MA30530B1 - Synthese de peptides insulinotropes - Google Patents
Synthese de peptides insulinotropesInfo
- Publication number
- MA30530B1 MA30530B1 MA31510A MA31510A MA30530B1 MA 30530 B1 MA30530 B1 MA 30530B1 MA 31510 A MA31510 A MA 31510A MA 31510 A MA31510 A MA 31510A MA 30530 B1 MA30530 B1 MA 30530B1
- Authority
- MA
- Morocco
- Prior art keywords
- fragments
- solution
- synthesis
- insulinotropic peptides
- solid phase
- Prior art date
Links
Classifications
-
- 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
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
-
- 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
- C07K14/605—Glucagons
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
- A61K38/26—Glucagons
-
- 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
- C07K14/62—Insulins
-
- 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)
- General Health & Medical Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Zoology (AREA)
- Gastroenterology & Hepatology (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Toxicology (AREA)
- Endocrinology (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (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
Synthèse de peptides insulinotropes La présente invention concerne la préparation de peptides insulinotropes qui sont synthétisés en utilisant une approche en phase solide et en solution (« hybride »). De manière générale, l'approche comprend la synthèse de trois fragments peptidiques intermédiaires différents en utilisant un processus chimique en phase solide. Un processus chimique en solution est ensuite utilisé pour ajouter des aminoacides supplémentaires à un des fragments. Puis les fragments sont couplés les uns aux autres dans la phase solide-solution. L'utilisation d'une pseudoproline dans un des fragments facilite la synthèse en phase solide de ce fragment et facilite également le couplage ultérieur, en solution, de ce fragment aux autres fragments. La présente invention est très utile pour former des peptides insulinotropes tels que le GLP-1(7-36) et ses analogues naturels et non naturels.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US81591906P | 2006-06-23 | 2006-06-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
MA30530B1 true MA30530B1 (fr) | 2009-06-01 |
Family
ID=38596729
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA31510A MA30530B1 (fr) | 2006-06-23 | 2008-12-25 | Synthese de peptides insulinotropes |
Country Status (33)
Country | Link |
---|---|
US (2) | US20080004429A1 (fr) |
EP (1) | EP2035451B1 (fr) |
JP (1) | JP4537495B2 (fr) |
KR (1) | KR101087859B1 (fr) |
CN (1) | CN101563364B (fr) |
AR (1) | AR061604A1 (fr) |
AT (1) | ATE466881T1 (fr) |
AU (1) | AU2007263043B2 (fr) |
BR (1) | BRPI0713575A2 (fr) |
CA (1) | CA2654610C (fr) |
CL (1) | CL2007001835A1 (fr) |
CR (1) | CR10463A (fr) |
CY (1) | CY1110186T1 (fr) |
DE (1) | DE602007006310D1 (fr) |
DK (1) | DK2035451T3 (fr) |
EC (1) | ECSP088999A (fr) |
ES (1) | ES2341588T3 (fr) |
HR (1) | HRP20100302T1 (fr) |
IL (1) | IL195421A0 (fr) |
MA (1) | MA30530B1 (fr) |
MX (1) | MX2008015935A (fr) |
MY (1) | MY144608A (fr) |
NO (1) | NO20084863L (fr) |
NZ (1) | NZ573093A (fr) |
PL (1) | PL2035451T3 (fr) |
PT (1) | PT2035451E (fr) |
RS (1) | RS51281B (fr) |
RU (1) | RU2448978C2 (fr) |
SI (1) | SI2035451T1 (fr) |
TW (1) | TWI331155B (fr) |
UA (1) | UA96602C2 (fr) |
WO (1) | WO2007147816A1 (fr) |
ZA (1) | ZA200810072B (fr) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5473925B2 (ja) | 2007-10-27 | 2014-04-16 | コーデン ファーマ コロラド インコーポレイテッド | 固相および溶液相の組み合わせ技法を使用するインスリン分泌性ペプチドの合成 |
EP2222695A2 (fr) * | 2007-12-11 | 2010-09-01 | F. Hoffmann-La Roche AG | Synthèse de peptides insulinotropiques mettant en uvre des techniques de combinaison de phases solides et en solution |
US20100317057A1 (en) * | 2007-12-28 | 2010-12-16 | Novo Nordisk A/S | Semi-recombinant preparation of glp-1 analogues |
US20100183876A1 (en) * | 2008-12-23 | 2010-07-22 | Hell Andre | Process for the Preparation of a Peptide Powder Form |
