[go: up one dir, main page]

SE8800169L - NEW PEPTIDE DERIVATIVES, THEIR PREPARATION AND USE - Google Patents

NEW PEPTIDE DERIVATIVES, THEIR PREPARATION AND USE

Info

Publication number
SE8800169L
SE8800169L SE8800169A SE8800169A SE8800169L SE 8800169 L SE8800169 L SE 8800169L SE 8800169 A SE8800169 A SE 8800169A SE 8800169 A SE8800169 A SE 8800169A SE 8800169 L SE8800169 L SE 8800169L
Authority
SE
Sweden
Prior art keywords
amino
preparation
peptide derivatives
new peptide
acid
Prior art date
Application number
SE8800169A
Other languages
Swedish (sv)
Other versions
SE8800169D0 (en
Inventor
A Hagenbach
R Metternich
E Pfenninger
B Weidmann
Original Assignee
Sandoz Ag
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 Sandoz Ag filed Critical Sandoz Ag
Publication of SE8800169D0 publication Critical patent/SE8800169D0/en
Publication of SE8800169L publication Critical patent/SE8800169L/en

Links

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
    • C07K5/06—Dipeptides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • 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
    • C07K5/0227—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the (partial) peptide sequence -Phe-His-NH-(X)2-C(=0)-, e.g. Renin-inhibitors with n = 2 - 6; for n > 6 see C07K5/06 - C07K5/10
    • 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
    • C07K5/06008—Dipeptides with the first amino acid being neutral
    • C07K5/06078—Dipeptides 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
    • C07K5/06—Dipeptides
    • C07K5/06191—Dipeptides containing heteroatoms different from O, S, or N
    • 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)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biophysics (AREA)
  • Biochemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Genetics & Genomics (AREA)
  • Cardiology (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

A compound of formula <IMAGE> where A is an acyl group; B and C are bonds or represent amino-acids with at least one amino-acid being present; R2 is a side chain of an amino-acid; R3 is H, OH, acyloxy or NH2; D is a bond, O, >NR1, or> CH-R1; Y is >CO, >SO2 or >P(O) NR4 R5; R1 is H or alkyl; and NR4 R5 is an amino function, These compounds have renin-inhibiting activity and are for use against hypertension and cardiac insufficiency.
SE8800169A 1987-01-21 1988-01-20 NEW PEPTIDE DERIVATIVES, THEIR PREPARATION AND USE SE8800169L (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE3701526 1987-01-21
DE3707339 1987-03-07

Publications (2)

Publication Number Publication Date
SE8800169D0 SE8800169D0 (en) 1988-01-20
SE8800169L true SE8800169L (en) 1988-07-22

Family

ID=25851692

Family Applications (1)

Application Number Title Priority Date Filing Date
SE8800169A SE8800169L (en) 1987-01-21 1988-01-20 NEW PEPTIDE DERIVATIVES, THEIR PREPARATION AND USE

Country Status (13)

Country Link
JP (1) JPS6419053A (en)
KR (1) KR880009041A (en)
AU (1) AU1037588A (en)
BE (1) BE1002212A5 (en)
CH (1) CH676988A5 (en)
DK (1) DK22588A (en)
FR (1) FR2609716A1 (en)
GB (1) GB2200115B (en)
IL (1) IL85136A0 (en)
IT (1) IT1219811B (en)
MY (1) MY102311A (en)
NL (1) NL8800100A (en)
SE (1) SE8800169L (en)

