IP Library Granted Patent US 7,135,566
Granted Patent B2
US 7,135,566 · App. 10/481,246 · Granted Nov 14, 2006

Process for producing sugar chain asparagine derivative

Assignees: Otsuka Chemical Co., Ltd.; Yasuhiro Kajihara
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Quick Facts
Patent No.
US 7,135,566
App. No.
10/481,246
Granted
Nov 14, 2006
Kind
B2
Abstract

The present invention provides a process for preparing a sugar chain asparagine derivative. According to the process, various isolated sugar chain asparagine derivatives useful in the field of the development of pharmaceuticals and the like can be conveniently obtained in a large amount as compared to that of the prior art. The present invention also provides a process for preparing a sugar chain asparagine and a process for preparing a sugar chain via a step for preparing a sugar chain asparagine derivative. The present invention further provides a novel sugar chain asparagine derivative, a sugar chain asparagine and a sugar chain.

Claims (54)

1. A process for preparing a sugar chain asparagine derivative derived from a sugar chain asparagine, comprising the steps of:

(a) introducing a fat-soluble protecting group selected from the group consisting of Fmoc and Boc groups into the sugar chain aspargine contained in a mixture of one or more sugar chain asparagines, to give a mixture of sugar chain asparagine derivatives; and

(b) subjecting the mixture of sugar chain asparagine derivatives or a mixture obtainable by hydrolyzing a sugar chain asparagine derivative contained in the mixture of sugar chain asparagine derivatives to chromatography, to separate each of the sugar chain asparagine derivatives therefrom.

2. The process according to claim 1 , further comprising the step of (b′): hydrolyzing the sugar chain asparagine derivative separated in step (b) with a glycosidase.

3. The process according to claim 1 or 2 , wherein the mixture of one or more sugar chain asparagines comprises a compound of the following formula, in which Asn denotes asparagine:

and/or a compound having one or more deletions of sugar residues in the above compound.

4. The process according to any one of claims 1 to 3 , wherein the fat-soluble protecting group is fluorenylmethoxycarbonyl (Fmoc) group.

5. The process according to any one of claims 1 to 3 , wherein the step (a) is a step of introducing Fmoc group into the sugar chain aspargine contained in a mixture of one or more sugar chain asparagines having a sialic acid residue at a non-reducing terminal, and introducing benzyl group into the sialic acid residue, to give a mixture of sugar chain asparagine derivatives.

6. A process for isolating a sugar chain aspargine from a mixture, comprising the steps of:

(a) introducing a fat-soluble protecting group selected from the group consisting of Fmoc and Boc groups into a sugar chain aspargine contained in a mixture of one or more sugar chain asparagines, to give a mixture of sugar chain asparagine derivatives;

(b) subjecting the mixture of sugar chain asparagine derivatives or a mixture obtainable by hydrolyzing a sugar chain asparagine derivative contained in the mixture of sugar chain asparagine derivatives to chromatography, to separate each of the sugar chain asparagine derivatives therefrom; and

(c) removing the protecting group from the sugar chain asparagine derivative separated in the step (b), to give the sugar chain asparagine.

7. The process according to claim 6 , further comprising the step of:

(b′) hydrolyzing the sugar chain asparagine derivative separated in step (b) with a glycosidase; and/or

(c′) hydrolyzing the sugar chain asparagine obtained in step (c) with a glycosidase.

8. The process according to claim 6 or 7 , wherein the mixture of one or more sugar chain asparagines comprises a compound of the following formula, in which Asn denotes asparagine:

and/or a compound having one or more deletions of sugar residues in the above compound.

9. The process according to any one of claims 6 to 8 , wherein the fat-soluble protecting group is Fmoc group.

10. The process according to any one of claims 6 to 8 , wherein the step (a) is a step of introducing Fmoc group into the sugar chain aspargine contained in a mixture of one or more sugar chain asparagines having a sialic acid residue at a non-reducing terminal, and introducing benzyl group into the sialic acid residue, to give a mixture of sugar chain asparagine derivatives.

11. A process for preparing a sugar chain from a mixture of sugar chain asparagines, comprising the steps of:

(a) introducing a fat-soluble protecting group selected from the group consisting of Fmoc and Boc groups into a sugar chain aspargine contained in a mixture of one or more sugar chain asparagines, to give a mixture of sugar chain asparagine derivatives;

(b) subjecting the mixture of sugar chain asparagine derivatives or a mixture obtainable by hydrolyzing a sugar chain asparagine derivative contained in the mixture of sugar chain asparagine derivatives to chromatography, to separate each of the sugar chain asparagine derivatives therefrom;

(c) removing the protecting group from the sugar chain asparagine derivative separated in the step (b), to give a sugar chain asparagine; and

(d) removing an asparagine residue from the sugar chain asparagine obtained in the step (c), to give the sugar chain.

12. The process claim 11 , further comprising the step of:

(b′) hydrolyzing the sugar chain asparagine derivative separated in step (b) with a glycosidase; and/or

(c′) hydrolyzing the sugar chain asparagine obtained in step (c) with a glycosidase; and/or

(d′) hydrolyzing the sugar chain obtained in step (d) with a glycosidase.

13. The process according to claim 11 or 12 , wherein the mixture of one or more sugar chain asparagines comprises a compound of the following formula, in which Asn denotes asparagine:

and/or a compound having one or more deletions of sugar residues in the above compound.

14. The process according to any one of claims 11 to 13 , wherein the fat-soluble protecting group is Fmoc group.

15. The process according to any one of claims 11 to 13 , wherein the step (a) is a step of introducing Fmoc group into the sugar chain aspargine contained in a mixture of one or more sugar chain asparagines having a sialic acid residue at a non-reducing terminal, and introducing benzyl group into the sialic acid residue, to give a mixture of sugar chain asparagine derivatives.

16. A sugar chain asparagine derivative having the general formula:

wherein Asn is asparagine, R 1 and R 2 , which may be identical or different, are H,

with proviso that a case where R 1 and R 2 are both H,

is excluded.

17. A sugar chain asparagine derivative having the general formula:

wherein one of R x and R y is

and the other is H,

18. A sugar chain asparagine having the general formula:

wherein Asn is asparagine, R 3 and R 4 , which may be identical or different, are H,

with proviso that (i) a case where R 3 and R 4 are

the same, (ii) a case where R3 is

and R 4 is H or

and

(iii) a case where R 3 is H and R 4 is

are excluded.

19. A sugar chain having the general formula:

wherein R 5 and R 6 , which may be identical or different, are H,

with proviso that (i) a case where R 5 and R 6 are the same, (ii) a case where one of R 5 and R 6 is

and the other is H or

and (iii) a case where R 5 is

and R 6 is

are excluded.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 6, 2013
From: OTSUKA CHEMICAL CO., LTD.
To: GLYTECH, INC.
Reel/Frame 030358/0088 →
CHANGE OF NAME Recorded Sep 3, 2009
From: OTSUKA CHEMICAL HOLDINGS CO., LTD.
To: OTSUKA CHEMICAL CO., LTD.
Reel/Frame 023180/0593 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 2, 2009
From: OTSUKA CHEMICAL CO., LTD.
To: OTSUKA CHEMICAL HOLDINGS CO., LTD.
Reel/Frame 023180/0098 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 18, 2003
From: KAJIHARA, YASUHIRO; SASAKI, KEN
To: OTSUKA CHEMICAL CO., LTD.; YASUHIRO KAJIHARA
Reel/Frame 015382/0919 →
Priority Claims (1)
JP 2001-185685 · Jun 19, 2001 · national
Continuity (1)
Related Publication 20040181054A1 · Sep 16, 2004