MX2015013463A - Sintesis de productos peptidicos que contienen imida ciclica. - Google Patents

Sintesis de productos peptidicos que contienen imida ciclica.

Info

Publication number
MX2015013463A
MX2015013463A MX2015013463A MX2015013463A MX2015013463A MX 2015013463 A MX2015013463 A MX 2015013463A MX 2015013463 A MX2015013463 A MX 2015013463A MX 2015013463 A MX2015013463 A MX 2015013463A MX 2015013463 A MX2015013463 A MX 2015013463A
Authority
MX
Mexico
Prior art keywords
cyclic imide
synthesis
containing peptide
peptide products
imide containing
Prior art date
Application number
MX2015013463A
Other languages
English (en)
Other versions
MX365465B (es
Inventor
Bernd Henkel
Original Assignee
Sanofi Aventis Deutschland
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sanofi Aventis Deutschland filed Critical Sanofi Aventis Deutschland
Publication of MX2015013463A publication Critical patent/MX2015013463A/es
Publication of MX365465B publication Critical patent/MX365465B/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/107—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides
    • C07K1/1072—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides by covalent attachment of residues or functional groups
    • C07K1/1077—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides by covalent attachment of residues or functional groups by covalent attachment of residues other than amino acids or peptide residues, e.g. sugars, polyols, fatty acids
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/006—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length of peptides containing derivatised side chain amino acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/04—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length on carriers
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/04—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length on carriers
    • C07K1/042—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length on carriers characterised by the nature of the carrier
    • 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
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30—Low-molecular-weight compounds
    • C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
    • C08G18/3819—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen
    • C08G18/3842—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen containing heterocyclic rings having at least one nitrogen atom in the ring
    • C08G18/3844—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen containing heterocyclic rings having at least one nitrogen atom in the ring containing one nitrogen atom in the ring
    • C08G18/3846—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen containing heterocyclic rings having at least one nitrogen atom in the ring containing one nitrogen atom in the ring containing imide groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/32—Polymers modified by chemical after-treatment
    • C08G65/329—Polymers modified by chemical after-treatment with organic compounds
    • C08G65/333—Polymers modified by chemical after-treatment with organic compounds containing nitrogen
    • C08G65/33331—Polymers modified by chemical after-treatment with organic compounds containing nitrogen containing imide group

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Medicinal Chemistry (AREA)
  • Biophysics (AREA)
  • Genetics & Genomics (AREA)
  • Analytical Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Toxicology (AREA)
  • Zoology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Immunology (AREA)
  • Biomedical Technology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Endocrinology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Cell Biology (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • Food Science & Technology (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Indole Compounds (AREA)

Abstract

La presente invención se relaciona con un método para sintetizar un producto peptídico que comprende al menos un grupo amida cíclica. Además, la invención se relaciona con un producto peptídico que comprende al menos un grupo imida cíclica, que está sustancialmente libre de productos de degradación. El producto peptídico puede usarse como un material de referencia para el control de calidad de los péptidos farmacéuticos, particularmente para el control de calidad de un agonista de GLP-1 como los péptidos exendina.
MX2015013463A 2013-03-21 2014-03-19 Sintesis de productos peptidicos que contienen imida ciclica. MX365465B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP13160380 2013-03-21
PCT/EP2014/055511 WO2014147129A1 (en) 2013-03-21 2014-03-19 Synthesis of cyclic imide containing peptide products

Publications (2)

Publication Number Publication Date
MX2015013463A true MX2015013463A (es) 2016-06-21
MX365465B MX365465B (es) 2019-06-04

Family

ID=47900953

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2015013463A MX365465B (es) 2013-03-21 2014-03-19 Sintesis de productos peptidicos que contienen imida ciclica.

Country Status (11)

Country Link
US (1) US10450343B2 (es)
EP (1) EP2976325B1 (es)
CN (1) CN105102427B (es)
AU (1) AU2014234314B2 (es)
CA (1) CA2907521C (es)
DK (1) DK2976325T3 (es)
ES (1) ES2624961T3 (es)
HU (1) HUE033371T2 (es)
MX (1) MX365465B (es)
SG (1) SG11201506885UA (es)
WO (1) WO2014147129A1 (es)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018032521A1 (zh) * 2016-08-19 2018-02-22 深圳市健元医药科技有限公司 一种利拉鲁肽的合成方法

