SG64917A1 - Method of peptide synthesis and new synthesis intermediates - Google Patents

Method of peptide synthesis and new synthesis intermediates

Info

Publication number
SG64917A1
SG64917A1 SG1996008443A SG1996008443A SG64917A1 SG 64917 A1 SG64917 A1 SG 64917A1 SG 1996008443 A SG1996008443 A SG 1996008443A SG 1996008443 A SG1996008443 A SG 1996008443A SG 64917 A1 SG64917 A1 SG 64917A1
Authority
SG
Singapore
Prior art keywords
synthesis
intermediates
new
peptide
amino acid
Prior art date
Application number
SG1996008443A
Other languages
English (en)
Inventor
Marc Anteunis
Frank Becu
Roland Callens
Georges Blondeel
Original Assignee
Solvay
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 Solvay filed Critical Solvay
Publication of SG64917A1 publication Critical patent/SG64917A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/06General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents
    • C07K1/061General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents using protecting groups
    • C07K1/062General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents using protecting groups for alpha- or omega-carboxy functions
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06Esters of carbamic acids
    • C07C271/08Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/22Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/006General 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/107General 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
    • C07K1/1072General 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
    • C07K1/1077General 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08Tripeptides
    • C07K5/0802Tripeptides with the first amino acid being neutral
    • C07K5/0804Tripeptides with the first amino acid being neutral and aliphatic
    • C07K5/081Tripeptides with the first amino acid being neutral and aliphatic the side chain containing O or S as heteroatoms, e.g. Cys, Ser
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Analytical Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Peptides Or Proteins (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Epoxy Compounds (AREA)
SG1996008443A 1992-03-20 1993-03-10 Method of peptide synthesis and new synthesis intermediates SG64917A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
BE9200273A BE1005720A3 (fr) 1992-03-20 1992-03-20 Procede de synthese peptidique et nouveaux intermediaires de synthese.

Publications (1)

Publication Number Publication Date
SG64917A1 true SG64917A1 (en) 1999-05-25

Family

ID=3886195

Family Applications (1)

Application Number Title Priority Date Filing Date
SG1996008443A SG64917A1 (en) 1992-03-20 1993-03-10 Method of peptide synthesis and new synthesis intermediates

Country Status (12)

Country Link
US (2) US5770692A (hu)
EP (1) EP0562659B1 (hu)
JP (1) JP3436559B2 (hu)
AT (1) ATE161269T1 (hu)
AU (1) AU664243B2 (hu)
BE (1) BE1005720A3 (hu)
CA (1) CA2092062C (hu)
DE (1) DE69315730T2 (hu)
ES (1) ES2112955T3 (hu)
HU (1) HU221619B1 (hu)
IL (1) IL105036A (hu)
SG (1) SG64917A1 (hu)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE1007184A3 (fr) * 1993-06-18 1995-04-18 Solvay Procede de preparation d'un amide d'alpha-aminoacide, utilisable en synthese peptidique.
SE9401079L (sv) * 1994-03-30 1995-10-01 Anders Unden Nya derivat av asparaginsyra och glutaminsyra som är skyddade på sidokedjans karboxylsyragrupp form av estrar som försvårar aspartimidbildning vid fastfassyntes av peptider
US6160122A (en) * 1996-06-28 2000-12-12 Abbott Laboratories Process for the preparation of a disubstituted thiazole
US6022989A (en) * 1996-06-28 2000-02-08 Abbott Laboratories Process for the preparation of an activated amino acid
US7635571B2 (en) * 2000-12-07 2009-12-22 Siemens Healthcare Diagnostics Products Gmbh Amplified signal in binding assays
WO2015030106A1 (ja) * 2013-09-02 2015-03-05 国立大学法人京都大学 Ggt阻害作用を有する化合物及びggtファミリー酵素阻害剤
JPWO2023085342A1 (hu) * 2021-11-10 2023-05-19

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT277965B (de) * 1966-02-04 1970-01-12 Geigy Ag J R Verfahren zur Herstellung neuer N<6>-Acyllysinester sowie ihrer Säureadditionssalze
DE1963734A1 (de) * 1969-12-19 1971-06-24 Bayer Ag Harnstoffderivate von Acylderivaten des KTI
JPS58198497A (ja) * 1982-05-14 1983-11-18 Kowa Co 新規アミノ配糖体及びその製法
FR2573765B1 (fr) * 1984-11-23 1988-06-10 Solvay Procede pour la synthese de peptides
US4800191A (en) * 1987-07-17 1989-01-24 Schally Andrew Victor LHRH antagonists
DE3918057C1 (hu) * 1989-06-02 1990-05-03 Degussa Ag, 6000 Frankfurt, De

Also Published As

Publication number Publication date
EP0562659A1 (fr) 1993-09-29
DE69315730D1 (de) 1998-01-29
HU9300799D0 (en) 1993-07-28
IL105036A (en) 1998-06-15
HU221619B1 (hu) 2002-12-28
AU3524993A (en) 1993-09-23
CA2092062A1 (fr) 1993-09-21
HUT65752A (en) 1994-07-28
ATE161269T1 (de) 1998-01-15
DE69315730T2 (de) 1998-07-02
CA2092062C (fr) 2003-08-05
JPH0641188A (ja) 1994-02-15
ES2112955T3 (es) 1998-04-16
EP0562659B1 (fr) 1997-12-17
AU664243B2 (en) 1995-11-09
US5965770A (en) 1999-10-12
US5770692A (en) 1998-06-23
JP3436559B2 (ja) 2003-08-11
BE1005720A3 (fr) 1993-12-28
IL105036A0 (en) 1993-07-08

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