SK121895A3 - Analogues of peptide yy and uses thereof - Google Patents
Analogues of peptide yy and uses thereof Download PDFInfo
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- SK121895A3 SK121895A3 SK1218-95A SK121895A SK121895A3 SK 121895 A3 SK121895 A3 SK 121895A3 SK 121895 A SK121895 A SK 121895A SK 121895 A3 SK121895 A3 SK 121895A3
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- Prior art keywords
- arg
- leu
- pyy
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/12—Drugs for disorders of the metabolism for electrolyte homeostasis
-
- 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
- C07K14/575—Hormones
- C07K14/57545—Neuropeptide Y
-
- 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)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Gastroenterology & Hepatology (AREA)
- Zoology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Genetics & Genomics (AREA)
- Endocrinology (AREA)
- Toxicology (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Measurement And Recording Of Electrical Phenomena And Electrical Characteristics Of The Living Body (AREA)
- Measuring Pulse, Heart Rate, Blood Pressure Or Blood Flow (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US3853493A | 1993-03-29 | 1993-03-29 | |
US10932693A | 1993-08-19 | 1993-08-19 | |
PCT/US1994/003380 WO1994022467A1 (en) | 1993-03-29 | 1994-03-29 | Analogs of peptide yy and uses thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
SK121895A3 true SK121895A3 (en) | 1996-10-02 |
Family
ID=26715298
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SK1218-95A SK121895A3 (en) | 1993-03-29 | 1994-03-29 | Analogues of peptide yy and uses thereof |
Country Status (14)
Country | Link |
---|---|
US (1) | US5604203A (xx) |
EP (1) | EP0692971A4 (xx) |
JP (1) | JPH08510205A (xx) |
KR (1) | KR960701653A (xx) |
CN (1) | CN1124927A (xx) |
AU (1) | AU685803B2 (xx) |
CA (1) | CA2157766A1 (xx) |
FI (1) | FI954559A (xx) |
HU (1) | HUT73494A (xx) |
NZ (1) | NZ265452A (xx) |
PL (1) | PL310897A1 (xx) |
SG (1) | SG52542A1 (xx) |
SK (1) | SK121895A3 (xx) |
WO (1) | WO1994022467A1 (xx) |
Families Citing this family (71)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5516653A (en) | 1993-12-28 | 1996-05-14 | Synaptic Pharmaceutical Corporation | DNA encoding a human neuropeptide Y/peptide YY/pancreatic polypeptide receptor (Y4) and uses thereof |
US5545549A (en) | 1994-02-03 | 1996-08-13 | Synaptic Pharmaceutical Corporation | DNA encoding a human neuropeptide Y/peptide YY (Y2) receptor and uses thereof |
US5602024A (en) | 1994-12-02 | 1997-02-11 | Synaptic Pharmaceutical Corporation | DNA encoding a hypothalamic atypical neuropeptide Y/peptide YY receptor (Y5) and uses thereof |
US5989920A (en) | 1994-12-02 | 1999-11-23 | Synaptic Pharmaceutical Corporation | Methods of modifying feeding behavior compounds useful in such methods and DNA encoding a hypothalmic atypical neuropeptide Y/peptide YY receptor Y5 |
US5912227A (en) * | 1995-01-27 | 1999-06-15 | North Carolina State University | Method of enhancing nutrient uptake |
US7048906B2 (en) | 1995-05-17 | 2006-05-23 | Cedars-Sinai Medical Center | Methods of diagnosing and treating small intestinal bacterial overgrowth (SIBO) and SIBO-related conditions |
US6861053B1 (en) | 1999-08-11 | 2005-03-01 | Cedars-Sinai Medical Center | Methods of diagnosing or treating irritable bowel syndrome and other disorders caused by small intestinal bacterial overgrowth |
