IL97298A - Vasoactive vasotocin derivatives and pharmaceutical compositions containing them - Google Patents

Vasoactive vasotocin derivatives and pharmaceutical compositions containing them

Info

Publication number: IL97298A
Authority: IL; Israel
Prior art keywords: phe; hgn; vasotocin; hmp; derivatives
Prior art date: 1990-02-27

Application number

IL9729891A

Other languages

English (en)

Other versions

IL97298A0 (en

Original Assignee

Ferring Ab

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.)

1990-02-27

Filing date

1991-02-20

Publication date

1995-08-31

1991-02-20 Application filed by Ferring Ab filed Critical Ferring Ab

1992-05-25 Publication of IL97298A0 publication Critical patent/IL97298A0/xx

1995-08-31 Publication of IL97298A publication Critical patent/IL97298A/en

Links

OXDZADMCOWPSOC-UHFFFAOYSA-N Argiprestocin Chemical class N1C(=O)C(N)CSSCC(C(=O)N2C(CCC2)C(=O)NC(CCCN=C(N)N)C(=O)NCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(CCC(N)=O)NC(=O)C(C(C)CC)NC(=O)C1CC1=CC=C(O)C=C1 OXDZADMCOWPSOC-UHFFFAOYSA-N 0.000 title claims abstract description 36
239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 12
230000002227 vasoactive effect Effects 0.000 title description 5
OLQOVQTWRIJPRE-UHFFFAOYSA-N 3-mercaptolactic acid Chemical group SCC(O)C(O)=O OLQOVQTWRIJPRE-UHFFFAOYSA-N 0.000 claims abstract description 4
-1 L-2-aminobutyryl Chemical group 0.000 claims abstract description 3
238000002360 preparation method Methods 0.000 claims description 6
YZJSUQQZGCHHNQ-UHFFFAOYSA-N Homoglutamine Chemical group OC(=O)C(N)CCCC(N)=O YZJSUQQZGCHHNQ-UHFFFAOYSA-N 0.000 claims description 4
XIGSAGMEBXLVJJ-YFKPBYRVSA-N L-homocitrulline Chemical compound NC(=O)NCCCC[C@H]([NH3+])C([O-])=O XIGSAGMEBXLVJJ-YFKPBYRVSA-N 0.000 claims description 4
COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 claims description 4
OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 claims description 4
125000000539 amino acid group Chemical group 0.000 claims description 4
150000008574 D-amino acids Chemical class 0.000 claims description 3
239000003085 diluting agent Substances 0.000 claims description 3
239000004480 active ingredient Substances 0.000 claims description 2
239000000654 additive Substances 0.000 claims description 2
238000007911 parenteral administration Methods 0.000 claims description 2
COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 claims description 2
OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 claims description 2
230000000996 additive effect Effects 0.000 claims 1
125000003295 alanine group Chemical group N[C@@H](C)C(=O)* 0.000 claims 1
230000000694 effects Effects 0.000 abstract description 19
230000002035 prolonged effect Effects 0.000 abstract description 5
125000001980 alanyl group Chemical group 0.000 abstract 1
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 24
230000036772 blood pressure Effects 0.000 description 19
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
238000004458 analytical method Methods 0.000 description 15
150000001413 amino acids Chemical class 0.000 description 14
KBZOIRJILGZLEJ-LGYYRGKSSA-N argipressin Chemical compound C([C@H]1C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CSSC[C@@H](C(N[C@@H](CC=2C=CC(O)=CC=2)C(=O)N1)=O)N)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCC(N)=O)C1=CC=CC=C1 KBZOIRJILGZLEJ-LGYYRGKSSA-N 0.000 description 13
239000000047 product Substances 0.000 description 12
108090000765 processed proteins & peptides Proteins 0.000 description 11
JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 10
230000002686 anti-diuretic effect Effects 0.000 description 9
238000004128 high performance liquid chromatography Methods 0.000 description 9
