IP Library Patent Application 17714240
Patent Application
App. No. 17/714,240

MIXTURE OF INOSITOL DERIVATIVES

Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US None
App. No.
17/714,240
Abstract

A mixture of inositol derivatives in which a sugar is bonded to inositol includes an inositol derivative (A10) in which total sugars bonded to one inositol molecule is 10 or more in terms of monosaccharide units. In addition, a mixture of inositol derivatives in which a sugar is bonded to inositol includes 5% by mass or more of an inositol derivative (A7), in which total sugars bonded to one inositol molecule is 7 or more in terms of monosaccharide units, with respect to a total amount of inositol derivatives (100% by mass).

Claims (27)

1 . A method of producing a mixture of inositol derivatives, comprising reacting an inositol and an oligosaccharide at a mass ratio of 1:3.5 to 1:4.5.

2 . The method according to claim 1 ,

wherein the mixture of inositol derivatives is a mixture of inositol derivatives in which a sugar is bonded to inositol, the mixture of inositol derivatives comprising an inositol derivative (A10) in which total sugars bonded to one inositol molecule is 10 or more in terms of monosaccharide units, and all of inositol derivatives in which total sugars bonded to one inositol molecule is 1 to 9 in terms of monosaccharide units, and

wherein the amount of an inositol derivative (A4) in which total sugars bonded to one inositol molecule is 4 or more in terms of monosaccharide units is 67% by mass or more with respect to total amount of inositol derivatives.

3 . The method according to claim 1 , wherein the reaction of the inositol and the oligosaccharide is performed for 30 to 70 hours.

4 . The method according to claim 3 , wherein the reaction of the inositol and oligosaccharide is performed in a buffer solution selected from the group consisting of a citrate buffer solution, a phosphate buffer solution, a Tris-HCl buffer solution, and a HEPES buffer solution.

5 . The method according to claim 4 , wherein the buffer solution is a citrate buffer solution.

6 . The method according to claim 1 ,

wherein the inositol is myo-inositol,

the oligosaccharide is cyclodextrin, and

the reaction is performed in the presence of cyclodextrin glucanotransferase.

7 . The method according to claim 2 ,

wherein the inositol is myo-inositol,

the oligosaccharide is cyclodextrin, and

the reaction is performed in the presence of cyclodextrin glucanotransferase.

8 . The method according to claim 3 ,

wherein the inositol is myo-inositol,

the oligosaccharide is cyclodextrin, and

the reaction is performed in the presence of cyclodextrin glucanotransferase.

9 . The method according to claim 4 ,

wherein the inositol is myo-inositol,

the oligosaccharide is cyclodextrin, and

the reaction is performed in the presence of cyclodextrin glucanotransferase.

10 . The method according to claim 5 ,

wherein the inositol is myo-inositol,

the oligosaccharide is cyclodextrin, and

the reaction is performed in the presence of cyclodextrin glucanotransferase.

Assignments (3)
CHANGE OF ADDRESS Recorded Feb 9, 2024
From: RESONAC CORPORATION
To: RESONAC CORPORATION
Reel/Frame 066547/0677 →
CHANGE OF NAME Recorded Jun 23, 2023
From: SHOWA DENKO K.K.
To: RESONAC CORPORATION
Reel/Frame 064082/0513 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 6, 2022
From: FUJITA, ICHIRO; YAMAKI, SHINJI; NAKAGAMI, YUKO
To: SHOWA DENKO K.K.
Reel/Frame 059617/0899 →