US6558708B1 (en) * | 1995-05-17 | 2003-05-06 | Cedars-Sinai Medical Center | Methods for manipulating upper gastrointestinal transit, blood flow, and satiety, and for treating visceral hyperalgesia |
FR2735983B1 (fr) * | 1995-06-29 | 1997-12-05 | Centre Nat Rech Scient | Peptide permettant de modifier l'activite du systeme immunitaire humain ou animal |
US6696409B1 (en) | 1996-06-05 | 2004-02-24 | Prince Of Wales Medical Research Institute Limited (Powmr Ltd.) | Neuropeptide Y agonists |
AU772915B2 (en) * | 1996-06-05 | 2004-05-13 | Prince Of Wales Medical Research Institute Limited | Neuropeptide Y agonists |
AUPO029096A0 (en) * | 1996-06-05 | 1996-07-04 | Crc For Biopharmaceutical Research Pty Ltd | Npy y2 agonists |
US6713265B1 (en) | 1997-06-04 | 2004-03-30 | Synaptic Pharmaceutical Corporation | Methods of modifying feeding behavior, compounds useful in such methods, and DNA encoding a hypothalamic atypical neuropeptide Y/peptide YY receptor (Y5) |
US5916869A (en) * | 1997-06-13 | 1999-06-29 | North Carolina State University | Method of treating birds in ovo |
EP1950223A3 (en) * | 1998-03-09 | 2009-05-13 | Zealand Pharma A/S | Pharmacologically active peptide conjugates having a reduced tendency towards enzymatic hydrolysis |
US6046167A (en) * | 1998-03-25 | 2000-04-04 | University Of Cincinnati | Peptide YY analogs |
US7745216B2 (en) * | 1999-02-10 | 2010-06-29 | Curis, Inc. | Methods and reagents for treating glucose metabolic disorders |
ES2353728T3 (es) | 1999-02-10 | 2011-03-04 | Curis, Inc. | Péptido yy (pyy) para tratar trastornos metabólicos de la glucosa. |
US7601691B2 (en) | 1999-05-17 | 2009-10-13 | Conjuchem Biotechnologies Inc. | Anti-obesity agents |
US6734166B1 (en) * | 2000-02-08 | 2004-05-11 | North Carolina State University | Method of reducing aluminum levels in the central nervous system |
RU2275207C2 (ru) | 2000-12-14 | 2006-04-27 | Амилин Фармасьютикалз, Инк. | Способ снижения доступности питательного вещества, способ подавления аппетита |
GB0121709D0 (en) * | 2001-09-07 | 2001-10-31 | Imp College Innovations Ltd | Food inhibition agent |
AU2002332054B2 (en) | 2001-09-24 | 2007-11-08 | Imperial Innovations Limited | Modification of feeding behavior |
US8058233B2 (en) * | 2002-01-10 | 2011-11-15 | Oregon Health And Science University | Modification of feeding behavior using PYY and GLP-1 |
WO2003057235A2 (en) | 2002-01-10 | 2003-07-17 | Imperial College Innovations Ltd | Modification of feeding behavior |
ATE494002T1 (de) * | 2002-06-14 | 2011-01-15 | Amylin Pharmaceuticals Inc | Prävention und/oder behandlung von colitis ulcerosa mit pyy oder pyyä3-36ü |
US7186692B2 (en) | 2002-12-17 | 2007-03-06 | Nastech Pharmaceutical Company Inc. | Compositions and methods for enhanced mucosal delivery and non-infused administration of Y2 receptor-binding peptides and methods for treating and preventing obesity |
US7229966B2 (en) | 2002-12-17 | 2007-06-12 | Nastech Pharmaceutical Company Inc. | Compositions and methods for enhanced mucosal delivery of Y2 receptor-binding peptides and methods for treating and preventing obesity |
JP2006516262A (ja) * | 2002-12-17 | 2006-06-29 | ナステック・ファーマシューティカル・カンパニー・インコーポレーテッド | Y2受容体結合ペプチドの粘膜送達促進のための組成物および方法ならびに肥満症の治療法および予防法 |
US7166575B2 (en) * | 2002-12-17 | 2007-01-23 | Nastech Pharmaceutical Company Inc. | Compositions and methods for enhanced mucosal delivery of peptide YY and methods for treating and preventing obesity |
GB0300571D0 (en) * | 2003-01-10 | 2003-02-12 | Imp College Innovations Ltd | Modification of feeding behaviour |
US7811989B2 (en) | 2003-01-17 | 2010-10-12 | Ipsen Pharma S.A.S. | Peptide YY analogs |
