US2017340584A1PendingUtilityA1
Modified taurine, and pharmaceutical composition for preventing or treating metabolic diseases containing same
Est. expiryDec 16, 2034(~8.4 yrs left)· nominal 20-yr term from priority
Inventors:Jonghyun Byun
A61P 9/10A61P 3/10A61P 7/02A61P 3/00A61P 27/02A61P 25/02A61P 3/04A61P 25/28A61P 25/00A61P 11/00A61P 13/12A61P 1/16A23L 33/10C07C 309/14A23V 2200/30A61K 31/198A61K 31/7004A61K 31/195A61K 31/70A61K 9/00A61K 31/145A61K 47/26A61K 31/185C07B 2200/13A61K 31/18A61K 31/352Y02P20/55A23V 2250/0644A61K 47/20A61K 9/08A23V 2002/00A61K 31/353A61K 47/183A61K 9/0019
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Claims
Abstract
The present invention relates to a modified taurine, and a pharmaceutical composition for preventing or treating metabolic disease or a food composition, which contains the modified taurine as an active ingredient. More specifically, the modified taurine of the present invention has physical properties different from those of existing taurine, and has significant effects on the prevention and treatment of metabolic syndrome, including antithrombotic effects.
Claims
exact text as granted — not AI-modified1 . A modified taurine produced by dissolving taurine with heating in a first polar solvent and adding a second polar solvent thereto,
wherein a difference in polarity between the first polar solvent and the second polar solvent is 5 or less, and wherein the ratios of absorption bands of 847/891, 1182/1256 and 1427/1458 at 847, 891, 1182, 1256, 1427 and 1458 cm −1 in the Raman spectrum of the modified taurine are all less than 1.
2 . The modified taurine of claim 1 , wherein an onset point where the modified taurine starts to melt ranges from 330° C. to 340° C.
3 . The modified taurine of claim 1 , wherein the modified taurine has a water solubility of 75-79 g/L.
4 . The modified taurine of claim 1 , wherein the absorption wavelength at 1650-2800 cm −1 in the FT-IR spectrum of the modified taurine differs from that of the taurine.
5 . The modified taurine of claim 1 , wherein the first polar solvent is water, and the second polar solvent contains a methyl group (—CH 3 ).
6 . The modified taurine of claim 5 , wherein the second polar solvent is any one or more selected from the group consisting of methanol, ethanol, butanol, acetic acid, acetone, propanol, chloroform, and ethyl acetate.
7 - 16 . (canceled)
17 . A method for producing a modified taurine, comprising the steps of:
dissolving taurine with heating in a first polar solvent; and adding a second polar solvent thereto to produce the modified taurine, wherein a difference in polarity between the first polar solvent and the second polar solvent is 5 or less, and wherein the first polar solvent is water, and the second polar solvent contains a methyl group (—CH 3 ).
18 . The method of claim 17 , wherein the second polar solvent is any one or more selected from the group consisting of methanol, ethanol, butanol, acetic acid, acetone, propanol, chloroform, and ethyl acetate.
19 . The method of claim 17 , wherein the ratios of absorption bands of 847/891, 1182/1256 and 1427/1458 at 847, 891, 1182, 1256, 1427 and 1458 cm −1 in the Raman spectrum of the modified taurine are all less than 1.
20 . The method of claim 17 , wherein an onset point where the modified taurine starts to melt ranges from 330° C. to 340° C.
21 . The method of claim 17 , wherein the modified taurine has a water solubility of 75-79 g/L.
22 . The method of claim 17 , wherein the absorption wavelength at 1650-2800 cm −1 in the FT-IR spectrum of the modified taurine differs from that of the taurine.
23 . A food composition for improving or alleviating metabolic disease, which contains the modified taurine of claim 1 .Join the waitlist — get patent alerts
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