Inhibition of the Interaction Between Viral Spike Proteins of SARS-CoV-2 and Human Angiotensin-Converting Enzyme 2 (hACE2)
Simple SummaryContent extracted from patent full text and abstract with AI.
This patent describes specific peptides (short chains of amino acids) designed to block the interaction between the SARS-CoV-2 viral spike protein and the human ACE2 receptor. By preventing this critical interaction, the peptides aim to stop the virus from entering human cells, offering a possible treatment for COVID-19.
Use CasesContent extracted from patent full text and abstract with AI.
- Therapeutic drug for treating COVID-19 patients
- Preventative treatment to reduce the risk of SARS-CoV-2 infection
- Research tool for studying virus-host interactions
- Potential base for developing new antiviral agents
BenefitsContent extracted from patent full text and abstract with AI.
- May directly inhibit SARS-CoV-2 infection by blocking viral entry into cells
- Could reduce severity and spread of COVID-19
- Provides a targeted approach with potentially fewer side effects compared to broad-spectrum antivirals
- Supports rapid development and adaptation to emerging viral variants
Technical Classifications (CPCs)
Main Classifications
Chemistry & Materials Science
Health, Food & Consumer Tech
Sub Classifications
Medical & Vet Science
Organic Chemistry
CPC Codes
Inventors & Applicants
Applicants
Forschungszentrum Juelich Gmbh
Patent Abstract
Described is a peptide comprising an amino acid sequence selected from the group consisting of SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4 and/or SEQ ID NO: 5, as well as homologues, fragments and parts thereof, its use for inhibiting the interaction of the viral spike protein of SARS-CoV-2 with the human angiotensin-converting enzyme hACE2, and such a peptide for use as a medicament, in particular for use in the treatment of COVID-19.
Key Information
Publication No.
DE102021005922A1
Family ID
86316929
Publication Date
2023-06-01
Application No.
DE102021005922A
Application Date
2021-11-30
Priority Date
2021-11-30
Granted
No
Possible Cooperation
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