CO4750673A1 - Derivados solubles compuestos de polipeptidos solubles y elementos que se unen a membrana - Google Patents
Derivados solubles compuestos de polipeptidos solubles y elementos que se unen a membranaInfo
- Publication number
- CO4750673A1 CO4750673A1 CO97039907A CO97039907A CO4750673A1 CO 4750673 A1 CO4750673 A1 CO 4750673A1 CO 97039907 A CO97039907 A CO 97039907A CO 97039907 A CO97039907 A CO 97039907A CO 4750673 A1 CO4750673 A1 CO 4750673A1
- Authority
- CO
- Colombia
- Prior art keywords
- membrane
- polypeptide
- elements
- group
- derivative
- Prior art date
Links
Classifications
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- 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)
- C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
- C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
- C12N9/64—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue
- C12N9/6421—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue from mammals
- C12N9/6424—Serine endopeptidases (3.4.21)
- C12N9/6456—Plasminogen activators
- C12N9/6462—Plasminogen activators u-Plasminogen activator (3.4.21.73), i.e. urokinase
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/54—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic compound
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/62—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
- A61K47/64—Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C323/39—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton at least one of the nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom
- C07C323/40—Y being a hydrogen or a carbon atom
- C07C323/41—Y being a hydrogen or an acyclic carbon atom
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
- C07C323/51—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/57—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups
- C07C323/58—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups with amino groups bound to the carbon skeleton
- C07C323/59—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being further substituted by nitrogen atoms, not being part of nitro or nitroso groups with amino groups bound to the carbon skeleton with acylated amino groups bound to the carbon skeleton
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
- C07K14/315—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Streptococcus (G), e.g. Enterococci
- C07K14/3153—Streptokinase
-
- 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
- C07K14/70596—Molecules with a "CD"-designation not provided for elsewhere
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y304/00—Hydrolases acting on peptide bonds, i.e. peptidases (3.4)
- C12Y304/21—Serine endopeptidases (3.4.21)
- C12Y304/21073—Serine endopeptidases (3.4.21) u-Plasminogen activator (3.4.21.73), i.e. urokinase
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biochemistry (AREA)
- Zoology (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Biophysics (AREA)
- Wood Science & Technology (AREA)
- Immunology (AREA)
- Biomedical Technology (AREA)
- General Engineering & Computer Science (AREA)
- Gastroenterology & Hepatology (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Cell Biology (AREA)
- Toxicology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
Un derivado soluble de un polipéptido soluble, (P)comprendiendo dicho derivado dos o más elementos heterológos que se unen a la membrana con baja afinidad hacia la membrana(W,X) asociados covalentemente con el polipéptido, donde dichos elementos son capaces de interaccionar, independientemente y con aditividad termodinámica, con componentes de membranas celulares o artificiales expuestas a fluidos extracelulares y donde todos los mencionados dos o más elementos exhiben baja afinidad hacia la membrana.2Un procedimiento para preparar un derivado según la reivindicación 1, procedimiento que comprende expresar ADN que codifica la porción polipeptídica de dicho derivado en una célula hospedadora recombinante y recuperar el producto y, después de esto, modificar después de la traducción el polipéptido para introducir químicamente elementos que se unen a la membrana. 