Family Cites Families (224)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3906031A (en) 1971-03-15 1975-09-16 Research Corp Novel 9-fluorenylmethoxycarbonyl compounds
US3835175A (en) 1971-03-15 1974-09-10 Research Corp 9-fluorenylmethanol haloformates, carbonates and thiocarbonates
US4108846A (en) 1977-02-01 1978-08-22 Hoffmann-La Roche Inc. Solid phase synthesis with base N alpha-protecting group cleavage
DE3542442A1 (de) 1985-11-30 1987-06-04 Hoechst Ag Verfahren zur herstellung von peptiden unter der verwendung von perchloraten
US5175254A (en) 1988-09-24 1992-12-29 Societe D'expansion Scientifque Expansia Solid phase peptide synthesis using a polyacrylic support in aqueous solution
GB8913089D0 (en) 1989-06-07 1989-07-26 Ciba Geigy Japan Ltd Novel endothelin derivative
US5296468A (en) 1989-10-30 1994-03-22 The Salk Institute For Biological Studies GnRH analogs
US5580957A (en) 1989-10-30 1996-12-03 The Salk Institute For Biological Studies GnRH analogs
US5352796A (en) 1989-10-30 1994-10-04 The Salk Institute For Biological Studies Amino acids useful in making GnRH analogs
US5169932A (en) 1989-10-30 1992-12-08 The Salk Institute For Biological Studies Gnrh analogs
EP0445801A3 (en) 1990-03-08 1992-07-01 Kuraray Co., Ltd. Peptide and its use
IT1241395B (it) 1990-04-02 1994-01-10 Eniricerche Spa Composti immunogenici,il procedimento per la loro sintesi e loro impiego per la preparazione di vaccini antimalaria
DE4014655A1 (de) 1990-05-08 1991-11-14 Behringwerke Ag Peptidamide, verfahren zu deren herstellung und diese enthaltende mittel als fibrin/thrombin-gerinnungsinhibitoren
TW295589B (es) 1990-08-30 1997-01-11 Hoechst Ag
DE4027675C2 (de) 1990-08-31 1997-05-07 Biotechnolog Forschung Gmbh Verfahren zur parallelen Herstellung von trägergebundenen oder freien Peptiden, trägergebundene Peptide und ihre Verwendung
IL101074A (en) 1991-03-14 1997-09-30 Salk Inst For Biological Studi GnRH ANALOGS AND THEIR PREPARATION
US5744450A (en) 1991-03-14 1998-04-28 The Salk Institute For Biological Studies GnRH analogs
SE9101472D0 (sv) 1991-05-15 1991-05-15 Trion Forskning & Utveckling Galanin antagonist
US5576296A (en) 1991-05-15 1996-11-19 Aktiebolaget Astra Galanin antagonist
GB9112825D0 (en) 1991-06-14 1991-07-31 Ici Plc Process for making peptides
JP3407260B2 (ja) 1991-08-09 2003-05-19 コルベツク，ヴインフリート ランチオニン架橋ペプチド
US6028168A (en) 1991-08-09 2000-02-22 Winfried Kolbeck Lanthionine bridged peptides
US5639603A (en) 1991-09-18 1997-06-17 Affymax Technologies N.V. Synthesizing and screening molecular diversity
CA2118806A1 (en) 1991-09-18 1993-04-01 William J. Dower Method of synthesizing diverse collections of oligomers
CA2104099A1 (en) 1991-12-18 1993-06-19 George A. Heavner Peptide inhibitors of inflammation mediated by selectins
US6709828B1 (en) 1992-03-06 2004-03-23 N.V. Innogenetics S.A. Process for the determination of peptides corresponding to immunologically important epitopes and their use in a process for determination of antibodies or biotinylated peptides corresponding to immunologically important epitopes, a process for preparing them and compositions containing them
KR20030096423A (ko) 1992-03-06 2003-12-31 엔. 브이. 이노제네틱스 소시에떼아노님 면역학적으로 중요한 에피토프에 상응하는 펩티드의 측정방법 및 면역학적으로 중요한 에피토프에 상응하는 항체또는 비오티닐화된 펩티드의 측정 방법에 상기 펩티드를사용하는 방법, 상기 펩티드의 제조방법 및 상기 펩티드를함유하는 조성물
US6667387B1 (en) 1996-09-30 2003-12-23 N.V. Innogenetics S.A. HCV core peptides
WO1993024526A1 (en) 1992-05-28 1993-12-09 Centocor, Inc. Peptide inhibitors of selectin binding
IE921942A1 (en) 1992-06-16 1993-12-29 Gary A Siwruk John S Eynon Liquid phase synthesis of peptides and peptide derivatives
US5516891A (en) 1992-06-16 1996-05-14 Kinerton, Ltd. Liquid phase synthesis of peptides and peptide derivatives