DTQVDTLACAAQTR-UHFFFAOYSA-N trifluoroacetic acid Substances OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 9
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
238000010265 fast atom bombardment Methods 0.000 description 8
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 7
238000001514 detection method Methods 0.000 description 7
230000014759 maintenance of location Effects 0.000 description 7
239000000126 substance Substances 0.000 description 7
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
238000001914 filtration Methods 0.000 description 6
238000001556 precipitation Methods 0.000 description 6
238000012360 testing method Methods 0.000 description 6
229960003726 vasopressin Drugs 0.000 description 6
GXBMIBRIOWHPDT-UHFFFAOYSA-N Vasopressin Natural products N1C(=O)C(CC=2C=C(O)C=CC=2)NC(=O)C(N)CSSCC(C(=O)N2C(CCC2)C(=O)NC(CCCN=C(N)N)C(=O)NCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(CCC(N)=O)NC(=O)C1CC1=CC=CC=C1 GXBMIBRIOWHPDT-UHFFFAOYSA-N 0.000 description 5
108010004977 Vasopressins Proteins 0.000 description 5
102000002852 Vasopressins Human genes 0.000 description 5
230000001965 increasing effect Effects 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 4
230000008878 coupling Effects 0.000 description 4
239000011347 resin Substances 0.000 description 4
229920005989 resin Polymers 0.000 description 4
238000004366 reverse phase liquid chromatography Methods 0.000 description 4
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
230000000740 bleeding effect Effects 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
238000010168 coupling process Methods 0.000 description 3
238000005859 coupling reaction Methods 0.000 description 3
238000001035 drying Methods 0.000 description 3
238000012986 modification Methods 0.000 description 3
230000004048 modification Effects 0.000 description 3
230000000144 pharmacologic effect Effects 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
239000007790 solid phase Substances 0.000 description 3
238000010532 solid phase synthesis reaction Methods 0.000 description 3
239000000243 solution Substances 0.000 description 3
238000003786 synthesis reaction Methods 0.000 description 3
210000002700 urine Anatomy 0.000 description 3
BJFIDCADFRDPIO-DZCXQCEKSA-N (2S)-N-[(2S)-6-amino-1-[(2-amino-2-oxoethyl)amino]-1-oxohexan-2-yl]-1-[[(4R,7S,10S,13S,16S,19R)-19-amino-7-(2-amino-2-oxoethyl)-10-(3-amino-3-oxopropyl)-16-[(4-hydroxyphenyl)methyl]-6,9,12,15,18-pentaoxo-13-(phenylmethyl)-1,2-dithia-5,8,11,14,17-pentazacycloeicos-4-yl]-oxomethyl]-2-pyrrolidinecarboxamide Chemical compound NCCCC[C@@H](C(=O)NCC(N)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H]1NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC=2C=CC=CC=2)NC(=O)[C@H](CC=2C=CC(O)=CC=2)NC(=O)[C@@H](N)CSSC1 BJFIDCADFRDPIO-DZCXQCEKSA-N 0.000 description 2
KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
OGNSCSPNOLGXSM-UHFFFAOYSA-N L-2,4-diaminobutyric acid group Chemical group NC(C(=O)O)CCN OGNSCSPNOLGXSM-UHFFFAOYSA-N 0.000 description 2
108010048179 Lypressin Proteins 0.000 description 2
208000001089 Multiple system atrophy Diseases 0.000 description 2
206010031127 Orthostatic hypotension Diseases 0.000 description 2
208000005735 Water intoxication Diseases 0.000 description 2
229940124538 antidiuretic agent Drugs 0.000 description 2
239000003160 antidiuretic agent Substances 0.000 description 2
125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 2
210000004899 c-terminal region Anatomy 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
230000029142 excretion Effects 0.000 description 2
229940088597 hormone Drugs 0.000 description 2
239000005556 hormone Substances 0.000 description 2
229910000040 hydrogen fluoride Inorganic materials 0.000 description 2
238000010253 intravenous injection Methods 0.000 description 2