3Un elemento peptídico que se une a la membrana con baja afinidad hacia la membrana, que comprende una o más modificaciones seleccionadas entre: un resto de cisteína terminal, opcionalmente activado en el grupo tiol; un grupo N-haloacetilo (en que halo significa cloro, bromo o yodo) localizado en el extremo N terminal del péptido o en un grupo e-amino de un resto de lisina; un grupo amido en el extremo C terminal; un grupo bloqueante N terminal; y un grupo N-acilo de ácido graso en el extremo N terminal o en un grupo e-amino de un resto de lisina, para la manufactura de un derivado polipéptido de acuerdo con la Reivindicación 1.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB9614871.3A GB9614871D0 (en) | 1996-07-15 | 1996-07-15 | Compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
CO4750673A1 true CO4750673A1 (es) | 1999-03-31 |
Family
ID=10796956
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CO97039907A CO4750673A1 (es) | 1996-07-15 | 1997-07-15 | Derivados solubles compuestos de polipeptidos solubles y elementos que se unen a membrana |
Country Status (17)
Country | Link |
---|---|
US (3) | US6713606B1 (es) |
EP (1) | EP0912730B1 (es) |
JP (1) | JP4177457B2 (es) |
AR (1) | AR007737A1 (es) |
AT (1) | ATE419345T1 (es) |
AU (1) | AU732725B2 (es) |
CA (1) | CA2260288A1 (es) |
CO (1) | CO4750673A1 (es) |
DE (1) | DE69739186D1 (es) |
DK (1) | DK0912730T3 (es) |
ES (1) | ES2321245T3 (es) |
GB (1) | GB9614871D0 (es) |
IL (3) | IL128034A0 (es) |
NZ (1) | NZ333722A (es) |
TW (1) | TW538048B (es) |
WO (1) | WO1998002454A2 (es) |
ZA (1) | ZA976216B (es) |
Families Citing this family (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9614871D0 (en) * | 1996-07-15 | 1996-09-04 | Smithkline Beecham Plc | Compounds |
US6210707B1 (en) | 1996-11-12 | 2001-04-03 | The Regents Of The University Of California | Methods of forming protein-linked lipidic microparticles, and compositions thereof |
GB9704519D0 (en) * | 1997-03-05 | 1997-04-23 | Smithkline Beecham Plc | Compounds |
IL136230A0 (en) | 1997-11-28 | 2001-05-20 | Roche Diagnostics Gmbh | An active hedgehog-protein-mutant, a process for its preparation and its use for pharmaceutical purposes |
EP0953576B1 (en) | 1998-04-30 | 2005-11-02 | Curis, Inc. | Active hedgehog protein conjugate, process for its production and use |
GB9815505D0 (en) * | 1998-07-16 | 1998-09-16 | Adprotech Plc | Polypeptide derivatives |
GB9905503D0 (en) * | 1999-03-10 | 1999-05-05 | Adprotech Plc | Novel compound formulations and methods of delivery |
GB0016811D0 (en) * | 2000-07-07 | 2000-08-30 | Adprotech Ltd | Lipid rafts |
GB0026924D0 (en) | 2000-11-03 | 2000-12-20 | Univ Cambridge Tech | Antibacterial agents |
GB0117193D0 (en) * | 2001-07-13 | 2001-09-05 | Adprotech Ltd | Protein modification reagents |
GB0123262D0 (en) * | 2001-09-27 | 2001-11-21 | Adprotech Ltd | Polymeric compounds |
GB0220936D0 (en) | 2002-09-05 | 2002-10-23 | Adprotech Ltd | Modified therapeutic agents |
FR2854897B1 (fr) * | 2003-05-12 | 2007-05-04 | Sederma Sa | Compositions cosmetiques ou dermopharmaceutiques pour reduire les signes du vieillissement cutane. |
US7858108B2 (en) * | 2003-10-21 | 2010-12-28 | Richard Nagler | Elutable surface coating |
US8454963B2 (en) * | 2003-11-13 | 2013-06-04 | Musc Foundation For Research Development | Tissue targeted complement modulators |
US8124097B2 (en) * | 2004-01-21 | 2012-02-28 | Case Western Reserve University | Hybrid and chimeric polypeptides that regulate activation of complement |
WO2005115430A1 (en) | 2004-05-27 | 2005-12-08 | Gropep Limited | Treatment of inflammatory airway disease |
