Search Results - "Ogunkoya, Ayodele O."
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Chemical Protein Synthesis by Chemoselective α-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline
Published in Angewandte Chemie International Edition (21-05-2012)“…The chemical synthesis of proteins from unprotected peptide segments uses KAHA ligation with 5‐oxaproline, which is incorporated readily into peptides by…”
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Tandem-Cleavage Linkers Improve the In Vivo Stability and Tolerability of Antibody–Drug Conjugates
Published in Bioconjugate chemistry (21-04-2021)“…Although peptide motifs represent the majority of cleavable linkers used in clinical-stage antibody–drug conjugates (ADCs), the sequences are often sensitive…”
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Sequential α-Ketoacid-Hydroxylamine (KAHA) Ligations: Synthesis of C-Terminal Variants of the Modifier Protein UFM1
Published in Angewandte Chemie International Edition (17-09-2012)“…3 for 3: Sequential α‐ketoacid–hydroxylamine (KAHA) ligations with 5‐oxaproline allow access to the modifier protein UFM1 (Ubiquitin‐fold modifier 1) with a…”
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Aspartic Acid Forming α‑Ketoacid–Hydroxylamine (KAHA) Ligations with (S)‑4,4-Difluoro-5-oxaproline
Published in Journal of organic chemistry (07-02-2020)“…The α-ketoacid-hydroxylamine (KAHA) ligation allows the coupling of unprotected peptide segments. Currently, the most applied hydroxylamine is the 5-membered…”
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Sequential [alpha]-Ketoacid-Hydroxylamine (KAHA) Ligations: Synthesis of C-Terminal Variants of the Modifier Protein UFM1
Published in Angewandte Chemie International Edition (17-09-2012)“…3 for 3: Sequential [alpha]-ketoacid-hydroxylamine (KAHA) ligations with 5-oxaproline allow access to the modifier protein UFM1 (Ubiquitin-fold modifier 1)…”
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A Novel HER2-targeted Antibody–drug Conjugate Offers the Possibility of Clinical Dosing at Trastuzumab-equivalent Exposure Levels
Published in Molecular cancer therapeutics (01-09-2020)“…Abstract Trastuzumab and the related ADC, ado-trastuzumab emtansine (T-DM1), both target HER2-overexpressing cells. Together, these drugs have treatment…”
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Corrigendum: Chemical Protein Synthesis by Chemoselective [alpha]-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline
Published in Angewandte Chemie International Edition (03-11-2014)Get full text
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Corrigendum: Chemical Protein Synthesis by Chemoselective α-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline
Published in Angewandte Chemie International Edition (03-11-2014)Get full text
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Chemical Protein Synthesis by Chemoselective [alpha]-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline
Published in Angewandte Chemie International Edition (21-05-2012)“…The chemical synthesis of proteins from unprotected peptide segments uses KAHA ligation with 5-oxaproline, which is incorporated readily into peptides by…”
Get full text
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Cover Picture: Chemical Protein Synthesis by Chemoselective [alpha]-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline (Angew. Chem. Int. Ed. 21/2012)
Published in Angewandte Chemie International Edition (21-05-2012)“…The chemical synthesis of proteins from unprotected peptide segments uses KAHA ligation with 5-oxaproline, which is incorporated readily into peptides by…”
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Berichtigung: Sequentielle α‐Ketosäurehydroxylamin(KAHA)‐Ligationen: Synthese C‐terminaler Varianten des Modifikationsproteins UFM1
Published in Angewandte Chemie (03-11-2014)Get full text
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Berichtigung: Chemical Protein Synthesis by Chemoselective [alpha]-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline
Published in Angewandte Chemie (03-11-2014)Get full text
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Berichtigung: Chemical Protein Synthesis by Chemoselective α-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline
Published in Angewandte Chemie (03-11-2014)Get full text
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Sequentielle α‐Ketosäurehydroxylamin(KAHA)‐Ligationen: Synthese C‐terminaler Varianten des Modifikationsproteins UFM1
Published in Angewandte Chemie (17-09-2012)“…3 für 3: Die sequentielle α‐Ketosäurehydroxylamin(KAHA)‐Ligation mit 5‐Oxaprolin eröffnet den einfachen Zugang zu C‐terminalen Amiden, Carbonsäuren und…”
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Chemical Protein Synthesis by Chemoselective α-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline
Published in Angewandte Chemie (21-05-2012)“…Die chemische Synthese von Proteinen ausgehend von ungeschützten Peptidsegmenten nutzt die KAHA‐Ligation mit 5‐Oxaprolin, das problemlos bei der…”
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Titelbild: Chemical Protein Synthesis by Chemoselective [alpha]-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline (Angew. Chem. 21/2012)
Published in Angewandte Chemie (21-05-2012)Get full text
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Titelbild: Chemical Protein Synthesis by Chemoselective α-Ketoacid-Hydroxylamine (KAHA) Ligations with 5-Oxaproline (Angew. Chem. 21/2012)
Published in Angewandte Chemie (21-05-2012)Get full text
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