Heparan sulfate (hs) oligosaccharides effect in liver ischemia reperfusion injury
US-2022265699-A1 · Aug 25, 2022 · US
US11633424B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11633424-B2 |
| Application number | US-201917254145-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 19, 2019 |
| Priority date | Jun 20, 2018 |
| Publication date | Apr 25, 2023 |
| Grant date | Apr 25, 2023 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Chondroitin sulfate compounds comprising chondroitin sulfate backbone 19 mer, CS-A 19 mer, CS-C 19 mer, CS-E 19 mer, C8 backbone 13 mer, C8-A 13 mer, CS-C 13 mer, CS-E 13 mer and/or combinations thereof are provided. Methods of treating histone toxicity in a subject are provided, the methods including administering to a subject a chondroitin sulfate compound to treat the histone toxicity in the subject. Pharmaceutical compositions for use in treating histone toxicity and/or sepsis are provided. Methods of treating sepsis in a subject are provided, the methods including administering to a subject a chondroitin sulfate compound to treat the sepsis in the subject.
Opening claim text (preview).
What is claimed is: 1. A method of treating histone toxicity in a subject, the method comprising: providing a subject in need of histone toxicity treatment; and administering to the subject a chondroitin sulfate (CS) compound, wherein the chondroitin sulfate compound comprises a CS backbone, CS-A, CS-E, CS-C and/or combinations thereof, and wherein the chondroitin sulfate compound comprises chondroitin sulfate backbone 19 mer, CS-A 19 mer, CS-C 19 mer, CS-E 19 mer, CS backbone 13 mer, CS-A 13 mer, CS-C 13 mer, CS-E 13 mer and/or combinations thereof, and wherein the histone toxicity in the subject is treated. 2. The method of claim 1 , wherein the subject is suffering from sepsis. 3. The method of claim 1 , wherein the subject is a human subject. 4. The method of claim 1 , wherein the chondroitin sulfate compound comprises one or more of the following structures: wherein R is selected from the group consisting of —H, alkyl, substituted alkyl, aryl, and substituted aryl, wherein n is 1, 2, 3, 4, 5, 6, 7 or 8. 5. The method of claim 1 , wherein the chondroitin sulfate compound is administered as part of a pharmaceutical composition. 6. The method of claim 1 , wherein the pharmaceutical composition comprises a CS compound and a pharmaceutically acceptable carrier or adjuvant for administration of the CS. 7. A method of treating sepsis in a subject, the method comprising: providing a subject in need of sepsis treatment; and administering to the subject a chondroitin sulfate compound, wherein the chondroitin sulfate compound comprises a CS backbone, CS-A, CS-E, CS-C and/or combinations thereof, and wherein the chondroitin sulfate compound comprises chondroitin sulfate backbone 19 mer, CS-A 19 mer, CS-C 19 mer, CS-E 19 mer, CS backbone 13 mer, CS-A 13 mer, CS-C 13 mer, CS-E 13 mer and/or combinations thereof wherein the sepsis in the subject is treated. 8. The method of claim 7 , wherein the subject is a human subject. 9. The method of claim 7 , wherein the chondroitin sulfate compound comprises one or more of the following structures: wherein R is selected from the group consisting of —H, alkyl, substituted alkyl, aryl, and substituted aryl, wherein n is 1, 2, 3, 4, 5, 6, 7 or 8. 10. The method of claim 7 , wherein the chondroitin sulfate compound is administered as part of a pharmaceutical composition. 11. The method of claim 7 , wherein the pharmaceutical composition comprises a CS compound and a pharmaceutically acceptable carrier or adjuvant for administration of the CS. 12. The method of claim 4 , wherein the alkyl is —CH 3 or —CH 2 CH 3 or the substituted aryl is a p-nitrophenyl group. 13. The method of claim 9 , wherein the alkyl is —CH 3 or —CH 2 CH 3 or the substituted aryl is a p-nitrophenyl group.
Sulfated polysaccharides, e.g. chondroitin sulfate, dermatan sulfate (A61K31/727 takes precedence) · CPC title
Antibacterial agents · CPC title
Antidotes · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.