Synfacts 2020; 16(05): 0614
DOI: 10.1055/s-0040-1707588
Peptide Chemistry
© Georg Thieme Verlag Stuttgart · New York

Acridine–Peptide Conjugates by Solid-Phase Synthesis

Contributor(s):
Hisashi Yamamoto
,
Tomohiro Hattori
Carlson CB, Beal PA. * University of Utah, Salt Lake City, USA
Solid-Phase Synthesis of Acridine–Peptide Conjugates and Their Analysis by Tandem Mass Spectrometry.

Org. Lett. 2000;
2: 1465-1468
Further Information

Publication History

Publication Date:
20 April 2020 (online)

 

Significance

With the growing range of applications of long-chain peptides, such as proteins, the development of appropriate analytical techniques is highly desirable. In 2000, Carlson and Beal prepared combinatorial libraries of acridine–peptide conjugates that could be helpful for the discovery of structure-specific nucleic acid ligands by affinity chromatography with mass spectrometry.


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Comment

9-Acridone-4-carboxylic acid was functionalized with aniline via a 9-triazolylacridine intermediate, and the product was used to synthesize acridine–peptide conjugates by solid-phase synthesis. The structures of the products could be determined from samples of less than 10 pmol by tandem mass spectrometry.


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