CN102414220A (zh) * | 2009-05-01 | 2012-04-11 | 霍夫曼-拉罗奇有限公司 | 使用固相和液相组合技术的促胰岛素肽合成 |
US20110313131A1 (en) | 2010-06-21 | 2011-12-22 | Christelle Carl | Reversed phase hplc purification of a glp-1 analogue |
US20120157382A1 (en) | 2010-12-21 | 2012-06-21 | Siegfried Krimmer | Pharmaceutical glp-1 compositions having an improved release profile |
DK2788110T3 (en) * | 2011-12-08 | 2019-02-11 | Pentair Water Pool & Spa Inc | AQUACULTURE SYSTEM AND PROCEDURE TO OPERATE A PUMP IN SUCH A SYSTEM |
RU2643515C2 (ru) | 2011-12-29 | 2018-02-02 | Ново Нордиск А/С | Дипептид, содержащий непротеиногенную аминокислоту |
CN104936610A (zh) | 2012-11-13 | 2015-09-23 | 益普生制药股份有限公司 | Glp-1类似物的纯化方法 |
WO2014077801A1 (fr) | 2012-11-13 | 2014-05-22 | Ipsen Pharma S.A.S. | Procédé de purification pour préparer du tasoglutide de haute pureté |
GR20140100479A (el) * | 2014-09-23 | 2016-05-05 | Novetide, Ltd., | Συνθεση λιραγλουτιδης |
CA3093221A1 (fr) | 2018-03-09 | 2019-09-12 | Enzypep B.V. | Synthese chimio-enzymatique de liraglutide, de semaglutide et de glp-1 |
EP3762408A1 (fr) | 2018-03-09 | 2021-01-13 | Enzypep B.V. | Synthèse chimio-enzymatique de semaglutide, de liraglutide et de glp-1 |
ES2938734T3 (es) * | 2018-10-09 | 2023-04-14 | Fresenius Kabi Ipsum S R L | Procedimiento para la fabricación de análogos de GLP-1 |
TWI738260B (zh) | 2019-03-25 | 2021-09-01 | 台灣神隆股份有限公司 | 純化利拉魯肽之方法 |
CN114401981A (zh) * | 2019-06-18 | 2022-04-26 | 北京费森尤斯卡比医药有限公司 | 胰高血糖素制造方法 |
EP3753946A1 (fr) | 2019-06-18 | 2020-12-23 | Fresenius Kabi iPSUM S.r.l. | Procédé amélioré pour la préparation de glucagon à pureté élevée |
US20230406900A1 (en) * | 2022-06-01 | 2023-12-21 | Scinopharm Taiwan, Ltd. | Process for preparing glucagon-like peptide-1 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6281335B1 (en) * | 1993-10-08 | 2001-08-28 | Coulter Corporation | Hybridoma and anti-KC-4 humanized monoclonal antibody |
US5705483A (en) * | 1993-12-09 | 1998-01-06 | Eli Lilly And Company | Glucagon-like insulinotropic peptides, compositions and methods |
EP0820296A4 (fr) * | 1995-04-14 | 1999-06-30 | Univ Tulane | Analogues du facteur liberant l'hormone de croissance |
UA65549C2 (uk) * | 1996-11-05 | 2004-04-15 | Елі Ліллі Енд Компані | Спосіб регулювання ожиріння шляхом периферійного введення аналогів та похідних glp-1 (варіанти) та фармацевтична композиція |
US6281331B1 (en) * | 1998-03-23 | 2001-08-28 | Trimeris, Inc. | Methods and compositions for peptide synthesis |
US6903186B1 (en) * | 1998-12-07 | 2005-06-07 | Societe De Conseils De Recherches Et D'applications Scientifiques, S.A.S | Analogues of GLP-1 |
US6514500B1 (en) * | 1999-10-15 | 2003-02-04 | Conjuchem, Inc. | Long lasting synthetic glucagon like peptide {GLP-!} |
US7238671B2 (en) | 2001-10-18 | 2007-07-03 | Bristol-Myers Squibb Company | Human glucagon-like-peptide-1 mimics and their use in the treatment of diabetes and related conditions |
WO2005063792A2 (fr) * | 2003-12-31 | 2005-07-14 | F. Hoffmann-La Roche Ag | Procedes pour recuperer un peptide clive a partir d'un support |
-
2007
- 2007-06-19 BR BRPI0713575-0A patent/BRPI0713575A2/pt not_active IP Right Cessation
- 2007-06-19 RS RSP-2010/0267A patent/RS51281B/sr unknown
- 2007-06-19 NZ NZ573093A patent/NZ573093A/en not_active IP Right Cessation
- 2007-06-19 EP EP07765481A patent/EP2035451B1/fr active Active
- 2007-06-19 AU AU2007263043A patent/AU2007263043B2/en not_active Ceased
- 2007-06-19 SI SI200730229T patent/SI2035451T1/sl unknown
- 2007-06-19 DK DK07765481.2T patent/DK2035451T3/da active
- 2007-06-19 CA CA2654610A patent/CA2654610C/fr not_active Expired - Fee Related
- 2007-06-19 JP JP2009515856A patent/JP4537495B2/ja not_active Expired - Fee Related
- 2007-06-19 WO PCT/EP2007/056052 patent/WO2007147816A1/fr active Application Filing
- 2007-06-19 UA UAA200900414A patent/UA96602C2/ru unknown
- 2007-06-19 CN CN200780023265.1A patent/CN101563364B/zh not_active Expired - Fee Related
- 2007-06-19 RU RU2009101969/04A patent/RU2448978C2/ru not_active IP Right Cessation
- 2007-06-19 AT AT07765481T patent/ATE466881T1/de active
