FI906204A - Menetelmä farmaseuttisesti vaikuttavien peptidiyhdisteiden valmistamiseksi - Google Patents

Menetelmä farmaseuttisesti vaikuttavien peptidiyhdisteiden valmistamiseksi Download PDF

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Publication number
FI906204A
FI906204A FI906204A FI906204A FI906204A FI 906204 A FI906204 A FI 906204A FI 906204 A FI906204 A FI 906204A FI 906204 A FI906204 A FI 906204A FI 906204 A FI906204 A FI 906204A
Authority
FI
Finland
Prior art keywords
preparation
pharmaceutically active
active peptide
peptide compounds
alkyl
Prior art date
Application number
FI906204A
Other languages
English (en)
Swedish (sv)
Other versions
FI93548B (fi
FI93548C (fi
FI906204A0 (fi
Inventor
Masaaki Matsuo
Daijiro Hagiwara
Hiroshi Miyake
Original Assignee
Fujisawa Pharmaceutical Co
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 Fujisawa Pharmaceutical Co filed Critical Fujisawa Pharmaceutical Co
Publication of FI906204A0 publication Critical patent/FI906204A0/fi
Publication of FI906204A publication Critical patent/FI906204A/fi
Publication of FI93548B publication Critical patent/FI93548B/fi
Application granted granted Critical
Publication of FI93548C publication Critical patent/FI93548C/fi

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Classifications

    • 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
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
    • C07K5/0202—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -NH-X-X-C(=0)-, X being an optionally substituted carbon atom or a heteroatom, e.g. beta-amino acids
    • 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
    • C07K5/06—Dipeptides
    • C07K5/06139—Dipeptides 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
FI906204A 1989-12-22 1990-12-17 Menetelmä farmaseuttisesti vaikuttavien peptidiyhdisteiden valmistamiseksi FI93548C (fi)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB8929070 1989-12-22
GB898929070A GB8929070D0 (en) 1989-12-22 1989-12-22 Peptide compounds,processes for preparation thereof and pharmaceutical composition comprising the same

Publications (4)

Publication Number Publication Date
FI906204A0 FI906204A0 (fi) 1990-12-17
FI906204A true FI906204A (fi) 1991-06-23
FI93548B FI93548B (fi) 1995-01-13
FI93548C FI93548C (fi) 1995-04-25

Family

ID=10668423

Family Applications (1)

Application Number Title Priority Date Filing Date
FI906204A FI93548C (fi) 1989-12-22 1990-12-17 Menetelmä farmaseuttisesti vaikuttavien peptidiyhdisteiden valmistamiseksi

Country Status (21)

Country Link
US (1) US5468731A (fi)
EP (1) EP0443132B1 (fi)
JP (1) JP2560919B2 (fi)
KR (1) KR0180223B1 (fi)
CN (2) CN1034869C (fi)
AT (1) ATE98651T1 (fi)
AU (1) AU640185B2 (fi)
CA (1) CA2032864C (fi)
DE (1) DE69005286T2 (fi)
DK (1) DK0443132T3 (fi)
ES (1) ES2060910T3 (fi)
FI (1) FI93548C (fi)
GB (1) GB8929070D0 (fi)
HK (1) HK18696A (fi)
HU (2) HUT56581A (fi)
IE (1) IE64570B1 (fi)
NO (1) NO177535C (fi)
PT (1) PT96324B (fi)
RU (1) RU2055078C1 (fi)
UA (1) UA27254C2 (fi)
ZA (1) ZA909901B (fi)

Families Citing this family (86)

