JPS5775957A - Peptide derivative - Google Patents
Peptide derivativeInfo
- Publication number
- JPS5775957A JPS5775957A JP55151610A JP15161080A JPS5775957A JP S5775957 A JPS5775957 A JP S5775957A JP 55151610 A JP55151610 A JP 55151610A JP 15161080 A JP15161080 A JP 15161080A JP S5775957 A JPS5775957 A JP S5775957A
- Authority
- JP
- Japan
- Prior art keywords
- protecting
- amino
- methylcoumarin
- lysine
- protecting group
- 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
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Peptides Or Proteins (AREA)
Abstract
NEW MATERIAL:A compound shown by the formula (R is H or amino-protecting group).
EXAMPLE: 7-(Nα-t-Butyloxycarbonyl-L-glutaminyl-Nε-carbobenzoxy-L-lysyl-Nσ,ω- dicarbobenzoxy-L-arginyl-Nε-carbobenzoxy-L-lysyl)amino-4-methylcoumarin.
USE: A substrate for enzyme. Useful for highly sensitive measurement, e.g., titer, purity, etc. of enzyme.
PROCESS: Nα-And Nε-protecting lysine is condensed through dehydration with 7- amino-4-methylcoumarin, and Nα protecting group is removed selectively. The prepared Nε-protecting lysine-4-methylcoumarin derivative is condensed through dehydration with a side chain- and Nα-protecting arginine, Nα- and Nε-protecting lysine and Nα-protecting glutamic acid successively. The side chain-protecting group is removed selectively, to give a compound shown by the formula. The reaction is preferably carried out at from 0°CW room temperature in a solvent, e.g., DMF, etc.
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP55151610A JPS5775957A (en) | 1980-10-29 | 1980-10-29 | Peptide derivative |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP55151610A JPS5775957A (en) | 1980-10-29 | 1980-10-29 | Peptide derivative |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5775957A true JPS5775957A (en) | 1982-05-12 |
Family
ID=15522290
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP55151610A Pending JPS5775957A (en) | 1980-10-29 | 1980-10-29 | Peptide derivative |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5775957A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6087120A (en) * | 1996-02-02 | 2000-07-11 | Haemoprobe B.V. | Measurement of complement activation by biomaterials by means of complement convertase cleavage of peptide substrates |
-
1980
- 1980-10-29 JP JP55151610A patent/JPS5775957A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6087120A (en) * | 1996-02-02 | 2000-07-11 | Haemoprobe B.V. | Measurement of complement activation by biomaterials by means of complement convertase cleavage of peptide substrates |
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