JP2003530311A5 - - Google Patents

Download PDF

Info

Publication number
JP2003530311A5
JP2003530311A5 JP2001537346A JP2001537346A JP2003530311A5 JP 2003530311 A5 JP2003530311 A5 JP 2003530311A5 JP 2001537346 A JP2001537346 A JP 2001537346A JP 2001537346 A JP2001537346 A JP 2001537346A JP 2003530311 A5 JP2003530311 A5 JP 2003530311A5
Authority
JP
Japan
Prior art keywords
seq
group
peptide
formula
wqeweqkitall
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
JP2001537346A
Other languages
English (en)
Japanese (ja)
Other versions
JP2003530311A (ja
Filing date
Publication date
Priority claimed from US09/349,205 external-priority patent/US6469136B1/en
Application filed filed Critical
Publication of JP2003530311A publication Critical patent/JP2003530311A/ja
Publication of JP2003530311A5 publication Critical patent/JP2003530311A5/ja
Ceased legal-status Critical Current

Links

JP2001537346A 1999-07-07 2000-07-05 ペプチド合成の方法および組成物 Ceased JP2003530311A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US09/349,205 US6469136B1 (en) 1999-07-07 1999-07-07 Methods and composition for peptide synthesis
US09/349,205 1999-07-07
PCT/US2000/035725 WO2001034635A2 (en) 1999-07-07 2000-07-05 Methods and compositions for peptide synthesis

Publications (2)

Publication Number Publication Date
JP2003530311A JP2003530311A (ja) 2003-10-14
JP2003530311A5 true JP2003530311A5 (https=) 2007-08-30

Family

ID=23371340

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2001537346A Ceased JP2003530311A (ja) 1999-07-07 2000-07-05 ペプチド合成の方法および組成物

Country Status (17)

Country Link
US (2) US6469136B1 (https=)
EP (1) EP1372686B1 (https=)
JP (1) JP2003530311A (https=)
KR (1) KR100631874B1 (https=)
CN (1) CN1267449C (https=)
AR (1) AR024686A1 (https=)
AT (1) ATE288278T1 (https=)
AU (1) AU4133701A (https=)
BR (1) BR0012249A (https=)
CA (1) CA2378086A1 (https=)
DE (1) DE60017955T2 (https=)
DK (1) DK1372686T3 (https=)
ES (1) ES2236043T3 (https=)
MX (1) MXPA02000021A (https=)
PT (1) PT1372686E (https=)
TW (1) TWI237640B (https=)
WO (1) WO2001034635A2 (https=)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6656906B1 (en) * 1998-05-20 2003-12-02 Trimeris, Inc. Hybrid polypeptides with enhanced pharmacokinetic properties
SK782002A3 (en) * 1999-07-21 2003-08-05 Lexigen Pharm Corp FC fusion proteins for enhancing the immunogenicity of protein and peptide antigens
WO2004013165A1 (en) * 2002-07-24 2004-02-12 F. Hoffmann-La Roche Ag Pegylated t1249 polypeptide
US20040158037A1 (en) * 2003-02-12 2004-08-12 Bohling James Charles Amino acid loaded trityl alcohol resins, method of production of amino acid loaded trityl alcohol resins and biologically active substances and therapeutics produced therewith
AU2004200485A1 (en) * 2003-02-25 2004-09-09 Rohm And Haas Company Method of manufacturing T-20 and T-1249 peptides at commercial scale, and T-20 and T-1249 compositions related thereto
PL2298347T3 (pl) * 2003-05-06 2016-03-31 Bioverativ Therapeutics Inc Białka chimeryczne czynnika krzepnięcia do leczenia zaburzenia hemostazy
TWI353991B (en) * 2003-05-06 2011-12-11 Syntonix Pharmaceuticals Inc Immunoglobulin chimeric monomer-dimer hybrids
US7348004B2 (en) 2003-05-06 2008-03-25 Syntonix Pharmaceuticals, Inc. Immunoglobulin chimeric monomer-dimer hybrids
WO2005063792A2 (en) * 2003-12-31 2005-07-14 F. Hoffmann-La Roche Ag Methods for recovering cleaved peptide from a support
EP1701976A2 (en) * 2003-12-31 2006-09-20 F.Hoffmann-La Roche Ag Peptide synthesis and deprotection with co-solvent
WO2005063800A2 (en) * 2003-12-31 2005-07-14 F. Hoffmann-La Roche Ag Peptide synthesis using decanting filter
ATE376556T1 (de) * 2003-12-31 2007-11-15 Hoffmann La Roche Verfahren zur peptidsynthese unter verwendung einer reduzierten menge an entschützungsmittel
ATE410437T1 (de) * 2003-12-31 2008-10-15 Hoffmann La Roche Verfahren und systeme zur rückgewinnung von peptiden
KR101276422B1 (ko) * 2004-03-15 2013-06-19 넥타르 테라퓨틱스 Hiv 유입 억제제의 중합체-기재 조성물 및 콘쥬게이트
ES2329270T3 (es) * 2004-12-30 2009-11-24 F. Hoffmann-La Roche Ag Sintesis del peptido t-1249 utilizando fragmentos intermediarios del ipeptido.
JP4886702B2 (ja) * 2004-12-30 2012-02-29 エフ.ホフマン−ラ ロシュ アーゲー ペプチド中間体断片を使用するペプチドt−20の合成
WO2006069779A1 (en) * 2004-12-30 2006-07-06 F. Hoffmann-La Roche Ag Preparing of peptides with excellent solubility
WO2006069697A1 (en) * 2004-12-30 2006-07-06 F. Hoffmann-La Roche Ag Colorimetrically assessing peptide characteristics
WO2006105199A2 (en) * 2005-03-30 2006-10-05 Trimeris, Inc. Compositions and methods for synthesis of peptide and related conjugate
TW200745163A (en) 2006-02-17 2007-12-16 Syntonix Pharmaceuticals Inc Peptides that block the binding of IgG to FcRn
CA2651070A1 (en) 2006-05-03 2007-11-15 Mallinckrodt Inc. Composition and method for the release of protected peptides from a resin
CN101195653B (zh) * 2006-12-08 2010-05-12 吉尔生化(上海)有限公司 亮丙瑞林的固液合成法
TW200911289A (en) * 2007-08-09 2009-03-16 Syntonix Pharmaceuticals Inc Immunomodulatory peptides
CN101874038A (zh) * 2007-09-25 2010-10-27 特里梅里斯公司 治疗性抗-hiv肽的合成方法
CN101835794A (zh) * 2007-10-27 2010-09-15 霍夫曼-拉罗奇有限公司 使用固相和溶液相组合技术的促胰岛素肽合成法
EP2222695A2 (en) * 2007-12-11 2010-09-01 F. Hoffmann-La Roche AG Insulinotropic peptide synthesis using solid and solution phase combination techniques
WO2010014909A1 (en) * 2008-08-01 2010-02-04 Syntonix Pharmaceuticals, Inc. Immunomodulatory peptides
TW201217527A (en) 2010-07-09 2012-05-01 Biogen Idec Hemophilia Inc Processable single chain molecules and polypeptides made using same
CN102268065A (zh) * 2011-06-23 2011-12-07 成都圣诺科技发展有限公司 氨基保护丝氨酸寡肽及其制备方法和用途
CN102603869B (zh) * 2012-03-27 2013-03-27 西安华澳丽康生物工程有限公司 六胜肽的合成方法
WO2014144549A1 (en) 2013-03-15 2014-09-18 Biogen Idec Ma Inc. Factor ix polypeptide formulations
US10450343B2 (en) 2013-03-21 2019-10-22 Sanofi-Aventis Deutschland Gmbh Synthesis of cyclic imide containing peptide products
CA2907454C (en) 2013-03-21 2021-05-04 Sanofi-Aventis Deutschland Gmbh Synthesis of hydantoin containing peptide products
CN108572171A (zh) * 2017-03-10 2018-09-25 江苏金斯瑞生物科技有限公司 一种检测哌啶残留的方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100358209B1 (ko) 1992-07-20 2003-01-24 듀크 유니버시티 Hiv복제를저해하는조성물
JP3401005B2 (ja) 1992-12-11 2003-04-28 ユニバーシティ オブ フロリダ 有害生物の防除のための材料および方法
WO1994028929A1 (en) 1993-06-07 1994-12-22 Genentech, Inc. Hiv envelope polypeptides
US6479055B1 (en) 1993-06-07 2002-11-12 Trimeris, Inc. Methods for inhibition of membrane fusion-associated events, including respiratory syncytial virus transmission
US5464933A (en) 1993-06-07 1995-11-07 Duke University Synthetic peptide inhibitors of HIV transmission
WO1999048513A1 (en) * 1998-03-23 1999-09-30 Trimeris, Inc. Methods and compositions for peptide synthesis
US6258782B1 (en) * 1998-05-20 2001-07-10 Trimeris, Inc. Hybrid polypeptides with enhanced pharmacokinetic properties
US6217666B1 (en) 1998-08-31 2001-04-17 Danieli Technology, Inc. Countercurrent reduction of oxides on moving metal