229960003837 lypressin Drugs 0.000 description 2
238000000034 method Methods 0.000 description 2
UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 2
WXEHBUMAEPOYKP-UHFFFAOYSA-N methylsulfanylethane Chemical compound CCSC WXEHBUMAEPOYKP-UHFFFAOYSA-N 0.000 description 2
230000036470 plasma concentration Effects 0.000 description 2
238000012453 sprague-dawley rat model Methods 0.000 description 2
VBVSINJSQBTTDR-YFKPBYRVSA-N (2,3,4,5,6-pentafluorophenyl) (2s)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate Chemical compound CC(C)(C)OC(=O)N[C@@H](C)C(=O)OC1=C(F)C(F)=C(F)C(F)=C1F VBVSINJSQBTTDR-YFKPBYRVSA-N 0.000 description 1
UHPQFNXOFFPHJW-UHFFFAOYSA-N (4-methylphenyl)-phenylmethanamine Chemical compound C1=CC(C)=CC=C1C(N)C1=CC=CC=C1 UHPQFNXOFFPHJW-UHFFFAOYSA-N 0.000 description 1
XXMFJKNOJSDQBM-UHFFFAOYSA-N 2,2,2-trifluoroacetic acid;hydrate Chemical compound [OH3+].[O-]C(=O)C(F)(F)F XXMFJKNOJSDQBM-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
101800001144 Arg-vasopressin Proteins 0.000 description 1
FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
102000004190 Enzymes Human genes 0.000 description 1
108090000790 Enzymes Proteins 0.000 description 1
206010020772 Hypertension Diseases 0.000 description 1
206010022998 Irritability Diseases 0.000 description 1
QWCKQJZIFLGMSD-VKHMYHEASA-N L-alpha-aminobutyric acid Chemical group CC[C@H](N)C(O)=O QWCKQJZIFLGMSD-VKHMYHEASA-N 0.000 description 1
150000008575 L-amino acids Chemical class 0.000 description 1
229930195725 Mannitol Natural products 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
125000000729 N-terminal amino-acid group Chemical group 0.000 description 1
206010030302 Oliguria Diseases 0.000 description 1
102100026383 Vasopressin-neurophysin 2-copeptin Human genes 0.000 description 1
101800003024 Vasotocin Proteins 0.000 description 1
150000003862 amino acid derivatives Chemical class 0.000 description 1
239000003708 ampul Substances 0.000 description 1
229940125782 compound 2 Drugs 0.000 description 1
229940126214 compound 3 Drugs 0.000 description 1
229940125898 compound 5 Drugs 0.000 description 1
230000001595 contractor effect Effects 0.000 description 1
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
230000007071 enzymatic hydrolysis Effects 0.000 description 1
238000006047 enzymatic hydrolysis reaction Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
238000004992 fast atom bombardment mass spectroscopy Methods 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
239000012467 final product Substances 0.000 description 1
238000001802 infusion Methods 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
238000011068 loading method Methods 0.000 description 1
238000011866 long-term treatment Methods 0.000 description 1
235000010355 mannitol Nutrition 0.000 description 1
239000000594 mannitol Substances 0.000 description 1
239000000203 mixture Substances 0.000 description 1
230000011224 negative regulation of urine volume Effects 0.000 description 1
125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 description 1
239000000813 peptide hormone Substances 0.000 description 1
230000002688 persistence Effects 0.000 description 1
239000002504 physiological saline solution Substances 0.000 description 1
230000001817 pituitary effect Effects 0.000 description 1
229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
210000002460 smooth muscle Anatomy 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
238000002560 therapeutic procedure Methods 0.000 description 1
238000011282 treatment Methods 0.000 description 1
230000002792 vascular Effects 0.000 description 1
230000003639 vasoconstrictive effect Effects 0.000 description 1
239000005526 vasoconstrictor agent Substances 0.000 description 1