JP2009508937A (ja) * | 2005-09-22 | 2009-03-05 | イエダ リサーチ アンド デベロップメント カンパニー リミテッド | T細胞免疫を調節するためのジアステレオマーペプチド |
JP2009529530A (ja) | 2006-03-09 | 2009-08-20 | インフラザイム・ファーマシューティカルズ・リミテッド | 新規の抗生物質組成物 |
EP2083841B1 (en) | 2006-10-20 | 2013-11-20 | Celldex Therapeutics, Inc. | SOLUBLE COMPLEMENT RECEPTOR TYPE I (sCR1) PROTEIN FOR USE IN THE TREATMENT OF AGE-RELATED MACULAR DEGENERATION AND OTHER DISEASES OF THE EYE |
EP2134373A4 (en) * | 2007-02-28 | 2014-04-02 | Yeda Res & Dev | CORE TARGETING SEQUENCES |
WO2010034015A2 (en) | 2008-09-22 | 2010-03-25 | The Regents Of The University Of Colorado, A Body Corporate | Modulating the alternative complement pathway |
CA2751673A1 (en) * | 2009-02-20 | 2010-08-26 | Ipsen Pharma S.A.S | Analogues of neuropeptide y having proline substitution at position 34 |
EP2419119B1 (en) * | 2009-04-16 | 2017-06-07 | Ruprecht-Karls-Universität Heidelberg | Muscle function enhancing peptide |
GB0915519D0 (en) | 2009-09-04 | 2009-10-07 | King S College London | Ntithrombotic compounds |
WO2011050334A1 (en) * | 2009-10-22 | 2011-04-28 | Yong Zhu | Compositions and methods for re-programming cells without genetic modification for treatment of obesity and related diseases |
US9295713B2 (en) | 2010-09-15 | 2016-03-29 | Celldex Therapeutics, Inc. | Treatment of chronic nephropathies using soluble complement receptor type I (sCR1) |
EP2632476B1 (en) | 2010-10-27 | 2017-06-14 | Celldex Therapeutics, Inc. | Method of improving transplant function using soluble complement receptor type i (scr1) |
BR112014013205A2 (pt) * | 2011-12-01 | 2020-10-27 | Protevobio, Inc. | proteína de fusão, seu uso e seu método de produção, composição farmacêutica, ácido nucleico, e kit |
US9987235B2 (en) | 2013-08-01 | 2018-06-05 | Nicholas L. Abbott | Methods and compositions for modifying mucous membranes |
US9695402B2 (en) | 2013-09-17 | 2017-07-04 | Yeda Research And Development Co. Ltd. | ERK-derived peptides and uses thereof |
GB201402267D0 (en) | 2014-02-10 | 2014-03-26 | Cambridge Entpr Ltd | Antibacterial agents |
GB2583560A (en) | 2018-12-11 | 2020-11-04 | Admirx Inc | Fusion protein constructs for complement associated disease |
CN110240656A (zh) * | 2019-04-24 | 2019-09-17 | 中山大学附属第三医院 | 一种融合蛋白及其制备方法与应用 |
CN110551177A (zh) * | 2019-08-29 | 2019-12-10 | 安徽瑞达健康产业有限公司 | 多肽、多肽衍生物、多肽-抗体复合物及制备、应用 |
GB201913804D0 (en) | 2019-09-25 | 2019-11-06 | Prostate Cancer Res Centre | Fusion polypeptides |
WO2024092160A2 (en) * | 2022-10-26 | 2024-05-02 | Flagship Pioneering Innovations Vii, Llc | Bifunctional proteases and uses thereof |
Family Cites Families (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4536391A (en) | 1982-11-17 | 1985-08-20 | Otsuka Pharmaceutical Co. | Process for preparing urokinase complex |
EP0114787B1 (de) * | 1983-01-25 | 1991-09-25 | Ciba-Geigy Ag | Neue Peptidderivate |
GB8334498D0 (en) | 1983-12-24 | 1984-02-01 | Beecham Group Plc | Compounds |
GB8400653D0 (en) | 1984-01-11 | 1984-02-15 | Beecham Group Plc | Conjugates |
GR860875B (en) | 1985-04-04 | 1986-07-29 | Beecham Group Plc | Novel compounds |
US5374548A (en) * | 1986-05-02 | 1994-12-20 | Genentech, Inc. | Methods and compositions for the attachment of proteins to liposomes using a glycophospholipid anchor |
JP2573007B2 (ja) * | 1987-12-28 | 1997-01-16 | 株式会社成和化成 | 修飾された動物毛粉末 |
US5256642A (en) | 1988-04-01 | 1993-10-26 | The Johns Hopkins University | Compositions of soluble complement receptor 1 (CR1) and a thrombolytic agent, and the methods of use thereof |
US5582968A (en) * | 1990-02-16 | 1996-12-10 | United Biomedical, Inc. | Branched hybrid and cluster peptides effective in diagnosing and detecting non-A, non-B hepatitis |
US6458360B1 (en) | 1990-04-25 | 2002-10-01 | The Johns Hopkins University | Soluble complement regulatory molecules |
US5326700A (en) | 1990-11-06 | 1994-07-05 | Eli Lilly And Company | DNA sequences encoding t-PA derivatives with cleavable sites |
