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Title: |
US6159936:
Compositions and methods for treating and preventing microbial and viral infections
[ Derwent Title ]

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Country: |
US United States of America

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Inventor: |
Lehrer, Robert I.; Santa Monica, CA
Harwig, Sylvia S. L.; Woodland Hills, CA
Kokryakov, Vladimir N.; St. Petersburg, Russian Federation

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Assignee: |
The Regents of the University of California, Oakland, CA
other patents from UNIVERSITY OF CALIFORNIA, THE REGENTS OF (599425) (approx. 4,840)
News, Profiles, Stocks and More about this company

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Published / Filed: |
2000-12-12
/ 1998-08-03

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Application Number: |
US1998000128345

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IPC Code: |
Advanced:
C07K 7/08;
C12N 15/12;
C12P 21/04;
A61K 38/00;
Core:
C07K 7/00;
more...
IPC-7:
A61K 38/04;
C07K 7/00;
C12N 15/12;
C12P 21/02;
C12P 21/04;

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ECLA Code: |
C07K7/08A;

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U.S. Class: |
Current:
514/013;
424/405;
435/069.1;
435/252.3;
435/320.1;
514/012;
530/326;
536/023.5;
Original:
514/013;
514/012;
424/405;
435/069.1;
435/252.3;
435/320.1;
530/236;
536/023.5;

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Field of Search: |
514/012,13
424/405
530/326
435/69.1,252.3,320.1
536/23.5

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Government Interest: |
This invention was made with funding from NIH Grant No. A122839. The U.S. Government has certain rights in this invention.

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Priority Number: |

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Abstract: |
Peptide-based compounds containing four invariant cysteine residues which have been optionally oxidized to contain two intramolecular disulfide bonds, or modified forms where the cysteines are replaced are useful as preservatives and in preventing, treating, or ameliorating viral or microbial infection in animals and plants, and in inactivating endotoxin. These compounds, in one embodiment, are of the formula:
A1 --A2 --A3 --A4 --A5 --A6 --A7 --A8 --A9 --A10 --A11 --A12 --A13 --A14 --A15 --A16 --(A17 --A18) (1)
- and the N-terminal acylated and/or C-terminal amidated or esterified forms thereof, which is either in the optionally --SH stablizied linear or in a cystine-bridged form
- wherein each of A1 and A9 is independently a basic amino acid;
- each of A2 and A3 is independently a small amino acid;
- each of A5, A7, A12, A14 and A16 is independently a hydrophobic amino acid;
- A4 is a basic or a small amino acid;
- A10 is a basic or a small amino acid or is proline;
- A11 is a basic or hydrophobic amino acid;
- A17 is not present or, if present, is a small amino acid;
- A18 is not present or, if present, is a basic amino acid; or a
- modified form of formula (1) and the N-terminal acylated and/or C-terminal amidated or esterified forms thereof wherein each of 1-4 cysteines is independently replaced by a hydrophobic amino acid or a small amino acid.

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Attorney, Agent or Firm: |
Pennie & Edmonds LLP ;

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Primary / Asst. Examiners: |
Achutamurthy, Ponnathapu; Moore, William W.

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INPADOC Legal Status: |
None
Family Legal Status Report

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Parent Case: |
This application is a continuation of application Ser. No. 08/499,523, filed Jul. 7, 1995, and issued as U.S. Pat. No. 5,804,558 on Sep. 8, 1998, which is a continuation-in-part of U.S. Ser. No. 08/451,832, filed May, 26, 1995, and now abandoned, which is a continuation-in-part of U.S. Ser. No. 08/243,879 filed May 17, 1994, and issued as U.S. Pat. No. 5,708,145 on Jan. 13, 1998, which is a continuation-in-part of U.S. Ser. No. 08/182,483 filed Jan. 13, 1994, and issued as U.S. Pat. No. 5,693,486 on Dec. 2, 1997, which is a continuation-in-part of U.S. Ser. No. 08/095,769 filed Jul. 26, 1993, and issued as U.S. Pat. No. 5,464,823 on Nov. 7, 1995, which is a continuation-in-part of U.S. Ser. No. 08/093,926 filed Jul. 20, 1993, and now abandoned. The contents of these applications are incorporated herein by reference.