WO1994005314A1 (en) 1992-09-08 1994-03-17 Centocor, Inc. Peptide inhibitors of leukocyte adhesion
US5563032A (en) 1992-10-21 1996-10-08 The United States Of America As Represented By The Department Of Health And Human Services Mosaic polypeptide and methods for detecting the hepatitis E virus
US5736315A (en) 1992-10-21 1998-04-07 National Institute Of Health Methods and compositions for detecting anti-hepatitis E virus activity
WO1994014836A1 (en) 1992-12-18 1994-07-07 Centocor, Inc. Peptide inhibitors of selectin binding
DE4244565A1 (de) 1992-12-30 1994-07-07 Forssmann Wolf Georg Verfahren und Anwendung des LPAP (Lymphocytoma Proliferation Activating Peptide
ES2133428T3 (es) 1993-02-19 1999-09-16 Hoffmann La Roche Fabricacion de amidas y peptidos, exenta de racemizacion, en presencia de cantidades cataliticas de un compuesto n-hidroxi.
JPH06256384A (ja) 1993-02-26 1994-09-13 Shimadzu Corp クリーベイジ装置
GB9319776D0 (en) 1993-09-24 1993-11-10 Medical Res Council Azapeptide synthesis
US5503805A (en) 1993-11-02 1996-04-02 Affymax Technologies N.V. Apparatus and method for parallel coupling reactions
US6165778A (en) 1993-11-02 2000-12-26 Affymax Technologies N.V. Reaction vessel agitation apparatus
CN1134156A (zh) 1993-11-02 1996-10-23 阿菲马克斯技术公司 合成和筛选多种分子
WO1995014787A1 (en) 1993-11-22 1995-06-01 Centocor, Inc. Peptide inhibitors of selecting binding
DE4341471A1 (de) 1993-12-02 1995-06-08 Schering Ag Tumor-Nekrose-Faktor-alpha-inaktivierende CDR-Peptide
US5502165A (en) 1994-04-04 1996-03-26 Merck & Co., Inc. Process for peptide segment condensation
US5614608A (en) 1995-01-20 1997-03-25 Selectide Corporation Apparatus and method for multiple synthesis of organic compounds on polymer support
AU5514396A (en) 1995-04-28 1996-11-18 Takeda Chemical Industries Ltd. Cyclic pentapeptide lh-rh receptor antagonists
GB9511474D0 (en) 1995-06-07 1995-08-02 Ciba Geigy Ag Antiviral peptoid compounds
DE19534988A1 (de) 1995-09-21 1997-03-27 Forssmann Wolf Georg Verfahren zur Herstellung und Anwendung synthetischer, biotinylierter Peptide
DE19543628A1 (de) 1995-11-24 1997-05-28 Forssmann Wolf Georg Humanes, im Blut zirkulierendes Peptid mit insulinotroper Wirkung (GCAP-II-(89-112), (Guanylyl Cyclase C Aktivierendes Peptid II) und seine GCAP-Analoga, insbesondere das GCAP-I-(99-115), seine Anwendung als pharmakologischer Wirkstoff und Benutzung seines Wirkungsprinzipes zur Bereitstellung neuer GC-C-abhängiger insulinotroper Wirkstoffe
TW505654B (en) 1996-07-30 2002-10-11 Hoffmann La Roche Synthesis of analogs of PTH and PTHrP
DK0929567T3 (da) 1996-09-09 2005-06-27 Zealand Pharma As Forbedret fastfase-peptidsyntese og middel til anvendelse af en sådan syntese
KR20000036015A (ko) 1996-09-09 2000-06-26 스타이니스 에바 알파-히드록시산 링커를 함유하는 펩티드 프로드럭
US7176282B1 (en) 1996-09-09 2007-02-13 Zealand Pharma A/S Solid-phase peptide synthesis and agent for use in such synthesis
WO1998031791A1 (en) 1997-01-21 1998-07-23 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Berlin Iga1 protease fragment as carrier peptide
NZ506839A (en) 1998-03-09 2003-05-30 Zealand Pharma As Pharmacologically active peptide conjugates having a reduced tendency towards enzymatic hydrolysis
WO2000018791A1 (en) * 1998-09-29 2000-04-06 Statens Serum Institut Ligand presenting assembly (lpa), method of preparation and uses thereof
JP3786533B2 (ja) 1998-11-12 2006-06-14 善彦 西村 ペプチド及び骨形成促進剤
IL143666A0 (en) 1998-12-11 2002-04-21 Coulter Pharm Inc Prodrug compounds and process for preparation thereof
US7425541B2 (en) 1998-12-11 2008-09-16 Medarex, Inc. Enzyme-cleavable prodrug compounds
FR2792631B1 (fr) 1999-04-21 2004-03-19 Pasteur Institut Support solide fonctionnalise pour la synthese de composes comportant au moins une fonction alpha oxoaldehyde et ses applications.
