HU176260B - Process for producing encephalin-analogue polypeptides - Google Patents
Process for producing encephalin-analogue polypeptides Download PDFInfo
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- HU176260B HU176260B HU77IE774A HUIE000774A HU176260B HU 176260 B HU176260 B HU 176260B HU 77IE774 A HU77IE774 A HU 77IE774A HU IE000774 A HUIE000774 A HU IE000774A HU 176260 B HU176260 B HU 176260B
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- 108010049589 leucyl-leucyl-leucine Proteins 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- HGVNLOSOAISYIT-KBPBESRZSA-N methyl (2s)-2-[[(2s)-2-amino-3-phenylpropanoyl]amino]-4-methylpentanoate Chemical compound COC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CC1=CC=CC=C1 HGVNLOSOAISYIT-KBPBESRZSA-N 0.000 description 1
- XELZGAJCZANUQH-UHFFFAOYSA-N methyl 1-acetylthieno[3,2-c]pyrazole-5-carboxylate Chemical compound CC(=O)N1N=CC2=C1C=C(C(=O)OC)S2 XELZGAJCZANUQH-UHFFFAOYSA-N 0.000 description 1
- ZGONRPXUNVTWTA-UHFFFAOYSA-N methyl 2-isocyanatoacetate Chemical compound COC(=O)CN=C=O ZGONRPXUNVTWTA-UHFFFAOYSA-N 0.000 description 1
- QVDXUKJJGUSGLS-LURJTMIESA-N methyl L-leucinate Chemical compound COC(=O)[C@@H](N)CC(C)C QVDXUKJJGUSGLS-LURJTMIESA-N 0.000 description 1
- 230000011987 methylation Effects 0.000 description 1
- 238000007069 methylation reaction Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 229960005181 morphine Drugs 0.000 description 1
- TUFOTJYGTCIWBE-UHFFFAOYSA-N n,n-dimethylformamide;4-methylbenzenesulfonic acid Chemical compound CN(C)C=O.CC1=CC=C(S(O)(=O)=O)C=C1 TUFOTJYGTCIWBE-UHFFFAOYSA-N 0.000 description 1
- 229960002009 naproxen Drugs 0.000 description 1
- CMWTZPSULFXXJA-VIFPVBQESA-N naproxen Chemical compound C1=C([C@H](C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-VIFPVBQESA-N 0.000 description 1
- 239000003176 neuroleptic agent Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 229960005489 paracetamol Drugs 0.000 description 1
- 238000005897 peptide coupling reaction Methods 0.000 description 1
- 238000010647 peptide synthesis reaction Methods 0.000 description 1
- 229960000482 pethidine Drugs 0.000 description 1
- 229960003893 phenacetin Drugs 0.000 description 1
- DDBREPKUVSBGFI-UHFFFAOYSA-N phenobarbital Chemical compound C=1C=CC=CC=1C1(CC)C(=O)NC(=O)NC1=O DDBREPKUVSBGFI-UHFFFAOYSA-N 0.000 description 1
- 229960002695 phenobarbital Drugs 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229910003446 platinum oxide Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- FNNIAKKPBXJGNJ-UHFFFAOYSA-N pyrazolidine-1-carboxylic acid Chemical compound OC(=O)N1CCCN1 FNNIAKKPBXJGNJ-UHFFFAOYSA-N 0.000 description 1
- 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 239000000932 sedative agent Substances 0.000 description 1
- 230000001624 sedative effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000011477 surgical intervention Methods 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- JDFUJAMTCCQARF-UHFFFAOYSA-N tatb Chemical compound NC1=C([N+]([O-])=O)C(N)=C([N+]([O-])=O)C(N)=C1[N+]([O-])=O JDFUJAMTCCQARF-UHFFFAOYSA-N 0.000 description 1
