JPS5634697A - Preparation of 5'-triphosphoryladnylyl-(2'-5')-adenylyl-(2'-5')-adenosine - Google Patents
Preparation of 5'-triphosphoryladnylyl-(2'-5')-adenylyl-(2'-5')-adenosineInfo
- Publication number
- JPS5634697A JPS5634697A JP11152479A JP11152479A JPS5634697A JP S5634697 A JPS5634697 A JP S5634697A JP 11152479 A JP11152479 A JP 11152479A JP 11152479 A JP11152479 A JP 11152479A JP S5634697 A JPS5634697 A JP S5634697A
- Authority
- JP
- Japan
- Prior art keywords
- group
- oligomer
- formula
- adenosine
- triphosphate
- 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
- Saccharide Compounds (AREA)
Abstract
PURPOSE: To prepare the titled compound having protein-synthesis inhibiting activity and useful as a carcinostatic agent, etc., by the total synthesis which comprises the conversion of the (2'-5')oligomer of adenosine-5'-monophosphate having a 3'-OH group protected with a specific group to 5'-triphosphate, and the elimination of the protecting group from the product.
CONSTITUTION: The objective compound of formula III (A is adenylyl) is prepared by (1) converting the (2'-5')oligomer of the adenosine-5'-mono-phosphate of formula II (NB is o-nitrobenzyl; n is 0, 1 or 2) to the 5'-triphosphate, and (2) eliminating the protecting group of the 3'-OH group. The oligomer of formula II can be prepared by converting the 3'-OH group of a compound of formula I (X is acyl or substituted or unsubstituted trityl) to o-nitro-4- and/or 5-substituted or unsubstituted benzyl group. The conversion to 5'-triphosphate is preferably carried out by reacting the oligomer with 1,1'-carbonylimidazole, and treating the reaction product with pyrophosphoric acid salt. The elimination of the protecting group is carried out preferably by the irradiation with ultraviolet rays having wavelength of ≥ 280nm.
COPYRIGHT: (C)1981,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11152479A JPS5634697A (en) | 1979-08-31 | 1979-08-31 | Preparation of 5'-triphosphoryladnylyl-(2'-5')-adenylyl-(2'-5')-adenosine |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11152479A JPS5634697A (en) | 1979-08-31 | 1979-08-31 | Preparation of 5'-triphosphoryladnylyl-(2'-5')-adenylyl-(2'-5')-adenosine |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5634697A true JPS5634697A (en) | 1981-04-06 |
JPS6121560B2 JPS6121560B2 (en) | 1986-05-27 |
Family
ID=14563508
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11152479A Granted JPS5634697A (en) | 1979-08-31 | 1979-08-31 | Preparation of 5'-triphosphoryladnylyl-(2'-5')-adenylyl-(2'-5')-adenosine |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5634697A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63226405A (en) * | 1987-03-16 | 1988-09-21 | Yasunobu Tomoto | Artificial ground structure for soft ground |
US4880918A (en) * | 1982-07-13 | 1989-11-14 | Eliezer Rapaport | Arrest and killing of tumor cells by adenosine 5-diphosphate and adenosine-5-triphosphate |
US5049372A (en) * | 1982-07-13 | 1991-09-17 | Eliezer Rapaport | Anticancer activities in a host by increasing blood and plasma adenosine 5'-triphosphate (ATP) levels |
US5227371A (en) * | 1982-07-13 | 1993-07-13 | Eliezer Rapaport | Utilization of adenine nucleotides and/or adenosine and inorganic phosphate for elevation of liver, blood and blood plasma adenosine 5'-triphosphate concentrations |
-
1979
- 1979-08-31 JP JP11152479A patent/JPS5634697A/en active Granted
Non-Patent Citations (1)
Title |
---|
CHEM. PHARM. BULL.=1977 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4880918A (en) * | 1982-07-13 | 1989-11-14 | Eliezer Rapaport | Arrest and killing of tumor cells by adenosine 5-diphosphate and adenosine-5-triphosphate |
US5049372A (en) * | 1982-07-13 | 1991-09-17 | Eliezer Rapaport | Anticancer activities in a host by increasing blood and plasma adenosine 5'-triphosphate (ATP) levels |
US5227371A (en) * | 1982-07-13 | 1993-07-13 | Eliezer Rapaport | Utilization of adenine nucleotides and/or adenosine and inorganic phosphate for elevation of liver, blood and blood plasma adenosine 5'-triphosphate concentrations |
JPS63226405A (en) * | 1987-03-16 | 1988-09-21 | Yasunobu Tomoto | Artificial ground structure for soft ground |
Also Published As
Publication number | Publication date |
---|---|
JPS6121560B2 (en) | 1986-05-27 |
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