WO2002062826A1 - Procede de fabrication des peptides - Google Patents
Procede de fabrication des peptides Download PDFInfo
- Publication number
- WO2002062826A1 WO2002062826A1 PCT/RU2002/000021 RU0200021W WO02062826A1 WO 2002062826 A1 WO2002062826 A1 WO 2002062826A1 RU 0200021 W RU0200021 W RU 0200021W WO 02062826 A1 WO02062826 A1 WO 02062826A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- sinτeza
- solution
- ποlucheniya
- peptides
- ρasτvορa
- 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.)
- Ceased
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/02—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length in solution
Definitions
- the invention relates to biology, and specifically, to the methods of receiving the drugs.
- Methods and devices of the invention can be used in biotechnology, medicine, pharmaceuticals, medical treatment, and medical treatment.
- E ⁇ ⁇ zv ⁇ lyae ⁇ on account s ⁇ zdaniya usl ⁇ vy for ⁇ vysheniya a ⁇ ivn ⁇ s ⁇ i and ⁇ yad ⁇ chn ⁇ g ⁇ movement i ⁇ n ⁇ v is ⁇ dny ⁇ ⁇ m ⁇ nen ⁇ v us ⁇ ani ⁇ available izves ⁇ n ⁇ m s ⁇ s ⁇ be ned ⁇ s ⁇ a ⁇ i, e ⁇ e ⁇ ivn ⁇ is ⁇ lz ⁇ va ⁇ ene ⁇ giyu sin ⁇ eza, snizi ⁇ v ⁇ emya sin ⁇ eza (uvelichi ⁇ ⁇ izv ⁇ di ⁇ eln ⁇ s ⁇ ) ⁇ ch ⁇ i ⁇ ln ⁇ s ⁇ yu us ⁇ ani ⁇ ⁇ tsess ⁇ chis ⁇ i ⁇ luchenn ⁇ g ⁇ ⁇ du ⁇ a.
- na ⁇ ime ⁇ on account is ⁇ lz ⁇ vaniya ba ⁇ a ⁇ eyn ⁇ g ⁇ ⁇ m ⁇ le ⁇ a ele ⁇ d ⁇ v and ⁇ vysheniya chis ⁇ y ⁇ luchaem ⁇ g ⁇ ⁇ du ⁇ a ele ⁇ iches ⁇ e ⁇ le s ⁇ zdayu ⁇ with ⁇ m ⁇ schyu ele ⁇ d ⁇ v of bi ⁇ l ⁇ giches ⁇ i ine ⁇ n ⁇ g ⁇ nemagni ⁇ n ⁇ g ⁇ ma ⁇ e ⁇ iala.
- ⁇ ⁇ aches ⁇ ve is ⁇ dny ⁇ ⁇ du ⁇ v is ⁇ lz ⁇ vali 10 ml e ⁇ vim ⁇ lya ⁇ n ⁇ g ⁇ ⁇ as ⁇ v ⁇ a, s ⁇ de ⁇ zhascheg ⁇ ⁇ 2u "5 ⁇ glu ⁇ amin ⁇ v ⁇ y ⁇ isl ⁇ y ( ⁇ i) a ⁇ ginina ( ⁇ g ⁇ ) and ⁇ i ⁇ ana ( ⁇ ga) in dis ⁇ illi ⁇ vann ⁇ y v ⁇ de.
- the temperature of the unit is 30 ° ⁇ .
- the synthesis ended with a change in the physical and chemical parameters, which depends on a change in the concentration of the final synthesis product. This time was 15 minutes. Then, the solution was cooled in 8 minutes to a temperature of 10 ° ⁇ . The isolation of the end product of the synthesis was carried out in a similar manner to Example 1. The results of the research showed that the synthesis of the product was performed, responsible for the standard (type 01i- ⁇ g ⁇ - ⁇ ga obtained by a well-known chemical process). The end of the product - 60% of the quantity of dry matter of the original components, the total amount of the life of the process - 38 min. Intended use.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Analytical Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| RU2001103251 | 2001-02-07 | ||
| RU2001103251/04A RU2001103251A (ru) | 2001-02-07 | Способ получения пептидов |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2002062826A1 true WO2002062826A1 (fr) | 2002-08-15 |
Family
ID=20245638
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/RU2002/000021 Ceased WO2002062826A1 (fr) | 2001-02-07 | 2002-01-30 | Procede de fabrication des peptides |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2002062826A1 (fr) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007084786A1 (fr) | 2006-01-20 | 2007-07-26 | Novartis Ag | Derives de pyrimidine utilises en tant qu’inhibiteurs de kinase pi-3 |
| WO2009080694A1 (fr) | 2007-12-20 | 2009-07-02 | Novartis Ag | Dérivés de thiazole utilisés comme inhibiteur de la pi 3 kinase |
| WO2011000905A1 (fr) | 2009-07-02 | 2011-01-06 | Novartis Ag | 2-carboxamide cycloamino urées substituées |
| EP2277595A2 (fr) | 2004-06-24 | 2011-01-26 | Novartis Vaccines and Diagnostics, Inc. | Composés pour potentialiser l'immunité |
| US7932262B2 (en) | 2006-04-06 | 2011-04-26 | Novartis Ag | Quinazolines for PDK1 inhibition |
| WO2012016970A1 (fr) | 2010-08-02 | 2012-02-09 | Novartis Ag | Forme cristalline de 1-(4-méthyl-5-[2-(2,2,2-trifluoro-1,1-diméthyléthyl)-pyridine-4-yl]-thiazol-2-yl)-amide du 2-amide de l'acide (s)-pyrrolidine-1,2-dicarboxylique et son utilisation comme inhibiteur de pi3k |
| WO2012104776A1 (fr) | 2011-01-31 | 2012-08-09 | Novartis Ag | Dérivés hétérocycliques inédits |
| WO2013061305A1 (fr) | 2011-10-28 | 2013-05-02 | Novartis Ag | Nouveaux dérivés de purine et utilisation de ceux-ci dans le traitement d'une maladie |
