US2020087349A1PendingUtilityA1
Broad-spectrum anti-infective peptides
Est. expiryJun 25, 2035(~8.9 yrs left)· nominal 20-yr term from priority
A61P 31/18C07K 14/005A61P 31/20A61K 9/08A61K 9/06C09D 189/00A61K 38/00A61P 31/12A61P 31/04C07K 14/1833A61P 31/14A61P 31/16A01N 47/44A61K 9/0019A61K 47/60C07K 14/001C07K 7/08A61K 9/0014A01N 25/04Y02A50/30
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Claims
Abstract
Provided herein are anti-infective peptides and uses thereof. Such anti-infective peptides are useful against bacteria and viruses. Also provided herein are compositions comprising said anti-infective peptides.
Claims
exact text as granted — not AI-modified1 . (canceled)
2 . A peptide of 16 to 26 amino acid residues in length comprising the following amino acid sequence:
X 1 X 2 SWLRDX 3 X 4 TX 5 LQSX 6 L, wherein X 1 is S or G; X 2 is S or G; X 3 is V; X 4 is W; X 5 is W or K; and X 6 is W, K or A (SEQ ID NO:13).
3 . A peptide of 16 to 26 amino acid residues in length comprising the following amino acid sequence: SGSWLRDVWTWLQSKL (SEQ ID NO:1).
4 - 7 . (canceled)
8 . The peptide of claim 3 , which consists of the following amino acid sequence: SGSWLRDVWTWLQSKL (SEQ ID NO:1).
9 - 10 . (canceled)
11 . The peptide of claim 8 , wherein the amino acid residues are L amino acids, D amino acids, or a mixture of D and L amino acids.
12 - 17 . (canceled)
18 . A pegylated peptide comprising the peptide as defined in claim 3 linked to one, two or more polyethylene glycol (PEG) polymers.
19 - 27 . (canceled)
28 . The pegylated peptide of claim 18 , wherein the one, two or more PEG polymers is linked to the N-terminus of the peptide, or the C-terminus of the peptide.
29 - 31 . (canceled)
32 . The pegylated peptide of claim 18 , which comprises the following structure: NH 2 -PEG12-Amide-PEG12-peptide.
33 - 47 . (canceled)
48 . The pegylated peptide of claim 18 , wherein each PEG polymer is in the molecular weight range of 500 to 5000 daltons.
49 . The pegylated peptide of claim 48 , wherein the one, two or more PEG polymers is branched or non-branched.
50 - 51 . (canceled)
52 . A composition comprising the peptide of claim 3 and a carrier.
53 . A composition comprising the pegylated peptide of claim 18 and a carrier.
54 - 59 . (canceled)
60 . A pharmaceutical composition comprising an effective amount of the peptide of claim 3 and a pharmaceutically acceptable carrier.
61 - 79 . (canceled)
80 . A method for treating a microorganism infection in a human, comprising administering to the human the pharmaceutical composition of claim 60 .
81 . (canceled)
82 . The method of claim 80 , wherein the microorganism is a bacteria or a virus.
83 . The method of claim 82 , wherein the bacteria is Gram-positive or Gram negative.
84 . The method of claim 83 , wherein the Gram-positive-bacteria is Staphylococcus aureus , enterococci, streptococci, Clostridium difficile, Propionibacterium acnes , or Bacillus anthracis.
85 . (canceled)
86 . The method of claim 83 , wherein the Gram-negative bacteria is Pseudomonas aeruginosa, Moraxella catarrhalis , or Haemophilus influenzae.
87 . The method of claim 82 , wherein the bacteria is Methicillin-sensitive Staphylococcus aureus , Methicillin-resistant Staphylococcus aureus , Vancomycin-sensitive enterococci, Vancomycin-resistant enterococci, penicillin-sensitive Streptococcus pneumoniae , penicillin-resistant Streptococcus pneumoniae , ciprofloxacin-resistant or clindamycin-resistant.
88 - 94 . (canceled)
95 . The method of claim 82 , wherein the virus belongs to the flaviviridae, togaviridae, filoviridae, arenaviridae, poxviridae, bunyaviridae, or retroviridae family.
96 . The method of claim 82 , wherein the virus is a dengue virus, Zika virus, Yellow Fever virus, Japanese encephalitis virus, Marburg virus, Chikungunya virus, Ebola virus, HIV, or influenza virus.
97 - 122 . (canceled)Join the waitlist — get patent alerts
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