US6469136B1 (en) 1999-07-07 2002-10-22 Trimeris, Inc. Methods and composition for peptide synthesis
US6703480B1 (en) 1999-11-24 2004-03-09 Palani Balu Peptide dimers as agonists of the erythropoientin (EPO) receptor, and associated methods of synthesis and use
FR2803594B1 (fr) 2000-01-11 2002-07-19 Centre Nat Rech Scient Oligomeres de mimes contraints non peptidiques de dipeptides ou de tripeptides, et leurs utilisations
DE60102899T2 (de) 2000-01-27 2005-03-31 Eli Lilly And Co., Indianapolis Verfahren zur lösung von glucagon-ähnlichen peptid-1 (glp-1) verbindungen
US6476186B1 (en) 2000-05-23 2002-11-05 Institute Of Nuclear Energy Research Process for preparing octreotide and derivatives thereof
AU7130101A (en) 2000-06-14 2001-12-24 Corixa Corp Enzyme-cleavable prodrug compounds
US20020058788A1 (en) 2000-08-25 2002-05-16 Sheppeck James E. Facile deprotection of Fmoc protected amino groups
NO314588B1 (no) 2000-09-04 2003-04-14 Bionor Immuno As HIV-peptider, antigener, vaksinesammensetning, immunoassay- testsett og en fremgangsmåte for å påvise antistoffer indusert av HIV
WO2002040512A2 (de) 2000-11-14 2002-05-23 Ipf Pharmaceuticals Gmbh Humanes beta-defensin-3
JP2004513191A (ja) 2001-01-04 2004-04-30 カウンシル・オブ・サイエンティフィック・アンド・インダストリアル・リサーチ ペプチドおよび小分子有機合成用の新しいリンカーに基づく固相支持体
GB0105069D0 (en) 2001-03-01 2001-04-18 Univ Ulster The Modified peptide
US20090281032A1 (en) 2001-03-01 2009-11-12 Peter Raymond Flatt Modified CCK peptides
BR0101088A (pt) 2001-03-19 2003-03-18 Biolab Sanus Farmaceutica Ltda Processo de isolamento e purificação de peptìdeos inibidores das vasopeptidases, com especificidade para o sìtio carboxìlico da enzima conversora da angiotensina, secretados pelas glândulas do veneno de serpentes (bpps), particularmente bothrops jararaca, ou produzidos endogenamente (evasins) possuindo ação vasodilatadora e anti-hipertensiva; processo de determinação da sequência de amido-ácidos dos peptìdios inibidores secretados pela glândula de veneno de serpentes (bpps) ou endógenos (evasins); processo de determinação da sequência de aminoácidos dos bpps por dedução do cdna dos precursores dessas moléculas expressos em tecidos de serpentes, especificamente bothrops jararaca. processo de determinação da sequência de aminoácidos dos evasins por dedução do cdna dos precursores dessas moléculas expressos em tecidos de serpentes, especificamente bothrops jararaca, processo de amplificação do cdna a partir das bibliotecas de cdna de pâncreas e/ou cérebro de serpentes, especificamente bothrops jararaca; processo de sìntese em fase sólida de peptìdeos inibidores das vasopeptidases com ação vasodilatadora e anti-hipertensiva, peptìdeos inibidores das vasopeptidases com ação anti-hipertensiva; utilização dos peptìdeos inibidores das vaso peptidases com ação vasodilatadora e anti-hipertensiva na obtenção de composições farmacêuticas; processo de determinação da atividade inibitória sobre as vasopeptidases e de atividade biológica sobre músculo liso, sistema cardiovascular e microcirculatório.
WO2002083606A1 (en) 2001-04-17 2002-10-24 University Of Alberta A linker system for the synthesis and screening of combinatorial libraries of polyamine derivatives on water compatible supports
CN1162446C (zh) 2001-05-10 2004-08-18 上海华谊生物技术有限公司 促胰岛素分泌肽衍生物
FR2825095B1 (fr) 2001-05-28 2003-09-26 Dev Des Antigenes Combinatoire Dispositif de presentation de polypeptides, utilisable comme "puce" pour la detection miniaturisee de molecules
AU2002326103A1 (en) 2001-08-24 2003-03-10 University Of British Columbia Solid-phase synthesis of oligosaccharides and glycopeptides using glycosynthases
EP1493747B1 (en) 2002-04-11 2012-12-19 Daiichi Sankyo Company, Limited Process for producing modified peptide
US6809190B2 (en) 2002-04-24 2004-10-26 Credia Japan Co., Ltd. Functional peptide nucleic acid and its production method