Similar Documents

Publication Publication Date Title
JP2003530311A5 (https=)
JP4405594B2 (ja) 改良型固相ペプチド合成及びかかる合成において利用するための試薬
JP2002507576A5 (https=)
FI90780B (fi) Tekohartsi
EP2873677B1 (en) Method of producing self-assembling peptide derivative
AU2010241171B2 (en) Method for the manufacture of degarelix
CA2654610A1 (en) Insulinotropic peptide synthesis
CA2324348A1 (en) Methods and compositions for peptide synthesis
EP0274999A2 (en) Resin support for solid phase peptide synthesis
AU705716B2 (en) Nalpha-2-(4-nitrophenulsulfonyl)ethoxycarbonyl-amino acids
Nishiuchi et al. Nin-Cyclohexyloxycarbonyl group as a new protecting group for tryptophan
CN117242083A (zh) 用于肽的化学合成的组合物
Limal et al. Solid-phase synthesis of N, N′-unsymmetrically substituted ureas: application to the synthesis of carbaza peptides
AU1480095A (en) PNA synthesis using a base-labile amino protecting group
CA1274340A (en) Resin support for solid phase peptide synthesis
WO1993005065A1 (en) Preparation of peptides by a solid-phase synthesis and intermediates therefor
JPWO2004092377A1 (ja) 新規な機能性ペプチド核酸およびその製法
JP4000453B2 (ja) 新規な機能性ペプチド核酸およびその製法
WO1999007874A1 (en) Process for producing lh-rh derivatives
CN110343147B (zh) 艾替班特的合成方法
Pande et al. Solid‐phase peptide synthesis on a novel hydrogenolysable linker–resin combination
JP3837633B2 (ja) 新規な機能性ペプチド核酸およびその製法
CN120574284A (zh) 一种三肽-29的合成方法
JP2948261B2 (ja) ペプチドモノマーの合成法
HU197030B (en) Process for producing new hexapeptides and pharmaceuticals comprising same