- IOGXOCVLYRDXLW-UHFFFAOYSA-N tert-butyl nitrite Chemical compound CC(C)(C)ON=O IOGXOCVLYRDXLW-UHFFFAOYSA-N 0.000 description 1
- 239000012414 tert-butyl nitrite Substances 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical class CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- ORQXBVXKBGUSBA-QMMMGPOBSA-N β-cyclohexyl-alanine Chemical class OC(=O)[C@@H](N)CC1CCCCC1 ORQXBVXKBGUSBA-QMMMGPOBSA-N 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
- C07K14/665—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans derived from pro-opiomelanocortin, pro-enkephalin or pro-dynorphin
- C07K14/70—Enkephalins
- C07K14/702—Enkephalins with at least 1 amino acid in D-form
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Biochemistry (AREA)
- Genetics & Genomics (AREA)
- Gastroenterology & Hepatology (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Zoology (AREA)
- Toxicology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biophysics (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB14362/76A GB1523812A (en) | 1976-04-08 | 1976-04-08 | Polypeptide |
| GB2106376 | 1976-05-21 | ||
| GB2205576 | 1976-05-27 | ||
| GB2929876 | 1976-07-14 | ||
| GB4483776 | 1976-10-28 | ||
| GB4483876 | 1976-10-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HU176260B true HU176260B (en) | 1981-01-28 |
Family
ID=27546664
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU77IE774A HU176260B (en) | 1976-04-08 | 1977-04-06 | Process for producing encephalin-analogue polypeptides |
Country Status (13)
| Country | Link |
|---|---|
| JP (1) | JPS52139039A (cs) |
| AU (1) | AU510760B2 (cs) |
| CS (1) | CS202568B2 (cs) |
| DD (1) | DD130348A5 (cs) |
| DE (1) | DE2715803A1 (cs) |
| DK (1) | DK158077A (cs) |
| FI (1) | FI771049A7 (cs) |
| FR (1) | FR2347336A1 (cs) |
| HU (1) | HU176260B (cs) |
| NZ (1) | NZ183712A (cs) |
| PL (1) | PL106210B1 (cs) |
| SE (1) | SE7704043L (cs) |
| SU (1) | SU904518A3 (cs) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2730851A1 (de) * | 1976-07-19 | 1978-01-26 | Sandoz Ag | Neu polypeptidderivate, ihre herstellung und verwendung |
| FR2359817A1 (fr) * | 1976-07-27 | 1978-02-24 | Reckitt & Colmann Prod Ltd | Nouveaux peptides, leur procede de preparation et composition therapeutique les contenant |
| NO773013L (no) * | 1976-09-01 | 1978-03-02 | David Howard Coy | Fremgangsmaate ved fremstilling av methionin-enkefalin-derivater |
| HU178001B (en) * | 1976-09-16 | 1982-02-28 | Gyogyszekutato Intezet | Process for preparing new pentapeptides with morphine-like activity and derivatives thereof |
| US4259234A (en) * | 1976-09-27 | 1981-03-31 | Eli Lilly And Company | Analgesic compounds |
| CH637626A5 (en) * | 1976-11-23 | 1983-08-15 | Wellcome Found | Process for the preparation of peptides |
| DE2862327D1 (en) * | 1977-07-22 | 1983-11-10 | Wellcome Found | Pentapeptide-n-alkylamides and their acid addition salts, methods for preparation of these compounds and pharmaceutical formulations containing them |
| GB1604850A (en) * | 1977-11-24 | 1981-12-16 | Wellcome Found | Biologically active peptides |
| US4178371A (en) * | 1977-12-15 | 1979-12-11 | Reckitt & Colman Products Limited | Tetrapeptide derivatives |