| WO2013173283A1 (fr) | 2012-05-16 | 2013-11-21 | Novartis Ag | Régime posologique pour un inhibiteur de pi-3 kinase |
| WO2017077445A1 (fr) | 2015-11-02 | 2017-05-11 | Novartis Ag | Schéma posologique pour un inhibiteur de la phosphatidylinositol 3-kinase |
| WO2018060833A1 (fr) | 2016-09-27 | 2018-04-05 | Novartis Ag | Schéma posologique pour l'alpelisib, un inhibiteur de la phosphatidylinositol 3-kinase spécifique de l'isoforme alpha |
| EP4000619A1 (fr) | 2013-12-06 | 2022-05-25 | Novartis AG | Schéma posologique d'un inhibiteur de la phosphatidylinositol 3-kinase sélectif de l'isoforme alpha |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU586165A1 (ru) * | 1976-07-14 | 1977-12-30 | Латвийский Филиал Всесоюзного Ордена Трудового Красного Знамени Научно-Исследовательского Института Химических Реакторов И Особо Чистых Химических Веществ "Иреа" | Способ получени окситоцина и дезаминоокситоцина |
| FR2536766A1 (fr) * | 1982-11-25 | 1984-06-01 | Sigma Tau Ind Farmaceuti | Procede et cellule electrolytiques pour la preparation de composes organiques |
| EP0201925A1 (fr) * | 1985-05-15 | 1986-11-20 | K.K. Musashino Kagaku Kenkyusho | Procédé pour la préparation d'un amino-acide libre à partir de son sel de métal alcalin |
| RU2100368C1 (ru) * | 1995-10-09 | 1997-12-27 | Вадим Викторович Новиков | Способ получения пептидов и устройство для его осуществления |
-
2002
- 2002-01-30 WO PCT/RU2002/000021 patent/WO2002062826A1/fr not_active Ceased
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU586165A1 (ru) * | 1976-07-14 | 1977-12-30 | Латвийский Филиал Всесоюзного Ордена Трудового Красного Знамени Научно-Исследовательского Института Химических Реакторов И Особо Чистых Химических Веществ "Иреа" | Способ получени окситоцина и дезаминоокситоцина |
| FR2536766A1 (fr) * | 1982-11-25 | 1984-06-01 | Sigma Tau Ind Farmaceuti | Procede et cellule electrolytiques pour la preparation de composes organiques |
| EP0201925A1 (fr) * | 1985-05-15 | 1986-11-20 | K.K. Musashino Kagaku Kenkyusho | Procédé pour la préparation d'un amino-acide libre à partir de son sel de métal alcalin |
| RU2100368C1 (ru) * | 1995-10-09 | 1997-12-27 | Вадим Викторович Новиков | Способ получения пептидов и устройство для его осуществления |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2277595A2 (fr) | 2004-06-24 | 2011-01-26 | Novartis Vaccines and Diagnostics, Inc. | Composés pour potentialiser l'immunité |
| WO2007084786A1 (fr) | 2006-01-20 | 2007-07-26 | Novartis Ag | Derives de pyrimidine utilises en tant qu’inhibiteurs de kinase pi-3 |
| EP2261223A1 (fr) | 2006-01-20 | 2010-12-15 | Novartis AG | Derives de pyrimidine utilises en tant qu inhibiteurs de kinase pi-3 |
| US7932262B2 (en) | 2006-04-06 | 2011-04-26 | Novartis Ag | Quinazolines for PDK1 inhibition |
| WO2009080694A1 (fr) | 2007-12-20 | 2009-07-02 | Novartis Ag | Dérivés de thiazole utilisés comme inhibiteur de la pi 3 kinase |
| WO2011000905A1 (fr) | 2009-07-02 | 2011-01-06 | Novartis Ag | 2-carboxamide cycloamino urées substituées |
| WO2012016970A1 (fr) | 2010-08-02 | 2012-02-09 | Novartis Ag | Forme cristalline de 1-(4-méthyl-5-[2-(2,2,2-trifluoro-1,1-diméthyléthyl)-pyridine-4-yl]-thiazol-2-yl)-amide du 2-amide de l'acide (s)-pyrrolidine-1,2-dicarboxylique et son utilisation comme inhibiteur de pi3k |
| WO2012104776A1 (fr) | 2011-01-31 | 2012-08-09 | Novartis Ag | Dérivés hétérocycliques inédits |
| WO2013061305A1 (fr) | 2011-10-28 | 2013-05-02 | Novartis Ag | Nouveaux dérivés de purine et utilisation de ceux-ci dans le traitement d'une maladie |
| WO2013173283A1 (fr) | 2012-05-16 | 2013-11-21 | Novartis Ag | Régime posologique pour un inhibiteur de pi-3 kinase |
| EP4000619A1 (fr) | 2013-12-06 | 2022-05-25 | Novartis AG | Schéma posologique d'un inhibiteur de la phosphatidylinositol 3-kinase sélectif de l'isoforme alpha |
| WO2017077445A1 (fr) | 2015-11-02 | 2017-05-11 | Novartis Ag | Schéma posologique pour un inhibiteur de la phosphatidylinositol 3-kinase |
| WO2018060833A1 (fr) | 2016-09-27 | 2018-04-05 | Novartis Ag | Schéma posologique pour l'alpelisib, un inhibiteur de la phosphatidylinositol 3-kinase spécifique de l'isoforme alpha |
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