Works by Lucena‐Agell, Daniel
Results: 21
Cover Feature: Synthesis and Structure‐Activity Relationship Studies of C(13)‐Desmethylene‐(−)‐Zampanolide Analogs (Chem. Eur. J. 36/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 36, p. 1, doi. 10.1002/chem.202301652
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- Article
Synthesis and Structure‐Activity Relationship Studies of C(13)‐Desmethylene‐(−)‐Zampanolide Analogs.
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- Chemistry - A European Journal, 2023, v. 29, n. 36, p. 1, doi. 10.1002/chem.202300703
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- Article
Maytansinol Functionalization: Towards Useful Probes for Studying Microtubule Dynamics.
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- Chemistry - A European Journal, 2023, v. 29, n. 5, p. 1, doi. 10.1002/chem.202203431
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- Article
Maytansinol Functionalization: Towards Useful Probes for Studying Microtubule Dynamics.
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- Chemistry - A European Journal, 2023, v. 29, n. 5, p. 1, doi. 10.1002/chem.202203431
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- Article
Front Cover: Maytansinol Functionalization: Towards Useful Probes for Studying Microtubule Dynamics (Chem. Eur. J. 5/2023).
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- Chemistry - A European Journal, 2023, v. 29, n. 5, p. 1, doi. 10.1002/chem.202300067
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- Article
Maytansinol Functionalization: Towards Useful Probes for Studying Microtubule Dynamics.
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- Chemistry - A European Journal, 2023, v. 29, n. 5, p. 1, doi. 10.1002/chem.202203431
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- Article
Synthese und Biologische Untersuchungen von C(13)/C(13′)‐Bis(desmethyl)disorazol Z**.
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- Angewandte Chemie, 2023, v. 135, n. 5, p. 1, doi. 10.1002/ange.202212190
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Design, synthesis and structure-activity relationship (SAR) studies of an unusual class of non-cationic fatty amine-tripeptide conjugates as novel synthetic antimicrobial agents.
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- Frontiers in Pharmacology, 2024, p. 1, doi. 10.3389/fphar.2024.1428409
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Structural insight into the stabilization of microtubules by taxanes.
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- eLife, 2023, p. 1, doi. 10.7554/eLife.84791
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N-alkylisatin-based microtubule destabilizers bind to the colchicine site on tubulin and retain efficacy in drug resistant acute lymphoblastic leukemia cell lines with less in vitro neurotoxicity.
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- Cancer Cell International, 2020, v. 20, n. 1, p. 1, doi. 10.1186/s12935-020-01251-6
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A fluorescence anisotropy assay to discover and characterize ligands targeting the maytansine site of tubulin.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-04535-8
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Synthesis and Biological Evaluation of C(13)/C(13′)‐Bis(desmethyl)disorazole Z**.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 5, p. 1, doi. 10.1002/anie.202212190
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- Article
Design, Synthesis, and in vitro Evaluation of Tubulin‐Targeting Dibenzothiazines with Antiproliferative Activity as a Novel Heterocycle Building Block.
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- ChemMedChem, 2021, v. 16, n. 19, p. 3003, doi. 10.1002/cmdc.202100383
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Effect of Clinically Used Microtubule Targeting Drugs on Viral Infection and Transport Function.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 7, p. 3448, doi. 10.3390/ijms23073448
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Mutational analysis of the Aspergillus ambient pH receptor PalH underscores its potential as a target for antifungal compounds.
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- Molecular Microbiology, 2016, v. 101, n. 6, p. 982, doi. 10.1111/mmi.13438
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Refining the pH response in Aspergillus nidulans: a modulatory triad involving PacX, a novel zinc binuclear cluster protein.
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- Molecular Microbiology, 2015, v. 98, n. 6, p. 1051, doi. 10.1111/mmi.13173
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Cover Feature: Maytansinol Derivatives: Side Reactions as a Chance for New Tubulin Binders (Chem. Eur. J. 2/2022).
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- Chemistry - A European Journal, 2022, v. 28, n. 2, p. 1, doi. 10.1002/chem.202104474
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Maytansinol Derivatives: Side Reactions as a Chance for New Tubulin Binders.
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- Chemistry - A European Journal, 2022, v. 28, n. 2, p. 1, doi. 10.1002/chem.202103520
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- Article
Synthesis of Morpholine‐Based Analogues of (−)‐Zampanolide and Their Biological Activity.
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- Chemistry - A European Journal, 2021, v. 27, n. 19, p. 5936, doi. 10.1002/chem.202003996
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Two Antagonistic Microtubule Targeting Drugs Act Synergistically to Kill Cancer Cells.
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- Cancers, 2020, v. 12, n. 8, p. 2196, doi. 10.3390/cancers12082196
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Ultrafast photochemistry produces superbright short-wave infrared dots for low-dose in vivo imaging.
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- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-16333-2
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