CA1108123A - Psychopharmacological peptides suitable for therapeutic administration - Google Patents
Psychopharmacological peptides suitable for therapeutic administrationInfo
- Publication number
- CA1108123A CA1108123A CA307,217A CA307217A CA1108123A CA 1108123 A CA1108123 A CA 1108123A CA 307217 A CA307217 A CA 307217A CA 1108123 A CA1108123 A CA 1108123A
- Authority
- CA
- Canada
- Prior art keywords
- peptide
- dimer
- asp
- group
- amino
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
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- 238000002360 preparation method Methods 0.000 claims description 15
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- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- JBFYUZGYRGXSFL-UHFFFAOYSA-N imidazolide Chemical compound C1=C[N-]C=N1 JBFYUZGYRGXSFL-UHFFFAOYSA-N 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000012442 inert solvent 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
- HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 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
- 229950003188 isovaleryl diethylamide 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
- 239000007788 liquid Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000006984 memory degeneration Effects 0.000 description 1
- 208000023060 memory loss Diseases 0.000 description 1
- 229910001463 metal phosphate Inorganic materials 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- WHQSYGRFZMUQGQ-UHFFFAOYSA-N n,n-dimethylformamide;hydrate Chemical compound O.CN(C)C=O WHQSYGRFZMUQGQ-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- NMHMNPHRMNGLLB-UHFFFAOYSA-N phloretic acid Chemical compound OC(=O)CCC1=CC=C(O)C=C1 NMHMNPHRMNGLLB-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 235000007686 potassium Nutrition 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229960003975 potassium Drugs 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 230000002633 protecting effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- UQDJGEHQDNVPGU-UHFFFAOYSA-N serine phosphoethanolamine Chemical compound [NH3+]CCOP([O-])(=O)OCC([NH3+])C([O-])=O UQDJGEHQDNVPGU-UHFFFAOYSA-N 0.000 description 1
- 125000002072 seryl group Chemical group 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000004289 sodium hydrogen sulphite Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- HAEPBEMBOAIUPN-UHFFFAOYSA-L sodium tetrathionate Chemical compound O.O.[Na+].[Na+].[O-]S(=O)(=O)SSS([O-])(=O)=O HAEPBEMBOAIUPN-UHFFFAOYSA-L 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 238000004809 thin layer chromatography Methods 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
- 125000002114 valyl group Chemical group 0.000 description 1
- MJIBOYFUEIDNPI-HBNMXAOGSA-L zinc 5-[2,3-dihydroxy-5-[(2R,3R,4S,5R,6S)-4,5,6-tris[[3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoyl]oxy]-2-[[3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoyl]oxymethyl]oxan-3-yl]oxycarbonylphenoxy]carbonyl-3-hydroxybenzene-1,2-diolate Chemical compound [Zn++].Oc1cc(cc(O)c1O)C(=O)Oc1cc(cc(O)c1O)C(=O)OC[C@H]1O[C@@H](OC(=O)c2cc(O)c(O)c(OC(=O)c3cc(O)c(O)c(O)c3)c2)[C@H](OC(=O)c2cc(O)c(O)c(OC(=O)c3cc(O)c(O)c(O)c3)c2)[C@@H](OC(=O)c2cc(O)c(O)c(OC(=O)c3cc(O)c(O)c(O)c3)c2)[C@@H]1OC(=O)c1cc(O)c(O)c(OC(=O)c2cc(O)c([O-])c([O-])c2)c1 MJIBOYFUEIDNPI-HBNMXAOGSA-L 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S930/00—Peptide or protein sequence
- Y10S930/01—Peptide or protein sequence
- Y10S930/26—Containing cys-cys disulfide bridge between nonadjacent cysteine residues
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biophysics (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Biomedical Technology (AREA)
- Genetics & Genomics (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (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 (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL7707781A NL7707781A (nl) | 1977-07-13 | 1977-07-13 | Psychofarmacologische peptiden. |
| NL77.07781 | 1977-07-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1108123A true CA1108123A (en) | 1981-09-01 |
Family
ID=19828866
