FI86432B - Foerfarande foer framstaellning av nya tillvaexthormon-frigoerande peptider. - Google Patents
Foerfarande foer framstaellning av nya tillvaexthormon-frigoerande peptider. Download PDFInfo
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- FI86432B FI86432B FI843141A FI843141A FI86432B FI 86432 B FI86432 B FI 86432B FI 843141 A FI843141 A FI 843141A FI 843141 A FI843141 A FI 843141A FI 86432 B FI86432 B FI 86432B
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- KFGRVLINLVVMJA-MITYVQBRSA-N chembl440262 Chemical compound C([C@H](N)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCN=C(N)N)C(O)=O)C1=CC=C(O)C=C1 KFGRVLINLVVMJA-MITYVQBRSA-N 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000002124 endocrine Effects 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
- 239000012530 fluid Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 125000000291 glutamic acid group Chemical group N[C@@H](CCC(O)=O)C(=O)* 0.000 description 1
- ZDXPYRJPNDTMRX-UHFFFAOYSA-N glutamine Natural products OC(=O)C(N)CCC(N)=O ZDXPYRJPNDTMRX-UHFFFAOYSA-N 0.000 description 1
- 125000003630 glycyl group Chemical group [H]N([H])C([H])([H])C(*)=O 0.000 description 1
- 244000144980 herd Species 0.000 description 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- AGPKZVBTJJNPAG-UHFFFAOYSA-N isoleucine Natural products CCC(C)C(N)C(O)=O AGPKZVBTJJNPAG-UHFFFAOYSA-N 0.000 description 1
- 229960000310 isoleucine Drugs 0.000 description 1
- 125000000741 isoleucyl group Chemical group [H]N([H])C(C(C([H])([H])[H])C([H])([H])C([H])([H])[H])C(=O)O* 0.000 description 1
- 210000004731 jugular vein Anatomy 0.000 description 1
- 229940070765 laurate Drugs 0.000 description 1
- 125000001909 leucine group Chemical group [H]N(*)C(C(*)=O)C([H])([H])C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000008176 lyophilized powder Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 229940105631 nembutal Drugs 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- WEXRUCMBJFQVBZ-UHFFFAOYSA-N pentobarbital Chemical compound CCCC(C)C1(CC)C(=O)NC(=O)NC1=O WEXRUCMBJFQVBZ-UHFFFAOYSA-N 0.000 description 1
- 238000010647 peptide synthesis reaction Methods 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 1
- COLNVLDHVKWLRT-QMMMGPOBSA-N phenylalanine group Chemical group N[C@@H](CC1=CC=CC=C1)C(=O)O COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 230000001817 pituitary effect Effects 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002953 preparative HPLC Methods 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 239000003488 releasing hormone Substances 0.000 description 1
- 125000003607 serino group Chemical group [H]N([H])[C@]([H])(C(=O)[*])C(O[H])([H])[H] 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 108010056001 somatotropin releasing hormone (1-29) Proteins 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- WROMPOXWARCANT-UHFFFAOYSA-N tfa trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.OC(=O)C(F)(F)F WROMPOXWARCANT-UHFFFAOYSA-N 0.000 description 1
- 125000000341 threoninyl group Chemical group [H]OC([H])(C([H])([H])[H])C([H])(N([H])[H])C(*)=O 0.000 description 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical class CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 239000004474 valine Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/575—Hormones
- C07K14/60—Growth hormone-releasing factor [GH-RF], i.e. somatoliberin
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Endocrinology (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Toxicology (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Gastroenterology & Hepatology (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Diabetes (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Ultra Sonic Daignosis Equipment (AREA)
- Medicinal Preparation (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Claims (5)
1. Förfarande för framställning av en terapeutiskt användbar peptid med formeln R^A-B-C-Ala-Ile-Phe-Thr-X-
5 Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu- Leu-Gln-Asp-Ile-Y-Ser-Arg-NH2 (I); väri R1 är väte eller en rakkedjad eller förgrenad C1-C6-alkanoyl; A är tyrosyl, D-tyrosyl eller histidyl; B är alanyl eller D-alanyl; C är aspartyl eller D-aspartyl; X är asparaginyl eller D-aspa-10 raginyl; Y är norleucyl eller metionyl; under förutsätt- ning att dä R1 är väte och B är alanyl och C är aspartyl och X är asparaginyl och Y är metionyl, kan A ej vara tyrosyl i formeln (I); och farmaceutiskt godtagbara salter därav; kännetecknat därav, att man kopplar en 15 C-terminalskyddad aminosyra tili ett harts i närvaro av ett koppiingsmedel; tvättar med ett inert lösningsmedel; avlägsnar skyddet i närvaro av en syra; upprepar stegvis denna sekvens i ändamälsenlig ordning med de övriga i formeln (I) definierade skyddade aminosyrorna och utgäende 20 frän peptidens C-terminala ända; acetylerar eventuellt peptidhartset och slutligen lösgör peptiden frän hartset för erhällande av peptiden med formeln (I).