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
- C07K7/16—Oxytocins; Vasopressins; Related peptides
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/24—Drugs for disorders of the endocrine system of the sex hormones
- A61P5/28—Antiandrogens
- 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
- A61P9/02—Non-specific cardiovascular stimulants, e.g. drugs for syncope, antihypotensives
- 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)
Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
General Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Medicinal Chemistry (AREA)
Genetics & Genomics (AREA)
Biophysics (AREA)
Molecular Biology (AREA)
Biochemistry (AREA)
Proteomics, Peptides & Aminoacids (AREA)
Bioinformatics & Cheminformatics (AREA)
Engineering & Computer Science (AREA)
Veterinary Medicine (AREA)
Animal Behavior & Ethology (AREA)
Public Health (AREA)
Pharmacology & Pharmacy (AREA)
Cardiology (AREA)
Heart & Thoracic Surgery (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
General Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Endocrinology (AREA)
Diabetes (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Peptides Or Proteins (AREA)
Polysaccharides And Polysaccharide Derivatives (AREA)
Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Saccharide Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Steroid Compounds (AREA)

IL9729891A 1990-02-27 1991-02-20 Vasoactive vasotocin derivatives and pharmaceutical compositions containing them IL97298A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
SE9000691A SE502644C2 (sv)	1990-02-27	1990-02-27	Vasoaktiva vasotocinderivat

Publications (2)

Publication Number	Publication Date
IL97298A0 IL97298A0 (en)	1992-05-25
IL97298A true IL97298A (en)	1995-08-31

Family

ID=20378692

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL9729891A IL97298A (en)	1990-02-27	1991-02-20	Vasoactive vasotocin derivatives and pharmaceutical compositions containing them

Country Status (19)

Country	Link
US (1)	US5459236A (de)
EP (1)	EP0517778B1 (de)
JP (1)	JP2957275B2 (de)
KR (1)	KR0171614B1 (de)
AT (1)	ATE137764T1 (de)
AU (1)	AU633198B2 (de)
CA (1)	CA2076749C (de)
DE (1)	DE69119409T2 (de)
DK (1)	DK0517778T3 (de)
ES (1)	ES2089196T3 (de)
FI (1)	FI109703B (de)
HU (1)	HU215121B (de)
IE (1)	IE62345B1 (de)
IL (1)	IL97298A (de)
MC (1)	MC2254A1 (de)
NO (1)	NO923333L (de)
RU (1)	RU2067586C1 (de)
SE (1)	SE502644C2 (de)
WO (1)	WO1991013092A1 (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6828415B2 (en)	1993-02-19	2004-12-07	Zentaris Gmbh	Oligopeptide lyophilisate, their preparation and use
PT710243E (pt) *	1993-06-29	2000-11-30	Ferring Bv	Sintese melhorada de peptidos ciclicos.
JO2937B1 (en) *	2004-08-11	2016-03-15	فيرينغ.بي.في	Tight muscles of the peptide vascular tensioner receptor
KR101194586B1 (ko) *	2006-02-10	2012-10-25	훼링 비.브이.	신규 화합물
WO2009037586A2 (en)	2007-08-14	2009-03-26	Ferring B.V.	Use of peptidic vasopressin receptor agonists
RU2454426C1 (ru) *	2011-04-06	2012-06-27	Федеральное государственное образовательное учреждение высшего профессионального образования Санкт-Петербургский государственный университет	Пептид калий-уретический
KR101304427B1 (ko)	2011-04-12	2013-09-05	한국과학기술연구원	재사용이 용이한 기공체 - 위성 나노입자 복합체 및 그 제조방법

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA1246055A (en) *	1980-03-24	1988-12-06	Joseph H. Cort	N-.omega.-substituted hormonogens of vasopressin and its synthetic analogs
SE469473B (sv) *	1987-10-07	1993-07-12	Ferring Ab	Vasoaktiva peptider