Families Citing this family (73)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6878728B1 (en) 1999-06-11 2005-04-12 Vertex Pharmaceutical Incorporated Inhibitors of aspartyl protease
US20040122000A1 (en) 1981-01-07 2004-06-24 Vertex Pharmaceuticals Incorporated. Inhibitors of aspartyl protease
DE3732971A1 (en) * 1987-09-30 1989-04-20 Hoechst Ag RENINE INHIBITING DIPEPTIDES, METHOD FOR THE PRODUCTION THEREOF, THE AGENTS CONTAINING THEM AND THEIR USE
DE3733296A1 (en) * 1987-10-02 1989-04-20 Merck Patent Gmbh AMINOSAEUREDERIVATE
EP0329295A1 (en) * 1988-02-01 1989-08-23 The Upjohn Company Renin inhibiting peptides with polar end groups
JP2524814B2 (en) * 1988-08-25 1996-08-14 キッセイ薬品工業株式会社 Method for producing α-hydroxy-β-amino acid
CA2010531A1 (en) * 1989-03-06 1990-09-06 Werner Neidhart Amino acid derivatives
US5185284A (en) * 1989-05-22 1993-02-09 Mitsubishi Denki Kabushiki Kaisha Method of making a semiconductor memory device
US5098924A (en) * 1989-09-15 1992-03-24 E. R. Squibb & Sons, Inc. Diol sulfonamide and sulfinyl renin inhibitors
TW225540B (en) * 1990-06-28 1994-06-21 Shionogi & Co
US5482947A (en) * 1990-11-19 1996-01-09 Talley; John J. Retroviral protease inhibitors
DE69130070T2 (en) * 1990-11-19 1999-04-29 Monsanto Co., St. Louis, Mo. RETROVIRAL PROTEASE INHIBITORS
US5475013A (en) * 1990-11-19 1995-12-12 Monsanto Company Retroviral protease inhibitors
US5475027A (en) * 1990-11-19 1995-12-12 G.D. Searle & Co. Retroviral protease inhibitors
ES2151975T3 (en) 1990-11-19 2001-01-16 Monsanto Co INHIBITORS OF RETROVIRIC PROTEASES.
ATE155779T1 (en) * 1990-11-19 1997-08-15 Monsanto Co RETROVIRAL PROTEASE INHIBITORS
US5614522A (en) * 1990-11-19 1997-03-25 G.D. Searle & Co. Retroviral protease inhibitors
US5602175A (en) * 1990-11-19 1997-02-11 G.D. Searle & Co. Retroviral protease inhibitors
DK0641333T3 (en) * 1992-05-20 1996-09-02 Monsanto Co Process for the preparation of intermediates useful in the synthesis of retrovirus protease inhibitors
DK0641325T3 (en) 1992-05-21 2001-04-17 Monsanto Co Inhibitors of retroviral protease
DK0656888T3 (en) * 1992-08-25 1998-02-09 Searle & Co Sulfonylalkanoylaminohydroxyethylaminosulfonamides useful as retroviral protease inhibitors
ES2103488T3 (en) * 1992-08-25 1997-09-16 Searle & Co N- (ALCANOYLAMINO-2-HYDROXYPROPIL) SULFONAMIDES USEFUL AS RETROVIRAL PROTEASE INHIBITORS.
US5968942A (en) * 1992-08-25 1999-10-19 G. D. Searle & Co. α- and β-amino acid hydroxyethylamino sulfonamides useful as retroviral protease inhibitors
US6022994A (en) 1992-08-25 2000-02-08 G. D. Searle &. Co. Succinoylamino hydroxyethylamino sulfonamides useful as retroviral protease inhibitors
DK0810209T3 (en) 1992-08-25 2002-08-12 Monsanto Co Alpha and beta amino acid hydroxyethylaminosulfonamides for use as inhibitors of retroviral proteases
US6743929B1 (en) 1992-08-25 2004-06-01 G. D. Searle & Co. Sulfonylalkanoylamino hydroxyethylamino sulfonamides useful as retroviral protease inhibitors
US7141609B2 (en) 1992-08-25 2006-11-28 G.D. Searle & Co. α- and β-amino acid hydroxyethylamino sulfonamides useful as retroviral protease inhibitors
US6046190A (en) * 1992-08-25 2000-04-04 G.D. Searle & Co. Hydroxyethylamino sulphonamides useful as retroviral protease inhibitors
US5830897A (en) * 1992-08-27 1998-11-03 G. D. Searle & Co. α- and β-amino acid hydroxyethylamino sulfonamides useful as retroviral protease inhibitors
IS2334B (en) 1992-09-08 2008-02-15 Vertex Pharmaceuticals Inc., (A Massachusetts Corporation) Aspartyl protease inhibitor of a new class of sulfonamides
US5723490A (en) * 1992-09-08 1998-03-03 Vertex Pharmaceuticals Incorporated THF-containing sulfonamide inhibitors of aspartyl protease
US5783701A (en) 1992-09-08 1998-07-21 Vertex Pharmaceuticals, Incorporated Sulfonamide inhibitors of aspartyl protease
US5578606A (en) * 1992-10-30 1996-11-26 G. D. Searle & Co. α- and β-amino acid hydroxyethylamino sulfonyl urea derivatives useful as retroviral protease inhibitors
US5756498A (en) * 1992-10-30 1998-05-26 G.D. Searle & Co. Sulfonylalkanoylamino hydroxyethylamino sulfonyl urea derivatives useful as retroviral protease inhibitors
US6337398B1 (en) 1992-10-30 2002-01-08 G.D. Searle & Co. Succinoylamino hydroxyethylamino sulfonyl urea derivatives useful as retroviral protease inhibitors
DK0666841T3 (en) * 1992-10-30 1997-02-10 Searle & Co Succinoylamino-hydroxyethylaminosulfamic acid derivatives for use as inhibitors of retroviral proteases
AU5547094A (en) 1992-10-30 1994-05-24 G.D. Searle & Co. Hydroxyethylamino sulfamic acid derivatives useful as retroviral protease inhibitors