GB0210183D0 (en) 2002-05-03 2002-06-12 Avecia Ltd Process
WO2003093302A2 (en) 2002-05-03 2003-11-13 Avecia Limited Process for the synthesis of peptides amides by side-chain attachement to a solid phase
WO2003095475A2 (en) 2002-05-10 2003-11-20 Pharmacia Corporation Peptide compounds and their use as protease substrates
ES2195787B1 (es) 2002-05-20 2005-06-01 Diverdrugs, S.L. Compuestos capaces de bloquear la respuesta a sustancias quimicas o estimulos termicos o mediadores de la inflamacion de los nociceptores, un metodo para su obtencion y composiciones que los continen.
BR0313019A (pt) 2002-08-09 2005-07-12 Yamanouchi Europ Bv Compostos que se ligam a p-selectina
AU2003273298B2 (en) 2002-09-08 2008-03-06 Applera Corporation Methods, compositions and libraries pertaining PNA dimer and PNA oligomer synthesis
CA2500295A1 (en) * 2002-10-02 2004-04-29 Zealand Pharma A/S Stabilized exendin-4 compounds
EP1445260A1 (de) 2003-02-04 2004-08-11 Jerini AG Verfahren zur Immobilisierung von chemischen Verbindungen an Festphasen
CA2521188C (en) 2003-04-08 2012-06-26 Novo Nordisk A/S Regeneration of chromatographic stationary phases
CN1771080B (zh) 2003-04-08 2010-12-15 诺沃挪第克公司 包括至少一个色谱处理步骤的生产治疗用多肽或其前体的方法
WO2004092377A1 (ja) 2003-04-15 2004-10-28 Credia Japan Co., Ltd. 新規な機能性ペプチド核酸およびその製法
EP1631597A4 (en) 2003-05-22 2007-07-11 Gryphon Therapeutics Inc SOLID PHASE CHEMICAL LIGATION CARRIED OUT WITH A MOBILE BONDING AGENT
WO2004105790A1 (en) 2003-06-03 2004-12-09 Novo Nordisk A/S Stabilized pharmaceutical peptide compositions
US7414106B2 (en) 2003-06-19 2008-08-19 Lawrence Livermore National Security, Llc Synthesis of peptide α-thioesters
US7902488B2 (en) 2003-06-23 2011-03-08 Cem Corporation Microwave-assisted peptide synthesis
US7393920B2 (en) 2003-06-23 2008-07-01 Cem Corporation Microwave-assisted peptide synthesis
EP1664109B1 (en) 2003-08-21 2009-07-22 Novo Nordisk A/S Purification of glucagon-like peptides
EP1701969B1 (en) 2003-12-31 2007-10-24 F.Hoffmann-La Roche Ag Process for peptide synthesis using a reduced amount of deprotection agent
FR2864830B1 (fr) 2004-01-06 2006-03-10 Centre Nat Rech Scient Procede de synthese sur support solide de composes peptidiques, notamment de composes peptidiques comportant un residu arginine
EP1713723A2 (en) * 2004-01-14 2006-10-25 William Marsh Rice University Fullerene based amino acids
EP1718671A2 (en) 2004-02-23 2006-11-08 Rheoscience A/S Peptide yy analogues
CA2458084A1 (en) 2004-03-12 2005-09-12 Dalton Chemical Laboratories Inc. Novel process for octreotide synthesis
US7534763B2 (en) 2004-07-02 2009-05-19 Bristol-Myers Squibb Company Sustained release GLP-1 receptor modulators
TW200611704A (en) 2004-07-02 2006-04-16 Bristol Myers Squibb Co Human glucagon-like-peptide-1 modulators and their use in the treatment of diabetes and related conditions
DK1771463T3 (da) 2004-07-16 2008-04-21 Lonza Ag Fremgangsmåde til peptidsyntese
JP4878031B2 (ja) 2004-10-12 2012-02-15 エフ．ホフマン−ラ ロシュ アーゲー 固相ペプチド合成法
EP1814908A4 (en) 2004-11-22 2009-07-01 Biosight Ltd Activated labeling reagents and method for their preparation and use
US7745570B2 (en) 2004-12-17 2010-06-29 Kansas State University Research Foundation PH dependent adhesive peptides
US8716221B2 (en) 2005-01-14 2014-05-06 Wuxi Grandchamp Pharmaceutical Technology Co., Ltd. Modified exendins and uses thereof
EP1845105A4 (en) 2005-01-14 2009-02-18 Wuxi Grandchamp Pharmaceutical MODIFIED EXENDINES AND CORRESPONDING USES
JP2008534639A (ja) 2005-04-08 2008-08-28 ロンザ ア−ゲ− Ｐｅｇ樹脂上におけるアルファ−ヘリックスのペプチド合成
KR20080012884A (ko) 2005-05-04 2008-02-12 론자 아게 펩타이드 합성 방법
CN1298732C (zh) 2005-05-17 2007-02-07 南京工业大学 多肽微波固相合成法
