JPS5626856A - Tetrapeptide - Google Patents
TetrapeptideInfo
- Publication number
- JPS5626856A JPS5626856A JP10238179A JP10238179A JPS5626856A JP S5626856 A JPS5626856 A JP S5626856A JP 10238179 A JP10238179 A JP 10238179A JP 10238179 A JP10238179 A JP 10238179A JP S5626856 A JPS5626856 A JP S5626856A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- protecting group
- tetrapeptide
- glycyl
- dipeptide
- 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.)
- Granted
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
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
NEW MATERIAL:The titled compound of formula I (X is Gly, Ala, Ser, etc.).
EXAMPLE: L-Tyrosyl-glycyl-glycyl-L-phenylalaninol.
USE: Useful as an analgesic, a narcotic antagonistic and an antidiarrheic drugs having an agonistic activity in the opiate acceptor and a prolonged duration with low toxicity, and including any of optical isomers and racemates.
PROCESS: A dipeptide of formula II (R3 is amino-protecting group; R4 is carboxyl- protecting group) is reacted with a dipeptide of formula III by the conventional peptide linkage forming method, e.g. the azide method, to give a tetrapeptide of formula IV, whose protecting group is eliminated by the conventional deprotection means to afford the tetrapeptide of formula I readily.
COPYRIGHT: (C)1981,JPO&Japio
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP54102381A JPS6055080B2 (en) | 1979-08-10 | 1979-08-10 | tetrapeptide |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP54102381A JPS6055080B2 (en) | 1979-08-10 | 1979-08-10 | tetrapeptide |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5626856A true JPS5626856A (en) | 1981-03-16 |
| JPS6055080B2 JPS6055080B2 (en) | 1985-12-03 |
Family
ID=14325867
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP54102381A Expired JPS6055080B2 (en) | 1979-08-10 | 1979-08-10 | tetrapeptide |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6055080B2 (en) |
-
1979
- 1979-08-10 JP JP54102381A patent/JPS6055080B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6055080B2 (en) | 1985-12-03 |
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