EP1462443A1 (en) * 1992-10-30 2004-09-29 G.D. Searle & Co. Sulfonylalkanoylamino hydroxyethylamino sulfamic acids useful as retroviral protease inhibitors
US5514801A (en) * 1992-12-29 1996-05-07 Monsanto Company Cyclic sulfone containing retroviral protease inhibitors
US5830888A (en) * 1993-04-16 1998-11-03 Monsanto Company Macrocyclic retroviral protease inhibitors
US5750648A (en) * 1993-08-20 1998-05-12 G.D. Searle & Co. Retroviral protease inhibitors and combinations thereof
US5602119A (en) * 1993-10-29 1997-02-11 Vazquez; Michael L. Succinoylamino hydroxyethylamino sulfamic acid derivatives useful as retroviral protease inhibitors
US6133444A (en) * 1993-12-22 2000-10-17 Perseptive Biosystems, Inc. Synthons for the synthesis and deprotection of peptide nucleic acids under mild conditions
CN1146201A (en) * 1994-03-07 1997-03-26 沃泰克斯药物股份有限公司 Sulphonamide derivatives as aspartyl protease inhibitors
EP1059285A3 (en) * 1994-07-07 2001-10-31 Pharm-Eco Laboratories, Inc. Process for the preparation of 1,3-diamino-2-propanol and 1,3-diamino-2-propanone derivatives
CA2194480A1 (en) * 1994-07-07 1996-01-25 Biman Pal Amino acid-derived diaminopropanols
US5475138A (en) * 1994-07-07 1995-12-12 Pharm-Eco Laboratories Incorporated Method preparing amino acid-derived diaminopropanols
US5831117A (en) * 1995-01-20 1998-11-03 G. D. Searle & Co. Method of preparing retroviral protease inhibitor intermediates
DE69637380T2 (en) 1995-01-20 2009-09-17 G.D. Searle Llc, Chicago BIS SULFONAMIDE HYDROXYETHYLAMINO DERIVATIVES AS INHIBITORS OF RETROVIRAL PROTEASES
US5756533A (en) * 1995-03-10 1998-05-26 G.D. Searle & Co. Amino acid hydroxyethylamino sulfonamide retroviral protease inhibitors
US6140505A (en) 1995-03-10 2000-10-31 G. D. Searle & Co. Synthesis of benzo fused heterocyclic sulfonyl chlorides
US6667307B2 (en) 1997-12-19 2003-12-23 G.D. Searle & Co. Sulfonylalkanoylamino hydroxyethylamino sulfonamide retroviral protease inhibitors
US5705500A (en) * 1995-03-10 1998-01-06 G.D. Searle & Co. Sulfonylalkanoylamino hydroxyethylamino sulfonamide retroviral protease inhibitors
US6407134B1 (en) 1995-03-10 2002-06-18 G. D. Searle & Co. Heterocyclecarbonyl amino acid hydroxyethylamino sulfonamide retroviral protease inhibitors
US6169085B1 (en) 1995-03-10 2001-01-02 G. D. Searle & Company Sulfonylalkanoylamino hydroxyethylamino sulfonamide retroviral protease inhibitors
US5776971A (en) 1995-03-10 1998-07-07 G.D. Searle & Co. Heterocyclecarbonyl amino acid hydroxyethylamino sulfonamide retroviral protease inhibitors
EP1188766A1 (en) 1995-03-10 2002-03-20 G.D. Searle & Co. Bis-amino acid hydroxyethylamino sulfonamide retroviral protease inhibitors
US7339078B2 (en) 1995-03-10 2008-03-04 G.D. Searle Llc Bis-amino acid hydroxyethylamino sulfonamide retroviral protease inhibitors
US6861539B1 (en) 1995-03-10 2005-03-01 G. D. Searle & Co. Bis-amino acid hydroxyethylamino sulfonamide retroviral protease inhibitors
US6150556A (en) 1995-03-10 2000-11-21 G. D. Dearle & Co. Bis-amino acid hydroxyethylamino sulfonamide retroviral protease inhibitors
US5985870A (en) * 1995-03-10 1999-11-16 G.D. Searle & Co. Sulfonylalkanoylamino hydroxyethylamino sulfonamide retroviral protease inhibitors
PT815124E (en) * 1995-03-10 2003-04-30 Searle & Co INHIBITORS RETROVIRAL PROTEASE SULFONAMIDE HYDROXYETHYLAMINO AMINOACIDES HETEROCYCLOCARBONYL
US5691372A (en) * 1995-04-19 1997-11-25 Vertex Pharmaceuticals Incorporated Oxygenated-Heterocycle containing sulfonamide inhibitors of aspartyl protease
US6004957A (en) * 1995-06-07 1999-12-21 Vertex Pharmaceuticals, Incorporated Sulfonamide inhibitors of aspartyl protease
US6063963A (en) * 1995-07-05 2000-05-16 Pharm-Eco Laboratories, Inc. Amino acid-derived diaminopropanols
EP0861249A1 (en) * 1995-11-15 1998-09-02 G.D. Searle & Co. Substituted sulfonylalkanoylamino hydroxyethylamino sulfonamide retroviral protease inhibitors
US6436989B1 (en) 1997-12-24 2002-08-20 Vertex Pharmaceuticals, Incorporated Prodrugs of aspartyl protease inhibitors
JPH11324710A (en) 1998-05-20 1999-11-26 Hitachi Ltd Gas turbine power plant
BR9912169A (en) 1998-06-19 2001-04-10 Vertex Pharma Aspartyl protease sulfonamide inhibitors
EP1095022A1 (en) 1998-07-08 2001-05-02 G.D. Searle & Co. Retroviral protease inhibitors
US6455734B1 (en) 2000-08-09 2002-09-24 Magnesium Diagnostics, Inc. Antagonists of the magnesium binding defect as therapeutic agents and methods for treatment of abnormal physiological states
JP3888095B2 (en) 2001-07-26 2007-02-28 株式会社日立製作所 Gas turbine equipment
US7251926B2 (en) 2001-07-26 2007-08-07 Hitachi, Ltd. Gas turbine installation