2. Förfarande enligt patentkravet 1 för framställ-ning av en petid med formeln I, kännetecknat 25 därav, att nämnda peptid har formeln Tyr-D-Ala-Asp-Ala- Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-NH2 och dess farmaceutiskt godtagbara sait; Tyr-Ala-D-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-30 Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-NH2 och dess farmaceu tiskt godtagbara sait; D-Tyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-NH2 och dess farmaceutiskt godtagbara sait; Ac-Tyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-35 Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu- 26 8 6 4 3 2 Gln-Asp-Ile-Met-Ser-Arg-NH2 och dess farmaceutiskt godtag-bara salt; Ac-His-D-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-NH2 och dess farmaceutiskt godtagbara 5 salt; Ac-D-Tyr-D-Ala-D-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr- Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-NH2 och dess farmaceutiskt godtagbara salt; Ac-D-Tyr-D-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-10 Ile-Met-Ser-Arg-NH2 och dess farmaceutiskt godtagbara salt; Tyr-Ala-Asp-Ala-Ile-Phe-Thr-D-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-NH2 och dess farmaceutiskt godtagbara salt; Tyr-D-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-15 Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Nle-Ser-Arg-NH2 och dess farmaceutiskt godtagbara salt; His-D-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-lle-Nle-Ser-Arg-NH2 och dess farmaceutiskt godtagbara salt; Tyr-D-Ala-Asp-Ala-Ile-Phe-Thr-20 D-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys- Leu-Leu-Gln-Asp-Ile-Nle-Ser-Arg-NH2 och dess farmaceutiskt godtagbara salt; Tyr-Ala-D-Asp-Ala-lle-Phe-Thr-D-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Nle-Ser-Arg-NH2 och dess farmaceutiskt godtag-25 bara salt; eller Tyr-D-Ala-D-Asp-Ala-Ile-Phe-Thr-D-Asn- Ser-Tyr-Arg-Lys-Val-Leu-Gly-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Nle-Ser-Arg-NH2 och dess farmaceutiskt godtagbara salt.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FI910205A FI910205A0 (fi) | 1983-08-10 | 1991-01-15 | Nya tillvaexthormon frigoerande peptider. |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US52206783A | 1983-08-10 | 1983-08-10 | |
| US52206783 | 1983-08-10 |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| FI843141A0 FI843141A0 (fi) | 1984-08-09 |
| FI843141A FI843141A (fi) | 1985-02-11 |
| FI86432B true FI86432B (fi) | 1992-05-15 |
| FI86432C FI86432C (sv) | 1992-08-25 |
Family
ID=24079327
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI843141A FI86432C (sv) | 1983-08-10 | 1984-08-09 | Förfarande för framställning av nya tillväxthormon-frigörande peptider |
Country Status (17)
| Country | Link |
|---|---|
| EP (1) | EP0136475B1 (sv) |
| JP (1) | JPH0684400B2 (sv) |
| KR (1) | KR850001772A (sv) |
| AT (1) | ATE60062T1 (sv) |
| AU (1) | AU575843B2 (sv) |
| CA (1) | CA1268898A (sv) |
| DE (1) | DE3483931D1 (sv) |