PE20061448A1 (es) 2005-05-26 2006-12-17 Bristol Myers Squibb Co Compuestos polipeptidos como moduladores del peptido 1 similar al glucagon humano
EP1805204A2 (en) 2005-09-14 2007-07-11 Novetide Ltd. Process for production of bivalirudin
EP1965823B1 (en) 2005-11-04 2016-05-18 Glaxosmithkline LLC Methods for administering hypoglycemic agents
CN100374462C (zh) 2005-11-21 2008-03-12 大连帝恩生物工程有限公司 截短胰高血糖素样肽1(sGLP-1)、制法及其应用
WO2007065691A2 (en) 2005-12-07 2007-06-14 Technische Universität München Small peptidic and peptido-mimetic affinity ligands for factor viii and factor viii-like proteins
WO2007114454A1 (ja) 2006-03-29 2007-10-11 Otsuka Chemical Co., Ltd. ペプチドのチオエステル化合物の製造方法
ES2283212B1 (es) 2006-03-31 2008-08-16 Lipotec S.A. Peptidos sinteticos utiles en el tratamiento de la piel y su uso en composiciones cosmeticas o dermofarmaceuticas.
FI20065208A0 (fi) 2006-03-31 2006-03-31 Karyon Oy Peptidikonjugaatteja
WO2007113386A1 (en) 2006-03-31 2007-10-11 Karyon-Ctt Ltd Peptide conjugates
WO2007139589A1 (en) 2006-05-26 2007-12-06 Bristol-Myers Squibb Company Sustained release glp-1 receptor modulators
GB2440388A (en) 2006-06-30 2008-01-30 Ucl Biomedica Plc Methods of linking a carbohydrate or polyalkylene oxide to a protein, precursors and the resultant products
US9766217B2 (en) 2006-09-08 2017-09-19 Novo Nordisk A/S Methods of optimizing chromatographic separation of polypeptides
WO2008044890A1 (en) 2006-10-12 2008-04-17 Dong Kook Pharm. Co., Ltd A method for preparing peptides using by solid phase synthesis
ES2322882B1 (es) 2006-10-25 2010-04-22 Lipotec Sa Peptidos inhibidores de la exocitosis neuronal.
EP1923397B1 (en) 2006-11-14 2009-10-28 NERVIANO MEDICAL SCIENCES S.r.l. Fluorinated amino acids and peptides
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
US7981998B2 (en) 2006-12-14 2011-07-19 Aileron Therapeutics, Inc. Bis-sulfhydryl macrocyclization systems
EP2094721B1 (en) 2006-12-14 2018-02-14 Aileron Therapeutics, Inc. Bis-sulfhydryl macrocyclization systems
KR20150116465A (ko) 2007-02-15 2015-10-15 인디애나 유니버시티 리서치 앤드 테크놀로지 코퍼레이션 글루카곤/ｇｌｐ-1 수용체 공동-항진물질
US20080287650A1 (en) 2007-03-01 2008-11-20 Avi Tovi High purity peptides
WO2008137165A1 (en) 2007-05-07 2008-11-13 President And Fellows Of Harvard College Anti-glycated cd59 antibodies and uses thereof
ATE520714T1 (de) 2007-06-15 2011-09-15 Zealand Pharma As Glucagonanaloga
JP2010531828A (ja) 2007-06-29 2010-09-30 ロンザ アーゲー プラムリンチドの製造方法
CN101357938B (zh) 2007-07-31 2013-07-03 周逸明 固相多肽合成Exenatide的制备方法
CN101357937B (zh) 2007-07-31 2012-11-07 上海苏豪逸明制药有限公司 固相多肽合成阿托西般的制备方法
WO2009059002A2 (en) * 2007-10-30 2009-05-07 The Regents Of The University Of Michigan Office Of Technology Transfer Macrocyclization of compounds from solid support using thioesterases
MX2010006044A (es) 2007-12-11 2010-06-23 Hoffmann La Roche Sintesis de peptidos insulinotropicos utilizando una combinacion de tecnicas en fase solida y en solucion.
KR101257330B1 (ko) 2008-02-06 2013-04-23 바이오콘 리미티드 펩타이드 정제 방법
ES2330291B1 (es) 2008-02-29 2010-10-18 Lipotec Sa Peptidos utiles en el tratamiento de la piel, mucosas y/o cuero cabelludo y su uso en composiciones cosmeticas o farmaceuticas.
CN101525370A (zh) 2008-03-06 2009-09-09 海南建邦制药科技有限公司 一种新型高效多肽合成缩合剂
CN101525368B (zh) 2008-03-06 2012-05-30 海南建邦制药科技有限公司 一种多肽合成脱保护剂
CN101255191A (zh) 2008-03-12 2008-09-03 中国药科大学 微波促进固相合成胰高血糖素样肽-1(glp-1)类似物及其应用
WO2009132231A2 (en) 2008-04-24 2009-10-29 Therimunex Pharmaceuticals, Inc. Peptidyl diacylglycerides
US20120149868A1 (en) 2008-05-15 2012-06-14 Novo Nordisk A/S Purification of peptides prepared by solid phase synthesis
BRPI0915282A2 (pt) 2008-06-17 2017-02-07 Univ Indiana Res & Tech Corp agonistas mistos baseados no gip para o tratamento de distúrbios metabólicos e obesidade
JP5775450B2 (ja) 2008-06-17 2015-09-09 インディアナ ユニバーシティー リサーチ アンド テクノロジー コーポレーションＩｎｄｉａｎａ Ｕｎｉｖｅｒｓｉｔｙ Ｒｅｓｅａｒｃｈ Ａｎｄ Ｔｅｃｈｎｏｌｏｇｙ Ｃｏｒｐｏｒａｔｉｏｎ グルカゴン／ｇｌｐ−１受容体コアゴニスト