US7780973B2 (en) * | 2003-12-15 | 2010-08-24 | Ethicon Endo-Surgery, Inc. | Method and device for minimally invasive implantation of biomaterial |
EP1789440A4 (en) * | 2004-02-11 | 2008-03-12 | Amylin Pharmaceuticals Inc | REASONS FOR THE FAMILY OF PANCREATIC POLYPEPTIDES AND POLYPEPTIDES CONTAINING THEM |
US8076288B2 (en) | 2004-02-11 | 2011-12-13 | Amylin Pharmaceuticals, Inc. | Hybrid polypeptides having glucose lowering activity |
BRPI0507594A (pt) * | 2004-02-11 | 2007-07-03 | Amylin Pharmaceuticals Inc | polipetìdeos hìbridos com propriedades selecionáveis |
CN1953763A (zh) * | 2004-03-17 | 2007-04-25 | 7Tm制药联合股份有限公司 | 用于治疗性干预的y4选择性受体激动剂 |
EA011860B1 (ru) * | 2004-03-17 | 2009-06-30 | 7ТиЭм ФАРМА А/С | Селективные агонисты рецептора y2 для терапевтического воздействия |
JP2007531714A (ja) * | 2004-03-17 | 2007-11-08 | 7ティーエム ファーマ エイ/エス | 治療的介入のためのy2/y4選択性レセプターアゴニスト |
CA2588594C (en) | 2004-12-13 | 2014-02-18 | Amylin Pharmaceuticals, Inc. | Pancreatic polypeptide family motifs, polypeptides and methods comprising the same |
US7410949B2 (en) * | 2005-01-18 | 2008-08-12 | Hoffmann-La Roche Inc. | Neuropeptide-2 receptor (Y-2R) agonists and uses thereof |
PA8660701A1 (es) * | 2005-02-04 | 2006-09-22 | Pfizer Prod Inc | Agonistas de pyy y sus usos |
US8283312B2 (en) * | 2005-02-04 | 2012-10-09 | The Research Foundation Of State University Of New York | Compositions and methods for modulating body weight and treating obesity-related disorders |
GB0504857D0 (en) * | 2005-03-09 | 2005-04-13 | Imp College Innovations Ltd | Novel compounds and their effects on feeding behaviour |
GB0511986D0 (en) * | 2005-06-13 | 2005-07-20 | Imp College Innovations Ltd | Novel compounds and their effects on feeding behaviour |
EP2330124B1 (en) * | 2005-08-11 | 2015-02-25 | Amylin Pharmaceuticals, LLC | Hybrid polypeptides with selectable properties |
BRPI0614649A2 (pt) * | 2005-08-11 | 2011-04-12 | Amylin Pharmaceuticals Inc | polipeptìdeos hìbridos com propriedades selecionáveis |
US8022035B2 (en) * | 2005-09-21 | 2011-09-20 | 7Tm Pharma A/S | Y4 selective receptor agonists for therapeutic interventions |
US7851590B2 (en) * | 2005-09-21 | 2010-12-14 | 7Tm Pharma A/S | Y2 selective receptor agonists for therapeutic interventions |
BRPI0616463A2 (pt) | 2005-09-29 | 2011-06-21 | Merck & Co Inc | composto, composição farmacêutica, e, uso de um composto |
US20070232537A1 (en) * | 2005-12-19 | 2007-10-04 | Nastech Pharmaceutical Company Inc. | Intranasal pyy formulations with improved transmucosal pharmacokinetics |
US20070197445A1 (en) * | 2006-01-18 | 2007-08-23 | University Of Cincinnati | Compounds for control of appetite |
CA2664113C (en) | 2006-09-22 | 2013-05-28 | Merck & Co., Inc. | Use of platencin and platensimycin as fatty acid synthesis inhibitors to treat obesity, diabetes and cancer |
TWI428346B (zh) | 2006-12-13 | 2014-03-01 | Imp Innovations Ltd | 新穎化合物及其等對進食行為影響 |
US20090099074A1 (en) * | 2007-01-10 | 2009-04-16 | Conjuchem Biotechnologies Inc. | Modulating food intake |
CA2682727C (en) | 2007-04-02 | 2016-03-22 | Banyu Pharmaceutical Co., Ltd. | Indoledione derivative |
GB0708226D0 (en) * | 2007-04-27 | 2007-06-06 | 7Tm Pharma As | Y-receptor agonists |
CA2758415C (en) | 2008-04-14 | 2019-06-04 | The General Hospital Corporation | Plectin-1 targeted agents for detection and treatment of pancreatic ductal adenocarcinoma |
US8299023B2 (en) | 2008-09-17 | 2012-10-30 | Hoffmann-La Roche Inc. | Neuropeptide-2 receptor (Y-2R) agonists |
