WO2007097254A1 - 新規イソジペプチド - Google Patents
新規イソジペプチド Download PDFInfo
- Publication number
- WO2007097254A1 WO2007097254A1 PCT/JP2007/052838 JP2007052838W WO2007097254A1 WO 2007097254 A1 WO2007097254 A1 WO 2007097254A1 JP 2007052838 W JP2007052838 W JP 2007052838W WO 2007097254 A1 WO2007097254 A1 WO 2007097254A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- formula
- isodipeptide
- hydrogen atom
- val
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/22—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 amino acids
-
- 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
Definitions
- the present invention relates to novel isodipeptides useful as synthetic units such as peptides.
- Non-Patent Documents 1 and 2 have developed the “0-acyl isopeptide method” as an efficient synthesis method for difficult sequence-containing peptides (see Non-Patent Documents 1 and 2). This method is to synthesize a 0-aglyceropeptide in which an amide bond is isomerized to an ester bond in a hydroxyl group-containing amino acid such as a serine residue, and then obtain a desired peptide by a 0-N intramolecular vicary rearrangement reaction. is there.
- Non-patent literature l Tetrahedoron Letters 45 (2004) 5965-5968
- Nonpatent literature 2 Chem. Commun., 2004, 124-125
- the inventors of the present invention have made further studies to find out that the following novel phosphopeptide (1) is used, in particular, as a synthesis unit in solid phase synthesis.
- the present inventors have completed the present invention by finding that the peptide of (1) can be conveniently synthesized in high yield and high purity.
- ⁇ represents an acid residue of a ⁇ -protected amino acid
- R a represents a protecting group of an amino group
- X a represents a carboxyl group, a hydrogen atom, an alkyl group, an aralkyl group, an aryl group or a hetero group
- Y represents a carboxyl group, a hydrogen atom or an alkyl group
- Z represents a hydrogen atom or an alkyl group
- n represents an integer of 0-3, with the proviso that Only means carboxyl group.
- the present invention relates to Formula (1)
- the alkyl group in X a and Y a of the formula (1) is not particularly limited, but is preferably A C1-C6 linear or branched alkyl group is mentioned. Also, it puts that Ararukiru group X a of the formula (1), Teroa reel to Ariru or in Ariru group or heteroaryl groups are methyl, nitro, or may have a substituent such as black hole.
- X a is a carboxyl group
- Y a is a hydrogen atom or an alkyl group
- n is 0 or an optically active isomer thereof
- X a is a hydrogen atom, an alkyl group, an aralkyl group, an aryl group or a heteroaryl group
- Y a is a carboxyl group
- n is 0 or an optically active peptide thereof.
- an amino protecting group of a common amino acid is targeted.
- Preferred protective groups are, for example, 9H-fluoren-9-ylmethoxy, which is desirable as a group in which only the protective group from which the ester bond in isopeptide (1) is cleaved is removed. Examples thereof include carboxyl (Fmo c), tert-butoxycarbol (Boc), benzyloxycarbol (Z), 2-chlorobenzilboxycarbol and the like.
- the amino acid residue of the N-protected amino acid shown by A when the amino acid has a side chain functional group such as a hydroxyl group or a further carboxyl group, it may be protected by a suitable known protective group. desirable.
- R a represents a hydrogen atom or a methyl group.
- Fmoc means 9H-fluorene-9-ylmethoxycarbo group
- Boc means ter t-butoxycarboyl group
- R b is the same as above.
- This compound (lb) is particularly useful for the synthesis of L-parin-L-threonine or L-parin-L-serine linked dipeptide as a component.
- the most preferable compound among isodipeptides (1) is a compound represented by the following formula (lc) (hereinafter simply referred to as ⁇ Boc-Thr (Fmoc-Val) -OH). ).
- the isodipeptide (1) according to the present invention is produced by a known esterification method using a carboxylic acid and an alcohol.
- N-protected amino acid represented by A-OH and the following formula (2)
- the diisopeptide (1) is produced by eliminating.
- Specific examples of the compound represented by the formula (2) preferably include amino acids having a hydroxyl group in a side chain such as threonine, serine, statin and norstatin.
- the N-protected amino acid represented by AOH is not particularly limited, and includes various types of amino acids such as a- or ⁇ -amino acids in which the amino group is protected.
- ⁇ -protected amino acid represented by ⁇ - ⁇ has a side chain functional group
- the above esterification reaction is carried out according to a conventional method.
- the solvent to be used include chloroform, dichloromethane and the like.
- the reaction temperature varies depending on the raw material used, and is usually around 25 ° C.
- the carboxyl-protecting group of compound (2a) is preferably a group which can be removed by hydrogenation, such as benzyl, p-trobenzyl or 4-pyridylmethyl. Be Furthermore, it is preferable to use a group which does not leave at this point and neither the protecting group of the above amino group of isodipeptide (1) by hydrogenation.
- the elimination treatment of the carboxyl group of compound (2b), which is an intermediate product, can be carried out, for example, by introducing hydrogen gas in the presence of Pd / C.
- the isodipeptide (1) thus obtained is isolated and purified by a conventional method to obtain a pure product, which is then used as a synthesis unit for the desired polypeptide synthesis.
- the compound represented by AOH as a raw material and the compound (2) may each have one or more asymmetric carbons. Therefore, depending on the type of raw material, the desired isopeptide can be obtained in the form of an optically active substance, a racemic mixture thereof, a diastereomer or a mixture thereof. For example, by using each optically active raw material, it is possible to obtain a distereomeric type of isodipeptide (see (lb) and (lc)).
- the desired resolution with high optical purity is carried out by performing optical resolution and separation according to the purpose according to the purpose. You can get a tide.
