ES2191061T3 - Antibioticos sinteticos. - Google Patents

Antibioticos sinteticos.

Info

Publication number
ES2191061T3
ES2191061T3 ES95933120T ES95933120T ES2191061T3 ES 2191061 T3 ES2191061 T3 ES 2191061T3 ES 95933120 T ES95933120 T ES 95933120T ES 95933120 T ES95933120 T ES 95933120T ES 2191061 T3 ES2191061 T3 ES 2191061T3
Authority
ES
Spain
Prior art keywords
compositions
disclosed
methods
synthetic antibiotics
growth
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.)
Expired - Lifetime
Application number
ES95933120T
Other languages
English (en)
Inventor
David L Edwards
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.)
Ceres Technologies Inc
Original Assignee
Ceres Technologies Inc
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
Application filed by Ceres Technologies Inc filed Critical Ceres Technologies Inc
Application granted granted Critical
Publication of ES2191061T3 publication Critical patent/ES2191061T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/04—Linear peptides containing only normal peptide links
    • C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 amino acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/04—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length on carriers
    • C07K1/047—Simultaneous synthesis of different peptide species; Peptide libraries
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08—Tripeptides
    • C07K5/0802—Tripeptides with the first amino acid being neutral
    • C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
    • C07K5/0808—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms, e.g. Val, Ile, Leu
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08—Tripeptides
    • C07K5/0802—Tripeptides with the first amino acid being neutral
    • C07K5/0812—Tripeptides with the first amino acid being neutral and aromatic or cycloaliphatic
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08—Tripeptides
    • C07K5/0821—Tripeptides with the first amino acid being heterocyclic, e.g. His, Pro, Trp
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10—Tetrapeptides
    • C07K5/1002—Tetrapeptides with the first amino acid being neutral
    • C07K5/1016—Tetrapeptides with the first amino acid being neutral and aromatic or cycloaliphatic
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10—Tetrapeptides
    • C07K5/1024—Tetrapeptides with the first amino acid being heterocyclic
    • 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)
  • Organic Chemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Biophysics (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Medicinal Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Peptides Or Proteins (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

LAS COMPOSICIONES DE ESTA INVENCION SE DIRIGEN A INHIBIR EL CRECIMIENTO DE MICRORGANISMOS , ESPECIALMENTE HONGOS. LAS COMPOSICIONES CONSISTEN DE ANTIBIOTICOS SINTETIZADOS QUIMICAMENTE INCLUYEN CIERTOS AMINOACIDOS. SE MUESTRAN METODOS PARA IDENTIFICAR COMPOSICIONES ANTIBIOTICAS PARTICULARES DE LAS BIBLIOTECAS DE TALES COMPOSICIONES. ADEMAS, SE MUESTRAN METODOS PARA PREVENIR EL CRECIMIENTO MICROBIANO EN PLANTAS Y ANIMALES.
ES95933120T 1994-09-13 1995-09-13 Antibioticos sinteticos. Expired - Lifetime ES2191061T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US08/305,768 US5602097A (en) 1994-09-13 1994-09-13 Synthetic antibiotics

Publications (1)

Publication Number Publication Date
ES2191061T3 true ES2191061T3 (es) 2003-09-01

Family

ID=23182264

Family Applications (1)

Application Number Title Priority Date Filing Date
ES95933120T Expired - Lifetime ES2191061T3 (es) 1994-09-13 1995-09-13 Antibioticos sinteticos.

Country Status (8)

