ES418929A1 - Procedure for the preparation of polipeptides. (Machine-translation by Google Translate, not legally binding) - Google Patents

Procedure for the preparation of polipeptides. (Machine-translation by Google Translate, not legally binding)

Info

Publication number
ES418929A1
ES418929A1 ES418929A ES418929A ES418929A1 ES 418929 A1 ES418929 A1 ES 418929A1 ES 418929 A ES418929 A ES 418929A ES 418929 A ES418929 A ES 418929A ES 418929 A1 ES418929 A1 ES 418929A1
Authority
ES
Spain
Prior art keywords
protecting group
hydrogen atom
radical
amino acids
peptide
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
ES418929A
Other languages
Spanish (es)
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.)
F Hoffmann La Roche AG
Original Assignee
F Hoffmann La Roche AG
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 F Hoffmann La Roche AG filed Critical F Hoffmann La Roche AG
Publication of ES418929A1 publication Critical patent/ES418929A1/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
    • C07K7/16Oxytocins; Vasopressins; Related peptides
    • 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
    • C07K5/10Tetrapeptides
    • C07K5/1002Tetrapeptides with the first amino acid being neutral
    • C07K5/1005Tetrapeptides with the first amino acid being neutral and aliphatic
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing 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)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Procedure for the preparation of polypeptides of the general formula **(See formula)** in which X represents the radical of an amino acid or a linear peptide of 2 to 6 amino acids and Q represents the radical of arginine or lysine, and where all amino acids with asymmetric center have L configuration, and of its non-toxic and pharmaceutically acceptable acid addition salts, characterized by: a) dissociate from a peptide of the general formula **(See formula)** in which R2 represents the optionally protected radical of an amino acid or a linear peptide of 2 to 6 amino acids; R2 represents a hydrogen atom or an amide protecting group, and Q'represents a grouping of the formula -RH-CH [- (CH2) 3 -NH-C (= NH) -NHR3] -CO- or -NH-CH [- (CH2) 4-NH-R4] -CO-, where R3 represents a hydrogen atom or a guanidine radical protecting group and R4 represents a hydrogen atom or an amine group protecting the lysine radical, provided that at least one of the radicals R1, R2 and R3 or R4 represents or contains a protecting group and wherein all amino acids with asymmetric center have L configuration, the protecting group or groups and optionally converting the free peptide obtained by reaction with an organic or inorganic acid, into a pharmaceutically acceptable and non-toxic acid addition salt; O well b) oxidizing a peptide of the general formula **(See formula)** in which X and Q have the same meaning as before, and R5 and R6 represent in each case a hydrogen atom or a sulfohydryl protecting group, and where all amino acids with an asymmetric center have an L configuration, with simultaneous or preliminary dissociation of the possibly existing protecting groups, and, if desired, converting the product obtained, by reaction with an organic or inorganic acid, into a pharmaceutically acceptable and non-toxic acid addition salt; O well c) oxidizing a peptide of the general formula **(See formula)** in which R1 represents the radical, possibly protected, of an amino acid or a linear peptide of 2 to 6 amino acids; R2 represents a hydrogen atom or an amide protecting group; Q'represents a grouping of the formula -NH-CH [- (CH2) 3-NH-C (= NH) -NHR3] -CO- or -NH- CH [- (CH2) 4-NH-R4] -CO-, where R3 represents a hydrogen atom or a guanidine radical protecting group, and R4 represents a hydrogen atom or an amino group protecting from the lysine radical, and R5 and R6 represent, in each case, a hydrogen atom or a sulfohydryl protecting group, provided that one, at least of the radicals R1, R2 and R3 or R4 represents or contains a protecting group, and wherein all amino acids with asymmetric center have L configuration, with simultaneous dissociation of the protecting group or groups and, if desired, converting the obtained product, by reaction with an organic or inorganic acid into a non-toxic and pharmaceutically acceptable acid addition salt. (Machine-translation by Google Translate, not legally binding)
ES418929A 1972-09-21 1973-09-20 Procedure for the preparation of polipeptides. (Machine-translation by Google Translate, not legally binding) Expired ES418929A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH1380372 1972-09-21

