JPS5645450A - Pentapeptide compound - Google Patents
Pentapeptide compoundInfo
- Publication number
- JPS5645450A JPS5645450A JP12165479A JP12165479A JPS5645450A JP S5645450 A JPS5645450 A JP S5645450A JP 12165479 A JP12165479 A JP 12165479A JP 12165479 A JP12165479 A JP 12165479A JP S5645450 A JPS5645450 A JP S5645450A
- Authority
- JP
- Japan
- Prior art keywords
- met
- pentapeptide
- condensation
- morphinelike
- tyn
- 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.)
- Pending
Links
Classifications
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Abstract
NEW MATERIAL:A pentapeptide expressed by the formula (Y is Met or Leu; Z is OH or NH2.
EXAMPLE: H-Tyn-D-Arg-Gly-Phe-Met-NH2.
USE: An analgesic agent having a morphinelike action with lower toxicity than the morphine.
PROCESS: Synthesized by the conventional liquid or solid phase method. The peptide chain is extended by the condensation methods, e.g. the stepwise elongation or fragment condensation method utilizing the azide, mixed acid anhydride or DCC method in a solvent, e.g. dimethylformamide. The final removal of the protecting group is carried out by the catalytic reduction or with hydrogen fluoride or acetic acid used generally in the field of peptides, and the purification by an ion exchange resin or partition chromatography.
COPYRIGHT: (C)1981,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12165479A JPS5645450A (en) | 1979-09-21 | 1979-09-21 | Pentapeptide compound |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12165479A JPS5645450A (en) | 1979-09-21 | 1979-09-21 | Pentapeptide compound |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5645450A true JPS5645450A (en) | 1981-04-25 |
Family
ID=14816590
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12165479A Pending JPS5645450A (en) | 1979-09-21 | 1979-09-21 | Pentapeptide compound |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5645450A (en) |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5356634A (en) * | 1976-09-01 | 1978-05-23 | Coy David Howard | Pharmaceutical composition |
-
1979
- 1979-09-21 JP JP12165479A patent/JPS5645450A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5356634A (en) * | 1976-09-01 | 1978-05-23 | Coy David Howard | Pharmaceutical composition |
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