* Cited by examiner, † Cited by third party
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US5654400A (en) * 1991-10-04 1997-08-05 Fujisawa Pharmaceutical Co., Ltd. Process for making peptide compounds having tachykinin antagonistic activity
DK0613458T3 (da) * 1991-11-12 1998-02-09 Pfizer Acykliske ethylendiaminderivater som substans P receptorantagonister
GB9200535D0 (en) * 1992-01-10 1992-02-26 Fujisawa Pharmaceutical Co New compound
PT655055E (pt) * 1992-08-13 2001-03-30 Warner Lambert Co Antagonistas de taquiquinina
DE4243496A1 (de) * 1992-09-03 1994-03-10 Boehringer Ingelheim Kg Neue Dipeptidderivate, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende pharmazeutische Zusammensetzungen
DE59309867D1 (de) * 1992-09-03 1999-12-16 Boehringer Ingelheim Pharma Neue aminosäurederivate, verfahren zu ihrer herstellung und diese verbindungen enthaltende pharmazeutische zusammensetzungen
FR2700472B1 (fr) 1993-01-19 1995-02-17 Rhone Poulenc Rorer Sa Association synergisante ayant un effet antagoniste des récepteurs NK1 et NK2.
WO1994020126A1 (en) * 1993-03-03 1994-09-15 Fujisawa Pharmaceutical Co., Ltd. Use of peptides for the manufacture of a medicament
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WO1995004551A1 (fr) * 1993-08-10 1995-02-16 Fujisawa Pharmaceutical Co., Ltd. Preparation absorbable par voie percutanee
EP1736152A3 (en) * 1993-10-29 2009-10-07 The Trustees Of Boston University Physiologically stable compositions of butyric acid as well as butyric acid salts and derivatives for treating wounds
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ITFI940009A1 (it) * 1994-01-19 1995-07-19 Menarini Farma Ind Antagonisti delle tachichinine, loro preparazione e formulazioni farmaceutiche che li contengono.
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FR2719312B1 (fr) * 1994-04-28 1996-06-14 Adir Nouveau pseudopeptides dérivés de neurokinines, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent.
SK142696A3 (en) * 1994-05-07 1997-06-04 Boehringer Ingelheim Kg Amino acids derivative, method for preparation thereof, pharmaceutical compositions containing said compounds (ii) and their use
FR2728165A1 (fr) 1994-12-19 1996-06-21 Oreal Utilisation d'un antagoniste de substance p pour le traitement des rougeurs cutanees d'origine neurogene
FR2728166A1 (fr) 1994-12-19 1996-06-21 Oreal Composition topique contenant un antagoniste de substance p
FR2728169A1 (fr) 1994-12-19 1996-06-21 Oreal Utilisation d'un antagoniste de substance p pour le traitement des prurits et des dysesthesies oculaires ou palpebrales
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Also Published As

Publication number Publication date
HUT56581A (en) 1991-09-30
PT96324B (pt) 1998-10-30
CN1159949A (zh) 1997-09-24
NO177535C (no) 1995-10-04
ZA909901B (en) 1991-10-30
UA27254C2 (uk) 2000-08-15
CA2032864A1 (en) 1991-06-23
AU6801090A (en) 1991-06-27
JP2560919B2 (ja) 1996-12-04
FI93548B (fi) 1995-01-13
NO905572L (no) 1991-06-24
CA2032864C (en) 2003-05-06
ES2060910T3 (es) 1994-12-01
US5468731A (en) 1995-11-21
GB8929070D0 (en) 1990-02-28
FI93548C (fi) 1995-04-25
EP0443132B1 (en) 1993-12-15
HU908443D0 (en) 1991-07-29
JPH04210996A (ja) 1992-08-03
NO177535B (no) 1995-06-26
HK18696A (en) 1996-02-09
RU2055078C1 (ru) 1996-02-27
NO905572D0 (no) 1990-12-21
FI906204A0 (fi) 1990-12-17
IE904581A1 (en) 1991-07-03
CN1034869C (zh) 1997-05-14
CN1064080A (zh) 1992-09-02
HU211558A9 (en) 1995-12-28
AU640185B2 (en) 1993-08-19
ATE98651T1 (de) 1994-01-15
DE69005286T2 (de) 1994-04-21
IE64570B1 (en) 1995-08-23
PT96324A (pt) 1991-09-30
DE69005286D1 (de) 1994-01-27
EP0443132A1 (en) 1991-08-28
KR0180223B1 (ko) 1999-04-01
KR910011891A (ko) 1991-08-07
DK0443132T3 (da) 1994-01-24

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Owner name: FUJISAWA PHARMACEUTICAL CO., LTD.

BB Publication of examined application
FG Patent granted

Owner name: FUJISAWA PHARMACEUTICAL CO., LTD.

MA Patent expired