Publications (1)

Publication Number Publication Date
ES418929A1 true ES418929A1 (en) 1976-03-01

Family

ID=4395476

Family Applications (1)

Application Number Title Priority Date Filing Date
ES418929A Expired ES418929A1 (en) 1972-09-21 1973-09-20 Procedure for the preparation of polipeptides. (Machine-translation by Google Translate, not legally binding)

Country Status (8)

Country Link
JP (1) JPS4969693A (en)
AU (1) AU5966773A (en)
BE (1) BE805132A (en)
DE (1) DE2347456A1 (en)
ES (1) ES418929A1 (en)
FR (1) FR2200001A1 (en)
NL (1) NL7312987A (en)
ZA (1) ZA735680B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0014815A3 (en) * 1978-12-20 1980-10-29 Ciba-Geigy Ag Peptide derivatives, process for their preparation and intermediates, and pharmaceutical compositions containing one of these compounds
IT1186733B (en) * 1985-06-05 1987-12-16 Eniricerche Spa TRIPEPTIDIC COMPOUNDS WITH HYPOTHENSIVE ACTION

Also Published As

Publication number Publication date
FR2200001A1 (en) 1974-04-19
ZA735680B (en) 1974-07-31
JPS4969693A (en) 1974-07-05
BE805132A (en) 1974-03-21
NL7312987A (en) 1974-03-25
DE2347456A1 (en) 1974-04-11
AU5966773A (en) 1975-02-27

Similar Documents

Publication Publication Date Title
ES440922A1 (en) Cyclization of cysteine-containing peptides
NO911787D0 (en) PEPTIDAMINES AND PROCEDURES FOR PREPARING THEREOF.
HUT70475A (en) New aminoacid derivates, process for producing the same and pharmaceutical compositions containing these compounds
ATE130312T1 (en) POLYPEPTIDE WITH MAIN REPEATING CELL ADHESIVE SEQUENCES.
ES403973A1 (en) (ile3,leu4)-vasopressin analogs and intermediates
ES418929A1 (en) Procedure for the preparation of polipeptides. (Machine-translation by Google Translate, not legally binding)
GB1109086A (en) Polypeptides
ES2104688T3 (en) A PROCEDURE FOR THE PREPARATION OF A TIO-3-CEFEM 3-SUBSTITUTED COMPOUND.
ES438799A1 (en) Vincaminic acid amides
GB1415471A (en) Phenylethylamine derivatives
ES438283A1 (en) Crystalline adducts of carbamoyl sulphoxides and urea in a 1:3 ratio
ES436399A1 (en) Tetracycline derivatives and process for preparing them
ES386846A1 (en) Hydroxamic acid derivatives of alphaaminooxy carboxylic acids
ES473090A1 (en) A peptide and the salts thereof, processes for their preparation and compositions containing them.
GB1231494A (en)
GB1270018A (en) Cysteine-containing peptides and their derivatives and a process for preparing them
GB1292094A (en) A phenylglycine derivative
GB1191522A (en) Derivatives of Cyclic Imides
JPS5225768A (en) Preparation of novel pentapeptides
ES416516A1 (en) A procedure for the preparation of nonapeptides. (Machine-translation by Google Translate, not legally binding)
JPS6416792A (en) Guanidine related compound containing tetraphenylborate ion, its production and use thereof in peptide synthesis
GB1115050A (en) O-(indolyl)-glycolic acid amides
ES8206446A1 (en) A procedure for the preparation of a peptide (Machine-translation by Google Translate, not legally binding)
ES435329A1 (en) 2,3,8,12b-tetrahydro-1h-3a 8-methanodibenzo-3,4,6,7-cyclohepta -1,2-c-pyrrole and derivatives thereof
ES463557A2 (en) N-(4-piperidyl)-benzamides and pharmaceutical compositions containing them