LT2393828T (lt) | 2009-02-03 | 2017-01-25 | Amunix Operating Inc. | Prailginti rekombinantiniai polipeptidai ir juos apimančios kompozicijos |
US9260500B2 (en) | 2009-07-02 | 2016-02-16 | Takeda Pharmaceutical Company Limited | Peptide and use thereof |
TW201138808A (en) | 2010-05-03 | 2011-11-16 | Bristol Myers Squibb Co | Serum albumin binding molecules |
DK2651398T3 (en) | 2010-12-16 | 2018-03-12 | Novo Nordisk As | Solid compositions comprising a GLP-1 agonist and a salt of N- (8- (2-hydroxybenzyl) amino) caprylic acid |
CA2865578C (en) | 2012-02-27 | 2023-01-17 | Amunix Operating Inc. | Xten conjugate compositions and methods of making same |
RS57727B1 (sr) | 2012-03-22 | 2018-12-31 | Novo Nordisk As | Kompozicije glp-1 peptida i njihovo dobijanje |
US9085637B2 (en) | 2013-11-15 | 2015-07-21 | Novo Nordisk A/S | Selective PYY compounds and uses thereof |
US10583172B2 (en) | 2013-11-15 | 2020-03-10 | Novo Nordisk A/S | HPYY(1-36) having a beta-homoarginine substitution at position 35 |
JP6731958B2 (ja) | 2015-06-12 | 2020-07-29 | ノヴォ ノルディスク アー/エス | 選択的pyy化合物及びその使用 |
MX2019002410A (es) | 2016-08-28 | 2019-09-18 | The State Of Israel Ministry Of Agriculture & Rural Development Agricultural Res Aro Volcani Center | Metodo para controlar infecciones fungicas en plantas. |
WO2019149880A1 (en) | 2018-02-02 | 2019-08-08 | Novo Nordisk A/S | Solid compositions comprising a glp-1 agonist, a salt of n-(8-(2-hydroxybenzoyl)amino)caprylic acid and a lubricant |
MX2022005676A (es) | 2019-11-13 | 2022-10-27 | Amunix Pharmaceuticals Inc | Polipéptidos xten con código de barras y composiciones de estos, y métodos para preparar y usar los mismos. |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS646294A (en) * | 1987-02-09 | 1989-01-10 | Ajinomoto Kk | Novel peptide derivative |
US5026685A (en) * | 1988-07-15 | 1991-06-25 | The Salk Institute For Biological Studies | NPY peptide analogs |
-
1994
- 1994-03-29 NZ NZ265452A patent/NZ265452A/en unknown
- 1994-03-29 HU HU9502833A patent/HUT73494A/hu unknown
- 1994-03-29 WO PCT/US1994/003380 patent/WO1994022467A1/en not_active Application Discontinuation
- 1994-03-29 KR KR1019950704035A patent/KR960701653A/ko not_active Application Discontinuation
- 1994-03-29 SK SK1218-95A patent/SK121895A3/sk unknown
- 1994-03-29 CN CN94192277A patent/CN1124927A/zh active Pending
- 1994-03-29 CA CA002157766A patent/CA2157766A1/en not_active Abandoned
- 1994-03-29 PL PL94310897A patent/PL310897A1/xx unknown
- 1994-03-29 SG SG1996005776A patent/SG52542A1/en unknown
- 1994-03-29 AU AU66214/94A patent/AU685803B2/en not_active Ceased
- 1994-03-29 JP JP6522278A patent/JPH08510205A/ja active Pending
- 1994-03-29 EP EP94913965A patent/EP0692971A4/en not_active Withdrawn
- 1994-10-24 US US08/329,151 patent/US5604203A/en not_active Expired - Lifetime
-
1995
- 1995-09-26 FI FI954559A patent/FI954559A/fi unknown
Also Published As
Publication number | Publication date |
---|---|
KR960701653A (ko) | 1996-03-28 |
EP0692971A1 (en) | 1996-01-24 |
FI954559A0 (fi) | 1995-09-26 |
US5604203A (en) | 1997-02-18 |
AU685803B2 (en) | 1998-01-29 |
CA2157766A1 (en) | 1994-10-13 |
AU6621494A (en) | 1994-10-24 |
NZ265452A (en) | 1997-09-22 |
JPH08510205A (ja) | 1996-10-29 |
HUT73494A (en) | 1996-08-28 |
FI954559A (fi) | 1995-09-26 |
EP0692971A4 (en) | 1997-11-12 |
SG52542A1 (en) | 1998-09-28 |
CN1124927A (zh) | 1996-06-19 |
HU9502833D0 (en) | 1995-11-28 |
PL310897A1 (en) | 1996-01-08 |
WO1994022467A1 (en) | 1994-10-13 |
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