| DK (1) | DK167361B1 (sv) |
| ES (2) | ES8606400A1 (sv) |
| FI (1) | FI86432C (sv) |
| HK (1) | HK73692A (sv) |
| IL (1) | IL72630A (sv) |
| NO (1) | NO165804C (sv) |
| NZ (1) | NZ209078A (sv) |
| PT (1) | PT79055B (sv) |
| SG (1) | SG28692G (sv) |
| ZA (1) | ZA846191B (sv) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4518586A (en) * | 1983-01-13 | 1985-05-21 | The Salk Institute For Biological Studies | GRF Analogs III |
| IL70530A (en) * | 1983-01-13 | 1986-09-30 | Salk Inst For Biological Studi | Synthetic peptides having growth hormone releasing factor activity and compositions containing them |
| PT79094B (en) * | 1983-08-29 | 1986-08-14 | Salk Inst For Biological Studi | Grf analogs |
| US4528190A (en) * | 1983-10-25 | 1985-07-09 | The Salk Institute For Biological Studies | GRF Analogs IV |
| DE3436819A1 (de) * | 1984-10-06 | 1986-04-17 | Hoechst Ag, 6230 Frankfurt | Arzneimittel mit grf-wirkung |
| CA1271600A (en) * | 1985-01-07 | 1990-07-10 | David Howard Coy | Growth hormone-releasing peptides and method of treating mammals therewith |
| EP0193910A3 (en) * | 1985-03-06 | 1988-11-23 | Sumitomo Pharmaceuticals Company, Limited | Synthesis of a derivative of grf and intermediate peptides |
| FR2594832B1 (fr) * | 1986-02-24 | 1990-05-25 | Sanofi Sa | Derives du facteur de liberation de l'hormone de croissance (grf) possedant des aminoacides modifies |
| FR2599038B1 (fr) * | 1986-05-26 | 1990-06-29 | Sanofi Sa | Procede de preparation de nonacosapeptides et peptides intermediaires |
| US5565606A (en) * | 1986-10-21 | 1996-10-15 | Hoechst Aktiengesellschaft | Synthesis of peptide aminoalkylamides and peptide hydrazides by the solid-phase method |
| DE3742633A1 (de) * | 1987-12-16 | 1989-06-29 | Hoechst Ag | Peptide mit beeinflussender wirkung auf die hypophyse von saeugern |
| IL86102A (en) * | 1987-05-11 | 1994-04-12 | Univ Tulane | Alkylated peptides that release growth hormone and their use |
| US5002931A (en) * | 1987-05-22 | 1991-03-26 | The Salk Institute For Biological Studies | GRF analogs VII |
| US4801456A (en) * | 1987-07-09 | 1989-01-31 | International Minerals & Chemical Corp. | Growth hormone-releasing factor analogs |
| USRE33699E (en) * | 1987-07-09 | 1991-09-24 | International Minerals & Chemical Corp. | Growth hormone-releasing factor analogs |
| ATE106895T1 (de) * | 1987-09-18 | 1994-06-15 | Hoffmann La Roche | Zyklische grf-analoga. |
| US4959352A (en) * | 1987-09-18 | 1990-09-25 | Hoffmann-La Roche Inc. | Cyclic growth hormone releasing factor analogs and method for the manufacture thereof |
| US5756458A (en) * | 1989-06-16 | 1998-05-26 | Pharmacia & Upjohn Company | Stabilized potent GRF analogs |
| DE69014115T2 (de) * | 1989-06-16 | 1995-05-24 | Upjohn Co | Stabilisierte, starke grf-analoga. |
| CN107936090B (zh) * | 2017-12-08 | 2021-09-24 | 陕西慧康生物科技有限责任公司 | 一种低成本合成ARK-Cu的方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ204456A (en) * | 1982-06-16 | 1987-05-29 | Salk Inst For Biological Studi | Synthetic pancreatic growth-hormone releasing factor |
