Synthesis of Novel Bis-statine-based Peptide Containing Ferrocenyl Moiety

Lijun Gu School of Chemistry and Biotechnology, Yunnan Nationalities University, Kunming, China; Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), Department of Chemistry, Northwest University, Xi'an, China

Feilong Liu Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), Department of Chemistry, Northwest University, Xi'an, China

Xiangguang Li Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), Department of Chemistry, Northwest University, Xi'an, China

Bo Gao Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), Department of Chemistry, Northwest University, Xi'an, China

Bingqin Yang Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), Department of Chemistry, Northwest University, Xi'an, ChinaCorrespondence[email protected]

Abstract

In a search for a new inhibitor of aspartyl protease, the ferrocenyl group was introduced from the C-terminus of statine to create a novel bis-statine-based peptide containing ferrocenyl moiety in solution. The target compound was characterized by infrared, ¹H NMR spectroscopy, mass spectrometry, and elemental analysis.

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ACKNOWLEDGMENTS

The authors thank the National Natural Science Foundation of China (No. 20572085) for financial support.

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Synthesis of Novel Bis-statine-based Peptide Containing Ferrocenyl Moiety

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Synthesis of Novel Bis-statine-based Peptide Containing Ferrocenyl Moiety

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