| FR2424253A1 (fr) * | 1978-04-27 | 1979-11-23 | Brun Lab Sa Le | Nouveaux derives de peptides analogues des enkephalines, leur procede de preparation et leur application therapeutique |
| US4278596A (en) * | 1978-08-08 | 1981-07-14 | American Home Products Corporation | Analgesic pentapeptides |
| CA1175810A (en) * | 1979-03-30 | 1984-10-09 | Frank A. Momany | Synthetic peptides having pituitary growth hormone releasing activity |
| DE2933947A1 (de) * | 1979-08-22 | 1981-03-12 | Hoechst Ag, 6000 Frankfurt | Neue peptidamide und verfahren zu ihrer herstellung. |
| JPS5692846A (en) * | 1979-12-27 | 1981-07-27 | Takeda Chem Ind Ltd | Tetrapeptide derivative and its preparation |
| FR2488253A1 (fr) * | 1980-08-08 | 1982-02-12 | Roques Bernard | Nouveaux peptides et leur application en therapeutique |
| US4495178A (en) * | 1983-10-06 | 1985-01-22 | G. D. Searle & Co. | Enkephalin analogs |
| JP2604268B2 (ja) * | 1990-04-09 | 1997-04-30 | 富士写真フイルム株式会社 | ペプチド誘導体両親媒性化合物、その中間体、ペプチド誘導体両親媒性化合物を用いたリポソームおよび薄膜 |
| US20070155803A1 (en) * | 2003-05-30 | 2007-07-05 | Prozymex A/S | Protease inhibitors |
| KR102016961B1 (ko) * | 2011-02-09 | 2019-09-02 | 노보자임스 에이/에스 | 피부질환 치료용 펩티드 |
| JP2013043885A (ja) * | 2011-08-26 | 2013-03-04 | Kansai Bunri Sogo Gakuen | デヒドロアミノ酸含有グリセロール誘導体 |
| CZ2012313A3 (cs) * | 2012-05-11 | 2013-05-29 | Zetor Tractors A.S. | Usporádání reverzacní dvoutoké prevodovky, zejména pro motorová vozidla a stavební stroje, s dvema vetvemi toku výkonu |
| EP3710467A4 (en) * | 2017-11-17 | 2021-08-04 | Cytogel Pharma, LLC | MU-OPIOID RECEPTOR POLYMERIC AGONISTS |
-
1977
- 1977-03-28 NZ NZ183712A patent/NZ183712A/xx unknown
- 1977-03-31 AU AU23819/77A patent/AU510760B2/en not_active Expired
- 1977-04-04 FI FI771049A patent/FI771049A7/fi not_active Application Discontinuation
- 1977-04-06 SE SE7704043A patent/SE7704043L/ not_active Application Discontinuation
- 1977-04-06 CS CS772289A patent/CS202568B2/cs unknown
- 1977-04-06 HU HU77IE774A patent/HU176260B/hu unknown
- 1977-04-06 DK DK158077A patent/DK158077A/da not_active IP Right Cessation
- 1977-04-07 FR FR7710668A patent/FR2347336A1/fr active Granted
- 1977-04-07 DD DD7700198316A patent/DD130348A5/xx unknown
- 1977-04-07 DE DE19772715803 patent/DE2715803A1/de not_active Withdrawn
- 1977-04-08 JP JP4023077A patent/JPS52139039A/ja active Pending
- 1977-04-08 PL PL1977197302A patent/PL106210B1/pl unknown
- 1977-04-08 SU SU772470259A patent/SU904518A3/ru active
Also Published As
| Publication number | Publication date |
|---|---|
| FR2347336A1 (fr) | 1977-11-04 |
| SU904518A3 (ru) | 1982-02-07 |
| CS202568B2 (en) | 1981-01-30 |
| JPS52139039A (en) | 1977-11-19 |
| SE7704043L (sv) | 1977-10-09 |
| FI771049A7 (cs) | 1977-10-09 |
| DD130348A5 (de) | 1978-03-22 |
| DK158077A (da) | 1977-10-09 |
| PL106210B1 (pl) | 1979-12-31 |
| NZ183712A (en) | 1979-10-25 |
| PL197302A1 (pl) | 1978-02-13 |
| DE2715803A1 (de) | 1977-10-27 |
| AU2381977A (en) | 1978-10-05 |
| AU510760B2 (en) | 1980-07-10 |
| FR2347336B1 (cs) | 1980-07-18 |
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