NO316924B1 - Materiale omfattende en pluralitet av selv-sammensatte peptider - Google Patents
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- NO316924B1 NO316924B1 NO19965142A NO965142A NO316924B1 NO 316924 B1 NO316924 B1 NO 316924B1 NO 19965142 A NO19965142 A NO 19965142A NO 965142 A NO965142 A NO 965142A NO 316924 B1 NO316924 B1 NO 316924B1
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- ZPNFWUPYTFPOJU-LPYSRVMUSA-N iniprol Chemical compound C([C@H]1C(=O)NCC(=O)NCC(=O)N[C@H]2CSSC[C@H]3C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@H](C(N[C@H](C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC=4C=CC(O)=CC=4)C(=O)N[C@@H](CC=4C=CC=CC=4)C(=O)N[C@@H](CC=4C=CC(O)=CC=4)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CSSC[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC=4C=CC=CC=4)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@H](CCCNC(N)=N)NC2=O)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CSSC[C@H](NC(=O)[C@H](CC=2C=CC=CC=2)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H]2N(CCC2)C(=O)[C@@H](N)CCCNC(N)=N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N2[C@@H](CCC2)C(=O)N2[C@@H](CCC2)C(=O)N[C@@H](CC=2C=CC(O)=CC=2)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(=O)N2[C@@H](CCC2)C(=O)N3)C(=O)NCC(=O)NCC(=O)N[C@@H](C)C(O)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H](C(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@H](C(=O)N1)C(C)C)[C@@H](C)O)[C@@H](C)CC)=O)[C@@H](C)CC)C1=CC=C(O)C=C1 ZPNFWUPYTFPOJU-LPYSRVMUSA-N 0.000 description 1
- 229940079322 interferon Drugs 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000002934 lysing effect Effects 0.000 description 1
- 235000010335 lysozyme Nutrition 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000000329 molecular dynamics simulation Methods 0.000 description 1
- 238000005232 molecular self-assembly Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000002547 new drug Substances 0.000 description 1
- FEMOMIGRRWSMCU-UHFFFAOYSA-N ninhydrin Chemical compound C1=CC=C2C(=O)C(O)(O)C(=O)C2=C1 FEMOMIGRRWSMCU-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012457 nonaqueous media Substances 0.000 description 1
- 229960003104 ornithine Drugs 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachloro-phenol Natural products OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 239000013034 phenoxy resin Substances 0.000 description 1
- 229920006287 phenoxy resin Polymers 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002704 polyhistidine Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000000734 protein sequencing Methods 0.000 description 1
- 230000017854 proteolysis Effects 0.000 description 1
- 230000006337 proteolytic cleavage Effects 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 238000012958 reprocessing Methods 0.000 description 1
- 230000000241 respiratory effect Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000004043 responsiveness Effects 0.000 description 1
- 101150106567 ser1 gene Proteins 0.000 description 1
- 239000012064 sodium phosphate buffer Substances 0.000 description 1
- 238000010532 solid phase synthesis reaction Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000013076 target substance Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- WROMPOXWARCANT-UHFFFAOYSA-N tfa trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.OC(=O)C(F)(F)F WROMPOXWARCANT-UHFFFAOYSA-N 0.000 description 1
- HNKJADCVZUBCPG-UHFFFAOYSA-N thioanisole Chemical compound CSC1=CC=CC=C1 HNKJADCVZUBCPG-UHFFFAOYSA-N 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000004627 transmission electron microscopy Methods 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 235000002374 tyrosine Nutrition 0.000 description 1
- 150000003668 tyrosines Chemical class 0.000 description 1
- 125000002987 valine group Chemical group [H]N([H])C([H])(C(*)=O)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- AFVLVVWMAFSXCK-UHFFFAOYSA-N α-cyano-4-hydroxycinnamic acid Chemical compound OC(=O)C(C#N)=CC1=CC=C(O)C=C1 AFVLVVWMAFSXCK-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
- C12N9/24—Hydrolases (3) acting on glycosyl compounds (3.2)
- C12N9/2402—Hydrolases (3) acting on glycosyl compounds (3.2) hydrolysing O- and S- glycosyl compounds (3.2.1)
- C12N9/2462—Lysozyme (3.2.1.17)
-
- 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
- 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
- C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Genetics & Genomics (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Zoology (AREA)
- Medicinal Chemistry (AREA)
- Biochemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Engineering & Computer Science (AREA)
- Gastroenterology & Hepatology (AREA)
- Wood Science & Technology (AREA)
- Biophysics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biotechnology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Immunology (AREA)
- Microbiology (AREA)
- Toxicology (AREA)
- General Engineering & Computer Science (AREA)
- Cell Biology (AREA)
- General Chemical & Material Sciences (AREA)
- Peptides Or Proteins (AREA)
