SU474137A3 - Способ получени модифицированных поли- -лизинов - Google Patents
Способ получени модифицированных поли- -лизиновInfo
- Publication number
- SU474137A3 SU474137A3 SU1914705A SU1914705A SU474137A3 SU 474137 A3 SU474137 A3 SU 474137A3 SU 1914705 A SU1914705 A SU 1914705A SU 1914705 A SU1914705 A SU 1914705A SU 474137 A3 SU474137 A3 SU 474137A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- added
- lysine
- hours
- solution
- units
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
- 239000000243 solution Substances 0.000 description 19
- 229920000642 polymer Polymers 0.000 description 16
- 239000012153 distilled water Substances 0.000 description 14
- 239000004472 Lysine Substances 0.000 description 10
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 9
- 229920001577 copolymer Polymers 0.000 description 9
- 239000012528 membrane Substances 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 9
- 235000011121 sodium hydroxide Nutrition 0.000 description 9
- -1 carboxyl - 2ethyl Chemical group 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 229920000729 poly(L-lysine) polymer Polymers 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000001913 cellulose Substances 0.000 description 5
- 229920002678 cellulose Polymers 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 238000000108 ultra-filtration Methods 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 235000019766 L-Lysine Nutrition 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 229910021538 borax Inorganic materials 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 238000000502 dialysis Methods 0.000 description 3
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 3
- 238000004108 freeze drying Methods 0.000 description 3
- GKKCIDNWFBPDBW-UHFFFAOYSA-M potassium cyanate Chemical compound [K]OC#N GKKCIDNWFBPDBW-UHFFFAOYSA-M 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- 235000010339 sodium tetraborate Nutrition 0.000 description 3
- 239000004328 sodium tetraborate Substances 0.000 description 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 2
- 235000018977 lysine Nutrition 0.000 description 2
- 150000004682 monohydrates Chemical class 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920000656 polylysine Polymers 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- RAJUSMULYYBNSJ-UHFFFAOYSA-N prop-1-ene-1-sulfonic acid Chemical group CC=CS(O)(=O)=O RAJUSMULYYBNSJ-UHFFFAOYSA-N 0.000 description 2
- 235000010288 sodium nitrite Nutrition 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- RVLHNHNPUBWSEE-UHFFFAOYSA-N 2,2-dioxooxathiolan-5-one Chemical compound O=C1CCS(=O)(=O)O1 RVLHNHNPUBWSEE-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 150000008545 L-lysines Chemical class 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- GQWMDCYHYQUTAO-UHFFFAOYSA-M sodium;3-ethoxy-3-oxopropane-1-sulfonate Chemical compound [Na+].CCOC(=O)CCS([O-])(=O)=O GQWMDCYHYQUTAO-UHFFFAOYSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- GINSRDSEEGBTJO-UHFFFAOYSA-N thietane 1-oxide Chemical compound O=S1CCC1 GINSRDSEEGBTJO-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- 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
- C07K1/006—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length of peptides containing derivatised side chain amino acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/001—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof by chemical synthesis
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
- C08G69/08—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from amino-carboxylic acids
- C08G69/10—Alpha-amino-carboxylic acids
-
- 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
- Y10S930/29—Polyamino acid or polypeptide with an uninterrupted series of peptide repeating units
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biophysics (AREA)
- Analytical Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Gastroenterology & Hepatology (AREA)
- Polyamides (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7215696A FR2182667B1 (cg-RX-API-DMAC7.html) | 1972-05-03 | 1972-05-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU474137A3 true SU474137A3 (ru) | 1975-06-14 |
Family
ID=9097906
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1914705A SU474137A3 (ru) | 1972-05-03 | 1973-04-28 | Способ получени модифицированных поли- -лизинов |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US3907755A (cg-RX-API-DMAC7.html) |
