SE8306145L - PROCEDURE FOR THE PREPARATION OF BESTATE ASSOCIATIONS - Google Patents

PROCEDURE FOR THE PREPARATION OF BESTATE ASSOCIATIONS

Info

Publication number
SE8306145L
SE8306145L SE8306145A SE8306145A SE8306145L SE 8306145 L SE8306145 L SE 8306145L SE 8306145 A SE8306145 A SE 8306145A SE 8306145 A SE8306145 A SE 8306145A SE 8306145 L SE8306145 L SE 8306145L
Authority
SE
Sweden
Prior art keywords
formula
image
optionally
compounds
hydroxybeta
Prior art date
Application number
SE8306145A
Other languages
Swedish (sv)
Other versions
SE8306145D0 (en
Inventor
H Umezawa
T Aoyagi
T Takita
R Nishizawa
T Saino
Original Assignee
Microbial Chem Res Found
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 Microbial Chem Res Found filed Critical Microbial Chem Res Found
Publication of SE8306145D0 publication Critical patent/SE8306145D0/en
Publication of SE8306145L publication Critical patent/SE8306145L/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/02Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Biophysics (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

For preparing the novel bestatin compounds of the formula <IMAGE> having R1 and R2 in accordance with the preceding Patent Claim 1, an alpha -hydroxybeta -amino acid of the formula <IMAGE> is used as the starting material. The latter is condensed, optionally after having protected the functional groups which are not to participate in the subsequent reaction, with a beta -amino acid of the formula <IMAGE> using a peptide-linking method. Protective groups which may optionally be present are subsequently removed. The optically pure diastereoisomers can be readily obtained from the compounds of the formula (III). The alpha -hydroxybeta -amino acids can be prepared by hydrolysing a corresponding cyanohydrin whose amino group is optionally protected. The novel compounds inhibit certain enzymes which decompose bleomycin and in this way amplify the anti-tumour activity of the bleomycins.
SE8306145A 1975-07-22 1983-11-09 PROCEDURE FOR THE PREPARATION OF BESTATE ASSOCIATIONS SE8306145L (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB30632/75A GB1510477A (en) 1975-07-22 1975-07-22 Peptides and to amino acid intermediates thereof

Publications (2)

Publication Number Publication Date
SE8306145D0 SE8306145D0 (en) 1983-11-09
SE8306145L true SE8306145L (en) 1983-11-09

Family

ID=10310676

Family Applications (3)

Application Number Title Priority Date Filing Date
SE7606736A SE431642B (en) 1975-07-22 1976-06-14 PROCEDURE FOR THE PREPARATION OF BESTATIN SOCIETIES
SE8001959A SE452318B (en) 1975-07-22 1980-03-13 AMINO ACIDS FOR USE AS INTERMEDIATES IN THE PRODUCTION OF BESTATIN
SE8306145A SE8306145L (en) 1975-07-22 1983-11-09 PROCEDURE FOR THE PREPARATION OF BESTATE ASSOCIATIONS

Family Applications Before (2)

Application Number Title Priority Date Filing Date
SE7606736A SE431642B (en) 1975-07-22 1976-06-14 PROCEDURE FOR THE PREPARATION OF BESTATIN SOCIETIES
SE8001959A SE452318B (en) 1975-07-22 1980-03-13 AMINO ACIDS FOR USE AS INTERMEDIATES IN THE PRODUCTION OF BESTATIN

Country Status (12)

Country Link
JP (2) JPS52136118A (en)
AU (1) AU506003B2 (en)
CA (1) CA1104156A (en)
CH (1) CH630892A5 (en)
CS (2) CS201034B2 (en)
DE (2) DE2632396C2 (en)
DK (1) DK149110C (en)
FR (1) FR2318863A1 (en)
GB (1) GB1510477A (en)
HU (1) HU183048B (en)
NL (1) NL7608064A (en)
SE (3) SE431642B (en)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2760007C2 (en) * 1977-06-07 1988-10-06 Microbial Chem Res Found
DE2725732C2 (en) 1977-06-07 1983-01-05 Zaidan Hojin Biseibutsu Kagaku Kenkyu Kai, Tokyo Bestatin analogs, processes for their preparation and pharmaceutical preparations containing these compounds
JPS6026099B2 (en) * 1977-09-21 1985-06-21 財団法人微生物化学研究会 Peptide, its acid salt and its production method
DK162288C (en) * 1978-11-25 1992-03-16 Nippon Kayaku Kk METHOD FOR PREPARING THREO-3-AMINO-2-HYDROXYBUTANOYL AMINO ACETIC ACIDS
US4370318A (en) * 1980-07-07 1983-01-25 Zaidan Hojin Biseibutsu Kagaku Kenkyu Kai Bestatin-related compounds as immunopotentiator
JPS5767516A (en) * 1980-09-24 1982-04-24 Microbial Chem Res Found Novel analgesic agent
JPH0810855Y2 (en) * 1989-07-20 1996-03-29 タナシン電機株式会社 Auto-reverse type tape recorder
USRE36718E (en) * 1993-06-29 2000-05-30 Kaneka Corporation Optically active aminoalcohol derivatives and method of producing same
HUP9901872A3 (en) * 1996-02-08 2001-06-28 Nippon Kayaku Kk Process for producing optically active cyanohydrins
BR9910092A (en) * 1998-05-01 2002-01-22 Abbott Lab Beta-amino acid inhibitors substituted for methionine aminopeptidase-2
US6242494B1 (en) 1998-05-01 2001-06-05 Abbott Laboratories Substituted β-amino acid inhibitors of methionine aminopeptidase-2

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5439477B2 (en) * 1974-07-01 1979-11-28

Also Published As

Publication number Publication date
DK149110B (en) 1986-01-27
SE8001959L (en) 1980-03-13
JPS52136118A (en) 1977-11-14
DE2632396A1 (en) 1977-02-03
SE8306145D0 (en) 1983-11-09
CA1104156A (en) 1981-06-30
SE7606736L (en) 1977-01-23
JPS5758338B2 (en) 1982-12-09
DE2660626C2 (en) 1985-07-11
FR2318863B1 (en) 1980-10-31
JPS6050780B2 (en) 1985-11-11
CS201033B2 (en) 1980-10-31
SE431642B (en) 1984-02-20
CS201034B2 (en) 1980-10-31
DK331276A (en) 1977-01-23
FR2318863A1 (en) 1977-02-18
GB1510477A (en) 1978-05-10
JPS5823654A (en) 1983-02-12
DK149110C (en) 1986-09-08
CH630892A5 (en) 1982-07-15
NL7608064A (en) 1977-01-25
DE2632396C2 (en) 1982-11-25
HU183048B (en) 1984-04-28
AU1591276A (en) 1978-01-19
SE452318B (en) 1987-11-23
AU506003B2 (en) 1979-12-13

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