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Designated Country: |
AL AM AP AZ BB BG BR BY CN CZ EE GE HU IS KE KG KP KR KZ LK LR LS LT BE CH FR GB GR IE IT LI FI

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Family: |
Show 65 known family members

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First Claim:
Show all 15 claims |
What is claimed is:
1. A purified and isolated or recombinantly produced compound which has antimicrobial or antiviral activity and which has the formula
A1 --A2 --A3 --A4 --A5 --A6 --A7 --A8 --A9 --A10 --A11 --A12 --A13 --A14 --A15 --A16 --A17 --A18 ( 1)
- or a pharmaceutically acceptable salt or an N-terminal acylated or a C-terminal amidated or esterified form thereof, which is either in a linear form or in a cystine-bridged form, wherein:
- each of A1 and A9 is independently a basic amino acid;
- each of A2 and A3 is independently a small amino acid;
- each of A5, A7, A12, A14 and A16 is independently a hydrophobic amino acid;
- A4 is a basic or a small amino acid;
- A10 is a basic or a small amino acid or is proline;
- A11 is a basic or a hydrophobic amino acid;
- A17 is not present or, if present, is a small amino acid;
- A18 is not present or, if present, is a basic amino acid; and
- each of C6, C8, C13 and C15 is independently selected from the group consisting of cysteine, a hydrophobic amino acid, a large polar amino acid and a small amino acid.

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Background / Summary: |
Show background / summary

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Drawing Descriptions: |
Show drawing descriptions

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Description: |
Show description

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Forward References: |
Show 8 U.S. patent(s) that reference this one

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U.S. References: |
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All U.S. references
| Forward references (8)
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Backward references (22)
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Citation Link

Buy PDF |
Patent |
Pub.Date |
Inventor |
Assignee |
Title |
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1985-09 |
Lehrer et al. |
The Regents of the University of California |
Cationic oligopeptides having microbicidal activity
|
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US4652639 |
1987-03 |
Stabinsky |
Amgen |
Manufacture and expression of structural genes
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US4659692 |
1987-04 |
Lehrer et al. |
The Regents of the University of California |
Cationic oligopeptides having microbicidal activity
|
 |
US4705777 |
1987-11 |
Lehrer et al. |
The Regents of the University of California |
Cationic oligopeptides having microbicidal activity
|
 |
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1992-02 |
Gabay et al. |
Cornell Research Foundation, Inc. and The Rockefeller University |
Antimicrobial proteins, compositions containing same and uses thereof
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1992-06 |
Gabay et al. |
Cornell Research Foundation |
Antimicrobial proteins, compositions containing same and uses thereof
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1992-12 |
Scott et al. |
Incyte Pharmaceuticals, Inc. |
Treatment of endotoxin-associated shock and preventation thereof using a BPI protein
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1993-08 |
Marra et al. |
INCYTE Pharmaceuticals, Inc. |
Pharmaceutical compositions comprising recombinant BPI proteins and a lipid carrier and uses thereof
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1994-05 |
Scott et al. |
Incyte Pharmaceuticals, Inc. |
Treatment of endotoxin-associated shock and prevention thereof using a BPI protein
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1994-08 |
Scott et al. |
INCYTE Pharamaceuticals, Inc. |
Recombinant, non-glycosylated bpi protein and uses thereof
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1994-08 |
Gabay et al. |
Cornell Research Foundation, Inc. |
Antimicrobial proteins, compositions containing same and uses thereof
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1995-06 |
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The Regents of the University of California |
Antibiotic cryptdin peptides and methods of their use
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1995-07 |
Zasloff et al. |
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DNA encoding tracheal antimicrobial peptides
|
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1995-09 |
Travis et al. |
Emory University |
Antimicrobial peptides
|
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1995-10 |
Pereira et al. |
Emory University |
Method of increasing monocyte chemotaxis with CAP37 and monocyte chemotactic portions thereof
|
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1995-10 |
Selsted et al. |
The Regents of the University of California |
Antimicrobial peptides antibodies and nucleic acid molecules from bovine neutrophils
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1995-11 |
Lehrer et al. |
The Regents of the University of California |
Mammalian antibiotic peptides
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1996-01 |
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Emory University |
Chemotactic, antibiotic and lipopolysaccharide-binding peptide fragments of CAP37
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1997-12 |
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IntraBiotics |
DNA sequences encoding protegrins and protegrin analogs and their use in recombinant methods of producing protegrins
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1998-01 |
Lehrer et al. |
University of California |
Immunglobulins reactive with protegrins
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1998-09 |
Lehrer et al. |
University of California |
Protegrins
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1999-11 |
Chang et al. |
IntraBiotics Pharmaceuticals, Inc. |
Fine-tuned protegrins
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