Country Link
US (1) US5602097A (es)
EP (1) EP0783316B1 (es)
AT (1) ATE228370T1 (es)
AU (1) AU3589895A (es)
CA (1) CA2199941C (es)
DE (1) DE69528993T2 (es)
ES (1) ES2191061T3 (es)
WO (1) WO1996008264A1 (es)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5885782A (en) * 1994-09-13 1999-03-23 Nce Pharmaceuticals, Inc. Synthetic antibiotics
US6020312A (en) * 1994-09-13 2000-02-01 Nce Pharmaceuticals, Inc. Synthetic antibiotics
AU4905497A (en) * 1996-10-11 1998-05-11 Pence, Inc. Antimicrobial peptide analogs of gramicidin s and compositions comprising them
EP1073768A2 (en) * 1998-04-24 2001-02-07 Hoechst Marion Roussel Method for screening antimycotic substances using essential genes from s. cerevisiae
EP0999284A1 (en) * 1998-09-11 2000-05-10 Hoechst Marion Roussel Method for screening antimycotic substances using essential genes from c.albicans, and said genes
GB9928323D0 (en) * 1999-11-30 2000-01-26 Cyclacel Ltd Peptides
WO2001098540A2 (en) * 2000-06-22 2001-12-27 San Diego State University Foundation Recombination modulators and methods for their production and use
ATE295687T1 (de) * 2000-08-18 2005-06-15 Univ Montana Res Dev Inst Gegen pflanzenkrankheiten verwendbare pseudomycine
US20060014674A1 (en) 2000-12-18 2006-01-19 Dennis Keith Methods for preparing purified lipopeptides
US20040109853A1 (en) * 2002-09-09 2004-06-10 Reactive Surfaces, Ltd. Biological active coating components, coatings, and coated surfaces
US20100233146A1 (en) * 2002-09-09 2010-09-16 Reactive Surfaces, Ltd. Coatings and Surface Treatments Having Active Enzymes and Peptides
US20100210745A1 (en) * 2002-09-09 2010-08-19 Reactive Surfaces, Ltd. Molecular Healing of Polymeric Materials, Coatings, Plastics, Elastomers, Composites, Laminates, Adhesives, and Sealants by Active Enzymes
US20050058689A1 (en) * 2003-07-03 2005-03-17 Reactive Surfaces, Ltd. Antifungal paints and coatings
US8618066B1 (en) 2003-07-03 2013-12-31 Reactive Surfaces, Ltd., Llp Coating compositions having peptidic antimicrobial additives and antimicrobial additives of other configurations
WO2011034931A2 (en) * 2009-09-15 2011-03-24 Reactive Surface, Ltd. Anti-fouling paints and coatings
US10412962B2 (en) 2015-11-25 2019-09-17 North Carolina Agricultural And Technical State University Antifungal compositions and methods of use thereof

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4324683A (en) * 1975-08-20 1982-04-13 Damon Corporation Encapsulation of labile biological material
NZ215865A (en) * 1985-04-22 1988-10-28 Commw Serum Lab Commission Method of determining the active site of a receptor-binding analogue
US5010175A (en) * 1988-05-02 1991-04-23 The Regents Of The University Of California General method for producing and selecting peptides with specific properties
US5182366A (en) * 1990-05-15 1993-01-26 Huebner Verena D Controlled synthesis of peptide mixtures using mixed resins
WO1992009300A1 (en) * 1990-11-21 1992-06-11 Iterex Pharmaceuticals Ltd. Partnership Synthesis of equimolar multiple oligomer mixtures, especially of oligopeptide mixtures
WO1994008010A1 (en) * 1992-09-28 1994-04-14 Monsanto Company Method of controlling plant pathogenic fungi
JPH06220088A (ja) * 1993-01-22 1994-08-09 Asahi Chem Ind Co Ltd アンジオテンシンｉ変換酵素を阻害するトリペプチドおよびその製造法ならびにそれを含む食品
US5440016A (en) * 1993-06-18 1995-08-08 Torrey Pines Institute For Molecular Studies Peptides of the formula (KFmoc) ZZZ and their uses

Also Published As

Publication number Publication date
CA2199941C (en) 2001-11-27
EP0783316A4 (en) 1999-05-26
DE69528993T2 (de) 2003-04-10
EP0783316A1 (en) 1997-07-16
WO1996008264A1 (en) 1996-03-21
DE69528993D1 (de) 2003-01-09
AU3589895A (en) 1996-03-29
CA2199941A1 (en) 1996-03-21
ATE228370T1 (de) 2002-12-15
US5602097A (en) 1997-02-11
EP0783316B1 (en) 2002-11-27

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