- 2007-06-19 KR KR1020087031096A patent/KR101087859B1/ko not_active IP Right Cessation
- 2007-06-19 MY MYPI20085211A patent/MY144608A/en unknown
- 2007-06-19 MX MX2008015935A patent/MX2008015935A/es active IP Right Grant
- 2007-06-19 DE DE602007006310T patent/DE602007006310D1/de active Active
- 2007-06-19 ES ES07765481T patent/ES2341588T3/es active Active
- 2007-06-19 PL PL07765481T patent/PL2035451T3/pl unknown
- 2007-06-19 PT PT07765481T patent/PT2035451E/pt unknown
- 2007-06-21 US US11/821,017 patent/US20080004429A1/en not_active Abandoned
- 2007-06-21 AR ARP070102735A patent/AR061604A1/es not_active Application Discontinuation
- 2007-06-22 CL CL200701835A patent/CL2007001835A1/es unknown
- 2007-06-22 TW TW096122579A patent/TWI331155B/zh not_active IP Right Cessation
-
2008
- 2008-11-19 NO NO20084863A patent/NO20084863L/no not_active Application Discontinuation
- 2008-11-20 IL IL195421A patent/IL195421A0/en unknown
- 2008-11-26 CR CR10463A patent/CR10463A/es not_active Application Discontinuation
- 2008-11-26 ZA ZA200810072A patent/ZA200810072B/xx unknown
- 2008-12-22 EC EC2008008999A patent/ECSP088999A/es unknown
- 2008-12-25 MA MA31510A patent/MA30530B1/fr unknown
-
2010
- 2010-05-27 HR HR20100302T patent/HRP20100302T1/hr unknown
- 2010-06-11 CY CY20101100519T patent/CY1110186T1/el unknown
-
2011
- 2011-05-11 US US13/105,435 patent/US20110213082A1/en not_active Abandoned
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MA30530B1 (fr) | Synthese de peptides insulinotropes | |
González-Montoya et al. | Bioactive peptides from germinated soybean with anti-diabetic potential by inhibition of dipeptidyl peptidase-IV, α-amylase, and α-glucosidase enzymes | |
TWI646112B (zh) | Pd-1/pd-l1及cd80(b7-1)/pd-l1蛋白質/蛋白質交互作用之大環狀抑制劑 | |
TWI255271B (en) | Analogues of GLP-1 | |
Ferder et al. | The world pandemic of vitamin D deficiency could possibly be explained by cellular inflammatory response activity induced by the renin-angiotensin system | |
JP5635529B2 (ja) | グルカゴン類似体 | |
MX2010006044A (es) | Sintesis de peptidos insulinotropicos utilizando una combinacion de tecnicas en fase solida y en solucion. | |
Thapa et al. | The emergence of cyclic peptides: The potential of bioengineered peptide drugs | |
WO2005076744A3 (fr) | Procede de preparation de conjugues peptides/oligonucleotides | |
JP2016147895A (ja) | 自己免疫疾患の治療方法及びそれに関する試薬 | |
JP2010001301A (ja) | Glp−1の類似体 | |
SA518391996B1 (ar) | نظائر عامل النمو الجلدي شبيه مجال أ ببدائل حمض دهني | |
Dekan et al. | Total synthesis of human hepcidin through regioselective disulfide‐bond formation by using the safety‐catch cysteine protecting group 4, 4′‐dimethylsulfinylbenzhydryl | |
WO2010059920A3 (fr) | Système et procédé pour générer une image en 2d à partir d'un ensemble de données de tomosynthèse | |
US9364449B2 (en) | Peptoid and synthetic oligomers, pharmaceutical compositions and methods of using same | |
Thomas et al. | Proline editing: a divergent strategy for the synthesis of conformationally diverse peptides | |
Lagu et al. | Selective PPARδ modulators improve mitochondrial function: potential treatment for duchenne muscular dystrophy (DMD) | |
MA31133B1 (fr) | Nouveau peptide d'actinomadura namibiensis | |
Tornøe et al. | Divergent protein synthesis of Bowman–Birk protease inhibitors, their hydrodynamic behavior and co-crystallization with α-chymotrypsin | |
Bojarska et al. | A Proline-Based Tectons and Supramolecular Synthons for Drug Design 2.0: A Case Study of ACEI | |
EA201171292A1 (ru) | Короткоцепочечные пептиды в качестве агониста рецептора паратиреоидного гормона (pth) | |
Majer et al. | Structure‐based subsite specificity mapping of human cathepsin D using statine‐based inhibitors | |
Gary et al. | Peptide Carbo cycles: From− SS–to− CC–via a Late-Stage “Snip-and-Stitch” | |
JP6517732B2 (ja) | Dpp−4阻害剤、血糖値上昇抑制剤およびdpp−4阻害用食品 | |
Rodhi et al. | A review on the types of amino acid at ultimate, penultimate and antepenultimate position in some dipeptidyl-peptidase IV inhibitory peptides based on molecular docking analysis |