| US4563352A (en) * | 1982-10-04 | 1986-01-07 | The Salk Institute For Biological Studies | Human pancreatic GRF |
| US4518586A (en) * | 1983-01-13 | 1985-05-21 | The Salk Institute For Biological Studies | GRF Analogs III |
| IL70530A (en) * | 1983-01-13 | 1986-09-30 | Salk Inst For Biological Studi | Synthetic peptides having growth hormone releasing factor activity and compositions containing them |
| DE3482387D1 (en) * | 1983-03-07 | 1990-07-05 | Hoffmann La Roche | Polypeptide. |
-
1984
- 1984-07-31 AU AU31334/84A patent/AU575843B2/en not_active Ceased
- 1984-08-01 NZ NZ209078A patent/NZ209078A/xx unknown
- 1984-08-06 DE DE8484109312T patent/DE3483931D1/de not_active Expired - Lifetime
- 1984-08-06 AT AT84109312T patent/ATE60062T1/de not_active IP Right Cessation
- 1984-08-06 EP EP84109312A patent/EP0136475B1/en not_active Expired - Lifetime
- 1984-08-08 CA CA000460517A patent/CA1268898A/en not_active Expired - Lifetime
- 1984-08-08 KR KR1019840004730A patent/KR850001772A/ko not_active Application Discontinuation
- 1984-08-09 PT PT79055A patent/PT79055B/pt not_active IP Right Cessation
- 1984-08-09 NO NO843195A patent/NO165804C/no unknown
- 1984-08-09 ZA ZA846191A patent/ZA846191B/xx unknown
- 1984-08-09 IL IL72630A patent/IL72630A/xx not_active IP Right Cessation
- 1984-08-09 FI FI843141A patent/FI86432C/sv not_active IP Right Cessation
- 1984-08-09 DK DK384084A patent/DK167361B1/da not_active IP Right Cessation
- 1984-08-09 ES ES535032A patent/ES8606400A1/es not_active Expired
- 1984-08-10 JP JP59166634A patent/JPH0684400B2/ja not_active Expired - Lifetime
-
1985
- 1985-07-31 ES ES545760A patent/ES8608540A1/es not_active Expired
-
1992
- 1992-03-09 SG SG286/92A patent/SG28692G/en unknown
- 1992-09-24 HK HK736/92A patent/HK73692A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES535032A0 (es) | 1986-05-01 |
| NZ209078A (en) | 1989-03-29 |
| ES8608540A1 (es) | 1986-07-16 |
| AU3133484A (en) | 1985-02-14 |
| PT79055A (en) | 1984-09-01 |
| FI843141A0 (fi) | 1984-08-09 |
| DK384084A (da) | 1985-02-11 |
| EP0136475A2 (en) | 1985-04-10 |
| ZA846191B (en) | 1985-03-27 |
| ES8606400A1 (es) | 1986-05-01 |
| ES545760A0 (es) | 1986-07-16 |
| NO843195L (no) | 1985-02-11 |
| EP0136475A3 (en) | 1987-03-11 |
| NO165804C (no) | 1991-04-10 |
| FI843141A (fi) | 1985-02-11 |
| JPS6057000A (ja) | 1985-04-02 |
| EP0136475B1 (en) | 1991-01-16 |
| FI86432C (sv) | 1992-08-25 |
| DK167361B1 (da) | 1993-10-18 |
| DE3483931D1 (de) | 1991-02-21 |
| DK384084D0 (da) | 1984-08-09 |
| AU575843B2 (en) | 1988-08-11 |
| PT79055B (en) | 1986-08-12 |
| JPH0684400B2 (ja) | 1994-10-26 |
| IL72630A (en) | 1988-11-30 |
| ATE60062T1 (de) | 1991-02-15 |
| NO165804B (no) | 1991-01-02 |
| CA1268898A (en) | 1990-05-08 |
| KR850001772A (ko) | 1985-04-01 |
| IL72630A0 (en) | 1984-11-30 |
| HK73692A (en) | 1992-10-02 |
| SG28692G (en) | 1992-05-15 |
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