- TFA tetrafluoroacetic acid
- all the constituent amino acids are L-amino acids.
- reaction conditions in each step in the above reaction process are as follows.
- a peptide containing various desired difficult sequences can be synthesized by using Fmoc-Va ⁇ OH instead of the above and using another amino acid protected by Fmoc or the like. Coupling reactions of other amino acids to amino acids or peptides are carried out by conventional methods in peptide synthesis. In addition, 0-N intramolecular asyl rearrangement reaction (Reaction vi) of the ester is also carried out by a known method (see Non-patent Document 1).
- Boc-Ser (Fmoc-Val) By substituting N- (t-butoxycarboyl) -L-serine benzyl ester (BocSer OBzl) for BocThroBzl according to the method of Example 1, Boc-Ser (Fmoc-Val) can be obtained. ) -OH can be synthesized.
- N-Acetylation was performed with Rumin (10.4 ⁇ L. 0.071 mmol).
- the protected peptide oil is TF in the presence of thionol (66.7 ⁇ L), m-taresol (66.7 ⁇ L) and ⁇ 0 (66.7 ⁇ L).
- the retention time on nm) was identical to that of peptide (3a) synthesized by conventional methods.
- isodipeptide (1) of the present invention as a synthetic unit of a peptide, side reactions such as racemization can be prevented, and a desired peptide can be synthesized completely automatically by a solid phase method.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Life Sciences & Earth Sciences (AREA)
- Peptides Or Proteins (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP07714368A EP1992611B1 (en) | 2006-02-22 | 2007-02-16 | Isodipeptide useful as a synthetic unit for making peptides |
JP2008501692A JP5097104B2 (ja) | 2006-02-22 | 2007-02-16 | 新規イソジペプチド |
DE602007007583T DE602007007583D1 (de) | 2006-02-22 | 2007-02-16 | Isodipeptid als syntheseeinheit zur herstellung von peptiden |
CA002638777A CA2638777A1 (en) | 2006-02-22 | 2007-02-16 | Novel isodipeptide |
AT07714368T ATE473208T1 (de) | 2006-02-22 | 2007-02-16 | Isodipeptid als syntheseeinheit zur herstellung von peptiden |
AU2007218747A AU2007218747B9 (en) | 2006-02-22 | 2007-02-16 | Novel isodipeptide |
DK07714368.3T DK1992611T3 (da) | 2006-02-22 | 2007-02-16 | Isodipeptid anvendelig som en syntetiskenhed til fremstilling af peptider |
US12/224,170 US20090318669A1 (en) | 2006-02-22 | 2007-02-16 | Novel Isodipeptide |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006044853 | 2006-02-22 | ||
JP2006-044853 | 2006-02-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2007097254A1 true WO2007097254A1 (ja) | 2007-08-30 |
Family
ID=38437294
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2007/052838 WO2007097254A1 (ja) | 2006-02-22 | 2007-02-16 | 新規イソジペプチド |
Country Status (9)
Country | Link |
---|---|
US (1) | US20090318669A1 (ja) |
EP (1) | EP1992611B1 (ja) |
JP (1) | JP5097104B2 (ja) |
AT (1) | ATE473208T1 (ja) |
AU (1) | AU2007218747B9 (ja) |
CA (1) | CA2638777A1 (ja) |
DE (1) | DE602007007583D1 (ja) |
DK (1) | DK1992611T3 (ja) |
WO (1) | WO2007097254A1 (ja) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113912675B (zh) * | 2021-09-23 | 2023-04-11 | 中国药科大学 | 一种具有镇痛活性的蜈蚣多肽及其应用 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08109180A (ja) * | 1994-10-11 | 1996-04-30 | Hamari Yakuhin Kogyo Kk | O→n分子内アシル転位型プロドラッグ |
JP4499383B2 (ja) * | 2003-07-11 | 2010-07-07 | 良明 木曽 | 水溶性プロドラッグ |
-
2007
- 2007-02-16 JP JP2008501692A patent/JP5097104B2/ja not_active Expired - Fee Related
- 2007-02-16 US US12/224,170 patent/US20090318669A1/en not_active Abandoned
- 2007-02-16 DK DK07714368.3T patent/DK1992611T3/da active
- 2007-02-16 AU AU2007218747A patent/AU2007218747B9/en not_active Ceased
- 2007-02-16 AT AT07714368T patent/ATE473208T1/de not_active IP Right Cessation
- 2007-02-16 DE DE602007007583T patent/DE602007007583D1/de active Active
- 2007-02-16 CA CA002638777A patent/CA2638777A1/en not_active Abandoned
- 2007-02-16 WO PCT/JP2007/052838 patent/WO2007097254A1/ja active Application Filing
- 2007-02-16 EP EP07714368A patent/EP1992611B1/en not_active Not-in-force
Non-Patent Citations (6)
Also Published As
Publication number | Publication date |
---|---|
EP1992611B1 (en) | 2010-07-07 |
EP1992611A4 (en) | 2009-04-01 |
JPWO2007097254A1 (ja) | 2009-07-09 |
CA2638777A1 (en) | 2007-08-30 |
AU2007218747B2 (en) | 2012-05-24 |
DK1992611T3 (da) | 2010-09-27 |
DE602007007583D1 (de) | 2010-08-19 |
EP1992611A1 (en) | 2008-11-19 |
US20090318669A1 (en) | 2009-12-24 |
ATE473208T1 (de) | 2010-07-15 |
AU2007218747B9 (en) | 2012-09-27 |
AU2007218747A1 (en) | 2007-08-30 |
JP5097104B2 (ja) | 2012-12-12 |
AU2007218747A2 (en) | 2008-11-06 |
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