Therapeutic compositions including gramicidin s peptidyl conjugates or imidazole-substituted fatty acids, variants thereof and uses thereof
AssigneeStealth BioTherapeutics Inc.
InventorD. Travis Wilson
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AssigneeStealth BioTherapeutics Inc.
InventorD. Travis Wilson
Estimating the term…
Disclosed herein are methods and compositions for the treatment and/or prevention of diseases or conditions comprising administration of Gramicidin S peptidyl conjugates (and/or derivatives, analogues, or pharmaceutically acceptable salts thereof), or imidazole-substituted fatty acids (and/or derivatives, analogues, or pharmaceutically acceptable salts thereof), alone or in combination with one or more active agents (e.g., an aromatic-cationic peptide). The present technology provides compositions related to aromatic-cationic peptides linked to imidazole-substituted fatty acids or Gramicidin S peptidyl conjugates of the present technology and uses of the same. In some embodiments, the aromatic-cationic peptide comprises 2′,6′-dimethyl-Tyr-D-Arg-Phe-Lys-NH2, Phe-D-Arg-Phe-Lys-NH2, or D-Arg-2′,6′-Dmt-Lys-Phe-NH2.
A peptide conjugate comprising an aromatic-cationic peptide conjugated to a Gramicidin S peptidyl conjugate, wherein the aromatic-cationic peptide is selected from the group consisting of:
A peptide conjugate comprising an imidazole-substituted fatty acid conjugated to an aromatic-cationic peptide, wherein the aromatic-cationic peptide is selected from the group consisting of:
-6. (canceled)
A method for delivering an aromatic-cationic peptide and/or a Gramicidin S peptidyl conjugate to a cell, the method comprising contacting the cell with a peptide conjugate, wherein the peptide conjugate comprises an aromatic-cationic peptide conjugated to a Gramicidin S peptidyl conjugate, wherein the aromatic-cationic peptide is selected from the group consisting of:
A method for delivering an aromatic-cationic peptide and/or an imidazole-substituted fatty acid to a cell, the method comprising contacting the cell with a peptide conjugate, wherein the peptide conjugate comprises an imidazole-substituted fatty acid conjugated to an aromatic-cationic peptide, wherein the aromatic-cationic peptide is selected from the group consisting of:
-13. (canceled)
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-35. (canceled)
Dependencies are inferred from the claim text.