CA1046441A - Peptide synthesis using pepsin - Google Patents

Peptide synthesis using pepsin

Info

Publication number
CA1046441A
CA1046441A CA225,715A CA225715A CA1046441A CA 1046441 A CA1046441 A CA 1046441A CA 225715 A CA225715 A CA 225715A CA 1046441 A CA1046441 A CA 1046441A
Authority
CA
Canada
Prior art keywords
formula
phe
peptide
leu
met
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.)
Expired
Application number
CA225,715A
Other languages
English (en)
French (fr)
Inventor
Yoshikazu Isowa
Takeshi Nagasawa
Katsumasa Kuroiwa
Koichi Narita
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nitto Boseki Co Ltd
Sagami Chemical Research Institute
Original Assignee
Nitto Boseki Co Ltd
Sagami Chemical Research Institute
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 Nitto Boseki Co Ltd, Sagami Chemical Research Institute filed Critical Nitto Boseki Co Ltd
Application granted granted Critical
Publication of CA1046441A publication Critical patent/CA1046441A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K7/00Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/04Linear peptides containing only normal peptide links
    • C07K7/22Tachykinins, e.g. Eledoisins, Substance P; Related peptides
    • 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)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • General Health & Medical Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Peptides Or Proteins (AREA)
CA225,715A 1974-04-24 1975-04-29 Peptide synthesis using pepsin Expired CA1046441A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4626174A JPS5443076B2 (de) 1974-04-24 1974-04-24

Publications (1)

Publication Number Publication Date
CA1046441A true CA1046441A (en) 1979-01-16

Family

ID=12742249

Family Applications (1)

Application Number Title Priority Date Filing Date
CA225,715A Expired CA1046441A (en) 1974-04-24 1975-04-29 Peptide synthesis using pepsin

Country Status (5)

Country Link
JP (1) JPS5443076B2 (de)
CA (1) CA1046441A (de)
DE (1) DE2518256C3 (de)
FR (1) FR2268792A1 (de)
NL (1) NL173183C (de)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4716151A (en) * 1984-08-16 1987-12-29 Rhone-Poulenc Sante Tripeptides and their use

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6027519B2 (ja) * 1977-11-02 1985-06-29 塩野義製薬株式会社 ペプチド誘導体の新規合成法
US4497801A (en) * 1982-09-17 1985-02-05 Fujisawa Pharmaceutical Co., Ltd. New peptides, process for preparation thereof and use thereof
DK15888D0 (da) * 1988-01-14 1988-01-14 Carlsberg Biotechnology Ltd Enzymatisk fremgangsmaade til fremstilling af immunmodulerende pentapeptider samt mellemprodukter til brug ved fremgangsmaaden

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS496660A (de) * 1972-05-09 1974-01-21

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4716151A (en) * 1984-08-16 1987-12-29 Rhone-Poulenc Sante Tripeptides and their use

Also Published As

Publication number Publication date
FR2268792B1 (de) 1980-12-12
DE2518256B2 (de) 1980-03-13
DE2518256A1 (de) 1975-11-06
DE2518256C3 (de) 1980-11-06
FR2268792A1 (en) 1975-11-21
NL7504254A (nl) 1975-10-28
NL173183C (nl) 1983-12-16
JPS50140686A (de) 1975-11-11
JPS5443076B2 (de) 1979-12-18

Similar Documents

Publication Publication Date Title
US4569967A (en) Synthesis of N-substituted peptide amides
CA1230069A (en) Modified protease inhibitors, process for their preparation, and pharmaceutical compositions prepared therefrom
US3972773A (en) Process for producing peptide
US4086136A (en) Process for producing a peptide using a serine or thiol proteinase
Finn et al. The synthesis of peptides by solution methods with emphasis on peptide hormones
US4645740A (en) Process for enzymatic replacement of the B-30 amino acid in insulins
US5032675A (en) Process for the production of glutamine derivatives
SK13232001A3 (sk) LH-RH-antagonisty so zlepšenými vlastnosťami rozpustnosti
CA1046441A (en) Peptide synthesis using pepsin
EP0037516A1 (de) N-omega substituierte Derivate der 1-Desamino-Vasopressin Analoga
Sawyer et al. Design, structure-activity, and molecular modeling studies of potent renin inhibitory peptides having N-terminal Nin-For-Trp (Ftr): angiotensinogen congeners modified by P1-P1'Phe-Phe, Sta, Leu. psi.[CH (OH) CH2] Val or Leu. psi.[CH2NH] Val substitutions
AU2002222439B2 (en) Process for the synthesis of a peptide having a tryptophan residue
Moroder et al. Studies on cytochrome c. Part I. Synthesis of the protected hexadecapeptide (sequence 1–16) of Baker's Yeast iso‐1‐cytochrome c
US4701499A (en) Synthesis of N-substituted peptide amides
EP1979370B1 (de) SELEKTIVE ENZYMATISCHE HYDROLYSE VON C-TERMINALEN tert-BUTYL-PEPTIDESTERN
ATE223927T1 (de) Mu-opioidligande: agonisten und antagonisten
US4569907A (en) Thiopeptolide substrates for vertebrate collagenase
GB1465235A (en) Process for preparing peptides
CA1059938A (en) Process for producing a peptide
US4474765A (en) Biologically active peptides
Nakase et al. Substrate recognition mechanism of carboxypeptidase Y
GANU et al. Synthesis and properties of cyclic peptides containing the activation site of plasminogen
GB2166139A (en) Biologically active penta- and heptapeptides
IE920664A1 (en) Process for the c-terminal modification of peptides having¹a c-terminal penultimate proline residue
Blake et al. ADRENOCORTICOTROPIN 52*. Synthesis and Biological Activity of Adrenocorticotropic Peptides with Cystine Bridges