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1245217A (en) * 1981-12-10 1988-11-22 Joshua S. Boger Renin inhibitory peptides having phe su13 xx deletion
JPS60163899A (en) * 1984-02-03 1985-08-26 Sankyo Co Ltd Renin-inhibiting peptide
EP0163237A3 (en) * 1984-05-29 1988-04-27 Merck & Co. Inc. Di- and tri-peptidal renin inhibitors
US4645759A (en) * 1984-06-22 1987-02-24 Abbott Laboratories Renin inhibiting compounds
FI88400C (en) * 1984-08-06 1993-05-10 Upjohn Co FRAMEWORK FOR THE FRAME STATION INHIBITION OF PEPTIDER
US4727060A (en) * 1984-11-13 1988-02-23 Ciba-Geigy Corporation Novel 5-amino-4-hydroxyvaleryl derivatives
EP0184855A3 (en) * 1984-12-14 1989-05-03 Abbott Laboratories Resin inhibiting compounds
KR870005013A (en) * 1985-11-29 1987-06-04 가와무라 요시부미 Lenin-inhibiting oligopeptides, methods of making and uses thereof
DE3601248A1 (en) * 1986-01-17 1987-07-23 Hoechst Ag SUBSTITUTED 4-AMINO-3-HYDROXYBUTTERIC ACID DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF, THESE AGENTS AND THEIR USE

