EP1242107A4 - Verfahren zur herstellung von durch pr-39 peptid vermittelte selektiver hemmung von ikappabaloha abbau - Google Patents

Verfahren zur herstellung von durch pr-39 peptid vermittelte selektiver hemmung von ikappabaloha abbau

Info

Publication number
EP1242107A4
EP1242107A4 EP00989492A EP00989492A EP1242107A4 EP 1242107 A4 EP1242107 A4 EP 1242107A4 EP 00989492 A EP00989492 A EP 00989492A EP 00989492 A EP00989492 A EP 00989492A EP 1242107 A4 EP1242107 A4 EP 1242107A4
Authority
EP
European Patent Office
Prior art keywords
selective inhibition
peptide mediated
mediated selective
ikappabalpha
degradation
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP00989492A
Other languages
English (en)
French (fr)
Other versions
EP1242107A1 (de
Inventor
Michael Simons
Youhe Gao
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Beth Israel Deaconess Medical Center Inc
Original Assignee
Beth Israel Deaconess Medical Center Inc
Beth Israel Hospital Association
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US09/474,967 external-priority patent/US7169604B1/en
Application filed by Beth Israel Deaconess Medical Center Inc, Beth Israel Hospital Association filed Critical Beth Israel Deaconess Medical Center Inc
Publication of EP1242107A1 publication Critical patent/EP1242107A1/de
Publication of EP1242107A4 publication Critical patent/EP1242107A4/de
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
    • C07K14/4702—Regulators; Modulating activity
    • C07K14/4705—Regulators; Modulating activity stimulating, promoting or activating activity
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
    • C07K14/4723—Cationic antimicrobial peptides, e.g. defensins
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Zoology (AREA)
  • Genetics & Genomics (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Toxicology (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
EP00989492A 1999-12-29 2000-12-27 Verfahren zur herstellung von durch pr-39 peptid vermittelte selektiver hemmung von ikappabaloha abbau Withdrawn EP1242107A4 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US474967 1999-12-29
US09/474,967 US7169604B1 (en) 1998-10-13 1999-12-29 Method for PR-39 peptide mediated selective inhibition of IκBα degradation
PCT/US2000/035293 WO2001047540A1 (en) 1999-12-29 2000-12-27 METHOD FOR PR-39 PEPTIDE MEDIATED SELECTIVE INHIBITION OF IλBα DEGRADATION

Publications (2)

Publication Number Publication Date
EP1242107A1 EP1242107A1 (de) 2002-09-25
EP1242107A4 true EP1242107A4 (de) 2004-10-06

Family

ID=23885707

Family Applications (1)

Application Number Title Priority Date Filing Date
EP00989492A Withdrawn EP1242107A4 (de) 1999-12-29 2000-12-27 Verfahren zur herstellung von durch pr-39 peptid vermittelte selektiver hemmung von ikappabaloha abbau

Country Status (4)

Country Link
EP (1) EP1242107A4 (de)
AU (1) AU2599001A (de)
CA (1) CA2397955A1 (de)
WO (1) WO2001047540A1 (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005537292A (ja) * 2002-07-31 2005-12-08 ヒャリテ−ウニヴェルズィテーツメディジン ベルリン 内皮機能障害の治療および／または低用量プロテアソーム阻害剤療法におけるプロテアソーム阻害剤の使用
ES2426441T3 (es) 2004-10-18 2013-10-23 Basf Beauty Care Solutions France S.A.S. Oligopéptidos y su uso en cosméticos
WO2006119183A2 (en) * 2005-05-03 2006-11-09 Trustees Of Dartmouth College Method for increasing cardiac mass and performance

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5489575A (en) * 1991-06-14 1996-02-06 Hans G. Boman Polypeptides and their use
WO1996032129A1 (en) * 1995-04-10 1996-10-17 Kansas State University Research Foundation Synthetic peptides that inhibit leukocyte superoxide anion production and/or attract leukocytes
WO1998035690A1 (en) * 1997-02-18 1998-08-20 Kansas State University Research Foundation Peptide modulation of reperfusion injury
WO2000057895A1 (en) * 1999-03-26 2000-10-05 Beth Israel Deaconess Medical Center Method for pr-39 peptide regulated stimulation of angiogenesis
WO2001030368A1 (en) * 1999-10-25 2001-05-03 Beth Israel Deaconess Medical Center Method for pr-39 peptide regulated stimulation of angiogenesis