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA307,217A Expired CA1108123A (en) | 1977-07-13 | 1978-07-12 | Psychopharmacological peptides suitable for therapeutic administration |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US4203975A (en]) |
| JP (1) | JPS5419934A (en]) |
| AU (1) | AU519567B2 (en]) |
| BE (1) | BE868953A (en]) |
| CA (1) | CA1108123A (en]) |
| DE (1) | DE2830489A1 (en]) |
| DK (1) | DK149454C (en]) |
| ES (1) | ES471672A1 (en]) |
| FI (1) | FI67367C (en]) |
| FR (1) | FR2397395A1 (en]) |
| GB (1) | GB2001076B (en]) |
| IE (1) | IE47547B1 (en]) |
| LU (1) | LU79960A1 (en]) |
| NL (1) | NL7707781A (en]) |
| SE (1) | SE443789B (en]) |
| ZA (1) | ZA783713B (en]) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU530062B2 (en) * | 1979-02-21 | 1983-06-30 | Akzo N.V. | Psycho-pharmacological peptides |
| JPH0195597U (en]) * | 1987-12-17 | 1989-06-23 | ||
| US5796673A (en) | 1994-10-06 | 1998-08-18 | Mosaid Technologies Incorporated | Delay locked loop implementation in a synchronous dynamic random access memory |
| WO2014188911A1 (ja) * | 2013-05-22 | 2014-11-27 | 独立行政法人産業技術総合研究所 | 光分解性架橋剤、光分解性ゲル、細胞培養器具、細胞配列・分別装置、細胞配列方法、細胞分別方法、組織体形成方法および組織体 |
| CA2924286C (en) * | 2013-09-17 | 2022-06-21 | Obi Pharma, Inc. | Compositions of a carbohydrate vaccine for inducing immune responses and uses thereof in cancer treatment |
| US10980894B2 (en) | 2016-03-29 | 2021-04-20 | Obi Pharma, Inc. | Antibodies, pharmaceutical compositions and methods |
| CN109379889A (zh) | 2016-04-22 | 2019-02-22 | 台湾浩鼎生技股份有限公司 | 通过经由globo系列抗原的免疫激活或免疫调节的癌症免疫疗法 |
| CA3032049C (en) | 2016-07-27 | 2023-11-07 | Obi Pharma, Inc. | Immunogenic/therapeutic glycan compositions and uses thereof |
| CN110062767B (zh) | 2016-07-29 | 2023-07-11 | 台湾浩鼎生技股份有限公司 | 人抗体、药物组合物和方法 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3803119A (en) * | 1970-04-20 | 1974-04-09 | Daiichi Seiyaku Co | Pantetheine-s-sulfonic acid derivatives and salts thereof |
| NL175293C (nl) * | 1972-02-08 | 1984-10-16 | Akzo Nv | Werkwijze ter bereiding of vervaardiging van een farmaceutisch preparaat met psychofarmacologische werking, alsmede werkwijze voor het bereiden van een van vasopressine afgeleid peptide. |
-
1977
- 1977-07-05 AU AU37780/78A patent/AU519567B2/en not_active Expired
- 1977-07-13 NL NL7707781A patent/NL7707781A/xx not_active Application Discontinuation
-
1978
- 1978-06-28 ZA ZA00783713A patent/ZA783713B/xx unknown
- 1978-06-28 IE IE1291/78A patent/IE47547B1/en unknown
- 1978-06-30 US US05/921,067 patent/US4203975A/en not_active Expired - Lifetime
- 1978-07-07 GB GB7829197A patent/GB2001076B/en not_active Expired
- 1978-07-07 FI FI782195A patent/FI67367C/fi not_active IP Right Cessation
- 1978-07-11 DE DE19782830489 patent/DE2830489A1/de not_active Withdrawn
- 1978-07-12 SE SE7807759A patent/SE443789B/sv not_active IP Right Cessation
- 1978-07-12 ES ES471672A patent/ES471672A1/es not_active Expired
- 1978-07-12 BE BE189247A patent/BE868953A/xx unknown
- 1978-07-12 LU LU79960A patent/LU79960A1/xx unknown
- 1978-07-12 CA CA307,217A patent/CA1108123A/en not_active Expired
- 1978-07-12 JP JP8500278A patent/JPS5419934A/ja active Granted
- 1978-07-13 DK DK314978A patent/DK149454C/da not_active IP Right Cessation
- 1978-07-13 FR FR7821087A patent/FR2397395A1/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| FR2397395B1 (en]) | 1981-01-16 |
| FI782195A7 (fi) | 1979-01-14 |
| DE2830489A1 (de) | 1979-01-25 |
| SE443789B (sv) | 1986-03-10 |
| NL7707781A (nl) | 1979-01-16 |
| FI67367B (fi) | 1984-11-30 |
| ZA783713B (en) | 1979-07-25 |
| US4203975A (en) | 1980-05-20 |
| IE47547B1 (en) | 1984-04-18 |
| JPS6220200B2 (en]) | 1987-05-06 |
| SE7807759L (sv) | 1979-01-14 |
| JPS5419934A (en) | 1979-02-15 |
| AU519567B2 (en) | 1981-12-10 |
| ES471672A1 (es) | 1979-09-16 |
| IE781291L (en) | 1979-01-13 |
| FR2397395A1 (fr) | 1979-02-09 |
| GB2001076A (en) | 1979-01-24 |
| GB2001076B (en) | 1982-01-27 |
| DK149454C (da) | 1986-11-17 |
| DK149454B (da) | 1986-06-16 |
| FI67367C (fi) | 1985-03-11 |
| LU79960A1 (fr) | 1979-04-09 |
| AU3778078A (en) | 1980-01-10 |
| DK314978A (da) | 1979-01-14 |
| BE868953A (fr) | 1979-01-12 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |