NO770650L - Fremgangsm}te til fremstilling av en forbindelse mellom en polyhydroksylpolymer og et prim{rt aminogruppeholdig stoff. - Google Patents
Fremgangsm}te til fremstilling av en forbindelse mellom en polyhydroksylpolymer og et prim{rt aminogruppeholdig stoff.Info
- Publication number
- NO770650L NO770650L NO770650A NO770650A NO770650L NO 770650 L NO770650 L NO 770650L NO 770650 A NO770650 A NO 770650A NO 770650 A NO770650 A NO 770650A NO 770650 L NO770650 L NO 770650L
- Authority
- NO
- Norway
- Prior art keywords
- polymer
- compound
- biologically active
- compounds
- reaction
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title description 33
- 229920000642 polymer Polymers 0.000 title description 29
- 239000000126 substance Substances 0.000 title description 19
- 238000000034 method Methods 0.000 title description 15
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 20
- 238000006243 chemical reaction Methods 0.000 description 19
- 239000007800 oxidant agent Substances 0.000 description 15
- 230000003647 oxidation Effects 0.000 description 14
- 238000007254 oxidation reaction Methods 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- -1 polyvinylene Polymers 0.000 description 13
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 13
- 239000000047 product Substances 0.000 description 13
- 229940088623 biologically active substance Drugs 0.000 description 10
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 10
- 229920001197 polyacetylene Polymers 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 239000013543 active substance Substances 0.000 description 9
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 8
- 102000004190 Enzymes Human genes 0.000 description 8
- 108090000790 Enzymes Proteins 0.000 description 8
- 239000012153 distilled water Substances 0.000 description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 7
- 239000007795 chemical reaction product Substances 0.000 description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 125000003172 aldehyde group Chemical group 0.000 description 6
- 239000000427 antigen Substances 0.000 description 6
- 102000036639 antigens Human genes 0.000 description 6
- 108091007433 antigens Proteins 0.000 description 6
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 6
- 108090000765 processed proteins & peptides Proteins 0.000 description 6
- 102000004169 proteins and genes Human genes 0.000 description 6
- 108090000623 proteins and genes Proteins 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000012876 carrier material Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 229960000583 acetic acid Drugs 0.000 description 4
- 230000004913 activation Effects 0.000 description 4
- 230000001588 bifunctional effect Effects 0.000 description 4
- 230000008878 coupling Effects 0.000 description 4
- 238000010168 coupling process Methods 0.000 description 4
- 238000005859 coupling reaction Methods 0.000 description 4
- 239000012636 effector Substances 0.000 description 4
- RWSXRVCMGQZWBV-WDSKDSINSA-N glutathione Chemical compound OC(=O)[C@@H](N)CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O RWSXRVCMGQZWBV-WDSKDSINSA-N 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- 230000003993 interaction Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 102000004506 Blood Proteins Human genes 0.000 description 3
- 108010017384 Blood Proteins Proteins 0.000 description 3
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 3
- 239000012190 activator Substances 0.000 description 3
- 239000003463 adsorbent Substances 0.000 description 3
- 150000001413 amino acids Chemical class 0.000 description 3
- 239000007809 chemical reaction catalyst Substances 0.000 description 3
- 239000012362 glacial acetic acid Substances 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 102000004196 processed proteins & peptides Human genes 0.000 description 3
- 125000006850 spacer group Chemical group 0.000 description 3
- 102000009027 Albumins Human genes 0.000 description 2
- 108010088751 Albumins Proteins 0.000 description 2
- 108010024636 Glutathione Proteins 0.000 description 2
- 239000002262 Schiff base Substances 0.000 description 2
- 150000004753 Schiff bases Chemical class 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- HAXFWIACAGNFHA-UHFFFAOYSA-N aldrithiol Chemical compound C=1C=CC=NC=1SSC1=CC=CC=N1 HAXFWIACAGNFHA-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 239000012954 diazonium Substances 0.000 description 2
- 150000001989 diazonium salts Chemical class 0.000 description 2
- 238000006193 diazotization reaction Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 229960003180 glutathione Drugs 0.000 description 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical compound OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 2
- 239000008363 phosphate buffer Substances 0.000 description 2
- 229920001184 polypeptide Polymers 0.000 description 2
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 2
- 239000012279 sodium borohydride Substances 0.000 description 2
- 229910000033 sodium borohydride Inorganic materials 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- JQWHASGSAFIOCM-UHFFFAOYSA-M sodium periodate Chemical compound [Na+].[O-]I(=O)(=O)=O JQWHASGSAFIOCM-UHFFFAOYSA-M 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- JMCRDEBJJPRTPV-UHFFFAOYSA-N 1,2-Ethenediol Chemical compound OC=CO JMCRDEBJJPRTPV-UHFFFAOYSA-N 0.000 description 1
- QWVCIORZLNBIIC-UHFFFAOYSA-N 2,3-dibromopropan-1-ol Chemical compound OCC(Br)CBr QWVCIORZLNBIIC-UHFFFAOYSA-N 0.000 description 1
- LGKDEBYYRWXEDL-UHFFFAOYSA-N 2-aminobenzenecarboximidamide Chemical compound NC(=N)C1=CC=CC=C1N LGKDEBYYRWXEDL-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000007868 Raney catalyst Substances 0.000 description 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 1
- 229910000564 Raney nickel Inorganic materials 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 238000001042 affinity chromatography Methods 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000005557 antagonist Substances 0.000 description 1
- 125000001769 aryl amino group Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical class C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000012280 lithium aluminium hydride Substances 0.000 description 1
- 229910052987 metal hydride Inorganic materials 0.000 description 1
- 150000004681 metal hydrides Chemical class 0.000 description 1
- ANORDWOIBSUYBN-UHFFFAOYSA-N n-chloro-1-phenylmethanamine Chemical compound ClNCC1=CC=CC=C1 ANORDWOIBSUYBN-UHFFFAOYSA-N 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 239000000813 peptide hormone Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000007659 semicarbazones Chemical class 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 230000036962 time dependent Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
- C08F8/32—Introducing nitrogen atoms or nitrogen-containing groups by reaction with amines
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polyamides (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2607766A DE2607766C3 (de) | 1976-02-26 | 1976-02-26 | Verfahren zur Herstellung von trägergebundenen biologisch aktiven Substanzen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO770650L true NO770650L (no) | 1977-08-29 |
Family
ID=5970898
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO770650A NO770650L (no) | 1976-02-26 | 1977-02-25 | Fremgangsm}te til fremstilling av en forbindelse mellom en polyhydroksylpolymer og et prim{rt aminogruppeholdig stoff. |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US4066581A (de) |
| JP (1) | JPS52103490A (de) |
| AU (1) | AU2262977A (de) |
| BE (1) | BE851917A (de) |
| DE (1) | DE2607766C3 (de) |
| DK (1) | DK83877A (de) |
| ES (1) | ES456118A1 (de) |
| FI (1) | FI770600A (de) |
| FR (1) | FR2342305A1 (de) |
| IL (1) | IL51529A0 (de) |
| IT (1) | IT1075122B (de) |
| LU (1) | LU76836A1 (de) |
| NL (1) | NL7701830A (de) |
| NO (1) | NO770650L (de) |
| SE (1) | SE7702125L (de) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4530974A (en) * | 1981-03-19 | 1985-07-23 | Board Of Regents, The University Of Texas System | Nonthrombogenic articles having enhanced albumin affinity |
| AU4660789A (en) * | 1988-11-23 | 1990-06-12 | Genentech Inc. | Polypeptide derivatives |
| US5446090A (en) * | 1993-11-12 | 1995-08-29 | Shearwater Polymers, Inc. | Isolatable, water soluble, and hydrolytically stable active sulfones of poly(ethylene glycol) and related polymers for modification of surfaces and molecules |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA667451A (en) * | 1963-07-23 | S. Newman Melvin | Vinylene carbonate and related products and processes | |
| CA667985A (en) * | 1963-08-06 | W. Gluesenkamp Earl | Polymerization of vinylene carbonate | |
| US2722525A (en) * | 1953-05-07 | 1955-11-01 | American Cyanamid Co | Polymerizable compositions containing an unsaturated carbonate and polymerization products thereof |
| DE1040789B (de) * | 1953-05-18 | 1958-10-09 | Monsanto Chemicals | Verfahren zur Herstellung von Polymerisaten und Mischpolymerisaten |
| US2847398A (en) * | 1953-05-18 | 1958-08-12 | Monsanto Chemicals | Vinylene carbonate-ethylene copolymer and method of producing same |
| US2794013A (en) * | 1953-12-23 | 1957-05-28 | American Cyanamid Co | Reaction products of vinylene carbonate and ammonia or primary amine |
| US2847402A (en) * | 1955-12-05 | 1958-08-12 | Monsanto Chemicals | High pressure homopolymerization and interpolymerization of vinylene carbonate |
| US2993030A (en) * | 1957-08-19 | 1961-07-18 | George E Ham | Process for polymerizing vinylene carbonate |
| US3037965A (en) * | 1958-04-14 | 1962-06-05 | Polaroid Corp | Water-insoluble hydrolyzed copolymer of vinylene carbonate and vinyl acetate |
| US3020290A (en) * | 1959-10-14 | 1962-02-06 | Jefferson Chem Co Inc | Preparation of unsaturated compounds |
| US3069391A (en) * | 1960-02-05 | 1962-12-18 | Du Pont | Polyhydroxymethylene polymers |
| NL286954A (de) * | 1962-01-03 | |||
| BE666318A (de) * | 1964-07-07 | 1966-01-03 | ||
| DE1494576A1 (de) * | 1965-02-03 | 1969-04-24 | Dynamit Nobel Ag | Verfahren zur Herstellung von Filmen,Folien und Fasern auf der Basis von Polyoxymethylenen |
| US3553310A (en) * | 1967-12-28 | 1971-01-05 | Miles Lab | Immunologically reactive particles |
| US3616229A (en) * | 1968-09-27 | 1971-10-26 | Monsanto Co | Polymer-enzyme products comprising plurality of enzymes covalently bound to polymer |
| US4011377A (en) * | 1971-02-11 | 1977-03-08 | Peter Duncan Goodearl Dean | Enzyme separation |
| US3847743A (en) * | 1971-08-24 | 1974-11-12 | American Cyanamid Co | Enzymes bound to carbonyl polymers |
| US4013514A (en) * | 1972-01-04 | 1977-03-22 | Monsanto Company | Preparing a reactor containing enzymes attached to dialdehyde cellulose |
| US3753861A (en) * | 1972-03-13 | 1973-08-21 | American Cyanamid Co | Binding enzymes to carbonyl polymers |
| US3944525A (en) * | 1973-10-03 | 1976-03-16 | Ciba-Geigy Corporation | Crosslinked resins prepared from an N,N'-bis-imide and a schiff base |
| GB1492937A (en) * | 1973-12-28 | 1977-11-23 | Beecham Group Ltd | Enzyme complexes and their use |
| US4025391A (en) * | 1974-06-15 | 1977-05-24 | Director Of National Food Research Institute | Preparation of bead-shaped immobilized enzyme |
| US4002531A (en) * | 1976-01-22 | 1977-01-11 | Pierce Chemical Company | Modifying enzymes with polyethylene glycol and product produced thereby |
-
1976
- 1976-02-26 DE DE2607766A patent/DE2607766C3/de not_active Expired
-
1977
- 1977-02-21 NL NL7701830A patent/NL7701830A/xx not_active Application Discontinuation
- 1977-02-21 ES ES456118A patent/ES456118A1/es not_active Expired
- 1977-02-24 AU AU22629/77A patent/AU2262977A/en not_active Expired
- 1977-02-24 IT IT20627/77A patent/IT1075122B/it active
- 1977-02-24 LU LU76836A patent/LU76836A1/xx unknown
- 1977-02-24 IL IL51529A patent/IL51529A0/xx unknown
- 1977-02-24 FI FI770600A patent/FI770600A/fi not_active Application Discontinuation
- 1977-02-24 US US05/771,766 patent/US4066581A/en not_active Expired - Lifetime
- 1977-02-25 SE SE7702125A patent/SE7702125L/xx unknown
- 1977-02-25 DK DK83877A patent/DK83877A/da unknown
- 1977-02-25 NO NO770650A patent/NO770650L/no unknown
- 1977-02-26 JP JP1982977A patent/JPS52103490A/ja active Pending
- 1977-02-28 BE BE175340A patent/BE851917A/xx unknown
- 1977-02-28 FR FR7705828A patent/FR2342305A1/fr not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| AU2262977A (en) | 1978-08-31 |
| LU76836A1 (de) | 1977-09-12 |
| JPS52103490A (en) | 1977-08-30 |
| US4066581A (en) | 1978-01-03 |
| DE2607766A1 (de) | 1977-09-01 |
| SE7702125L (sv) | 1977-08-27 |
| FI770600A (de) | 1977-08-27 |
| NL7701830A (nl) | 1977-08-30 |
| FR2342305A1 (fr) | 1977-09-23 |
| IL51529A0 (en) | 1977-04-29 |
| ES456118A1 (es) | 1978-02-01 |
| DE2607766C3 (de) | 1978-12-07 |
| BE851917A (de) | 1977-08-29 |
| DE2607766B2 (de) | 1978-04-20 |
| DK83877A (da) | 1977-08-27 |
| IT1075122B (it) | 1985-04-22 |
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