- Materials For Medical Uses (AREA)
- Manufacturing Of Micro-Capsules (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9506806.0A GB9506806D0 (en) | 1995-04-01 | 1995-04-01 | Improvements relating to polymers |
| PCT/GB1996/000743 WO1996031528A1 (fr) | 1995-04-01 | 1996-03-28 | Peptides formant des enveloppes a pli beta et gels obtenus a partir de ces peptides |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO965142D0 NO965142D0 (no) | 1996-12-02 |
| NO965142L NO965142L (no) | 1997-01-30 |
| NO316924B1 true NO316924B1 (no) | 2004-06-28 |
Family
ID=10772373
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19965142A NO316924B1 (no) | 1995-04-01 | 1996-12-02 | Materiale omfattende en pluralitet av selv-sammensatte peptider |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US20020132974A1 (fr) |
| EP (1) | EP0759933B1 (fr) |
| JP (1) | JPH10505106A (fr) |
| AT (1) | ATE217323T1 (fr) |
| AU (1) | AU5155196A (fr) |
| CA (1) | CA2191872C (fr) |
| DE (1) | DE69621085T2 (fr) |
| ES (1) | ES2180748T3 (fr) |
| GB (1) | GB9506806D0 (fr) |
| NO (1) | NO316924B1 (fr) |
| WO (1) | WO1996031528A1 (fr) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0939766A2 (fr) | 1996-05-24 | 1999-09-08 | The Regents Of The University Of Minnesota | Synthese de peptides formant des feuillets beta solubles |
| US5955577A (en) * | 1996-06-27 | 1999-09-21 | Regents Of The University Of Minnesota | Method for synthesizing a water-soluble β-sheet forming peptide |
| US5964295A (en) | 1996-10-09 | 1999-10-12 | Schlumberger Technology Corporation, Dowell Division | Methods and compositions for testing subterranean formations |
| US6435277B1 (en) | 1996-10-09 | 2002-08-20 | Schlumberger Technology Corporation | Compositions containing aqueous viscosifying surfactants and methods for applying such compositions in subterranean formations |
| US6258859B1 (en) | 1997-06-10 | 2001-07-10 | Rhodia, Inc. | Viscoelastic surfactant fluids and related methods of use |
| US6071720A (en) * | 1998-04-29 | 2000-06-06 | Incyte Pharmaceuticals, Inc. | Delayed rectifier potassium channel subunit |
| EP1268976B1 (fr) | 2000-04-05 | 2011-10-05 | Sofitech N.V. | Diminution de la viscosite de fluides a base de tensio-actifs visco-elastiques |
| US6908888B2 (en) | 2001-04-04 | 2005-06-21 | Schlumberger Technology Corporation | Viscosity reduction of viscoelastic surfactant based fluids |
| US7084095B2 (en) | 2001-04-04 | 2006-08-01 | Schlumberger Technology Corporation | Methods for controlling the rheological properties of viscoelastic surfactants based fluids |
| GB0108767D0 (en) * | 2001-04-07 | 2001-05-30 | Univ Leeds | Coatings |
| GB0117011D0 (en) * | 2001-07-12 | 2001-09-05 | Univ Leeds | Peptide barrels |
| CA2476427A1 (fr) | 2002-02-20 | 2003-08-28 | Regents Of The University Of Minnesota | Mimetiques peptidiques partiels et procedes associes |
| WO2010019651A1 (fr) | 2008-08-13 | 2010-02-18 | Dow Global Technologies Inc. | Fibres enrobées d'un peptide |
| EP2318584A1 (fr) * | 2008-08-13 | 2011-05-11 | Dow Global Technologies LLC | Procédé de production de fibres enrobées de peptides |
| US8546338B2 (en) | 2010-12-08 | 2013-10-01 | Johnson & Johnson Consumer Companies, Inc. | Self-assembling hydrogels based on dicephalic peptide amphiphiles |
| JP6490897B2 (ja) * | 2013-12-27 | 2019-03-27 | 株式会社メニコンネクト | 自己組織化ペプチドゲル |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06502993A (ja) * | 1990-11-28 | 1994-04-07 | イー・アイ・デユポン・ドウ・ヌムール・アンド・カンパニー | 人工遺伝子からの構造タンパク質 |
| ATE250628T1 (de) * | 1993-10-14 | 2003-10-15 | Scripps Research Inst | Rohr bestehend aus zyklischen peptiden |
-
1995
- 1995-04-01 GB GBGB9506806.0A patent/GB9506806D0/en active Pending
-
1996
- 1996-03-28 ES ES96908230T patent/ES2180748T3/es not_active Expired - Lifetime
- 1996-03-28 AT AT96908230T patent/ATE217323T1/de not_active IP Right Cessation
- 1996-03-28 DE DE69621085T patent/DE69621085T2/de not_active Expired - Fee Related
- 1996-03-28 CA CA002191872A patent/CA2191872C/fr not_active Expired - Fee Related
- 1996-03-28 JP JP8530070A patent/JPH10505106A/ja not_active Ceased
- 1996-03-28 WO PCT/GB1996/000743 patent/WO1996031528A1/fr active IP Right Grant
- 1996-03-28 US US08/750,187 patent/US20020132974A1/en not_active Abandoned
- 1996-03-28 EP EP96908230A patent/EP0759933B1/fr not_active Expired - Lifetime
- 1996-03-28 AU AU51551/96A patent/AU5155196A/en not_active Abandoned
- 1996-12-02 NO NO19965142A patent/NO316924B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| NO965142L (no) | 1997-01-30 |
| EP0759933A1 (fr) | 1997-03-05 |
| NO965142D0 (no) | 1996-12-02 |
| AU5155196A (en) | 1996-10-23 |
| DE69621085D1 (de) | 2002-06-13 |
| ATE217323T1 (de) | 2002-05-15 |
| ES2180748T3 (es) | 2003-02-16 |
| US20020132974A1 (en) | 2002-09-19 |
| GB9506806D0 (en) | 1995-05-24 |
| DE69621085T2 (de) | 2002-12-19 |
| WO1996031528A1 (fr) | 1996-10-10 |
| JPH10505106A (ja) | 1998-05-19 |
| CA2191872A1 (fr) | 1996-10-10 |
| CA2191872C (fr) | 2004-08-10 |
| EP0759933B1 (fr) | 2002-05-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM1K | Lapsed by not paying the annual fees |