JPS5463072A - Decapeptide derivative and its preparation - Google Patents
Decapeptide derivative and its preparationInfo
- Publication number
- JPS5463072A JPS5463072A JP12763777A JP12763777A JPS5463072A JP S5463072 A JPS5463072 A JP S5463072A JP 12763777 A JP12763777 A JP 12763777A JP 12763777 A JP12763777 A JP 12763777A JP S5463072 A JPS5463072 A JP S5463072A
- Authority
- JP
- Japan
- Prior art keywords
- protecting group
- carboxyl
- derivative
- compound
- preparation
- 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
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Peptides Or Proteins (AREA)
Abstract
NEW MATERIAL:Decapeptide derivative of formula I [X1 is H, amino-protecting group; Y1,2 are carboxyl-protecting group; Y3 is NH2, carboxyl-protecting group; Z1 is H, OH-protecting group. SO3X (X is alkali metal such as K, Na, base such as triethylamine, H); Z2 is H, OH-protecting group].
EXAMPLE: A compound II (Z is benzyloxycarbonyl; Bzl is benzyl).
USE: Raw material of caerulein which is a physiologically active peptide.
PROCESS: The compound I can be prepared by the fragment condensation of 1 mole of a tetrapeptide derivative III (Y4 is OH, carboxyl-protecting group such as methyl ester) with 1-2 moles of a hexapeptide derivative IV or its acid salt, in the presence of proteinase, in an aqueous medium of pH2-11, at a temperature lower than the deactivation temp. of the enzyme, for about several tens sec. to 20 hours.
COPYRIGHT: (C)1979,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP52127637A JPS6023680B2 (en) | 1977-10-26 | 1977-10-26 | Decapeptide derivatives and their production method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP52127637A JPS6023680B2 (en) | 1977-10-26 | 1977-10-26 | Decapeptide derivatives and their production method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5463072A true JPS5463072A (en) | 1979-05-21 |
JPS6023680B2 JPS6023680B2 (en) | 1985-06-08 |
Family
ID=14965013
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP52127637A Expired JPS6023680B2 (en) | 1977-10-26 | 1977-10-26 | Decapeptide derivatives and their production method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6023680B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0106282A2 (en) * | 1982-10-08 | 1984-04-25 | Shionogi & Co., Ltd. | Production of caerulein intermediate |
-
1977
- 1977-10-26 JP JP52127637A patent/JPS6023680B2/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0106282A2 (en) * | 1982-10-08 | 1984-04-25 | Shionogi & Co., Ltd. | Production of caerulein intermediate |
EP0106282A3 (en) * | 1982-10-08 | 1986-05-14 | Shionogi & Co., Ltd. | Production of caerulein intermediate |
Also Published As
Publication number | Publication date |
---|---|
JPS6023680B2 (en) | 1985-06-08 |
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