TWI395752B (zh) 2008-09-03 2013-05-11 Scinopharm Taiwan Ltd 製造比伐蘆汀（ｂｉｖａｌｉｒｕｄｉｎ）之方法
TW201012829A (en) 2008-09-22 2010-04-01 Ipsen Mfg Ireland Ltd Process for the synthesis of (Aib8,35)hGLP-1(7-36)-NH2
AU2009294875C1 (en) 2008-09-22 2015-05-14 Aileron Therapeutics, Inc. Methods for preparing purified polypeptide compositions
CA2745499A1 (en) 2008-12-05 2010-06-10 Angiochem Inc. Peptide therapeutic conjugates and uses thereof
MX2011005963A (es) 2008-12-05 2011-09-01 Angiochem Inc Conjugados de neurotensina o analogos de neurotensina y sus usos.
BRPI0922691A2 (pt) 2008-12-05 2018-11-06 Angiochem Inc conjugados de leptina e análogo de leptina e usos dos mesmos
ES2439499T3 (es) 2008-12-15 2014-01-23 Zealand Pharma A/S Análogos de glucagón
CN102282167B (zh) 2008-12-15 2014-08-13 西兰制药公司 胰高血糖素类似物
CA2747112A1 (en) 2008-12-15 2010-06-24 Zealand Pharma A/S Glucagon analogues
NZ593813A (en) 2008-12-15 2013-02-22 Zealand Pharma As Glucagon analogues
CN101463081B (zh) 2009-01-12 2012-07-04 华东师范大学 一种glp-1衍生物
CN101463078B (zh) 2009-01-12 2011-07-27 华东师范大学 一种Exendin-4衍生物及其固相化学合成
CN101538324B (zh) 2009-01-13 2013-01-16 深圳翰宇药业股份有限公司 一种制备艾塞那肽的方法
ES2349972B1 (es) 2009-02-16 2011-11-24 Lipotec, S.A. Péptidos útiles en el tratamiento y/o cuidado de la piel, mucosas y/o cuero cabelludo y su uso en composiciones cosméticas o farmacéuticas.
WO2010096052A1 (en) 2009-02-19 2010-08-26 Merck Sharp & Dohme Corp. Oxyntomodulin analogs
MX337830B (es) 2009-04-17 2016-03-16 Lipotec Sa Peptidos utiles en el tratamiento y/o cuidado de la piel y/o cabello y su uso en composiciones cosmeticas o farmaceuticas.
CN101555274B (zh) 2009-05-15 2013-08-21 海南双成药业股份有限公司 一种多肽固相合成比法卢定粗品的制备方法
IN2012DN00377A (es) 2009-06-16 2015-08-21 Univ Indiana Res & Tech Corp
NZ597981A (en) 2009-07-13 2014-02-28 Zealand Pharma As Acylated glucagon analogues
CA2768386A1 (en) 2009-07-24 2011-01-27 Lipotec, S.A. Compounds which inhibit muscle contraction
ES2358829B1 (es) 2009-10-23 2012-06-25 Lipotec, S.A. Péptidos útiles en el tratamiento y/o cuidado de la piel, mucosas y/o cabello y su uso en composiciones cosméticas o farmacéuticas.
US8703701B2 (en) 2009-12-18 2014-04-22 Indiana University Research And Technology Corporation Glucagon/GLP-1 receptor co-agonists
EP2528618A4 (en) 2010-01-27 2015-05-27 Univ Indiana Res & Tech Corp GLUCAGON ANTAGONISTE AND GIP AGONISTS CONJUGATES AND COMPOSITIONS FOR THE TREATMENT OF METABOLISM DISEASES AND ADIPOSITAS
EP2542565A1 (en) 2010-03-01 2013-01-09 Novo Nordisk A/S Preparative rp-hplc method for purifying peptides
CA2792663A1 (en) 2010-03-26 2011-09-29 Novo Nordisk A/S Novel glucagon analogues
US8620595B2 (en) 2010-03-26 2013-12-31 University Of Manitoba Methods for determining the retention of peptides in reverse phase chromatography using linear solvent strength theory
AR080592A1 (es) 2010-03-26 2012-04-18 Lilly Co Eli Peptido con actividad para el gip-r y glp-1-r, formulacion famaceutica que lo comprende, su uso para preparar un medicamento util para el tratamiento de diabetes mellitus y para inducir la perdida de peso
CN102918177B (zh) 2010-05-31 2015-09-09 株式会社捷太格特 覆盖部件的制造方法
EP2579435B1 (en) 2010-06-01 2016-11-30 Honda Motor Co., Ltd. Controller for dc/dc converter
US20110313131A1 (en) 2010-06-21 2011-12-22 Christelle Carl Reversed phase hplc purification of a glp-1 analogue
AR081975A1 (es) 2010-06-23 2012-10-31 Zealand Pharma As Analogos de glucagon
CN101906150B (zh) 2010-06-28 2013-01-09 上海昂博生物技术有限公司 一种比法卢定的制备方法
WO2012057624A1 (en) 2010-10-25 2012-05-03 Pepscan Systems B.V. Novel bicyclic peptide mimetics
CN103189384A (zh) 2010-10-29 2013-07-03 隆萨有限公司 形成二酮哌嗪的二肽连接子
SG191194A1 (en) 2010-12-22 2013-07-31 Univ Indiana Res & Tech Corp Glucagon analogs exhibiting gip receptor activity
