V.ae butted.rl.o slashed.se, Denmark

Ole Buchardt


Average Co-Inventor Count = 3.0

ph-index = 1

Forward Citations = 10(Granted Patents)


Company Filing History:


Years Active: 1996

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1 patent (USPTO):Explore Patents

Title: Ole Buchardt: Innovator in Peptide Chemistry

Introduction

Ole Buchardt is a distinguished inventor known for his contributions to the field of peptide chemistry. He is based in Denmark and has made significant strides in the preparation of C-terminally amidated peptides. His innovative approach has implications for various applications in biochemistry and pharmaceuticals.

Latest Patents

Ole Buchardt holds a patent for a process titled "Process for the preparation of C-terminally amidated peptides." This patent describes a method for preparing C-terminally amidated peptides, specifically Peptide-NH.sub.2. The process involves two main steps: first, a substrate component is reacted with a nucleophile component in the presence of trypsin or a carboxypeptidase. The second step involves the non-enzymatic chemical cleavage of the first reaction product to yield the C-terminally amidated product. This innovative method allows for the C-terminal amidation of various types of peptides, showcasing Buchardt's expertise in the field.

Career Highlights

Ole Buchardt is associated with Carlsberg A/S, where he continues to advance his research in peptide synthesis. His work has garnered attention for its potential applications in drug development and therapeutic interventions. With a focus on enzymatic synthesis, Buchardt's contributions are paving the way for new advancements in peptide chemistry.

Collaborations

Throughout his career, Ole Buchardt has collaborated with notable colleagues, including Klaus Breddam and Dennis B Henriksen. These partnerships have enriched his research and expanded the impact of his innovations in the scientific community.

Conclusion

Ole Buchardt's work in peptide chemistry exemplifies the importance of innovation in the field of biochemistry. His patented process for preparing C-terminally amidated peptides represents a significant advancement that could influence future research and applications.

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