US5580563A (en) * | 1992-05-01 | 1996-12-03 | Tam; James P. | Multiple antigen peptide system having adjuvant properties, vaccines prepared therefrom and methods of use thereof |
DE69328098T2 (de) * | 1992-06-24 | 2000-08-24 | Adprotech Plc | Lösliche derivate des complement type-rezeptors (cr1) |
US5456909A (en) | 1992-08-07 | 1995-10-10 | T Cell Sciences, Inc. | Glycoform fractions of recombinant soluble complement receptor 1 (sCR1) having extended half-lives in vivo |
US5856300A (en) * | 1994-05-12 | 1999-01-05 | T Cell Sciences, Inc. | Compositions comprising complement related proteins and carbohydrates, and methods for producing and using said compositions |
PT730608E (pt) * | 1993-05-17 | 2002-09-30 | Avant Immunotherapeutics Inc | Composicoes compreendendo hidratos de carbono e proeinas relacionadas pelo complemento e metodos para produzir e utilizar as referidas composicoes |
WO1995023512A1 (en) * | 1994-03-03 | 1995-09-08 | Alexion Pharmaceuticals, Inc. | Terminal complement inhibitor fusion genes and proteins |
GB9614871D0 (en) | 1996-07-15 | 1996-09-04 | Smithkline Beecham Plc | Compounds |
US5776689A (en) | 1996-07-19 | 1998-07-07 | The Regents Of The University Of California | Protein recruitment system |
WO2000020867A1 (en) | 1998-10-01 | 2000-04-13 | Alexey Vladimirovich Titievsky | A novel ret-independent signaling pathway for gdnf |
GB0220936D0 (en) * | 2002-09-05 | 2002-10-23 | Adprotech Ltd | Modified therapeutic agents |
-
1996
- 1996-07-15 GB GBGB9614871.3A patent/GB9614871D0/en active Pending
-
1997
- 1997-07-08 AT AT97933665T patent/ATE419345T1/de not_active IP Right Cessation
- 1997-07-08 AU AU36939/97A patent/AU732725B2/en not_active Ceased
- 1997-07-08 JP JP50560898A patent/JP4177457B2/ja not_active Expired - Fee Related
- 1997-07-08 DE DE69739186T patent/DE69739186D1/de not_active Expired - Lifetime
- 1997-07-08 IL IL12803497A patent/IL128034A0/xx active IP Right Grant
- 1997-07-08 NZ NZ333722A patent/NZ333722A/xx unknown
- 1997-07-08 WO PCT/EP1997/003715 patent/WO1998002454A2/en active Application Filing
- 1997-07-08 ES ES97933665T patent/ES2321245T3/es not_active Expired - Lifetime
- 1997-07-08 CA CA002260288A patent/CA2260288A1/en not_active Abandoned
- 1997-07-08 DK DK97933665T patent/DK0912730T3/da active
- 1997-07-08 EP EP97933665A patent/EP0912730B1/en not_active Expired - Lifetime
- 1997-07-14 AR ARP970103142A patent/AR007737A1/es unknown
- 1997-07-14 ZA ZA976216A patent/ZA976216B/xx unknown
- 1997-07-15 CO CO97039907A patent/CO4750673A1/es unknown
- 1997-07-18 TW TW086110188A patent/TW538048B/zh not_active IP Right Cessation
-
1999
- 1999-01-13 IL IL128034A patent/IL128034A/en not_active IP Right Cessation
-
2000
- 2000-07-07 US US09/612,314 patent/US6713606B1/en not_active Expired - Fee Related
-
2003
- 2003-12-23 US US10/742,887 patent/US7655617B2/en not_active Expired - Fee Related
-
2004
- 2004-12-30 IL IL16605104A patent/IL166051A0/xx unknown
-
2008
- 2008-08-15 US US12/192,560 patent/US20100286367A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
IL128034A0 (en) | 1999-11-30 |
DE69739186D1 (de) | 2009-02-12 |
US6713606B1 (en) | 2004-03-30 |
US7655617B2 (en) | 2010-02-02 |
EP0912730A2 (en) | 1999-05-06 |
IL166051A0 (en) | 2006-01-15 |
DK0912730T3 (da) | 2009-04-27 |
AR007737A1 (es) | 1999-11-10 |
ES2321245T3 (es) | 2009-06-03 |
GB9614871D0 (en) | 1996-09-04 |
US20040266684A1 (en) | 2004-12-30 |
AU3693997A (en) | 1998-02-09 |
WO1998002454A3 (en) | 1998-04-02 |
ATE419345T1 (de) | 2009-01-15 |
IL128034A (en) | 2007-03-08 |
TW538048B (en) | 2003-06-21 |
CA2260288A1 (en) | 1998-01-22 |
JP4177457B2 (ja) | 2008-11-05 |
AU732725B2 (en) | 2001-04-26 |
ZA976216B (en) | 1999-04-14 |
US20100286367A1 (en) | 2010-11-11 |
WO1998002454A2 (en) | 1998-01-22 |
JP2000515370A (ja) | 2000-11-21 |
NZ333722A (en) | 2000-09-29 |
EP0912730B1 (en) | 2008-12-31 |
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