EP2655395B1 (en) 2010-12-23 2018-03-07 Universiteit Gent Method for cross-linking peptides
CN102643339B (zh) 2011-02-21 2014-04-09 天津药物研究院 一种glp-1类似物、制备方法及其应用
CN102174082B (zh) 2011-02-23 2014-08-27 上海昂博生物技术有限公司 一种艾塞那肽的制备方法
ES2397889B1 (es) 2011-03-25 2014-02-07 Lipotec, S.A. PÉPTIDOS MODULADORES DE PGC-1Alfa.
CN102718858B (zh) 2011-03-29 2014-07-02 天津药物研究院 胰高血糖素样肽-1类似物单体、二聚体及其制备方法与应用
EP2694095B1 (en) 2011-04-05 2018-03-07 Longevity Biotech, Inc. Compositions comprising glucagon analogs and methods of making and using the same
CN102786590A (zh) 2011-05-19 2012-11-21 江苏豪森药业股份有限公司 分枝型peg修饰的glp-1类似物及其可药用盐
US8933196B2 (en) 2011-05-20 2015-01-13 National Central University Peptide chromatographic purification assisted by combining of solubility parameter and solution conformation energy calculations
CN102286076B (zh) 2011-06-23 2014-03-12 成都圣诺科技发展有限公司 比伐卢定的制备方法
CN102286092B (zh) 2011-09-14 2014-01-01 深圳翰宇药业股份有限公司 利拉鲁肽的固相合成方法
NL2007536C2 (en) 2011-10-05 2013-04-08 Academisch Ziekenhuis Leiden Lumc Adjuvant compound.
RU2625793C2 (ru) 2011-12-23 2017-07-19 Ипсен Мэньюфэкчеринг Айэлэнд Лимитед Способ синтеза терапевтических пептидов
CN102411801A (zh) 2011-12-27 2012-04-11 湖南超氏信息集成有限公司 一种挂起排队方法
CN102584944B (zh) 2012-02-06 2014-12-17 成都圣诺生物科技股份有限公司 一种依非巴特的制备方法
CN103242443A (zh) 2012-02-06 2013-08-14 长春百克生物科技股份公司 一种胸腺素α1及其类似物的制备方法
CN102584982B (zh) 2012-02-10 2014-02-05 深圳翰宇药业股份有限公司 一种纯化固相合成利拉鲁肽粗肽的方法
CN102558338B (zh) 2012-02-10 2014-09-17 深圳翰宇药业股份有限公司 一种合成利西拉来的方法
BR112014025621B1 (pt) 2012-04-16 2023-01-17 Lubrizol Advanced Materials, Inc Composto, composição cosmética ou farmacêutica, e, uso de um composto
US20130289241A1 (en) 2012-04-26 2013-10-31 Shanghai Ambiopharm, Inc. Method for preparing exenatide
AU2013262069C1 (en) 2012-05-16 2019-01-31 Aptarion Biotech Ag Enzymatic synthesis of L-nucleic acids
CN102875663B (zh) 2012-09-26 2014-06-11 深圳翰宇药业股份有限公司 利西拉来的纯化方法
CN104994924B (zh) 2013-01-29 2017-09-22 诺伊兰健康科学私人有限公司 使用在反相柱上的替代固定相纯化有机化合物
CN103965285B (zh) 2013-02-06 2016-12-28 北京大学 一种以超顺磁纳米颗粒为固相进行多肽合成及同步构建多肽磁纳米探针的方法
CN103333237B (zh) 2013-05-07 2015-03-11 海南双成药业股份有限公司 一种固相片段法合成艾塞那肽
JP2016527231A (ja) 2013-07-15 2016-09-08 ノース カロライナ ステイト ユニヴァーシティ プロテアーゼ耐性ペプチドリガンド
US9263194B2 (en) 2013-09-06 2016-02-16 Gwangju Institute Of Science And Technology Porphyrin-peptoid conjugate and the preparation process thereof
WO2015038919A1 (en) 2013-09-15 2015-03-19 Stc. Unm Method for atomic layer deposition
CN103536912B (zh) 2013-09-30 2015-05-13 重庆理工大学 一种猪圆环病毒2型表位肽疫苗及其制备方法
CN103613655B (zh) 2013-11-20 2015-05-13 陕西东大生化科技有限责任公司 一种低成本纯化艾塞那肽的方法
BR112016012391A2 (pt) 2013-12-01 2017-09-26 Univ Copenhagen composto, e, método para fabricar o composto
HU230584B1 (hu) 2014-02-28 2017-01-30 Szegedi Tudományegyetem Eljárás peptidek előállítására
CN104086631A (zh) 2014-07-10 2014-10-08 成都天台山制药有限公司 卡贝缩宫素和制法
RU2696276C2 (ru) 2014-08-07 2019-08-01 Ф. Хоффманн-Ля Рош Аг Способы получения аналогов окситоцина
US9688750B2 (en) 2014-10-07 2017-06-27 Ann And Robert H. Lurie Children's Hospital Of Chicago Anti-nodal antibodies and methods of using same
CN105585612B (zh) 2014-10-20 2020-05-05 北京益生康华医药技术有限公司 八肽修饰的地塞米松、制备、纳米结构和应用
US10344069B2 (en) 2014-10-31 2019-07-09 Auro Peptides Ltd. Process for the preparation of liraglutide
WO2016084100A2 (en) 2014-11-26 2016-06-02 Alaparthi Lakshmi Prasad Novel and efficient method for large scale synthesis of romidepsin
US10308677B2 (en) 2014-12-19 2019-06-04 Cem Corporation Coupling method for peptide synthesis at elevated temperatures
CN105111303B (zh) 2015-06-23 2019-07-26 济南康和医药科技有限公司 一种固液结合制备利拉鲁肽的方法
CA3018627A1 (en) 2016-03-23 2017-09-28 Bachem Holding Ag Purification of glucagon-like peptide 1 analogs

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