Abstract: The present invention provides peptides that are synthetic modifications of Polar Assonant (PA) peptide including C-terminal PEGylation. The invention further provides methods of using least one synthetic peptide for regulating the complement system and interacting with neutrophils to alter their binding and activity.
Type:
Application
Filed:
September 27, 2021
Publication date:
January 11, 2024
Applicant:
REALTA LIFE SCIENCES, INC.
Inventors:
Neel K. KRISHNA, Kenji CUNNION, Ulrich THIENEL
Abstract: The present invention provides synthetic peptides. The invention is directed to modifications of a synthetic peptide of 15 amino acids from the Polar Assortant (PA) peptide, which is a scrambled peptide derived from human Astrovirus protein. In some embodiments, the invention is directed to pharmaceutical formulations of the peptides including lipid-based formulations and formulations suitable for intravenous administration.
Abstract: The present invention provides synthetic peptides. The invention is directed to modifications of a synthetic peptide of 15 amino acids from the Polar Assonant (PA) peptide, which is a scrambled peptide derived from human astrovirus protein. In some embodiments, the invention is directed to peptides that are modifications of PA including sarcosine substitutions at certain amino acid positions that are stapled and/or have D-enantiomeric substitutions of certain amino acids. The invention further provides methods of selecting at least one synthetic peptide for treating various conditions.
Type:
Application
Filed:
November 1, 2021
Publication date:
September 28, 2023
Applicant:
REALTA LIFE SCIENCES, INC.
Inventors:
Neel K. KRISHNA, Kenji CUNNION, Ulrich THIENEL
Abstract: The present invention provides synthetic peptides. The invention is directed to modifications of a synthetic peptide of 15 amino acids from the Polar Assortant (PA) peptide, which is a scrambled peptide derived from human astrovirus protein. In some embodiments, the invention is directed to peptides that are modifications of PA including sarcosine substitutions at certain amino acid positions that are stapled and/or have D-enantiomeric substitutions of certain amino acids. The invention further provides methods of selecting at least one synthetic peptide for treating various conditions.