Also Published As

Publication number Publication date
MY102311A (en) 1992-05-28
GB2200115B (en) 1990-11-14
IT8847556A0 (en) 1988-01-21
NL8800100A (en) 1988-08-16
IT1219811B (en) 1990-05-24
SE8800169D0 (en) 1988-01-20
BE1002212A5 (en) 1990-10-16
JPS6419053A (en) 1989-01-23
GB2200115A (en) 1988-07-27
GB8801040D0 (en) 1988-02-17
CH676988A5 (en) 1991-03-28
DK22588A (en) 1988-07-22
AU1037588A (en) 1988-09-01
FR2609716A1 (en) 1988-07-22
IL85136A0 (en) 1988-06-30
DK22588D0 (en) 1988-01-19
KR880009041A (en) 1988-09-13

Similar Documents

Publication Publication Date Title
SE8800169L (en) NEW PEPTIDE DERIVATIVES, THEIR PREPARATION AND USE
OA06421A (en) Process for the preparation of N- (vinblastinoyl-23) derivatives of amino acids and peptides.
NO890921D0 (en) PROCEDURE FOR THE PREPARATION OF AMINO ACID DERIVATIVES.
FI102379B1 (en) Uranium protected amino acid N-carboxyanhydrides
KR920012051A (en) Biphenylyl compound
SE8501392L (en) CYCLOSPORINES, THEIR PREPARATION AND USE
DE3788397D1 (en) SYNTHETIC HTLV III PEPTIDE COMPOSITIONS AND THEIR USE.
GR3001889T3 (en) Prodrug compounds, process for the preparation thereof and sustained release preparation comprising the same
ATE19088T1 (en) PEPTIDE AND ITS USE.
ATE24917T1 (en) PEPTIDE DERIVATIVES, THEIR PREPARATION AND USE AS ANTI-ELASTASIC AGENTS.
ES2088011T3 (en) EXCITING AMINO ACID ANTAGONISTS.
ES2081817T3 (en) POLYPEPTIDE WITH MAIN SEQUENCES REPEATED THAT ARE FIXED IN THE CELL.
MY106287A (en) Acid addition salts of amidated taurine or glycine, their preparation and use
ES2045067T3 (en) PROCEDURE FOR PREPARING NEW TIAZOL COMPOUNDS.
BG97123A (en) DERIVATIVES OF HUMAN BILE SALTS, LIPASE AND PHARMACEUTICAL COMPOSITIONS BASED THEREOF
ES2051711T3 (en) PROCEDURE FOR PREPARING 2-OXO-1 - (((SUBSTITUTED SULFONIL) AMINO) -CARBONYL) -AZETIDINS.
FI895568A0 (en) Process for the preparation of therapeutically useful aminodiol derivatives
ES2052535T3 (en) SYNTHESIS OF AMINO-ALKYL-AMIDES OF PEPTIDES OR HYDRAZIDES OF PEPTIDES THROUGH A SOLID PHASE METHOD.
FI932206A0 (en) This heterocyclic compound is an antagonist of excitatory amino acid receptors, which can be used as an exciter
DK158729C (en) N- (3-TRIFLUORMETHYLPHENYL) -N&#39;-PROPARGYLPIPERAZINE, PHARMACEUTICAL PREPARATIONS CONTAINING IT, ITS USE, AND A PROCEDURE FOR THE PREPARATION OF A PHARMACEUTICAL PREPARATION
ES2077021T3 (en) PEPTIDES THAT HAVE RENINE INHIBITING ACTIVITY, ITS PREPARATION AND USE.
IT1186766B (en) METHOD FOR THE PREPARATION OF IMMUNOGLOBULINS FOR INTRAVENOUS USE
SE8605513D0 (en) NEW PEPTID AND IMMUNOLOGICALLY ACTIVE ASSOCIATIONS
ATE85346T1 (en) PHOSPHORYLATED DERIVATIVES OF CARDIODILATIN/ANFPEPTIDEN.
IT1211138B (en) ANTI-HYPERTENSIVE COMPOUND PROCEDURE FOR ITS PREPARATION AND RELATED PHARMACEUTICAL COMPOSITIONS.

Legal Events

Date Code Title Description
NAV Patent application has lapsed

Ref document number: 8800169-8

Effective date: 19910801

Format of ref document f/p: F