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5654273A (en) * 1994-09-22 1997-08-05 Children's Medical Center Corporation Synducin mediated modulation of tissue repair

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5489575A (en) * 1991-06-14 1996-02-06 Hans G. Boman Polypeptides and their use
WO1996032129A1 (en) * 1995-04-10 1996-10-17 Kansas State University Research Foundation Synthetic peptides that inhibit leukocyte superoxide anion production and/or attract leukocytes
WO1998035690A1 (en) * 1997-02-18 1998-08-20 Kansas State University Research Foundation Peptide modulation of reperfusion injury
WO2000057895A1 (en) * 1999-03-26 2000-10-05 Beth Israel Deaconess Medical Center Method for pr-39 peptide regulated stimulation of angiogenesis
WO2001030368A1 (en) * 1999-10-25 2001-05-03 Beth Israel Deaconess Medical Center Method for pr-39 peptide regulated stimulation of angiogenesis

Non-Patent Citations (7)

* Cited by examiner, † Cited by third party
Title
GAO Y ET AL: "Inhibition of ubiquitin-proteasome pathway-mediated I-kappaBalpha degradation by a naturally occuring antibacterial peptide", JOURNAL OF CLINICAL INVESTIGATION, NEW YORK, NY, US, vol. 106, no. 3, August 2000 (2000-08-01), pages 439 - 448, XP002180614, ISSN: 0021-9738 *
GAO YOUHE ET AL: "PR39 interacts with proteasome and modulates HIF-1alpha level in ECV cells", MOLECULAR BIOLOGY OF THE CELL, vol. 9, no. SUPPL., November 1998 (1998-11-01), & 38TH ANNUAL MEETING OF THE AMERICAN SOCIETY FOR CELL BIOLOGY; SAN FRANCISCO, CALIFORNIA, USA; DECEMBER 12-16, 1998, pages 123A, XP008033931, ISSN: 1059-1524 *
HOFFMEYER M R ET AL: "PR-39, a potent neutrophil inhibitor, attenuates myocardial ischemia-reperfusion injury in mice.", AMERICAN JOURNAL OF PHYSIOLOGY. HEART AND CIRCULATORY PHYSIOLOGY. DEC 2000, vol. 279, no. 6, December 2000 (2000-12-01), pages H2824 - H2828, XP002292143, ISSN: 0363-6135 *
LI J ET AL: "CARDIAC-SPECIFIC OVEREXPRESSION OF PR-39 INDUCES ANGIOGENESIS, MYOCARDIAL HYPERTROPHY AND INCREASED MICROVASCULAR REACTIVITY", CIRCULATION, AMERICAN HEART ASSOCIATION, DALLAS, TX, US, vol. 98, no. 17, October 1998 (1998-10-01), pages 1794, XP002929855, ISSN: 0009-7322 *
LI J ET AL: "Macrophage-dependent regulation of syndecan gene expression", CIRCULATION RESEARCH 1997 UNITED STATES, vol. 81, no. 5, 1997, pages 785 - 796, XP008033955, ISSN: 0009-7330 *
LI J ET AL: "PR39, a peptide regulator of angiogenesis", NATURE MEDICINE, NATURE AMERICA, NEW YORK, US, vol. 6, no. 1, January 2000 (2000-01-01), pages 49 - 55, XP002968105, ISSN: 1078-8956 *
See also references of WO0147540A1 *

Also Published As

Publication number Publication date
AU2599001A (en) 2001-07-09
EP1242107A1 (de) 2002-09-25
CA2397955A1 (en) 2001-07-05
WO2001047540A1 (en) 2001-07-05

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Legal Events

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Ipc: 7C 07K 14/47 B

Ipc: 7A 61K 38/16 B

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