1,5-Disubstituted 1,2,3-Triazoles as Amide Bond Isosteres Yield Novel Tumor-Targeting Minigastrin Analogs-Reference-Cited by-同舟云学术

1,5-Disubstituted 1,2,3-Triazoles as Amide Bond Isosteres Yield Novel Tumor-Targeting Minigastrin Analogs

Author:

Grob Nathalie M.¹,Schibli Roger¹²,Béhé Martin²^ORCID,Valverde Ibai E.³^ORCID,Mindt Thomas L.⁴⁵⁶

Affiliation:

1. Department of Chemistry and Applied Biosciences, ETH Zurich, 8093 Zürich, Switzerland

2. Center for Radiopharmaceutical Sciences, Division of Biology and Chemistry, Paul Scherrer Institute, 5232 Villigen, Switzerland

3. Institut de Chimie Moléculaire de l’Université de Bourgogne, UMR CNRS 6302, Université de Bourgogne Franche-Comté, 21000 Dijon, France

4. Ludwig Boltzmann Institute Applied Diagnostics, General Hospital of Vienna, 1090 Vienna, Austria

5. Department of Inorganic Chemistry, Faculty of Chemistry, University of Vienna, 1090 Vienna, Austria

6. Department of Biomedical Imaging and Image Guided Therapy, Medical University of Vienna, 1090 Vienna, Austria

Funder

European Commission

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Universit? de Bourgogne

Conseil r?gional de Bourgogne-Franche-Comt?

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Link

Reference43 articles.

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2. A Concise Account of Synthetic Approaches to 1,2,3-Triazoles;Organic Preparations and Procedures International;2024-06-18