| JP (1) | JPS4948785A (cg-RX-API-DMAC7.html) |
| BE (1) | BE798994A (cg-RX-API-DMAC7.html) |
| CA (1) | CA994759A (cg-RX-API-DMAC7.html) |
| DE (1) | DE2322310A1 (cg-RX-API-DMAC7.html) |
| FR (1) | FR2182667B1 (cg-RX-API-DMAC7.html) |
| GB (1) | GB1402397A (cg-RX-API-DMAC7.html) |
| IL (1) | IL42178A (cg-RX-API-DMAC7.html) |
| NL (1) | NL7305784A (cg-RX-API-DMAC7.html) |
| SE (1) | SE401189B (cg-RX-API-DMAC7.html) |
| SU (1) | SU474137A3 (cg-RX-API-DMAC7.html) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1081627B (it) * | 1977-07-27 | 1985-05-21 | Snam Progetti | Procedimento per la preparazione di materiali biocompatibili e manufatti cosi' ottenuti |
| US4171916A (en) * | 1977-11-18 | 1979-10-23 | Ishikawajima-Harima Heavy Industries Co., Ltd. | Apparatus and method for measuring the consistency of a pulp suspension |
| US4297477A (en) * | 1979-01-05 | 1981-10-27 | Toray Industries, Incorporated | Polyamide having --NH--(CH2)4 --CH(NRR')--CO--units |
| FR2461724A1 (fr) * | 1979-07-20 | 1981-02-06 | Christine Fougnot | Polymeres substitues par des groupes leur conferant des proprietes anti-coagulantes et leur procede de preparation, objets constitues par et/ou comprenant lesdits polymeres et leurs procedes de fabrication, application desdits objets en chirurgie et en medecine, et compositions pharmaceutiques contenant lesdits polymeres substitues |
| FR2489343A1 (fr) * | 1980-08-29 | 1982-03-05 | Weck Alain De | Nouveaux polymeres de lysine utilisables comme supports pour la preparation de produits de diagnostic et produits obtenus |
| CS252559B1 (en) * | 1985-03-22 | 1987-09-17 | Frantisek Rypacek | Polymer stabilizer of emulsion type water in oil |
| JP2807287B2 (ja) * | 1989-10-13 | 1998-10-08 | 株式会社医学生物学研究所 | ペプチドおよびその用途 |
| AUPO104396A0 (en) * | 1996-07-17 | 1996-08-08 | Biomolecular Research Institute Limited | Antiviral linear polymers |
| AUPO104496A0 (en) * | 1996-07-17 | 1996-08-08 | Biomolecular Research Institute Limited | Angiogenic inhibitory compounds |
| FR2781485B1 (fr) | 1998-07-21 | 2003-08-08 | Denis Barritault | Polymeres biocompatibles leur procede de preparation et les compositions les contenant |
| DE102005056592A1 (de) * | 2005-11-25 | 2007-05-31 | Basf Ag | Herstellung und Verwendung von hochfunktionellen, hoch-oder hyperverzweigten Polylysinen |
| AR074881A1 (es) * | 2008-12-24 | 2011-02-16 | Synthon Bv | Un proceso para purificar una mezcla de polimeros |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB721067A (en) * | 1952-10-09 | 1954-12-29 | Ilford Ltd | Improvements in or relating to the production of silver halide photographic emulsions |
| GB834227A (en) * | 1955-01-22 | 1960-05-04 | Fred Mayer | Poly-n-quaternary ammonium electrolytes and í¡í¡ thereof |
| GB822192A (en) * | 1956-08-29 | 1959-10-21 | Ilford Ltd | Improvements in or relating to the production of photographic emulsions |
| NL131219C (cg-RX-API-DMAC7.html) * | 1966-06-28 | |||
| GB1221469A (en) * | 1967-11-22 | 1971-02-03 | Kyowa Hakko Kogyo Kk | Glutamic acid polymer coatings |
| GB1218879A (en) * | 1968-04-03 | 1971-01-13 | Kyowa Hakko Kogyo Kk | Polyamino acid solution |
-
1972
- 1972-05-03 FR FR7215696A patent/FR2182667B1/fr not_active Expired
-
1973
- 1973-04-25 NL NL7305784A patent/NL7305784A/xx not_active Application Discontinuation
- 1973-04-28 SU SU1914705A patent/SU474137A3/ru active
- 1973-04-30 US US355407A patent/US3907755A/en not_active Expired - Lifetime
- 1973-05-01 JP JP48047687A patent/JPS4948785A/ja active Pending
- 1973-05-02 SE SE7306120A patent/SE401189B/xx unknown
- 1973-05-02 IL IL42178A patent/IL42178A/en unknown
- 1973-05-02 GB GB2078273A patent/GB1402397A/en not_active Expired
- 1973-05-02 BE BE130656A patent/BE798994A/xx unknown
- 1973-05-02 CA CA170,277A patent/CA994759A/fr not_active Expired
- 1973-05-03 DE DE2322310A patent/DE2322310A1/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| NL7305784A (cg-RX-API-DMAC7.html) | 1973-11-06 |
| GB1402397A (en) | 1975-08-06 |
| BE798994A (fr) | 1973-11-05 |
| JPS4948785A (cg-RX-API-DMAC7.html) | 1974-05-11 |
| SE401189B (sv) | 1978-04-24 |
| IL42178A0 (en) | 1973-07-30 |
| DE2322310A1 (de) | 1973-11-22 |
| FR2182667B1 (cg-RX-API-DMAC7.html) | 1978-03-03 |
| IL42178A (en) | 1976-06-30 |
| CA994759A (fr) | 1976-08-10 |
| US3907755A (en) | 1975-09-23 |
| FR2182667A1 (cg-RX-API-DMAC7.html) | 1973-12-14 |
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