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Fast Cyclization of a Proline‐Derived Self‐Immolative Spacer Improves the Efficacy of Carbamate Prodrugs.
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- Angewandte Chemie, 2020, v. 132, n. 10, p. 4205, doi. 10.1002/ange.201916394
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- Article
Affinity Enhancement of Protein Ligands by Reversible Covalent Modification of Neighboring Lysine Residues.
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- Angewandte Chemie, 2018, v. 130, n. 52, p. 17424, doi. 10.1002/ange.201811650
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- Article
Synthesis of Noncoded Amino Acids Bearing a Salicylaldehyde Tag for the Design of Reversible‐Covalent Peptides.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 22, p. 1, doi. 10.1002/ejoc.202400229
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- Article
Affinity Enhancement of Protein Ligands by Reversible Covalent Modification of Neighboring Lysine Residues.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 52, p. 17178, doi. 10.1002/anie.201811650
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- Article
Metallaphotoredox C−O and C−N Cross‐Coupling Using Donor‐Acceptor Cyanoarene Photocatalysts.
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- ChemCatChem, 2022, v. 14, n. 23, p. 1, doi. 10.1002/cctc.202200990
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- Article
Advanced Pyrrolidine‐Carbamate Self‐Immolative Spacer with Tertiary Amine Handle Induces Superfast Cyclative Drug Release.
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- ChemMedChem, 2022, v. 17, n. 15, p. 1, doi. 10.1002/cmdc.202200279
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- Article
Synthesis and Biological Evaluation of RGD and isoDGR–Monomethyl Auristatin Conjugates Targeting Integrin α<sub>V</sub>β<sub>3</sub>.
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- ChemMedChem, 2019, v. 14, n. 9, p. 938, doi. 10.1002/cmdc.201900049
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- Article
Functionalized 2‐Hydroxybenzaldehyde‐PEG Modules as Portable Tags for the Engagement of Protein Lysine ϵ‐Amino Groups.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 11, p. 1763, doi. 10.1002/ejoc.202100160
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- Article
Synthesis and Biological Evaluation of Paclitaxel Conjugates Involving Linkers Cleavable by Lysosomal Enzymes and α<sub>V</sub>β<sub>3</sub>‐Integrin Ligands for Tumor Targeting.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 23, p. 2902, doi. 10.1002/ejoc.201800447
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- Article
Synthesis, Characterization, and Biological Evaluation of a Dual-Action Ligand Targeting α<sub>v</sub>β<sub>3</sub> Integrin and VEGF Receptors.
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- ChemistryOpen, 2015, v. 4, n. 5, p. 633, doi. 10.1002/open.201500062
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- Article
Amine‐Carbamate Self‐Immolative Spacers Counterintuitively Release 3° Alcohol at Much Faster Rates than 1° Alcohol Payloads.
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- ChemBioChem, 2024, v. 25, n. 8, p. 1, doi. 10.1002/cbic.202400174
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- Article
A Tight Contact: The Expanding Application of Salicylaldehydes in Lysine‐Targeting Covalent Drugs.
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- ChemBioChem, 2024, v. 25, n. 7, p. 1, doi. 10.1002/cbic.202300743
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- Article
Targeted Small‐Molecule Conjugates: The Future is Now.
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- ChemBioChem, 2020, v. 21, n. 23, p. 3321, doi. 10.1002/cbic.202000507
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- Article
Multimeric Presentation of RGD Peptidomimetics Enhances Integrin Binding and Tumor Cell Uptake.
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- Chemistry - A European Journal, 2020, v. 26, n. 33, p. 7492, doi. 10.1002/chem.202001115
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- Article
Frontispiece: Innovative Linker Strategies for Tumor‐Targeted Drug Conjugates.
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- Chemistry - A European Journal, 2019, v. 25, n. 65, p. N.PAG, doi. 10.1002/chem.201986561
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- Article
Innovative Linker Strategies for Tumor‐Targeted Drug Conjugates.
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- Chemistry - A European Journal, 2019, v. 25, n. 65, p. 14740, doi. 10.1002/chem.201903127
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- Article
Neutrophil Elastase Promotes Linker Cleavage and Paclitaxel Release from an Integrin‐Targeted Conjugate.
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- Chemistry - A European Journal, 2019, v. 25, n. 7, p. 1696, doi. 10.1002/chem.201805447
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- Article
Frontispiece: Multivalency Increases the Binding Strength of RGD Peptidomimetic-Paclitaxel Conjugates to Integrin α<sub>V</sub>β<sub>3</sub>.
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- Chemistry - A European Journal, 2017, v. 23, n. 58, p. n/a, doi. 10.1002/chem.201703093
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- Article
Multivalency Increases the Binding Strength of RGD Peptidomimetic-Paclitaxel Conjugates to Integrin α<sub>V</sub>β<sub>3</sub>.
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- Chemistry - A European Journal, 2017, v. 23, n. 58, p. 14410, doi. 10.1002/chem.201703093
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- Publication type:
- Article
Fast Cyclization of a Proline‐Derived Self‐Immolative Spacer Improves the Efficacy of Carbamate Prodrugs.
- Published in:
- Angewandte Chemie International Edition, 2020, v. 59, n. 10, p. 4176, doi. 10.1002/anie.201916394
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- Publication type:
- Article
Ex vivo mass spectrometry-based biodistribution analysis of an antibody-Resiquimod conjugate bearing a protease-cleavable and acid-labile linker.
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- Frontiers in Pharmacology, 2023, p. 1, doi. 10.3389/fphar.2023.1320524
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- Article
RGD Cyclopeptide Equipped with a Lysine‐Engaging Salicylaldehyde Showing Enhanced Integrin Affinity and Cell Detachment Potency.
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- Chemistry - A European Journal, 2023, v. 29, n. 19, p. 1, doi. 10.1002/chem.202203768
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- Article
Impact of a Central Scaffold on the Binding Affinity of Fragment Pairs Isolated from DNA-Encoded Self-Assembling Chemical Libraries.
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- ChemMedChem, 2017, v. 12, n. 21, p. 1748, doi. 10.1002/cmdc.201700569
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- Article
Synthesis and Biological Evaluation of RGD Peptidomimetic-Paclitaxel Conjugates Bearing Lysosomally Cleavable Linkers.
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- Chemistry - A European Journal, 2015, v. 21, n. 18, p. 6921, doi. 10.1002/chem.201500158
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- Article
Cyclic isoDGR and RGD Peptidomimetics Containing Bifunctional Diketopiperazine Scaffolds are Integrin Antagonists.
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- Chemistry - A European Journal, 2015, v. 21, n. 16, p. 6265, doi. 10.1002/chem.201406567
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- Article
Cyclic isoDGR Peptidomimetics as Low-Nanomolar α<sub>v</sub>β<sub>3</sub> Integrin Ligands.
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- Chemistry - A European Journal, 2013, v. 19, n. 11, p. 3563, doi. 10.1002/chem.201204639
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- Article