WO2005090387A3 - Derives de peptide d'histone h2a et analogues, et methodes d'utilisation - Google Patents

Derives de peptide d'histone h2a et analogues, et methodes d'utilisation Download PDF

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Publication number
WO2005090387A3
WO2005090387A3 PCT/IL2005/000328 IL2005000328W WO2005090387A3 WO 2005090387 A3 WO2005090387 A3 WO 2005090387A3 IL 2005000328 W IL2005000328 W IL 2005000328W WO 2005090387 A3 WO2005090387 A3 WO 2005090387A3
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WO
WIPO (PCT)
Prior art keywords
treating
protecting against
methods
histone
analogs
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Application number
PCT/IL2005/000328
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English (en)
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WO2005090387A2 (fr
Inventor
Uri Wormser
Original Assignee
Univ Jerusalem Yissum Res Dev
Uri Wormser
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.)
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Publication date
Application filed by Univ Jerusalem Yissum Res Dev, Uri Wormser filed Critical Univ Jerusalem Yissum Res Dev
Publication of WO2005090387A2 publication Critical patent/WO2005090387A2/fr
Publication of WO2005090387A3 publication Critical patent/WO2005090387A3/fr
Priority to US11/527,162 priority Critical patent/US7528227B2/en
Priority to US11/750,408 priority patent/US7605132B2/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10Tetrapeptides
    • C07K5/1002Tetrapeptides with the first amino acid being neutral
    • C07K5/1005Tetrapeptides with the first amino acid being neutral and aliphatic
    • C07K5/1008Tetrapeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atoms, i.e. Gly, Ala
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/46Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • C07K5/06008Dipeptides with the first amino acid being neutral
    • C07K5/06017Dipeptides with the first amino acid being neutral and aliphatic
    • C07K5/06026Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atom, i.e. Gly or Ala
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • C07K5/06008Dipeptides with the first amino acid being neutral
    • C07K5/06017Dipeptides with the first amino acid being neutral and aliphatic
    • C07K5/06034Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms
    • C07K5/06043Leu-amino acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • C07K5/06008Dipeptides with the first amino acid being neutral
    • C07K5/06078Dipeptides with the first amino acid being neutral and aromatic or cycloaliphatic
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • C07K5/06086Dipeptides with the first amino acid being basic
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • C07K5/0802Tripeptides with the first amino acid being neutral
    • C07K5/0804Tripeptides with the first amino acid being neutral and aliphatic
    • C07K5/0806Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atoms, i.e. Gly, Ala
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • C07K5/0815Tripeptides with the first amino acid being basic
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • C07K5/0819Tripeptides with the first amino acid being acidic
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10Tetrapeptides
    • C07K5/1002Tetrapeptides with the first amino acid being neutral
    • C07K5/1016Tetrapeptides with the first amino acid being neutral and aromatic or cycloaliphatic
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10Tetrapeptides
    • C07K5/1019Tetrapeptides with the first amino acid being basic
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10Tetrapeptides
    • C07K5/1021Tetrapeptides with the first amino acid being acidic

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Zoology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Toxicology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)

Abstract

L'invention concerne des peptides dérivés d'un segment d'histone H2A humain correspondant à des résidus d'acides aminé 36-44 d'histone H2A humain qui, lorsqu'ils sont administrés à des animaux, sont capables de réduire ou d'atténuer la gravité de lésions induites par de stimuli nocifs. Sont également décrites des compositions pharmaceutiques et des méthodes d'utilisation de ces peptides. Ces compositions pharmaceutiques conviennent pour le traitement et la prévention de maladies inflammatoires et de maladies auto-immunes, pour le traitement et la prévention de dégâts tissulaires, pour l'inhibition de l'activité de la métalloprotéinase ainsi que pour le traitement et la prévention de maladies associées à la dégradation de la matrice extracellulaire ou des tissus conjonctifs.
PCT/IL2005/000328 2001-08-29 2005-03-23 Derives de peptide d'histone h2a et analogues, et methodes d'utilisation WO2005090387A2 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US11/527,162 US7528227B2 (en) 2004-03-23 2006-09-25 Histone H2A peptide derivatives and uses thereof
US11/750,408 US7605132B2 (en) 2001-08-29 2007-05-18 Protective factors against inflammation, burns and noxious stimuli

