10.1002/anie.201506192
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- Article
The mechanism of patellamide macrocyclization revealed by the characterization of the PatG macrocyclase domain.
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- Nature Structural & Molecular Biology, 2012, v. 19, n. 8, p. 767, doi. 10.1038/nsmb.2340
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Encapsulation Induces Helical Folding of Alkanes ( We thank E. Bosa for valuable advice on NMR experiments. We are grateful to the Skaggs Institute for Research, the NASA Astrobiology Institute, and the National Institutes of Health (GM 50174) for financial support. L.T. and A.S. are Skaggs Postdoctoral Fellows. )
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- Angewandte Chemie, 2003, v. 115, n. 44, p. 5657, doi. 10.1002/ange.200352235
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Encapsulation Induces Helical Folding of Alkanes ( We thank E. Bosa for valuable advice on NMR experiments. We are grateful to the Skaggs Institute for Research, the NASA Astrobiology Institute, and the National Institutes of Health (GM 50174) for financial support. L.T. and A.S. are Skaggs Postdoctoral Fellows. )
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- Angewandte Chemie International Edition, 2003, v. 42, n. 44, p. 5499, doi. 10.1002/anie.200352235
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- Article
Acetylcholine Recognition by a Deep, Biomimetic Pocket ( This research was supported by the Skaggs Institute for Chemical Biology and the NIH (GM 27932). E.C.U. thanks the Deutsche Forschungsgemeinschaft for fellowship support. The authors thank Prof. Pablo Ballester for helpful discussions. )
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- Angewandte Chemie, 2003, v. 115, n. 27, p. 3258, doi. 10.1002/ange.200351174
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- Article
Acetylcholine Recognition by a Deep, Biomimetic Pocket ( This research was supported by the Skaggs Institute for Chemical Biology and the NIH (GM 27932). E.C.U. thanks the Deutsche Forschungsgemeinschaft for fellowship support. The authors thank Prof. Pablo Ballester for helpful discussions. )
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- Angewandte Chemie International Edition, 2003, v. 42, n. 27, p. 3150, doi. 10.1002/anie.200351174
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- Article