Analogs of temporin-SHa and uses thereof

US9522942B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9522942-B2
Application numberUS-201013257018-A
CountryUS
Kind codeB2
Filing dateMar 18, 2010
Priority dateMar 19, 2009
Publication dateDec 20, 2016
Grant dateDec 20, 2016

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The present invention relates to novel antimicrobial peptides, to pharmaceutical compositions comprising said peptides, and to the uses thereof, in particular as antimicrobial drugs, disinfectants, pesticides or preservatives. The present invention also relates to a transgenic plant expressing said novel peptides.

First claim

Opening claim text (preview).

The invention claimed is: 1. A non-natural peptide of between 13 and 100 amino acids selected from the group consisting of: a) a peptide containing the sequence F-L-X 1 -G-I-V-G-M-L-G-K-L-F (SEQ ID NO: 2) or a pharmaceutically acceptable salt thereof; b) a retropeptide or retro-inverso peptide of a peptide containing the sequence F-L-X 1 -G-I-V-G-M-L-G-K-L-F (SEQ ID NO: 2) or a pharmaceutically acceptable salt thereof; and c) a peptide containing the sequence of SEQ ID NO: 2 shortened by 1 or 2 amino acids at the N-terminal end or a pharmaceutically acceptable salt thereof; wherein said non-natural peptide or said pharmaceutically acceptable salt thereof as shown in group a), b) and c) exhibits antimicrobial activity and wherein X 1 is an amino acid selected from the group consisting of R (arginine), H (histidine) and K (lysine). 2. The non-natural peptide according to claim 1 , wherein X 1 represents K (lysine). 3. A method for treating a microbial infection comprising administering a therapeutically effective dose of a non-natural peptide according to claim 1 to a subject in need of treatment for said microbial infection. 4. The method according to claim 3 , wherein the microbial infection is an infection due to a bacterium, a virus, a fungus or a parasite. 5. The method according to claim 4 , wherein the parasite belongs to the genus Leishmania. 6. A method for treating an infection of a plant by a phytopathogen comprising administering an effective dose of a non-natural peptide according to claim 1 to said plant. 7. A method for improving conservation of a food product comprising applying an effective dose of a non-natural peptide according to claim 1 to said food product. 8. A method of disinfecting a surface, a liquid or a gas comprising applying an effective dose of a non-natural peptide according to claim 1 to said surface, liquid or gas. 9. The non-natural peptide according to claim 1 , wherein X 1 represents H (histidine). 10. The non-natural peptide according to claim 1 , wherein X 1 represents R (arginine). 11. The non-natural peptide according to claim 1 , wherein said non-natural peptide has a size of 13 amino acids. 12. The non-natural peptide according to claim 1 , wherein said non-natural peptide contains the amino acid sequence of SEQ ID NO: 2. 13. The non-natural peptide according to claim 1 , wherein said non-natural peptide is a retropeptide or retro-inverso peptide of a peptide containing the amino acid sequence of SEQ ID NO: 2. 14. The non-natural peptide according to claim 1 , wherein said non-natural peptide contains the amino acid sequence of SEQ ID NO: 2 shortened by 1 or 2 amino acids at the N-terminal end. 15. The non-natural peptide according to claim 1 , wherein said pharmaceutically acceptable salt is a hydrochloric acid salt, hydrobromic acid salt, sulphuric acid salt, phosphoric acid salt; acetic acid salt, citric acid salt, maleic acid salt, malic acid salt, succinic acid salt, ascorbic acid salt, tartaric acid salt, sodium salt, potassium salt, calcium salt, magnesium salt or ammonium salt.

Assignees

Inventors

Classifications

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9522942B2 cover?
The present invention relates to novel antimicrobial peptides, to pharmaceutical compositions comprising said peptides, and to the uses thereof, in particular as antimicrobial drugs, disinfectants, pesticides or preservatives. The present invention also relates to a transgenic plant expressing said novel peptides.
Who is the assignee on this patent?
Ladram Ali, Sereno Denis, Abbassi Feten, and 6 more
What technology area does this patent fall under?
Primary CPC classification C07K14/463. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Dec 20 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).