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US55533404P 2004-03-23 2004-03-23
US60/555,334 2004-03-23

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US11/527,162 Continuation-In-Part US7528227B2 (en) 2001-08-29 2006-09-25 Histone H2A peptide derivatives and uses thereof

Publications (2)

Publication Number Publication Date
WO2005090387A2 WO2005090387A2 (fr) 2005-09-29
WO2005090387A3 true WO2005090387A3 (fr) 2006-02-02

Family

ID=34964143

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IL2005/000328 WO2005090387A2 (fr) 2001-08-29 2005-03-23 Derives de peptide d'histone h2a et analogues, et methodes d'utilisation

Country Status (1)

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Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL1866328T3 (pl) 2005-03-22 2011-05-31 Rohto Pharma Peptydy zwiększające wytwarzanie kolagenu lub kwasu hialuronowego
WO2008010218A1 (fr) * 2006-07-17 2008-01-24 Yissum Research Development Company Of The Hebrew University Of Jerusalem Peptides dérivés de l'histone h2a humaine et leurs procédés d'utilisation
EP2558110B1 (fr) 2010-04-11 2015-06-03 Yissum Research Development Company of the Hebrew University of Jerusalem Ltd. Extrait et peptides dérivés du groupe oryza sativa japonica et leurs utilisations
US9518107B2 (en) 2010-08-31 2016-12-13 Yissum Research Development Company Of The Hebrew University Of Jerusalem, Ltd. Pharmaceutical compositions containing polypeptides derived from α-1 antitrypsin and methods of use thereof
EP2611459B1 (fr) 2010-08-31 2019-12-11 Yissum Research Development Company of the Hebrew University of Jerusalem, Ltd. Polypeptides dérivés d'alpha-1 antitrypsin pour l'utilisation dans le traitement de l'inflammation
US10570174B2 (en) 2015-02-08 2020-02-25 Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. Peptides for the treatment of malignant proliferative diseases
CN106397575A (zh) * 2016-10-20 2017-02-15 上海懿贝瑞生物医药科技有限公司 一种具有胞外组蛋白毒性抑制作用的多肽制备方法及用途
CN112745379A (zh) * 2021-01-22 2021-05-04 浙江辉肽生命健康科技有限公司 具有氨基酸结构rdnkktriipr的生物活性肽及其制备方法和应用

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0489577A1 (fr) * 1990-12-03 1992-06-10 Celltech Limited Dérivés peptidyliques
WO1998009985A2 (fr) * 1996-09-03 1998-03-12 Yeda Research And Development Co. Ltd. Peptides anti-inflammatoires et leurs utilisations
WO2003017920A2 (fr) * 2001-08-29 2003-03-06 Yissum Research Development Company Of The Hebrew University Of Jerusalem Facteurs de protection contre des inflammations, des brulures et des stimuli nocifs
EP1297753A1 (fr) * 2001-10-01 2003-04-02 Societe Des Produits Nestle S.A. Peptides pour l'utilisation comme flavour

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0489577A1 (fr) * 1990-12-03 1992-06-10 Celltech Limited Dérivés peptidyliques
WO1998009985A2 (fr) * 1996-09-03 1998-03-12 Yeda Research And Development Co. Ltd. Peptides anti-inflammatoires et leurs utilisations
WO2003017920A2 (fr) * 2001-08-29 2003-03-06 Yissum Research Development Company Of The Hebrew University Of Jerusalem Facteurs de protection contre des inflammations, des brulures et des stimuli nocifs
EP1297753A1 (fr) * 2001-10-01 2003-04-02 Societe Des Produits Nestle S.A. Peptides pour l'utilisation comme flavour

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