1990
- 1990-02-27 SE SE9000691A patent/SE502644C2/sv not_active IP Right Cessation
1991
- 1991-02-20 IL IL9729891A patent/IL97298A/en not_active IP Right Cessation
- 1991-02-26 DE DE69119409T patent/DE69119409T2/de not_active Expired - Fee Related
- 1991-02-26 AT AT91905375T patent/ATE137764T1/de not_active IP Right Cessation
- 1991-02-26 CA CA002076749A patent/CA2076749C/en not_active Expired - Fee Related
- 1991-02-26 ES ES91905375T patent/ES2089196T3/es not_active Expired - Lifetime
- 1991-02-26 AU AU73424/91A patent/AU633198B2/en not_active Ceased
- 1991-02-26 RU SU5052869/04A patent/RU2067586C1/ru not_active IP Right Cessation
- 1991-02-26 KR KR1019920702039A patent/KR0171614B1/ko not_active Expired - Fee Related
- 1991-02-26 HU HU9202748A patent/HU215121B/hu not_active IP Right Cessation
- 1991-02-26 WO PCT/SE1991/000154 patent/WO1991013092A1/en not_active Ceased
- 1991-02-26 US US07/923,895 patent/US5459236A/en not_active Expired - Fee Related
- 1991-02-26 MC MC91SE9100154D patent/MC2254A1/xx unknown
- 1991-02-26 JP JP3505030A patent/JP2957275B2/ja not_active Expired - Fee Related
- 1991-02-26 DK DK91905375.1T patent/DK0517778T3/da active
- 1991-02-26 IE IE64891A patent/IE62345B1/en not_active IP Right Cessation
- 1991-02-26 EP EP91905375A patent/EP0517778B1/de not_active Expired - Lifetime
1992
- 1992-08-26 NO NO92923333A patent/NO923333L/no unknown
- 1992-08-26 FI FI923820A patent/FI109703B/fi active

Also Published As

Publication number	Publication date
NO923333L (no)	1992-10-16
CA2076749C (en)	2001-02-20
JPH05504575A (ja)	1993-07-15
DE69119409D1 (de)	1996-06-13
RU2067586C1 (ru)	1996-10-10
WO1991013092A1 (en)	1991-09-05
EP0517778B1 (de)	1996-05-08
FI109703B (fi)	2002-09-30
SE9000691D0 (sv)	1990-02-27
SE9000691L (sv)	1991-08-28
IE62345B1 (en)	1995-01-25
HUT61580A (en)	1993-01-28
DE69119409T2 (de)	1996-09-05
SE502644C2 (sv)	1995-11-27
AU7342491A (en)	1991-09-18
US5459236A (en)	1995-10-17
EP0517778A1 (de)	1992-12-16
JP2957275B2 (ja)	1999-10-04
DK0517778T3 (da)	1996-08-19
ES2089196T3 (es)	1996-10-01
KR0171614B1 (ko)	1999-02-01
IE910648A1 (en)	1991-08-28
ATE137764T1 (de)	1996-05-15
AU633198B2 (en)	1993-01-21
CA2076749A1 (en)	1991-08-28
MC2254A1 (fr)	1993-03-25
FI923820L (fi)	1992-08-26
HU9202748D0 (en)	1992-12-28
KR920703003A (ko)	1992-12-17
NO923333D0 (no)	1992-08-26
FI923820A0 (fi)	1992-08-26
HU215121B (hu)	1998-09-28
IL97298A0 (en)	1992-05-25

Legal Events

Date	Code	Title
1997-06-10	KB	Patent renewed
2001-06-14	KB	Patent renewed
2006-01-15	MM9K	Patent not in force due to non-payment of renewal fees

Publication	Publication Date	Title
US4481139A (en)	1984-11-06	Peptide antagonists of substance P
US4766108A (en)	1988-08-23	Tyr-Arg-vasopressin antagonists
US5204328A (en)	1993-04-20	Peptides having atrial natriuretic factor activity
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